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Leukocyte Telomere Length and All-Cause Mortality: A Between-Within Twin Study With Time-Dependent Effects Using Generalized Survival Models

机译:白细胞端粒长度和全因死亡率:双胞胎在双胞胎中,使用广义存活模型与时间依赖性效果

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摘要

Although previous studies examining leukocyte telomere length (LTL) and all-cause mortality controlled for several confounders, the observed association could be biased due to unmeasured confounders, including familial factors. We aimed to examine the association of LTL with all-cause mortality in a Swedish twin sample while adjusting for familial factors and allowing for time-dependent effects. A total of 366 participants (174 twin pairs and 18 individuals) were recruited from the Swedish Twin Registry. LTL was assessed using the Southern blot method. All-cause mortality data were obtained through linkage with the Swedish Population Registry, updated through November 15, 2017. To control for familial factors within twin pairs, we applied a between-within shared frailty model based on generalized survival models. Overall, 115 (31.4%) participants were men and 251 (68.6%) were women. The average age of the study participants when blood was drawn was 79.1 years, and follow-up duration ranged from 10 days to 25.7 years (mean = 10.2 years). During the follow-up period, 341 (93.2%) participants died. Shorter LTL was associated with higher mortality rates when controlling for familial factors in the between-within shared frailty model. We found significant time-dependent effects of LTL on all-cause mortality, where the mortality rate ratios were attenuated with increasing age.
机译:尽管先前的研究检查了白细胞端粒长度(LT1)和对几个混淆控制的全因死亡率,但由于未测量的混乱,包括家族因素,所观察到的关联可能被偏见。我们旨在检查LTL与瑞典双胞胎样品中的所有原因死亡率的关联,同时调整家庭因素并允许时间依赖的影响。瑞典双人登记处共招募了366名参与者(174人双对和18个个人)。使用Southern印迹法评估LT1。通过与瑞典人口登记处的联系获得全局死亡率数据,于2017年11月15日更新。为了控制双对中的家族因素,我们在基于广义生存模型的共享体内模型中应用了一系列的共用体内模型。总体而言,115(31.4%)参与者是男性,251名(68.6%)是妇女。研究参与者的平均年龄为79.1岁,随访时间为10天至25.7岁(平均= 10.2岁)。在随访期间,341(93.2%)参与者死亡。当在共享体内模型中的内部内部的家族性因素控制家族因素时,较短的LTL与较高的死亡率有关。我们发现LTL对全因死亡率的显着时间依赖性作用,其中增长的死亡率比率随着年龄的增加而衰减。

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