{"id":158506,"date":"2014-11-12T11:46:17","date_gmt":"2014-11-12T16:46:17","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/study-to-assess-if-knowing-about-genetic-risk-for-kidney-disease-changes-a-persons-lifestyle.php"},"modified":"2014-11-12T11:46:17","modified_gmt":"2014-11-12T16:46:17","slug":"study-to-assess-if-knowing-about-genetic-risk-for-kidney-disease-changes-a-persons-lifestyle","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/genetic-medicine\/study-to-assess-if-knowing-about-genetic-risk-for-kidney-disease-changes-a-persons-lifestyle.php","title":{"rendered":"Study to Assess if Knowing About Genetic Risk For Kidney Disease Changes a Person&#39;s Lifestyle"},"content":{"rendered":"<p><p>Contact Information         <\/p>\n<p>      Available for logged-in reporters only    <\/p>\n<p>    Newswise  (NEW YORK  November 10)  The Icahn School    of Medicine at Mount Sinais Institute for Personalized    Medicine is launching a study designed to learn whether    patients, who are aware of their genetic predisposition to    chronic kidney disease, are more inclined to engage in    proactive lifestyle modification with their primary care    physician.  <\/p>\n<p>    Chronic kidney disease affects about 26 million American    adults. Many studies have shown that African Americans are up    to seven times more likely than any other population to develop    high blood pressure and subsequent complications, such as    kidney disease. A large fraction of the kidney disease    disparity is attributable to variations, or differences, in a    single gene called apolipoprotein L1 (APOL1). In Mount Sinais    specialized laboratory, variations in the APOL1 gene can be    identified with a simple blood test.  <\/p>\n<p>    Erwin Bottinger, MD, Director, Charles Bronfman Institute for    Personalized Medicine in the Icahn School of Medicine at Mount    Sinai is one of the studys Principal Investigators. Many    patients do not have their blood pressure adequately controlled    to minimize the risk for complications such as kidney disease.    We will test whether sharing genetic risk information with    patients and alerting their doctors through a patient's    electronic health record, will achieve better control of blood    pressure to reduce kidney disease risk.  <\/p>\n<p>    Dr. Bottinger and Co-Principal Investigator Carol Horowitz, MD,    MPH, are seeking to enroll approximately two thousand African    American participants with hypertension for their year-long    study: Genetic testing to Understand and Address Renal Disease    Disparities (The GUARDD Study). Funded by the National Human    Genome Research Institute (NHGRI) the study will be conducted    in a network of community health centers and primary care    facilities in Northern Manhattan and the South Bronx,    affiliated with the Icahn School of Medicines Institute for    Family Health and at primary care facilities of The Mount Sinai    Health System.  <\/p>\n<p>    At the first study visit, all study participants will be asked    to complete medical and family health histories, blood    pressure, height, and weight measurements. If eligible, each    individual will be randomly assigned to one of two groups.    Group 1 will have blood drawn for genetic testing and return    within 4 weeks later to discuss the results with a member of    the research team. They will also be given printed information    to share with their primary care physician. Those participants    will return after 3 months and 12 months for a blood pressure    check and to complete follow-up surveys.  <\/p>\n<p>    Individuals in Group 2 will receive the genetic testing until    the end of the study but will be asked to return at 3 and 12    months for the same measurements as those in Group 1. Primary    care providers for patients enrolled in the study will also    receive the results of the APOL1 genetic test and information    about the test through alerts in the patients electronic    medical record.  <\/p>\n<p>    We are translating the latest scientific developments for both    patients and their primary care physicians, says Dr. Horowitz.    While we cant guarantee results, we are hopeful participants    who know they carry the APOL1 gene variant will engage in    proactive behaviors, under their doctors supervision to    forestall renal failure often associated with hypertension.  <\/p>\n<p>    Neil Calman, MD, President and Chief Executive Officer of the    Institute for Family Health, and Professor and Chair of Family    Medicine and Community Health at Mount Sinai said, Armed with    this genetic information, African Americans with high blood    pressure who carry variations in this gene will be able to    focus on the management of their high blood pressure with their    primary care providers, helping to prevent the onset of the    devastating effects of kidney failure.  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>See original here: <\/p>\n<p><a target=\"_blank\" href=\"http:\/\/www.newswise.com\/articles\/view\/625992\/?sc=rsmn\/RK=0\/RS=n1gKyGyONaz0T.NNr.LHf1hXr50-\" title=\"Study to Assess if Knowing About Genetic Risk For Kidney Disease Changes a Person&#39;s Lifestyle\">Study to Assess if Knowing About Genetic Risk For Kidney Disease Changes a Person&#39;s Lifestyle<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Contact Information Available for logged-in reporters only Newswise (NEW YORK November 10) The Icahn School of Medicine at Mount Sinais Institute for Personalized Medicine is launching a study designed to learn whether patients, who are aware of their genetic predisposition to chronic kidney disease, are more inclined to engage in proactive lifestyle modification with their primary care physician. Chronic kidney disease affects about 26 million American adults <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/genetic-medicine\/study-to-assess-if-knowing-about-genetic-risk-for-kidney-disease-changes-a-persons-lifestyle.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-158506","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\/158506"}],"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=158506"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/158506\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=158506"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=158506"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=158506"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}