{"id":179930,"date":"2015-02-02T18:47:55","date_gmt":"2015-02-02T23:47:55","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/obamas-precision-medicine-database-how-safe-and-private-is-the-patient-data.php"},"modified":"2015-02-02T18:47:55","modified_gmt":"2015-02-02T23:47:55","slug":"obamas-precision-medicine-database-how-safe-and-private-is-the-patient-data","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/genetic-medicine\/obamas-precision-medicine-database-how-safe-and-private-is-the-patient-data.php","title":{"rendered":"Obamas &#39;Precision Medicine&#39; Database: How Safe And Private Is The Patient Data?"},"content":{"rendered":"<p><p>    Scientific progress sometimes requires a leap of faith. And    patients who volunteer their records to a national genomic    database under President Obamas new initiative for precision    medicine will be taking a big one.  <\/p>\n<p>    In the young field of genomics, scientists are still drawing    the ethical road map for open-ended exploration and realizing    the privacy implications for what they might uncover. In the    meantime, those who sign up for genomic studies are essentially    along for the ride.  <\/p>\n<p>    President Obama is asking Congress to embark down a new path in    medicine to create treatments for diseases that have long    stumped the scientific community. Obamas 2016 budget proposal    grants $215 million to    advance the field of precision medicine, an approach in which    experts toss out their one-size-fits-all strategy to develop    drugs or therapies that target the genetic makeup and lifestyle    choices of each patient.  <\/p>\n<p>    As part of the proposal, the Obama administration intends to    give $130 million to the National Institutes of Health (NIH) to    build a database of records that will include biological    samples, test results, medical histories and genomic profiles    of a million or more Americans. Theproject should present    unprecedented opportunities for researchers but also a host of    new challenges for an administration with a dicey record of    data protection at    HealthCare.gov and a history ofelectronic surveillance in    the name of national security.  <\/p>\n<p>    I think this is a bold initiative, says Michael Zimmer, an    expert in Internet privacy issues at University of    Wisconsin-Madison. What I'm hoping here is that, given the    sensitivity of this data, they will engage with the right    communities and do it in a transparent way.  <\/p>\n<p>    Francis Collins, director of the NIH, has confirmed to    International Business Times that many of the genomes included    in the database will be gleaned from a network of 200 groups of    scientists around the country who have enrolled, or are    enrolling, at least 10,000 participants each for the studies.    It should be possible to build the precision medicine    initiative largely from existing studies, saving a great deal    of time and money, he says.  <\/p>\n<p>    Of course, amassing the data will only be half of the    challenge; the federal government must also keep it safe.    Holding a persons genomic and medical records is like having a    window into their lifestyle, family history and possible    future, and the risk is that such intimate information could be    abused or misused if found in the wrong hands.  <\/p>\n<p>    Some patient protections are already in place. The Common Rule, by which    most federal agencies abide, prohibits research on human    subjects without their consent except in special situations.    The Privacy Rule of the Health Insurance Portability and    Accountability Act also generally prohibits research on or the    disclosure of information related to a patient's health without    their consent among many universities and hospitals that may    contribute to the nationwide study. And should this information    ever leak out, Congress also passed the Genetic Information    Nondiscrimination Act in 2008 to prevent insurers or    employers from holding genetic findings against a person.    Regardless, concerns still loom large in the minds of privacy    advocates.  <\/p>\n<p>    Pam Dixon, founder of a nonprofit concerned with privacy issues    called the World Privacy Forum, argues that    genomic data can be mishandled in ways that might impact an    individuals family or children as well as themselves -- for    instance, detecting an inheritable disease or predisposition    for a late-onset illness. She thinks these concerns merit extra    layers of protection. We cannot miss the mark on this one,    she says.  <\/p>\n<p>    The administration plans to grant $5 million to the Office of    the National Coordinator for Health Information Technology for    the sole purpose of ensuring data security. Zimmer takes this    investment as a sign that the administration is making privacy    a priority from the start.  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Follow this link:<\/p>\n<p><a target=\"_blank\" href=\"http:\/\/www.ibtimes.com\/obamas-precision-medicine-database-how-safe-private-patient-data-1802570\/RK=0\/RS=wM9Vku.hB41r4fa7d8HdzWPT2.U-\" title=\"Obamas &#39;Precision Medicine&#39; Database: How Safe And Private Is The Patient Data?\">Obamas &#39;Precision Medicine&#39; Database: How Safe And Private Is The Patient Data?<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Scientific progress sometimes requires a leap of faith.  <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/genetic-medicine\/obamas-precision-medicine-database-how-safe-and-private-is-the-patient-data.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-179930","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\/179930"}],"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=179930"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/179930\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=179930"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=179930"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=179930"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}