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Study challenges view that sickle cell trait increases mortality risk
Surprising findings from a study of health records of thousands of African-American soldiers show that a common genetic condition poses far less risk than previously thought.
Health experts have long believed that sickle cell gene variants, which occur in about 1 in 13 African-Americans, increase the risk of premature death, even when people carry only a single copy of the variant. But health records of nearly 50,000 active-duty U.S. Army soldiers between 2011 and 2014 shows that’s not the case, according to a study led by researchers at the Stanford University School of Medicine.
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This platform is made possible through a partnership with the Sickle Cell Disease Association of America, Inc. (SCDAA) and its member organizations. SCDAA's mission is to advocate for people affected by sickle cell conditions and empower community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure.