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瑞典老年男性白细胞端粒长度与死亡率的纵向变化

Longitudinal changes in leukocyte telomere length and mortality in elderly Swedish men.

作者信息

Yuan Xiaotian, Kronström Magnus, Hellenius Mai-Lis, Cederholm Tommy, Xu Dawei, Sjögren Per

机构信息

Department of Medicine, Division of Hematology, and Center for Molecular Medicine, Karolinska Institutet and Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden.

Department of Public Health and Caring Sciences, Unit of Clinical Nutrition and Metabolism, Uppsala University, Uppsala, Sweden.

出版信息

Aging (Albany NY). 2018 Oct 29;10(10):3005-3016. doi: 10.18632/aging.101611.

Abstract

Telomere length (TL) is considered an indicator of aging and age-related diseases, but longitudinal studies on TL changes and mortality are few. We therefore analyzed TL and longitudinal changes in TL in relation to all-cause, cardiovascular, and cancer mortality in 247 elderly Swedish men. TL was determined by the qPCR method at ages 71 and 81 and subsequent mortality cases were identified from the Swedish cause-of-death registry. Cox proportional hazard ratios were calculated during a mean follow-up of 7.4 years, during which 178 deaths occurred. Short telomeres at baseline was strongly associated with mortality risks, with a 40 to 70% increased risk of all-cause mortality, and a 2-fold increased risk of cancer mortality. Longitudinal changes in TL revealed shortening in 83% of individuals, whilst 10% extended their telomeres. TL attrition did not predict all-cause or cancer mortality, but we found a 60% decreased risk for cardiovascular mortality in those who shortened their telomeres. Our data show an increased risk of mortality in individuals with short baseline telomeres, but no relations to all-cause, and cancer mortality for changes in TL. Intriguingly, our data indicate lower risk of cardiovascular mortality with shortening of telomeres. The latter should be interpreted cautiously.

摘要

端粒长度(TL)被视为衰老及与年龄相关疾病的一个指标,但关于TL变化与死亡率的纵向研究较少。因此,我们分析了247名瑞典老年男性的TL及其纵向变化与全因死亡率、心血管疾病死亡率和癌症死亡率的关系。通过qPCR方法在71岁和81岁时测定TL,并从瑞典死因登记处识别随后的死亡病例。在平均7.4年的随访期间计算Cox比例风险比,在此期间有178人死亡。基线端粒短与死亡风险密切相关,全因死亡率风险增加40%至70%,癌症死亡率风险增加两倍。TL的纵向变化显示83%的个体端粒缩短,而10%的个体端粒延长。端粒损耗不能预测全因死亡率或癌症死亡率,但我们发现端粒缩短的个体心血管死亡率风险降低60%。我们的数据表明基线端粒短的个体死亡风险增加,但TL变化与全因死亡率和癌症死亡率无关。有趣的是,我们的数据表明端粒缩短时心血管死亡率风险较低。对此应谨慎解读。

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