Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Department of Epidemiology, Harvard School of Public Health, Boston, MA, USA.
Depress Anxiety. 2018 May;35(5):431-439. doi: 10.1002/da.22732. Epub 2018 Feb 27.
Although depression and anxiety have been associated with shorter telomeres in cross-sectional studies, the data regarding the prospective relations of depression and anxiety to accelerated telomere length shortening are limited and findings are mixed. We prospectively examined relations of baseline depression and phobic anxiety to subsequent 11-year change in relative leukocyte telomere lengths (LTLs).
We selected 1,250 women from a subcohort of the Nurses' Health Study who provided blood specimens at both blood collections (1989-1990 and 2000-2001). Depression was defined by self-reported regular antidepressant use or presence of severe depressive symptoms; anxiety symptoms were assessed using the Crown-Crisp Experiential Index. Using quantitative real-time polymerase chain reaction assay, LTLs were measured as the copy number ratio of telomere repeat to a single control gene. Changes in LTLs were defined in three ways: absolute change, symmetrized percent change, and decile shift.
Overall, there were no statistically significant associations of depression or phobic anxiety to subsequent 11-year LTL shortening, despite a point estimates in the direction of greater telomere shortening among participants with versus without depression, across all three metrics of telomere change. The strongest predictor of LTL change was baseline telomere length, and regression-to-the-mean was observed.
Baseline depression and phobic anxiety were not significantly associated with 11-year attrition in LTLs among 1,250 mid-life and older women. However, a suggestion of depression and greater subsequent LTL attrition, while not statistically significant, may warrant further inquiry, particularly in prospective studies with larger sample sizes and broader windows of the lifespan.
尽管横断面研究表明抑郁和焦虑与端粒较短有关,但关于抑郁和焦虑与端粒长度缩短加速之间前瞻性关系的数据有限,且研究结果存在差异。我们前瞻性地研究了基线抑郁和恐惧症焦虑与随后 11 年相对白细胞端粒长度(LTL)变化的关系。
我们从护士健康研究的一个子队列中选择了 1250 名女性,她们在两次采血时(1989-1990 年和 2000-2001 年)提供了血样。抑郁的定义是定期使用抗抑郁药或有严重抑郁症状;焦虑症状采用 Crown-Crisp 体验指数评估。使用实时定量聚合酶链反应测定法,将端粒重复序列与单个对照基因的拷贝数比作为 LTL 进行测量。LTL 变化以三种方式定义:绝对变化、对称百分比变化和十分位变化。
总体而言,抑郁或恐惧症焦虑与随后 11 年的 LTL 缩短之间没有统计学上的显著关联,尽管在所有三种端粒变化指标中,与没有抑郁的参与者相比,有抑郁的参与者的端粒缩短幅度更大。LTL 变化的最强预测因子是基线端粒长度,且存在回归平均值现象。
在 1250 名中年和老年女性中,基线抑郁和恐惧症焦虑与 11 年 LTL 缩短无显著相关性。然而,虽然没有统计学意义,但抑郁和更大的随后 LTL 缩短的提示可能需要进一步研究,特别是在具有更大样本量和更广泛寿命窗口的前瞻性研究中。