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Bloodborne, Transhumanism and Cosmic Cyberpunk – Kotaku UK (blog)

Posted: August 22, 2017 at 5:45 am

With all its morbid decadence, the richly-layered Gothic imagination and cosmic horror of Bloodborne tends to overshadow some of its more (post)modern influences. Bloodborne isnt a traditionalist, after all, but a punk: or to be more precise, a cyberpunk. It may not havesinister corporations or hackers, yet this sci-fi renegade still conjures the rebellious ghost in the machine.

Most obviously, theres the overpowering presence of that looming megalopolis Yharnam as dependent on monumental, almost brutalist architecture as any good futuristic urban sprawl. The social dynamics within Yharnam echo the politics of cyberpunk, the hegemonic power of the Healing Church pitted against the social outcasts roaming the grimy streets. Dangerous social experiments and unchecked technological advancements have led to a Victorian dystopia. There are even cyberspaces, simulated, subordinate worlds in the form of the Dreams, which can be accessed and even hacked by those who are privy to secret knowledge.

Yharnham:

Ridley Scott'sBlade Runner:

And just like cyberpunk, the world of Bloodborne is held captive by the promise of transhumanism the idea that humankind will, one day, be able to transcend our fleshlylimitations and become something more. Whether it is Deus Ex or Bloodborne, the tool for this quasi-religious endeavour is cutting edge research and technology. In Deus Ex, that means body modification through nanotech or even merging consciousnesses with an omnipresent AI. In Bloodborne, its the Healing Church and Byrgenwerth researching into the old ones and their blood that drives this change: aiming to transform humans, in theory, into celestial beings that have entirely discarded their humanity. Not unlike in Blade Runner, the eye becomes an omnipresent symbol of self-directed evolution and the dangerous knowledge necessary to pursue it.

However, Bloodborneisa punk that refuses to slavishly follow in the tracks of those that came before. The differences are the most fascinating thing here. The futuristic vision of transhumanism, whether it is presented as a utopian promise or a dystopian threat, is seen as an evolutionary culmination or perhaps even singularity that severs the umbilical cord that connects us to our evolutionary history. The human is a product of natural processes, distant cousin of the apes. The posthuman the product of transhumanism is something different (strangely, it is our human arrogance that leads to this fallacy of teleological evolution.)

Blade Runner

Eye of a Blood-Drunk Hunter

Bloodbornes idea of transhumanism is recognisable, but different. Its still a morally complex idea, both pursued by individuals and institutions while also causing societal upheaval, but its vector is in the opposite direction. The path to transcendence doesnt lead the inhabitants of Yharnam away from humankinds evolutionary history, but confronts it head-on in a retrogressive journey. The first enemies our hunter encounters are beastmen, many of them recognisably human but some, like the werewolves or Vicar Amelia, almost devoid of human characteristics. Theyre hairy and canine, clearly mammalian despite their deformities. So far, this is in keeping with stories like Robert Louis Stevensons The Strange Case of Dr. Jekyll and Mr. Hyde or H.P. Lovecrafts tales of human degeneracy, such as Facts Concerning the Late Arthur Jermyn and His Family, in which a British nobleman burns himself alive after discovering that one of his ancestors was an ape goddess from the Congo. These stories play with our post-Darwinian revulsion at being the offspring of mere animals.

But as you progress through Bloodborne, the hunter descends deeper down the evolutionary ladder. Soon, enemies resemble snakes, insects, arachnids. Later, they become more alien still, strange variations of squids, snails, slugs (that is, molluscs) or even fungi. They have names like Celestial Emissary, or Celestial Child and are closely related to the Great Ones, some of whom, like Ebrietas or Kos, share similarities with the games mollusc-like creatures. Bloodborne displays a special fascination with mushrooms and molluscs, as well as the creatures of the ocean (especially in The Old Hunters DLC). These creatures are associated with the primordial, the early origins of life on earth, and their strange forms, both beautiful and disturbing, gives them a semblance of otherworldliness. And since they dont seem to belong to this world, perhaps they originally visited earth from unknown regions of the cosmos?

Kos

Ebrietas, Daughter of the Cosmos

Celestial Child

Nudibranch, Nembrotha Kubaryana. Photo by Nick Hobgood

Nudibranch, Nembrotha Cristata. Photo by Chriswan Sungkono.

Nudibranch, Tritoniopsis Elegans. Photo by Sean Murray.

From this anthropocentric perspective, becoming like these creatures means getting closer to the miraculous origins of life, when the earth and the cosmos had yet to be disentangled. The transhumanism of Bloodborne thus turns the usual teleological view of human evolution on its head; the forces of evolution, whether natural or self-directed, will not bring humans closer to the gods, but have instead distanced them from the celestial spring of life. To fulfil their atavistic yearning to return to the lap of the cosmos, the inhabitants of Yharnam must regress to earlier evolutionary stages. The horror and tragedy of turning into wolf-like beasts, therefore, isnt just due to a revulsion to our animal ancestors or the destruction they cause, but the knowledge that those beastmen didnt regress far enough. If only they hadnt gotten lost in this evolutionary valley, they could have emerged on the other side as transcendental beings, as kin not of the earth, but the cosmos. At least, thats one way of looking at the complex picture Bloodborne paints.

The transcended hunter as slug-like Great One in Bloodbornes true ending

The beautiful thing about this is that it doesnt just fly in the face of transhumanism as it is usually understood, but the most problematic aspects of Lovecrafts work, too. The ugly concept of degeneracy, with all its overt racism, was an integral part of Lovecrafts fictional worlds. The ancient and unambiguously evil powers of the Great Old Ones is tied to primitives and mongrels, marginalised humans seen as genetically impure and degraded. They are easily manipulated by the old gods and worship them in the hidden and remote corners of the earth.

In Bloodborne, the blame of Yharnams ruin is dramatically shifted. The hidden corners of worship arent foreign jungles or secluded villages, but the sacred spaces of a church that is the backbone and centre of a sprawling megalopolis; the mysteries of the Great Ones are still secret knowledge, but secrets of a powerful, manipulative elite (as you would expect in the conspiracy-filled worlds of cyberpunk stories). But while this elites endeavours clearly lead to a horrific dystopia, the moral issues of this regressive transhumanism stay ambiguous throughout. The degenerate beastmen are hapless, unfortunate victims rather than villains. The experiment of transcendence through reverse evolution seems doomed to fail, but it is not at all clear whether that goal is inherently misguided. After all, the Great Ones seem amoral rather than evil (not unlike the people of Yharnam), and the hunter is no stranger to the allure these celestial beings exert through their disturbing kind of beauty. Perhaps their apparent darkness stems purely from the human minds failing to comprehend their true nature? Either way, Lovecrafts ideas of degeneracy doesnt entirely fit into Bloodbornes world.

Being kin to both the Lovecraftian as well as cyberpunk, Bloodborne, too, is a kind of mongrel. But this impurity is precisely what enables it to distinguish itself and comment meaningfully on its ancestral genres. It reshapes its influences by letting disparate ideas collide and creates something fresh from the wreckage. Its not unique in its subversion of transhumanist idealism or Lovecraftian racist tropes, but the way it combines these separate issues in a seamless if ambiguous whole is entirely original.

Bloodborne is both a cyberpunk dystopia in which the end point of self-directed evolution is not a disembodied mind, but a slug or a squid, as well as a tale of cosmic horror where that dubious degeneracy stems not from shady outsiders or social outcasts, but squarely from within organised mainstream religion and science. It shares with cyberpunk an awareness and distaste for the unequal power dynamics in a world governed by the amoral ambitions of hegemonies, but, like Lovecraft, looks backwards to our distant origins rather than to the future. And soBloodborne transcends its influences, and challenges us on new planes of existence.

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Ambrosia: the startup harvesting the blood of the young | Society … – The Guardian

Posted: August 22, 2017 at 5:45 am

What we now call intergenerational fairness has suffered a lot lately, and its not about to be improved by the news that the Baby Boomers are sucking the blood of the young. Although, in fairness, they are only after the plasma.

In Monterey, California, a new startup has emerged, offering transfusions of human plasma: 1.5 litres a time, pumped in across two days, harvested uniquely from young adults.

Ambrosia, the vampiric startup concerned, is run by a 32-year-old doctor called Jesse Karmazin, who bills $8,000 (6,200) a pop for participation in what he has dubbed a study. So far, he has 600 clients, with a median age of 60. The blood is collected from local blood banks, then separated and combined it takes multiple donors to make one package.

Its no coincidence his scheme is based near San Francisco. The idea has become faddish in tech circles. While anti-ageing products usually hold more appeal with women, two-thirds of the more than 65 participants who have signed up for this trial are men. Mike Judges Silicon Valley sitcom recently parodied the notion, with arch-tech guru Gavin Belson relying on a blood boy following him around to donate pints of sticky red at inopportune moments.

That fictionalised account may well be based on the real-life adventures of Peter Thiel, the PayPal founder, who has expressed interest in having transfusions (Gawker even reported that he was spending $40,000 (31,000) a quarter on regular transfusions from 18-year-olds).He, and various other thinkers who radiate out towards the death-evading transhumanist movement, are fascinated by heterochronic parabiosis the sewing together of two animals in order to create a living chimera. Studies going back decades show the regenerative effects of one organism being joined to another. In the 17th century, Robert Boyle he of Boyles Law suggested replacing the blood of the old with the blood of the young.

In 2012, the University of Cambridges Dr Robin Franklin led a group that showed blood from young mice could replace myelin sheaths crucial for combatting MS in older mice. But it was a 2014 Harvard report that seems to have kickstarted the present revival of interest in transfusions. There, scientists injecting old mice with the plasma of a younger generation found it improved their memory and their ability to learn. Conversely, injecting old blood into young seemed to knobble the young rodents.

The scientific community has rolled its eyes at the trial element of Ambrosia. There is no control group and, with participation costing so much, no one involved is very randomised. Despite these criticisms of the science, Dr Karmazin is still reporting positive results. His team has found that levels of carcino-embryonic antigens fell by around 20%, as did the level of amyloids proteins involved in cancer and Alzheimers disease respectively.

Improvements in sleep seem to be the most glittering prize to emerge so far: As people get older, they have much more difficulty sleeping, Dr Karmazin noted. Improve that and you get benefits in mood, immune system, weight management and much else.

It answers the question: how do you sleep at night after leeching the blood out of busboys and students? Just fine, thanks.

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Bio-inspired Materials Give Boost to Regenerative Medicine – Bioscience Technology

Posted: August 22, 2017 at 5:43 am

What if one day, we could teach our bodies to self-heal like a lizards tail, and make severe injury or disease no more threatening than a paper cut?

Or heal tissues by coaxing cells to multiply, repair or replace damaged regions in loved ones whose lives have been ravaged by stroke, Alzheimers or Parkinsons disease?

Such is the vision, promise and excitement in the burgeoning field of regenerative medicine, now a major ASU initiative to boost 21st-century medical research discoveries.

ASU Biodesign Institute researcher Nick Stephanopoulos is one of several rising stars in regenerative medicine. In 2015, Stephanopoulos, along with Alex Green and Jeremy Mills, were recruited to the Biodesign Institutes Center for Molecular Design and Biomimetics (CMDB), directed by Hao Yan, a world-recognized leader in nanotechnology.

One of the things that that attracted me most to the ASU and the Biodesign CMDB was Haos vision to build a group of researchers that use biological molecules and design principles to make new materials that can mimic, and one day surpass, the most complex functions of biology, Stephanopoulos said.

I have always been fascinated by using biological building blocks like proteins, peptides and DNA to construct self-assembled structures, devices and materials, and the interdisciplinary and highly collaborative team in the CMDB is the ideal place to put this vision into practice.

Yans research center uses DNA and other basic building blocks to build their nanotechnology structures only at a scale 1,000 times smaller than the width of a human hair.

Theyve already used nanotechnology to build containers to specially deliver drugs to tissues, build robots to navigate a maze or nanowires for electronics.

To build a manufacturing industry at that tiny scale, their bricks and mortar use a colorful assortment of molecular Legos. Just combine the ingredients, and these building blocks can self-assemble in a seemingly infinite number of ways only limited by the laws of chemistry and physics and the creative imaginations of these budding nano-architects.

Learning from nature

The goal of the Center for Molecular Design and Biomimetics is to usenatures design rulesas an inspiration in advancing biomedical, energy and electronics innovation throughself-assembling moleculesto create intelligent materials for better component control and for synthesis intohigher-order systems, said Yan, who also holds the Milton Glick Chair in Chemistry and Biochemistry.

Prior to joining ASU, Stephanopoulos trained with experts in biological nanomaterials, obtaining his doctorate with the University of California Berkeleys Matthew Francis, and completed postdoctoral studies with Samuel Stupp at Northwestern University. At Northwestern, he was part of a team that developed a new category of quilt-like, self-assembling peptide and peptide-DNA biomaterials for regenerative medicine, with an emphasis in neural tissue engineering.

Weve learned from nature many of the rules behind materials that can self-assemble. Some of the most elegant complex and adaptable examples of self-assembly are found in biological systems, Stephanopoulos said.

Because they are built from the ground-up using molecules found in nature, these materials are also biocompatible and biodegradable, opening up brand-new vistas for regenerative medicine.

Stephanopoulos tool kit includes using proteins, peptides, lipids and nucleic acids like DNA that have a rich biological lexicon of self-assembly.

DNA possesses great potential for the construction of self-assembled biomaterials due to its highly programmable nature; any two strands of DNA can be coaxed to assemble to make nanoscale constructs and devices with exquisite precision and complexity, Stephanopoulos said.

Proof all in the design

During his time at Northwestern, Stephanopoulos worked on a number of projects and developed proof-of-concept technologies for spinal cord injury, bone regeneration and nanomaterials to guide stem cell differentiation.

Now, more recently, in a new studyin Nature Communications, Stephanopoulos and his colleague Ronit Freeman in the Stupp laboratory successfully demonstrated the ability to dynamically control the environment around stem cells, to guide their behavior in new and powerful ways.

In the new technology, materials are first chemically decorated with different strands of DNA, each with a unique code for a different signal to cells.

To activate signals within the cells, soluble molecules containing complementary DNA strands are coupled to short protein fragments, called peptides, and added to the material to create DNA double helices displaying the signal.

By adding a few drops of the DNA-peptide mixture, the material effectively gives a green light to stem cells to reproduce and generate more cells. In order to dynamically tune the signal presentation, the surface is exposed to a soluble single-stranded DNA molecule designed to grab the signal-containing strand of the duplex and form a new DNA double helix, displacing the old signal from the surface.

This new duplex can then be washed away, turning the signal off. To turn the signal back on, all that is needed is to now introduce a new copy of single-stranded DNA bearing a signal that will reattach to the materials surface.

One of the findings of this work is the possibility of using the synthetic material to signal neural stem cells to proliferate, then at a specific time selected by the scientist, trigger their differentiation into neurons for a while, before returning the stem cells to a proliferative state on demand.

One potential use of the new technology to manipulate cells could help cure a patient with neurodegenerative conditions like Parkinsons disease.

The patients own skin cells could be converted to stem cells using existing techniques. The new technology could help expand the newly converted stem cells back in the lab and then direct their growth into specific dopamine-producing neurons before transplantation back to the patient.

People would love to have cell therapies that utilize stem cells derived from their own bodies to regenerate tissue, Stupp said. In principle, this will eventually be possible, but one needs procedures that are effective at expanding and differentiating cells in order to do so. Our technology does that.

In the future, it might be possible to perform this process entirely within the body. The stem cells would be implanted in the clinic, encapsulated in the type of material described in the new work, and injected into a particular spot. Then the soluble peptide-DNA molecules would be given to the patient to bind to the material and manipulate the proliferation and differentiation of transplanted cells.

Scaling the barriers

One of the future challenges in this area will be to develop materials that can respond better to external stimuli and reconfigure their physical or chemical properties accordingly.

Biological systems are complex, and treating injury or disease will in many cases necessitate a material that can mimic the complex spatiotemporal dynamics of the tissues they are used to treat, Stephanopoulos said.

It is likely that hybrid systems that combine multiple chemical elements will be necessary; some components may provide structure, others biological signaling and yet others a switchable element to imbue dynamic ability to the material.

A second challenge, and opportunity, for regenerative medicine lies in creating nanostructures that can organize material across multiple length scales. Biological systems themselves are hierarchically organized: from molecules to cells to tissues, and up to entire organisms.

Consider that for all of us, life starts simple, with just a single cell. By the time we reach adulthood, every adult human body is its own universe of cells, with recent estimates of 37 trillion or so. The human brain alone has 100 billion cells or about the same number of cells as stars in the Milky Way galaxy.

But over the course of a life, or by disease, whole constellations of cells are lost due to the ravages of time or the genetic blueprints going awry.

Collaborative DNA

To overcome these obstacles, much more research funding and recruitment of additional talent to ASU will be needed to build the necessary regenerative medicine workforce.

Last year, Stephanopoulos research received a boost with funding from the U.S. Air Forces Young Investigator Research Program (YIP).

The Air Force Office of Scientific ResearchYIP award will facilitate Nicks research agenda in this direction, and is a significant recognition of his creativity and track record at the early stage of his careers, Yan said.

Theyll need this and more to meet the ultimate challenge in the development of self-assembled biomaterials and translation to clinical applications.

Buoyed by the funding, during the next research steps, Stephanopoulos wants to further expand horizons with collaborations from other ASU colleagues to take his research teams efforts one step closer to the clinic.

ASU and the Biodesign Institute also offer world-class researchers in engineering, physics and biology for collaborations, not to mention close ties with the Mayo Clinic or a number of Phoenix-area institutes so we can translate our materials to medically relevant applications, Stephanopoulos said.

There is growing recognition that regenerative medicine in the Valley could be a win-win for the area, in delivering new cures to patients and building, person by person, a brand-new medicinal manufacturing industry.

Stephanopoulos recent research was carried out at Stupps Northwesterns Simpson Querrey Institute for BioNanotechnology. The National Institute of Dental and Craniofacial Research of the National Institutes of Health (grant 5R01DE015920) provided funding for biological experiments, and the U.S. Department of Energy, Office of Science, Basic Energy Sciences provided funding for the development of the new materials (grants DE-FG01-00ER45810 and DE-SC0000989 supporting an Energy Frontiers Research Center on Bio-Inspired Energy Science (CBES)).

The paper is titled Instructing cells with programmable peptide DNA hybrids. Samuel I. Stupp is the senior author of the paper, and post-doctoral fellows Ronit Freeman and Nicholas Stephanopoulos are primary authors.

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New method for the 3D printing of living tissues – Scientist Live

Posted: August 22, 2017 at 5:43 am

Scientists at the University of Oxford have developed a new method to 3D-print laboratory- grown cells to form living structures.

The approach could revolutionise regenerative medicine, enabling the production of complex tissues and cartilage that would potentially support, repair or augment diseased and damaged areas of the body.

In research published in the journal Scientific Reports, an interdisciplinary team from the Department of Chemistry and the Department of Physiology, Anatomy and Genetics at Oxford and the Centre for Molecular Medicine at Bristol, demonstrated how a range of human and animal cells can be printed into high-resolution tissue constructs.

Interest in 3D printing living tissues has grown in recent years, but, developing an effective way to use the technology has been difficult, particularly since accurately controlling the position of cells in 3D is hard to do.

They often move within printed structures and the soft scaffolding printed to support the cells can collapse on itself.

As a result, it remains a challenge to print high-resolution living tissues. But, led by Professor Hagan Bayley, Professor of Chemical Biology in Oxfords Department of Chemistry, the team devised a way to produce tissues in self-contained cells that support the structures to keep their shape.

The cells were contained within protective nanolitre droplets wrapped in a lipid coating that could be assembled, layer-by-layer, into living structures.

Producing printed tissues in this way improves the survival rate of the individual cells, and allowed the team to improve on current techniques by building each tissue one drop at a time to a more favourable resolution.

To be useful, artificial tissues need to be able to mimic the behaviours and functions of the human body. The method enables the fabrication of patterned cellular constructs, which, once fully grown, mimic or potentially enhance natural tissues.

Dr Alexander Graham, lead author and 3D Bioprinting Scientist at OxSyBio (Oxford Synthetic Biology), said: We were aiming to fabricate three-dimensional living tissues that could display the basic behaviours and physiology found in natural organisms. To date, there are limited examples of printed tissues, which have the complex cellular architecture of native tissues. Hence, we focused on designing a high-resolution cell printing platform, from relatively inexpensive components, that could be used to reproducibly produce artificial tissues with appropriate complexity from a range of cells including stem cells.

The researchers hope that, with further development, the materials could have a wide impact on healthcare worldwide. Potential applications include shaping reproducible human tissue models that could take away the need for clinical animal testing.

The team completed their research last year, and have since taken steps towards commercialising the technique and making it more widely available. In January 2016, OxSyBio officially spun-out from the Bayley Lab. The company aims to commercialise the technique for industrial and biomedical purposes.

Over the coming months they will work to develop new complementary printing techniques, that allow the use of a wider range of living and hybrid materials, to produce tissues at industrial scale. Dr Sam Olof, Chief Technology Officer at OxSyBio, said: There are many potential applications for bioprinting and we believe it will be possible to create personalised treatments by using cells sourced from patients to mimic or enhance natural tissue function. In the future, 3D bio-printed tissues maybe also be used for diagnostic applications for example, for drug or toxin screening.

Dr Adam Perriman from the University of Bristols School of Cellular and Molecular Medicine, added: The bioprinting approach developed with Oxford University is very exciting, as the cellular constructs can be printed efficiently at extremely high resolution with very little waste. The ability to 3D print with adult stem cells and still have them differentiate was remarkable, and really shows the potential of this new methodology to impact regenerative medicine globally

The full citation for the paper is High-resolution patterned cellular constructs by droplet-based 3D printingA.D. Graham et. al. Scientific Reports 7, Article number: 7004 (2017).

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Spanish town struggles to reconcile locals as extremist cell – Medicine Hat News

Posted: August 21, 2017 at 4:44 am

By Lori Hinnant, Alex Oller And Joseph Wilson, The Associated Press on August 20, 2017.

RIPOLL, Spain They were brothers and boyhood friends from a town with no unfamiliar faces. They were linked by Moroccan roots and equally tied by their upbringings in Ripoll, an ancient hub in the Catalan foothills known for its monastery and passageways dotted with cafes and kebab shops.

But most recently, police believe, the young men were drawn together by an imam and an alleged plot to murder on a massive scale an extraordinary secret for 12 people to keep for months on end.

In the suspected extremist cells final days, the group accumulated more than 100 gas canisters, blew up a house in a botched effort to make bombs, drove a van through Barcelonas storied Las Ramblas promenade, and attacked beachside tourists, Spanish authorities said.

The Islamic State group claimed responsibility for the attacks that killed at least 14 people and left scores wounded. Five of the dozen were shot dead by police.

Now, Ripoll is cut off by police roadblocks as the search for an alleged cell member thought to still be on the run continues. Families and friends in the town are torn between horror at the bloodshed and grief for the children they thought they knew.

We dont know whether to cry and mourn them or what to do, said Wafa Marsi, who knew the attackers and stood with their weeping mothers on Saturday as they clustered in small groups in the town square. They have killed 13 or 14 people and wounded a hundred, and we dont know what to do.

What the families finally did, after fiercely debating the issue, was denounce the attack, some holding up homemade signs reading Not in our name.

Police have identified 12 members of the cell, but three remained unaccounted for Sunday. Two are believed to have been killed when the house where the plot was hatched exploded Wednesday, Catalan police official Josep Lluis Trapero told reporters Sunday.

Complicating the manhunt for the suspected fugitive and any other possible accomplices, though, was the fact that police so far have been unable to pinpoint who remained at large. The explosion in Alcanar, 300 kilometres (186 miles) south of Ripoll, nearly obliterated the bomb makers along with the house. A police official has said the imam, Abdelbaki Es Satty, is thought to be one of them.

Trapero declined to confirm that Younes Abouyaaquoub, a 22-year-old Moroccan, was the one at large and the suspected driver of the van that plowed down the Las Ramblas promenade Thursday, killing 13 people and injuring 120. Another attack hours later killed one person and injured others in Cambrils, a seaside town south of the city.

We are working in that line, Trapero said. But he added: We dont know where he is.

Another police official did confirm that three vans tied to the investigation were rented with Abouyaaquoubs credit card: The one used in the Las Ramblas carnage, another found in Ripoll, where all the main attack suspects lived, and a third found in Vic, on the road between the two.

Police are investigating whether a man found stabbed to death inside a car in Barcelona may have been killed by an attacker as well.

Police believe the cell members had planned to fill the vans with explosives and create a massive attack in the Catalan capital. Trapero confirmed that more than 100 tanks of butane gas were found at the Alcanar house that exploded, as well as ingredients of the explosive TATP, which was used by the Islamic State group in attacks in Paris and Brussels.

Our thesis is that the group had planned one or more attacks with explosives in the city of Barcelona, he said. The plot was foiled when the house in Alcanar blew up Wednesday night.

None of the 12 had any known history of violent extremism, Spanish police have said.

Trapero confirmed the imam was part of the investigation, but said police had no solid evidence that he was responsible for radicalizing the young men in the cell. Es Satty in June abruptly quit working at a mosque in Ripoll and has not been seen since.

Dont criminalize the mosques because the overwhelming majority of them are places of worship. They are places where people pray, Trapero said. In fact, even though there is an imam implicated in the group, it doesnt mean that the mosque is where they were radicalized.

One woman who was close to multiple attackers and who heard Es Sattys sermons said the imam repeatedly preached about jihad and killing infidels. She spoke on condition of anonymity, fearing she would be attacked for speaking out.

I feel like I could have done something. I feel a little bit guilty now, she said. Everybody knew it. It was an open secret. But I cant say it because these people are dangerous and they could come after me. I dont trust anybody now.

Es Sattys former mosque denounced the deadly attacks, but denied Es Satty was anything other than a normal imam.

Hammou Minaj, secretary of the mosque who knew the attackers as well, described Es Satty as an easygoing preacher.

Its hard to get an imam. When you get one, youre always happy, Minaj said.

The mosque is on a main artery in Ripoll named Progress, occupying an unmarked corner storefront. The Muslim community took the space when it outgrew the towns other mosque, which held just 40 worshippers. Es Satty preached first at the smaller space and eventually lost his job in late 2015 for reasons that the president, Ali Yassine, did not specify.

Es Satty then left to look for work as an imam in Belgium from January to March 2016, according to Hans Bonte, mayor of the Belgian city of Vilvoorde.

Vilvoorde is known for Islamic State recruiting and jihadi activity. Police there contacted the Catalan department of justice and were told Es Satty had no links to extremist violence.

With what we know today, this is remarkable and an eye-opener for everybody, Bonte told De Morgen newspaper.

But Catalonia itself has become increasingly known as a centre of extremism and for tensions within the Muslim community on how to handle it. Nearly one-third of the arrests in Spain for alleged links to the Islamic State group were made in Catalonia, according to an analysis last year by Fernano Reinares of the Royal Institute Elcano, a Spanish think-tank founded by the king.

When Es Satty returned to Ripoll, he again landed a job as imam this time at the new mosque. But at the beginning of the summer, Es Satty announced he wanted a three-month vacation in Morocco and the mosque let him go. His apartment was empty on Saturday.

Ripoll resident Marsi, as well others who spoke with the AP on condition of anonymity, admitted tensions brewed at times between the two mosques, although Marsi pointed out that the differences were not over religious content.

I cant vouch for anybody else, but I can guarantee 100 per cent that there was zero radicalization in either mosque. If the imam had said something about jihad, the people of Ripoll would have ousted him. The women, in particular, are raging right now, Marsi emphasized.

The size of the cell and the close family connections among the attack suspects recalled the November 2015 attacks in Paris, where Islamic State adherents struck the national stadium, a concert hall and bars and restaurants nearly simultaneously, leaving 130 people dead.

Catalan authorities have not released the names of those killed, but Spanish media have reported widely that at least three sets of brothers were among the cells alleged members.

Brothers radicalizing together are a common theme among extremists. They share unbreakable bonds, an ability to keep secrets, and an airtight communication channel. A pair of brothers carried out suicide bombings in March 2016 in Brussels. Two brothers gunned down the staff members of satirical newspaper Charlie Hebdo in Paris in January 2015. Dzhokhar and Tamerlan Tsarnaev, who bombed the Boston Marathon in 2013, were brothers originally from Chechnya.

On Sunday, many in Ripoll said they didnt see themselves in either the young men who had once seemed familiar or the imam now implicated in the investigation

Those people that heard him talk about jihad and didnt say anything, are they happy now? Why didnt they stop him? Hassan Azzidi, who was holding a sign that read Not in the name of Islam, said.

He added: We are taught not to kill animals for sport, let alone humans.

___

Wilson contributed from Barcelona. Angela Charlton in Paris; Nicole Winfield in Rome; Mystyslav Chernov in Ripoll, Spain; and Oleg Cetinic in Alcanar, Spain contributed.

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New Study Reveals Stem Cells from Young Hearts May Help Reverse the Aging Process – Futurism

Posted: August 21, 2017 at 4:44 am

In BriefA new study from the Cedars-Sinai Heart Institute reveals that stem cells taken from younger rats provided older rats with youthful vigor when injected into their hearts. After a month, the rats ran longer, and regrew hair faster.

Old hearts may find new life, according to a new study, which shows that stem cells taken from younger hearts can be used to reverse the aging process. This could potentially cause older hearts to act and perform like younger ones.Click to View Full Infographic

The study, conducted by the Cedars-Sinai Heart Institute and published by the European Heart Journal, set out to observe the effects of cardiac stem cells on various aspects of the heart, including its function and structure. Prior applications of Cardiosphere-derived cells (CDC) resulted in positive effects, but this was the first time its effects in the aging process were tested. This is different from the tests performed last month at the Albert Einstein College of Medicine, where the hypothalamus region of the brain was discovered to be a key part of aging in mice.

Cedars-Sinai researchers instead took CDC cells from newborn mice and injected it into the hearts of older mice, while another group of older mice were injected with saline. Blood, echocardiographic, haemodynamic and treadmill stress tests were performed on all mice after injections, with the older groups tested 1 month later.

The mice given the Cardiosphere-derived cells saw a number of benefits compared to their saline counterparts. They had improved heart functionality, were able to exercise 20 percent longer, regrew hair at a faster rate, and had longer heart cell telomeres. This is important because telomeres are compounds found at the ends of chromosomes whose shortening is directly correlated to the aging process.

The way the cells work to reverse aging is fascinating, said Cedars-Sinai Heart Institute Director and Lead Researcher Eduardo Marbn, MD, PhD. They secrete tiny vesicles that are chock-full of signaling molecules such as RNA and proteins. The vesicles from young cells appear to contain all the needed instructions to turn back the clock.

Tests on ratshave shown that CDCs have shown cardiac and systemic rejuvenation on the aging process, but there is much work to do before the anti-aging treatment is tested on people, let alone over the table. Lilian Griorian-Shamagian, MD, PhD, who was co-primary researcher on the study, notes that its still unclear if the cells actually extend the lifespan of the rats, rather than simply providing a new heart in an old body. Its also unknown if CDCs need to be taken from younger hearts in order to be effective. If any CDCs, regardless of their origin, can be used, it could lead to a new round of tests comparing the effects of CDCs from the young to the CDCs from the old or middle-aged.

If stem cells were used for medical purposes, they couldhelp those suffering from heart failure, or the Duchenne muscular dystrophy Marbn and his team are hoping to treat. Beyond that, it could lessen the number of deaths caused by heart disease, which is currently responsible for over 610,000 deaths a year.

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Let’s Use Pigs as Organ Donors – First Things

Posted: August 21, 2017 at 4:43 am

There are approximately 120,000 Americans on the organ transplant waiting list, about as many people as live in Charleston, South Carolina and Hartford, Connecticut. Many of these peoples lives will ultimately be saved, after long and harrowing waitsas former Vice President Dick Cheneys was. But others on the list will die before their turn comes up and a suitable donor is found.

These tragic deaths are putting increasing pressure on organ transplant ethics. Some jump the queue and travel to China to buy organsmany of which come from executed political prisoners. Others pay destitute people in developing countries for a kidney; this exploitation of the desperate poor became so rampant that Pakistan outlawed live organ donations to non-relatives and the Philippines banned organ transplant surgeries for non-citizens. Here in the U.S., public intellectuals such as Sally Satel of the American Enterprise Institutewho received a kidney from a live donorargue for changing the law to permit organ sales. Of course, people in Satels socioeconomic class would never be the sellers.

Meanwhile, many bioethicists argue that we should eliminate the dead donor rule that requires donors of vital organs to be deceased before procurement. If these advocates get their way, doctors will be allowed to euthanize seriously incapacitated patients by means of organ harvesting.

Fortunately, organ transplant medicine remains a highly ethical enterprise (although some believe that using brain death to determine readiness for organ procurement is highly questionable). But the waiting lists continue to grow, a fact measured in sleepless nights of desperation and the tragedy of avoidable deaths. This is why the news that scientists have made progress in genetically altering pigs to use in human organ transplantation is so exciting.

Specifically, scientists are learning to alter pig organs to avoid tissue rejection when the organs are transplanted and, more recently, have used a gene-editing technique to help prevent interspecies infections. From the New York Times story:

Some might feel squeamish at having an animal organ implanted into their bodies. But if the choice is between death and receiving a pig kidney, most would take the kidney. And why not? Animal body parts are already transplanted into humansfor example, pig heart valves. If it is acceptable to receive part of an animal organ to save human life, why not the entire thing?

Still, some would certainly object. Utilitarian bioethicists such as Peter Singer might claim that killing pigs for their organswhile sparing cognitively disabled humanswould amount to unethical speciesism, because it would treat humans as having greater value than pigs, based solely on their humanity. Singer rejects human exceptionalism, arguing that an individualwhether animal or humanearns the moral status of person based on the individuals mental capacities. Non-personsagain, whether human or animalhave lesser value and may be used for the benefit of persons. In this view, since pigs have greater mental capacities than people with, say, the capacities of a Terri Schiavo, cognitively disabled humans should be used as organ sources before pigs. (Singer has specifically argued that people in a persistent vegetative state should have been used in creating the hepatitis vaccine instead of chimpanzees.) If we ever accept such a philosophy, it will mark the end of universal human rights, since human non-persons could be exploited and killed for the benefit of persons.

The loudest wailing over pig-organ donation will undoubtedly come from animal rights activists. Animal rights ideology (which must be distinguished from animal welfare) holds that the capacity to suffersometimes called painienceis the proper measure of moral value. Since both animals and humans experience pain, they are morally equal. Hence, raising and killing pigs for their organs would be equivalent to killing racial minorities for the same purpose.

That is nonsense. Racism is an invidious evil because it treats intrinsic equalse.g., human beingsas if they were unequal. But there is a hierarchy of moral worth, with humans at the apex. Not only are pigs not our moral equals, but they cannot possess rights, since they are inherently incapable of assuming duties. It would not be wrong to raise these animals to save human lives. Assuming the safety issue is solved, it would be immoral not to.

This does not mean that the grim good of using pig organs would have to be a permanent policy. We must hope that an even more ethical means of supplying organs will be developed, one that would obviate the need to use sentient animals. Scientists have already learned how to change our skin cells into stem cells, and from there into particular organ tissue. Research is advancing on using these induced pluripotent stem cells to repair damaged hearts and lungs, with hope that some day this technology might even be harnessed to grow new organs from a patients own flesh.

Should that hoped-for day arrive, there will be no further moral justification for using pigs for organsany more than it is currently justifiable to hunt whales for their oil. Then we could stop the pig organ harvest and resume arguing about the ethics of eating bacon.

Wesley J. Smith is a senior fellow at the Discovery Institutes Center on Human Exceptionalism. He is the author of A Rat is a Pig is a Dog is a Boy: The Human Cost of the Animal Rights Movement.

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Binge-Watching TV? You May Not Sleep Well – HealthCentral.com

Posted: August 21, 2017 at 4:43 am

Binge-Watching TV? You May Not Sleep Well

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Poor sleep quality, increased fatigue, and insomnia in young adults are associated with binge-watching television, according to researchers. Watching multiple episodes of the same television show in succession in one sitting, on a television, computer, or mobile device raises your level of cognitive alertness, which interferes with sleep.

The researchers, whose study was published in the Journal of Clinical Sleep Medicine, looked at binge-watching and sleep habits in 423 young adults between 18 and 25. Study participants completed an online survey assessing their regular TV watching, binge-watching, sleep quality, fatigue, insomnia, and alertness before going to sleep. Average binge-watching lasted 3 hours and 8 minutes and three to four episodes.

Study results suggest that more than 80 percent of young adults identify as binge-watchers, and 20.2 percent binge-watch television at least a few times per week. Binge-watchers reported more fatigue and insomnia and higher levels of alertness before going to sleep than those who dont binge-watch television. The bingers were also 98 percent more likely to have poor sleep quality.

Sourced from: Journal of Clinical Sleep Medicine

Published On: Aug 15th 2017

How a Low-Calorie Diet May Slow Aging

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Previous research suggests that a lifelong low-calorie diet can boost longevity, but a new mouse study demonstrates, for the first time, how restricting calories may affect circadian rhythm and, in turn, the aging process. The study was conducted by researchers at the Center for Epigenetics & Metabolism at the University of California, Irvine, and the results were published in Cell.

According to the researchers, our circadian rhythm, or biological clock, changes as a result of aging, and these changes are based in part on the metabolism of energy within our cells. In a study involving 6-monthold and 18-month-old mice, the researchers determined that older cells process energy less efficiently than younger cells. But when a group of older mice were fed a diet with 30 percent fewer calories for a period of six months, the energy process was rejuvenated promoting healthy aging.

A companion study from the Barcelona Institute for Research in Biomedicine in Spain tested body clock function in stem cells collected from older and younger mice. This study confirmed that a low-calorie diet helps protect circadian rhythm function.

Sourced from: ScienceDaily

Published On: Aug 15th 2017

Don't Look at the Sun! Solar Eclipse Safety Tips

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In the absence of cloud cover, a total solar eclipse will be visible on Monday, August 21 in a 70-mile wide band across the entire continental United States, from central Oregon through South Carolina. In a total solar eclipse, the moon moves in between the earth and the sun, completely blocking out the sun for a short period of time. Prior to the total eclipse, which will last about two minutes, and in other areas of the country, and other parts of North and Central America, a partial solar eclipse will be visible.

Ahead of this amazing event, the U.S. Centers for Disease Control and Prevention (CDC) is warning that viewing a partial solar eclipse without proper eye protection even very briefly can cause permanent vision loss and blindness. Looking directly at the sun can damage the retinas, light-sensitive parts of the eye that transmit what we see to our brain. Retinal damage can occur without pain and, according to the CDC, it can take a few hours, or even days, for symptoms like an inability to see colors or loss of central vision to develop. Anyone who experiences vision changes after viewing the solar eclipse next week should contact an eye care professional immediately.

The only way to look directly at the sun safely when its not eclipsed or is partly eclipsed is with a special solar filter or a handheld solar viewer. Goggles, homemade filters, and dark sunglasses do not offer enough protection. Avoid looking at the sun through an unfiltered camera including a smartphone telescope, binoculars, or any other device. You can also make your own simple and inexpensive pinhole projector to safely view the eclipse, but be sure to follow instructions for making and using the projector carefully.

Sourced from: CDC

Published On: Aug 15th 2017

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Heritability of IQ – Wikipedia

Posted: August 21, 2017 at 4:42 am

Research on heritability of IQ infers, from the similarity of IQ in closely related persons, the proportion of variance of IQ among individuals in a study population that is associated with genetic variation within that population. This provides a maximum estimate of genetic versus environmental influence for phenotypic variation in IQ in that population. "Heritability", in this sense, "refers to the genetic contribution to variance within a population and in a specific environment".[1] In other words, heritability is a mathematical estimate that indicates how much of a traits variation can be attributed to genes. There has been significant controversy in the academic community about the heritability of IQ since research on the issue began in the late nineteenth century.[2]Intelligence in the normal range is a polygenic trait, meaning it's influenced by more than one gene.[3][4]

The general figure for the heritability of IQ, according to an authoritative American Psychological Association report, is 0.45 for children, and rises to around 0.75 for late teens and adults.[5][6] In simpler terms, IQ goes from being weakly correlated with genetics, for children, to being strongly correlated with genetics for late teens and adults. The heritability of IQ increases with age and reaches an asymptote at 1820 years of age and continues at that level well into adulthood.[7] Recent studies suggest that family and parenting characteristics are not significant contributors to variation in IQ scores;[8] however, poor prenatal environment, malnutrition and disease can have deleterious effects.[9][10]

"Heritability" is defined as the proportion of variance in a trait which is attributable to genetic variation within a defined population in a specific environment.[1] Heritability takes a value ranging from 0 to 1; a heritability of 1 indicates that all variation in the trait in question is genetic in origin and a heritability of 0 indicates that none of the variation is genetic. The determination of many traits can be considered primarily genetic under similar environmental backgrounds. For example, a 2006 study found that adult height has a heritability estimated at 0.80 when looking only at the height variation within families where the environment should be very similar.[11] Other traits have lower heritabilities, which indicate a relatively larger environmental influence. For example, a twin study on the heritability of depression in men calculated it as 0.29, while it was 0.42 for women in the same study.[12] Contrary to popular[citation needed] belief, two parents of higher IQ will not necessarily produce offspring of equal or higher intelligence. In fact, according to the concept of regression toward the mean, parents whose IQ is at either extreme are more likely to produce offspring with IQ closer to the mean (or average).[13][14]

There are a number of points to consider when interpreting heritability:

Various studies have found the heritability of IQ to be between 0.7 and 0.8 in adults and 0.45 in childhood in the United States.[6][18][19] It may seem reasonable to expect that genetic influences on traits like IQ should become less important as one gains experiences with age. However, that the opposite occurs is well documented. Heritability measures in infancy are as low as 0.2, around 0.4 in middle childhood, and as high as 0.8 in adulthood.[7] One proposed explanation is that people with different genes tend to seek out different environments that reinforce the effects of those genes.[6] The brain undergoes morphological changes in development which suggests that age-related physical changes could also contribute to this effect.[20]

A 1994 article in Behavior Genetics based on a study of Swedish monozygotic and dizygotic twins found the heritability of the sample to be as high as 0.80 in general cognitive ability; however, it also varies by trait, with 0.60 for verbal tests, 0.50 for spatial and speed-of-processing tests, and 0.40 for memory tests. In contrast, studies of other populations estimate an average heritability of 0.50 for general cognitive ability.[18]

In 2006, The New York Times Magazine listed about three quarters as a figure held by the majority of studies.[21]

There are some family effects on the IQ of children, accounting for up to a quarter of the variance. However, adoption studies show that by adulthood adoptive siblings aren't more similar in IQ than strangers,[22] while adult full siblings show an IQ correlation of 0.24. However, some studies of twins reared apart (e.g. Bouchard, 1990) find a significant shared environmental influence, of at least 10% going into late adulthood.[19]Judith Rich Harris suggests that this might be due to biasing assumptions in the methodology of the classical twin and adoption studies.[23]

There are aspects of environments that family members have in common (for example, characteristics of the home). This shared family environment accounts for 0.25-0.35 of the variation in IQ in childhood. By late adolescence it is quite low (zero in some studies). There is a similar effect for several other psychological traits. These studies have not looked into the effects of extreme environments such as in abusive families.[6][22][24][25]

The American Psychological Association's report "Intelligence: Knowns and Unknowns" (1995) states that there is no doubt that normal child development requires a certain minimum level of responsible care. Severely deprived, neglectful, or abusive environments must have negative effects on a great many aspects of development, including intellectual aspects. Beyond that minimum, however, the role of family experience is in serious dispute. There is no doubt that such variables as resources of the home and parents' use of language are correlated with children's IQ scores, but such correlations may be mediated by genetic as well as (or instead of) environmental factors. But how much of that variance in IQ results from differences between families, as contrasted with the varying experiences of different children in the same family? Recent twin and adoption studies suggest that while the effect of the shared family environment is substantial in early childhood, it becomes quite small by late adolescence. These findings suggest that differences in the life styles of families whatever their importance may be for many aspects of children's lives make little long-term difference for the skills measured by intelligence tests.

Although parents treat their children differently, such differential treatment explains only a small amount of non-shared environmental influence. One suggestion is that children react differently to the same environment due to different genes. More likely influences may be the impact of peers and other experiences outside the family.[6][24] For example, siblings grown up in the same household may have different friends and teachers and even contract different illnesses. This factor may be one of the reasons why IQ score correlations between siblings decreases as they get older.[26]

Certain single-gene genetic disorders can severely affect intelligence. Phenylketonuria is an example,[27] with publications demonstrating the capacity of phenylketonuria to produce a reduction of 10 IQ points on average.[28] Meta-analyses have found that environmental factors, such as iodine deficiency, can result in large reductions in average IQ; iodine deficiency has been shown to produce a reduction of 12.5 IQ points on average.[29]

The APA report "Intelligence: Knowns and Unknowns" (1995) also stated that:

"We should note, however, that low-income and non-white families are poorly represented in existing adoption studies as well as in most twin samples. Thus it is not yet clear whether these studies apply to the population as a whole. It remains possible that, across the full range of income and ethnicity, between-family differences have more lasting consequences for psychometric intelligence."[6]

A study (1999) by Capron and Duyme of French children adopted between the ages of four and six examined the influence of socioeconomic status (SES). The children's IQs initially averaged 77, putting them near retardation. Most were abused or neglected as infants, then shunted from one foster home or institution to the next. Nine years later after adoption, when they were on average 14 years old, they retook the IQ tests, and all of them did better. The amount they improved was directly related to the adopting family's socioeconomic status. "Children adopted by farmers and laborers had average IQ scores of 85.5; those placed with middle-class families had average scores of 92. The average IQ scores of youngsters placed in well-to-do homes climbed more than 20 points, to 98."[21][30]

Stoolmiller (1999) argued that the range of environments in previous adoption studies were restricted. Adopting families tend to be more similar on, for example, socio-economic status than the general population, which suggests a possible underestimation of the role of the shared family environment in previous studies. Corrections for range restriction to adoption studies indicated that socio-economic status could account for as much as 50% of the variance in IQ.[31]

On the other hand, the effect of this was examined by Matt McGue and colleagues (2007), who wrote that "restriction in range in parent disinhibitory psychopathology and family socio-economic status had no effect on adoptive-sibling correlations [in] IQ"[32]

Turkheimer and colleagues (2003) argued that the proportions of IQ variance attributable to genes and environment vary with socioeconomic status. They found that in a study on seven-year-old twins, in impoverished families, 60% of the variance in early childhood IQ was accounted for by the shared family environment, and the contribution of genes is close to zero; in affluent families, the result is almost exactly the reverse.[33]

In contrast to Turkheimer (2003), a study by Nagoshi and Johnson (2005) concluded that the heritability of IQ did not vary as a function of parental socioeconomic status in the 949 families of Caucasian and 400 families of Japanese ancestry who took part in the Hawaii Family Study of Cognition.[34]

Asbury and colleagues (2005) studied the effect of environmental risk factors on verbal and non-verbal ability in a nationally representative sample of 4-year-old British twins. There was not any statistically significant interaction for non-verbal ability, but the heritability of verbal ability was found to be higher in low-SES and high-risk environments.[35]

Harden and colleagues (2007) investigated adolescents, most 17 years old, and found that, among higher income families, genetic influences accounted for approximately 55% of the variance in cognitive aptitude and shared environmental influences about 35%. Among lower income families, the proportions were in the reverse direction, 39% genetic and 45% shared environment."[36]

Rushton and Jensen (2010) criticized many of these studies for being done on children or adolescents. They argued that heritability increases during childhood and adolescence, and even increases greatly between 1620 years of age and adulthood, so one should be cautious drawing conclusions regarding the role of genetics from studies where the participants are not adults. Furthermore, the studies typically did not examine if IQ gains due to adoption were on the general intelligence factor (g). When the studies by Capron and Duyme were re-examined, IQ gains from being adopted into high SES homes were on non-g factors. By contrast, the adopted children's g mainly depended on their biological parents SES, which implied that g is more difficult to environmentally change.[17] The most cited adoption projects that sought to estimate the heritability of IQ were those of Texas,[37] Colorado[38] and Minnesota[39] that were started in the 1970s. These studies showed that while the adoptive parents' IQ does correlate with adoptees' IQ in early life, when the adoptees reach adolescence the correlation has faded and disappeared. The correlation with the biological parent seemed to explain most of the variation.

A 2011 study by Tucker-Drob and colleagues reported that at age 2, genes accounted for approximately 50% of the variation in mental ability for children being raised in high socioeconomic status families, but genes accounted for negligible variation in mental ability for children being raised in low socioeconomic status families. This gene-environment interaction was not apparent at age 10 months, suggesting that the effect emerges over the course of early development.[40]

A 2012 study based on a representative sample of twins from the United Kingdom, with longitudinal data on IQ from age two to age fourteen, did not find evidence for lower heritability in low-SES families. However, the study indicated that the effects of shared family environment on IQ were generally greater in low-SES families than in high-SES families, resulting in greater variance in IQ in low-SES families. The authors noted that previous research had produced inconsistent results on whether or not SES moderates the heritability of IQ. They suggested three explanations for the inconsistency. First, some studies may have lacked statistical power to detect interactions. Second, the age range investigated has varied between studies. Third, the effect of SES may vary in different demographics and different countries.[41]

A 2017 King's College London study suggests that genes account for nearly 50 per cent of the differences between whether children are socially mobile or not.[42]

A meta-analysis by Devlin and colleagues (1997) of 212 previous studies evaluated an alternative model for environmental influence and found that it fits the data better than the 'family-environments' model commonly used. The shared maternal (fetal) environment effects, often assumed to be negligible, account for 20% of covariance between twins and 5% between siblings, and the effects of genes are correspondingly reduced, with two measures of heritability being less than 50%. They argue that the shared maternal environment may explain the striking correlation between the IQs of twins, especially those of adult twins that were reared apart.[2] IQ heritability increases during early childhood, but whether it stabilizes thereafter remains unclear.[2][old info] These results have two implications: a new model may be required regarding the influence of genes and environment on cognitive function; and interventions aimed at improving the prenatal environment could lead to a significant boost in the population's IQ.[2]

Bouchard and McGue reviewed the literature in 2003, arguing that Devlin's conclusions about the magnitude of heritability is not substantially different from previous reports and that their conclusions regarding prenatal effects stands in contradiction to many previous reports.[43] They write that:

Chipuer et al. and Loehlin conclude that the postnatal rather than the prenatal environment is most important. The Devlin et al. (1997a) conclusion that the prenatal environment contributes to twin IQ similarity is especially remarkable given the existence of an extensive empirical literature on prenatal effects. Price (1950), in a comprehensive review published over 50 years ago, argued that almost all MZ twin prenatal effects produced differences rather than similarities. As of 1950 the literature on the topic was so large that the entire bibliography was not published. It was finally published in 1978 with an additional 260 references. At that time Price reiterated his earlier conclusion (Price, 1978). Research subsequent to the 1978 review largely reinforces Prices hypothesis (Bryan, 1993; Macdonald et al., 1993; Hall and Lopez-Rangel, 1996; see also Martin et al., 1997, box 2; Machin, 1996).[43]

Dickens and Flynn (2001) argued that the "heritability" figure includes both a direct effect of the genotype on IQ and also indirect effects where the genotype changes the environment, in turn affecting IQ. That is, those with a higher IQ tend to seek out stimulating environments that further increase IQ. The direct effect can initially have been very small but feedback loops can create large differences in IQ. In their model an environmental stimulus can have a very large effect on IQ, even in adults, but this effect also decays over time unless the stimulus continues. This model could be adapted to include possible factors, like nutrition in early childhood, that may cause permanent effects.

The Flynn effect is the increase in average intelligence test scores by about 0.3% annually, resulting in the average person today scoring 15 points higher in IQ compared to the generation 50 years ago.[44] This effect can be explained by a generally more stimulating environment for all people. The authors suggest that programs aiming to increase IQ would be most likely to produce long-term IQ gains if they taught children how to replicate outside the program the kinds of cognitively demanding experiences that produce IQ gains while they are in the program and motivate them to persist in that replication long after they have left the program.[45][46] Most of the improvements have allowed for better abstract reasoning, spatial relations, and comprehension. Some scientists have suggested that such enhancements are due to better nutrition, better parenting and schooling, as well as exclusion of the least intelligent, genetically inferior, people from reproduction. However, Flynn and a group of other scientists share the viewpoint that modern life implies solving many abstract problems which leads to a rise in their IQ scores.[44]

More recent research has illuminated genetic factors underlying IQ stability and change. Genome-wide association studies have demonstrated that the genes involved in intelligence remain fairly stable over time.[47] Specifically, in terms of IQ stability, "genetic factors mediated phenotypic stability throughout this entire period [age 0 to 16], whereas most age-to-age instability appeared to be due to non-shared environmental influences".[48][49] These findings have been replicated extensively and observed in the United Kingdom,[50] the United States,[48][51] and the Netherlands.[52][53][54][55] Additionally, researchers have shown that naturalistic changes in IQ occur in individuals at variable times.[56]

Spatial ability has been shown to be unifactorial (a single score accounts well for all spatial abilities), and is 69% heritable in a sample of 1,367 twins from the ages 19 through 21.[57] Further only 8% of spatial ability can be accounted for by a shared environmental factors like school and family.[58] Of the genetically determined portion of spacial ability, 24% is shared with verbal ability (general intelligence) and 43% was specific to spatial ability alone.[59]

A 2009 review article identified over 50 genetic polymorphisms that have been reported to be associated with cognitive ability in various studies, but noted that the discovery of small effect sizes and lack of replication have characterized this research so far.[60] Another study attempted to replicate 12 reported associations between specific genetic variants and general cognitive ability in three large datasets, but found that only one of the genotypes was significantly associated with general intelligence in one of the samples, a result expected by chance alone. The authors concluded that most reported genetic associations with general intelligence are probably false positives brought about by inadequate sample sizes. Arguing that common genetic variants explain much of the variation in general intelligence, they suggested that the effects of individual variants are so small that very large samples are required to reliably detect them.[61] Genetic diversity within individuals is heavily correlated with IQ.[62]

A novel molecular genetic method for estimating heritability calculates the overall genetic similarity (as indexed by the cumulative effects of all genotyped single nucleotide polymorphisms) between all pairs of individuals in a sample of unrelated individuals and then correlates this genetic similarity with phenotypic similarity across all the pairs. A study using this method estimated that the lower bounds for the narrow-sense heritability of crystallized and fluid intelligence are 40% and 51%, respectively. A replication study in an independent sample confirmed these results, reporting a heritability estimate of 47%.[63] These findings are compatible with the view that a large number of genes, each with only a small effect, contribute to differences in intelligence.[61]

The relative influence of genetics and environment for a trait can be calculated by measuring how strongly traits covary in people of a given genetic (unrelated, siblings, fraternal twins, or identical twins) and environmental (reared in the same family or not) relationship. One method is to consider identical twins reared apart, with any similarities which exists between such twin pairs attributed to genotype. In terms of correlation statistics, this means that theoretically the correlation of tests scores between monozygotic twins would be 1.00 if genetics alone accounted for variation in IQ scores; likewise, siblings and dizygotic twins share on average half of their alleles and the correlation of their scores would be 0.50 if IQ were affected by genes alone (or greater if, as is undoubtedly the case, there is a positive correlation between the IQs of spouses in the parental generation). Practically, however, the upper bound of these correlations are given by the reliability of the test, which is 0.90 to 0.95 for typical IQ tests[64]

If there is biological inheritance of IQ, then the relatives of a person with a high IQ should exhibit a comparably high IQ with a much higher probability than the general population. In 1982, Bouchard and McGue reviewed such correlations reported in 111 original studies in the United States. The mean correlation of IQ scores between monozygotic twins was 0.86, between siblings, 0.47, between half-siblings, 0.31, and between cousins, 0.15.[65]

The 2006 edition of Assessing adolescent and adult intelligence by Alan S. Kaufman and Elizabeth O. Lichtenberger reports correlations of 0.86 for identical twins raised together compared to 0.76 for those raised apart and 0.47 for siblings.[66] These number are not necessarily static. When comparing pre-1963 to late 1970s data, researches DeFries and Plomin found that the IQ correlation between parent and child living together fell significantly, from 0.50 to 0.35. The opposite occurred for fraternal twins.[67]

Another summary:

Although IQ differences between individuals are shown to have a large hereditary component, it does not follow that mean group-level disparities (between-group differences) in IQ necessarily have a genetic basis. The Flynn effect is one example where there is a large difference between groups(past and present) with little or no genetic difference. An analogy, attributed to Richard Lewontin,[70] illustrates this point:

Suppose two handfuls are taken from a sack containing a genetically diverse variety of corn, and each grown under carefully controlled and standardized conditions, except that one batch is lacking in certain nutrients that are supplied to the other. After several weeks, the plants are measured. There is variability of growth within each batch, due to the genetic variability of the corn. Given that the growing conditions are closely controlled, nearly all the variation in the height of the plants within a batch will be due to differences in their genes. Thus, within populations, heritabilities will be very high. Nevertheless, the difference between the two groups is due entirely to an environmental factordifferential nutrition. Lewontin didn't go so far as to have the one set of pots painted white and the other set black, but you get the idea. The point of the example, in any case, is that the causes of between-group differences may in principle be quite different from the causes of within-group variation.[71]

Arthur Jensen has written in agreement that this is technically correct, but he has also stated that a high heritability increases the probability that genetics play a role in average group differences.[72][73]

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TPR Lifeline: Clinical Genetics Is A Growing Field – Texas Public Radio

Posted: August 21, 2017 at 4:42 am

We all have about 24,000 genes. How those genes are structured and interact can determine our current health and our future health.

Modern medicine includes specialists in this field called Clinical Geneticists. In todays TPR Lifeline, Bioscience-Medicine reporter Wendy Rigby talks to Baylor College of Medicines Scott McLean, MD, about his work at the Childrens Hospital of San Antonio.

Rigby: Dr. McLean, what is clinical genetics?

McLean: Clinical genetics is the medical specialty that uses genetic information to improve your genetic health or to understand the basis for a variety of medical conditions.

Those of us who have had children in Texas know that while youre still in the hospital, you get some genetic testing done. What is that called and what are you looking for?

We have newborn screening which is actually a blood test that is given to all babies 24 and 48 hours of age. The blood test involves collecting that blood on a piece of paper, filter paper, and sending that to the Texas State Department of Health Services in Austin where they do a series of tests.

This is the foot prick?

This is where you prick the heel. It seem awfully cruel. Babies cry. Parents dont like it. But its actually a wonderful test because it allows us to screen for over 50 conditions.

Give us some examples. What are some of the genetic conditions we might have heard of?

Well, the initial condition that was screened for in newborn screening in the United States was PKU which stands for Phenylketonuria. This is a condition that results in intellectual disability and seizures. We can change that outcome if we are able to identify the condition early enough and change the diet.

Lets say a child comes in to Childrens Hospital of San Antonio. Doctors are having trouble figuring out whats going on. Are you called in to consult?

Most of our patients that we see in the outpatient clinic are sent to us by consultation from physicians in the community or from nurseries, neonatal intensive care units. They range from situations such as multiple birth defects, to autism, intellectual disability, seizures, encephalopathy, blindness, deafness. Theres a whole gamut of reasons that folks come to see us.

When these children become grownups, does that information that youve learned about them help them out if theyre planning to have their own children in the future?

So when pediatric patients make the transition from pediatric care to adult care, its very common for information and ideas to get lost. And we certainly would hope that people remember that. Sometimes when we have identified a situation in a little baby, I tell the parents that I want them to put a sticky note on the last page of their baby book so that when they are showing the baby book to their childs fiance and they get to the last page, it reminds them you need to go back to see the geneticist because theres this genetic situation that you need to have a nice long chat about so that you can plan your family as carefully as possible.

Right. So the work youre doing today could help someone 30 years in the future.

Well, genetics is a very unique specialty in that regard because when we see a patient were not thinking about their next year of life or their next two years of life or the next month. We do think about that. But this is a lifelong diagnosis and a lifelong situation. So I often joke with my patients that Im going to try to put them on the 90-year plan. What we figure out now about their genetics is going to be helpful for them throughout their entire lifespan, at least up until 90 years. And then after that theyre on their own. But well get them to 90.

So its an exciting time to be in the field.

Very exciting. I think the era of gene therapy which for many people we thought was never going to happen, its very promising because we have new technologies that I think are going to allow for advances in that area.

Dr. Scott McLean with Baylor College of Medicine and the Childrens Hospital of San Antonio, thanks for the information.

Youre quite welcome.

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TPR Lifeline: Clinical Genetics Is A Growing Field - Texas Public Radio

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