Physician-Training Stress and Accelerated Cellular Aging

损耗 实习 端粒 医学 老年学 长寿 神经质 心理学 队列 内科学 遗传学 人格 生物 医学教育 DNA 牙科 社会心理学
作者
Kathryn K. Ridout,Samuel J. Ridout,Constance Guille,Douglas A. Mata,Huda Akil,Srijan Sen
出处
期刊:Biological Psychiatry [Elsevier]
卷期号:86 (9): 725-730 被引量:27
标识
DOI:10.1016/j.biopsych.2019.04.030
摘要

Background Stress is a key precipitant for many common diseases, but established biological markers to track stress and guide investigations into mechanisms linking stress and disease are lacking. Cross-sectional studies have identified correlations between stress and telomere attrition, but no large, longitudinal studies examining the impacts of chronic stress on telomere length exist. Residency training for physicians is a well-established stressful experience and can be used as a prospective stress model. Methods In a longitudinal cohort study of 250 interns (first-year residents) at 55 United States hospital systems serving during the 2015–2016 academic year, we examined associations between measures of the residency experience and saliva-measured telomere attrition. Results Telomere length shortened significantly over the course of internship year, from mean ± SD of 6465.1 ± 876.8 base pairs before internship to 6321.5 ± 630.6 base pairs at the end of internship (t246 = 2.69; p = .008). Stressful early family environments and neuroticism were significantly associated with shorter preinternship telomere length. Longer work hours were associated with greater telomere intern telomere loss over the year (p = .002). Of note, the mean telomere attrition during internship year was six times greater than the typical annual attrition rate identified in a recent meta-analysis. Conclusions This work implicates telomere attrition as a biologically measurable consequence of physician training, with the magnitude of attrition associated with workload. Identification of an objective, biological sequela of residency stress may help to facilitate the development of effective interventions. Further, the findings implicate telomere attrition as an objective biomarker to follow the pathologic effects of stress, in general.
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