{"id":176298,"date":"2015-01-21T17:46:59","date_gmt":"2015-01-21T22:46:59","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/usc-neuroscientists-lead-global-enigma-consortium-to-crack-brains-genetic-code.php"},"modified":"2015-01-21T17:46:59","modified_gmt":"2015-01-21T22:46:59","slug":"usc-neuroscientists-lead-global-enigma-consortium-to-crack-brains-genetic-code","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/genetic-medicine\/usc-neuroscientists-lead-global-enigma-consortium-to-crack-brains-genetic-code.php","title":{"rendered":"USC neuroscientists lead global ENIGMA consortium to crack brain&#39;s genetic code"},"content":{"rendered":"<p><p>  Global research alliance ENIGMA finds 8 common gene mutations  leading to brain age in over 30,000 brain scans that may some day  unlock mysteries of Alzheimer's, autism and other neurological  disorders<\/p>\n<p>    LOS ANGELES -- In the largest collaborative study of the brain    to date, researchers from the Keck School of Medicine of the    University of Southern California (USC) led a global consortium    of 190 institutions to identify eight common genetic mutations    that appear to age the brain an average of three years. The    discovery could lead to targeted therapies and interventions    for Alzheimer's disease, autism and other neurological    conditions.  <\/p>\n<p>    An international team of roughly 300 scientists known as the    Enhancing Neuro Imaging Genetics through Meta Analysis (ENIGMA)    Network pooled brain scans and genetic data worldwide to    pinpoint genes that enhance or break down key brain regions in    people from 33 countries. This is the first high-profile study    since the National Institutes of Health (NIH) launched its Big    Data to Knowledge (BD2K) centers of excellence in 2014. The    research was published Wednesday, Jan. 21, in the peer-reviewed    journal Nature.  <\/p>\n<p>    \"ENIGMA's scientists screen brain scans and genomes worldwide    for factors that help or harm the brain -- this crowd-sourcing    and sheer wealth of data gives us the power to crack the    brain's genetic code,\" said Paul Thompson, Ph.D., Keck School    of Medicine of USC professor and principal investigator of    ENIGMA. \"Our global team discovered eight genes that may erode    or boost brain tissue in people worldwide. Any change in those    genes appears to alter your mental bank account or brain    reserve by 2 or 3 percent. The discovery will guide research    into more personalized medical treatments for Alzheimer's,    autism, depression and other disorders.\"  <\/p>\n<p>    The study could help identify people who would most benefit    from new drugs designed to save brain cells, but more research    is necessary to determine if the genetic mutations are    implicated in disease.  <\/p>\n<p>    The ENIGMA researchers screened millions of \"spelling    differences\" in the genetic code to see which ones affected the    size of key parts of the brain in magnetic resonance images    (MRIs) from 30,717 individuals. The MRI analysis focused on    genetic data from seven regions of the brain that coordinate    movement, learning, memory and motivation. The group identified    eight genetic variants associated with decreased brain volume,    several found in over one-fifth of the world's population.    People who carry one of those eight mutations had, on average,    smaller brain regions than brains without a mutation but of    comparable age; some of the genes are implicated in cancer and    mental illness.  <\/p>\n<p>    In October 2014, the NIH invested nearly $32 million in its Big    Data Initiative, creating 12 research hubs across the United    States to improve the utility of biomedical data. USC's two    BD2K centers of excellence, including ENIGMA, were awarded a    total of $23 million over four years.  <\/p>\n<p>    \"The ENIGMA Center's work uses vast datasets as engines of    biomedical discovery; it shows how each individual's genetic    blueprint shapes the human brain,\" said Philip Bourne, Ph.D.,    associate director for data science at the NIH. \"This 'Big    Data' alliance shows what the NIH Big Data to Knowledge (BD2K)    Program envisions achieving with our 12 Centers of Excellence    for Big Data Computing.\"  <\/p>\n<p>    ###  <\/p>\n<p>    Other USC co-authors include Derrek P. Hibar, Neda Jahanshad    and Arthur Toga. ENIGMA was supported in part by a Consortium    grant (U54 EB020403) from the NIH BD2K Initiative, supported by    a cross-NIH partnership, and by public and private agencies    worldwide.  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Read more: <\/p>\n<p><a target=\"_blank\" href=\"http:\/\/www.eurekalert.org\/pub_releases\/2015-01\/uosc-012115.php\/RK=0\/RS=aWbY_fPQP5zjXlhn8jt0tbtB72I-\" title=\"USC neuroscientists lead global ENIGMA consortium to crack brain&#39;s genetic code\">USC neuroscientists lead global ENIGMA consortium to crack brain&#39;s genetic code<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Global research alliance ENIGMA finds 8 common gene mutations leading to brain age in over 30,000 brain scans that may some day unlock mysteries of Alzheimer's, autism and other neurological disorders LOS ANGELES -- In the largest collaborative study of the brain to date, researchers from the Keck School of Medicine of the University of Southern California (USC) led a global consortium of 190 institutions to identify eight common genetic mutations that appear to age the brain an average of three years. The discovery could lead to targeted therapies and interventions for Alzheimer's disease, autism and other neurological conditions <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/genetic-medicine\/usc-neuroscientists-lead-global-enigma-consortium-to-crack-brains-genetic-code.php\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"limit_modified_date":"","last_modified_date":"","_lmt_disableupdate":"","_lmt_disable":"","footnotes":""},"categories":[5],"tags":[],"class_list":["post-176298","post","type-post","status-publish","format-standard","hentry","category-genetic-medicine"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/176298"}],"collection":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/comments?post=176298"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/176298\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=176298"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=176298"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=176298"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}