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Paternal age is positively linked to telomere length of children

机译:父亲年龄与儿童端粒长度成正比

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Summary Telomere length is linked to age-associated diseases, with shorter telomeres in blood associated with an increased probability of mortality from infection or heart disease. Little is known about how human telomere length is regulated despite convincing data from twins that telomere length is largely heritable, uniform in various tissues during development until birth and variable between individuals. As sperm cells show increasing telomere length with age, we investigated whether age of fathers at conception correlated with telomere length of their offspring. Telomere length in blood from 125 random subjects was shown to be positively associated with paternal age (+22?bp?yr?1, 95% confidence interval 5.2–38.3, P ?=?0.010), and paternal age was calculated to affect telomere length by up to 20% of average telomere length per generation. Males lose telomeric sequence faster than females (31?bp?yr?1, 17.6–43.8, P ??1, 3.5–24.8, P
机译:小结端粒长度与年龄相关疾病有关,血液中端粒较短会导致感染或心脏病死亡的可能性增加。尽管来自双胞胎的数据令人信服,端粒长度在很大程度上可遗传,在发育至出生期间在各个组织中均一,并且个体之间存在差异,但人们对端粒长度的调控知之甚少。由于精子细胞的端粒长度随着年龄的增长而增加,因此我们研究了受孕父亲的年龄是否与其后代的端粒长度相关。研究显示,来自125名随机受试者的血液中端粒长度与父亲年龄呈正相关(+22?bp?yr ?1 ,95%置信区间5.2–38.3,P?=?0.010),并且父本年龄经计算可影响端粒长度,最高可达每代平均端粒长度的20%。雄性失去端粒序列的速度比雌性快(31?bp?yr ?1 ,17.6–43.8,P ?? 1 ,3.5–24.8,P

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