全基因组关联研究(GWAS)确定的疾病风险等位基因不会影响人类的长寿。
Genome-wide association study (GWAS)-identified disease risk alleles do not compromise human longevity.
机构信息
Molecular Epidemiology, Leiden University Medical Center, 2300 RC, Leiden, The Netherlands.
出版信息
Proc Natl Acad Sci U S A. 2010 Oct 19;107(42):18046-9. doi: 10.1073/pnas.1003540107. Epub 2010 Oct 4.
A set of currently known alleles increasing the risk for coronary artery disease, cancer, and type 2 diabetes as identified by genome-wide association studies was tested for compatibility with human longevity. Here, we show that nonagenarian siblings from long-lived families and singletons older than 85 y of age from the general population carry the same number of disease risk alleles as young controls. Longevity in this study population is not compromised by the cumulative effect of this set of risk alleles for common disease.
一套由全基因组关联研究确定的与冠心病、癌症和 2 型糖尿病风险增加相关的已知等位基因,被测试其与人类长寿的兼容性。在这里,我们发现,来自长寿家族的 90 岁以上的兄弟姐妹和来自普通人群的 85 岁以上的单身个体,与年轻对照者携带相同数量的疾病风险等位基因。在本研究人群中,这些常见疾病风险等位基因的累积效应并未影响到长寿。