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The association of telomere length with paternal history of premature myocardial infarction in the European Atherosclerosis Research Study II

机译:欧洲动脉粥样硬化研究II中端粒长度与早发性心肌梗死的父亲病史的关系

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摘要

Inter-individual variability in telomere length is highly heritable and has been correlated with risk of coronary heart disease (CHD). Our aim was to determine the association of mean leukocyte telomere length with paternal history of premature myocardial infarction (MI). Mean leukocyte telomere length was measured with real-time polymerase chain reactions in 369 male students (18–28 years) with a paternal history of MI before the age of 55, recruited from 14 European universities, serving as cases and 396 age-matched controls with no paternal history of CHD. Overall, cases had borderline significantly shorter mean length (~550 bp), adjusted for age and geographical region, than controls (p = 0.05). A significant difference in telomere length across the geographical regions of Europe was observed (p < 0.0001), with shorter mean length in the Baltic and South and the longest in the Middle. The case–control difference (∼2.24 kb) in mean length was highly significant only in the Baltic region (p < 0.0001). There is suggestive evidence that, in young men, the biological expression of a paternal history of premature MI is at least in part mediated through inherited short telomeres. The association with paternal history of MI is strongly seen only in the Baltic compared to the rest of Europe, but this is not explained by shorter telomere length in this region.Electronic supplementary materialThe online version of this article (doi:10.1007/s00109-008-0347-x) contains supplementary material, which is available to authorized users.
机译:端粒长度的个体差异是高度遗传的,并且与冠心病(CHD)的风险相关。我们的目的是确定平均白细胞端粒长度与早发性心肌梗死(MI)的父亲病史的关联。从欧洲14所大学招募了369名年龄与年龄匹配的对照组的369名年龄在55岁之前的MI父系病史的男生(18-28岁),通过实时聚合酶链反应测量了平均白细胞端粒长度没有冠心病的父亲病史。总体而言,根据年龄和地理区域进行调整后,病例的边界线平均长度(〜550bp)明显短于对照组(p = 0.05)。整个欧洲地理区域的端粒长度存在显着差异(p <0.0001),波罗的海和南部的平均长度较短,而中部的长度最长。仅在波罗的海地区(p <0.0001),病例对照平均长度的差异(〜2.24kb)才具有显着性。有暗示性的证据表明,在年轻人中,MI的父亲病史的生物学表达至少部分是通过遗传的短端粒介导的。与欧洲其他地区相比,仅在波罗的海地区才强烈发现与MI的父亲史有关,但这不能通过该地区端粒长度较短来解释。电子补充材料本文的在线版本(doi:10.1007 / s00109-008) -0347-x)包含补充材料,授权用户可以使用。

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