{"id":106025,"date":"2014-02-04T09:45:21","date_gmt":"2014-02-04T14:45:21","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/new-hope-as-researchers-discover-genetic-mutations-that-cause-rare-and-deadly-lung-disease.php"},"modified":"2014-02-04T09:45:21","modified_gmt":"2014-02-04T14:45:21","slug":"new-hope-as-researchers-discover-genetic-mutations-that-cause-rare-and-deadly-lung-disease","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/genetic-medicine\/new-hope-as-researchers-discover-genetic-mutations-that-cause-rare-and-deadly-lung-disease.php","title":{"rendered":"New Hope As Researchers Discover Genetic Mutations That Cause Rare and Deadly Lung Disease"},"content":{"rendered":"<p><p>Contact Information         <\/p>\n<p>      Available for logged-in reporters only    <\/p>\n<p>    Newswise  SALT LAKE CITY  A team of researchers, led by    physicians and scientists at Intermountain Medical Center and    ARUP Laboratories in Salt Lake City, has made a medical    breakthrough by discovering genetic mutations that cause a rare    and deadly lung disease.  <\/p>\n<p>    The disease, pulmonary capillary hemangiomatosis or PCH, is a    rare cause of pulmonary hypertension, which occurs    predominantly in young adults. PCH affects less than one in a    million people, and has been extremely difficult and expensive    to diagnose, as well as challenging to treat.  <\/p>\n<p>    This genetic discovery offers new hope.  <\/p>\n<p>    This is a significant finding. This discovery should advance    our understanding of this rare pulmonary vascular disorder and    other related disorders, said Greg Elliott, MD, MACP, senior    investigator of the study and medical director of the Pulmonary    Hypertension Center at Intermountain Medical Center in Murray,    Utah, and professor of medicine at the University of Utah    School of Medicine.  <\/p>\n<p>    Results of the study will be published in the February issue of    the journal CHEST, the official publication of the American    College of Chest Physicians. The study is embargoed by CHEST    until Feb 4 at 6am, EST.  <\/p>\n<p>    Dr. Elliott and his team at Intermountain Medical Center and    the University of Utah School of Medicine collaborated with    researchers from Columbia University, Vanderbilt University and    Mayo Clinic-Scottsdale.  <\/p>\n<p>    To find the genetic mutation, the research team used a    relatively new technology  whole exome sequencing  performed    at ARUP Laboratories in Salt Lake City to test DNA samples.    They discovered the genetic mutations in Eukaryotic Translation    Initiation Factor 2 Alpha Kinase 4. EIF2AK4 is a protein    responsible for down-regulating protein synthesis when cells    are exposed to stress.  <\/p>\n<p>    Researchers found that in patients with the genetic mutations,    their bodies don't properly regulate blood vessels in the lung.    As a result, the capillaries in the lungs proliferate and the    patient develops pulmonary hypertension.  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>See more here: <\/p>\n<p><a target=\"_blank\" href=\"http:\/\/www.newswise.com\/articles\/view\/613156\/?sc=rsmn\" title=\"New Hope As Researchers Discover Genetic Mutations That Cause Rare and Deadly Lung Disease\">New Hope As Researchers Discover Genetic Mutations That Cause Rare and Deadly Lung Disease<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Contact Information Available for logged-in reporters only Newswise SALT LAKE CITY A team of researchers, led by physicians and scientists at Intermountain Medical Center and ARUP Laboratories in Salt Lake City, has made a medical breakthrough by discovering genetic mutations that cause a rare and deadly lung disease.  <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/genetic-medicine\/new-hope-as-researchers-discover-genetic-mutations-that-cause-rare-and-deadly-lung-disease.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-106025","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\/106025"}],"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=106025"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/106025\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=106025"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=106025"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=106025"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}