Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Department of Psychology, College of Humanities, Arts, and Social Sciences, University of California, Riverside, Riverside, California.
Am J Epidemiol. 2018 Oct 1;187(10):2186-2191. doi: 10.1093/aje/kwy128.
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.
尽管先前的研究在控制了多种混杂因素的情况下,检查了白细胞端粒长度(LTL)和全因死亡率之间的关系,但由于未测量的混杂因素(包括家族因素),观察到的关联可能存在偏差。我们旨在在调整家族因素并允许时间依赖性效应的情况下,在瑞典双胞胎样本中检查 LTL 与全因死亡率之间的关联。共招募了 366 名参与者(174 对双胞胎和 18 名个体)来自瑞典双胞胎登记处。使用Southern blot 方法评估 LTL。通过与瑞典人口登记处链接获取全因死亡率数据,截至 2017 年 11 月 15 日进行更新。为了控制双胞胎内的家族因素,我们基于广义生存模型应用了基于对之间的共享脆弱性模型。总体而言,115 名(31.4%)参与者为男性,251 名(68.6%)为女性。抽取血液时研究参与者的平均年龄为 79.1 岁,随访时间从 10 天到 25.7 年(平均为 10.2 年)。在随访期间,有 341 名(93.2%)参与者死亡。在基于对之间的共享脆弱性模型中控制家族因素时,较短的 LTL 与较高的死亡率相关。我们发现 LTL 对全因死亡率有显著的时间依赖性影响,随着年龄的增加,死亡率比值减弱。