Abstract

BackgroundShort or long sleep duration is proposed as a potential risk factor for all-cause mortality in the older people, yet the results of published studies are not often reproducible.MethodsLiterature retrieval, study selection and data extraction were completed independently and in duplicate. Only prospective cohort studies were included. Effect-size estimates are expressed as hazard ratio (HR) and 95% confidence interval (CI).ResultsSummary data from 28 articles, involving a total of 95,259 older people, were meta-analyzed. Overall analyses revealed a remarkably significant association between long sleep duration and all-cause mortality (adjusted HR = 1.24, 95% CI: 1.16–1.33, P < .001), whereas only marginal significance was observed for short sleep duration (adjusted HR = 1.04; 95% CI: 1.00–1.09; P = .033). Funnel plots suggested no publication bias for short sleep duration (P = .392). The probability of publication bias was high for long sleep duration (P = .020), yet the trim-and-fill method strengthened its significance in predicting all-cause mortality. In subgroup analyses, the association of long sleep duration with all-cause mortality was statistically significant in both women (HR = 1.48; 95% CI: 1.18–1.86; P = .001) and men (HR = 1.31; 95% CI: 1.10–1.58; P = .003). By contrast, with regard to short sleep duration, statistical significance was observed in men (HR = 1.13; 95% CI: 1.04–1.24; P = .007), but not in women (HR = 1.00; 95% CI: 0.85–1.18; P = .999) (Two-sample Z test P = .099). Besides gender, geographic region, sleep survey method, baseline age and follow-up interval were identified as possible causes of between-study heterogeneity in subgroup analyses. Further dose-response regression analyses revealed that trend estimation was more obvious for long sleep duration (regression coefficient: 0.13; P < .001) than for short sleep duration (regression coefficient: 0.02; P = .046).ConclusionsOur findings indicate a significantly increased risk of all-cause mortality associated with long sleep duration, especially in women, as well as with short sleep duration in men only.

Highlights

  • Short or long sleep duration is proposed as a potential risk factor for all-cause mortality in the older people, yet the results of published studies are not often reproducible

  • In 2016, da Silva and colleagues conducted a meta-analysis by pooling the results of 27 cohort studies, and they found a significant association of both long and short sleep duration with increased allcause mortality risk in the older people, and the association was more evident for long sleep duration [18]

  • The association of long sleep duration with all-cause mortality was statistically significant in both women (HR = 1.48; 95% confidence interval (CI): 1.18–1.86; P = .001) and men (HR = 1.31; 95% CI: 1.10–1.58; P = .003) (Two-sample Z test P = .205)

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Summary

Introduction

Short or long sleep duration is proposed as a potential risk factor for all-cause mortality in the older people, yet the results of published studies are not often reproducible. The results of other studies have failed to provide any supportive data on sleep duration and mortality in the older people [19,20,21]. The reasons for these inconsistent reports are multifactorial, possibly relating to inadequate statistical power of individual studies, different backgrounds and characteristics of study groups, and lack of adjustment for confounding factors. Given the accumulating data afterwards, there is a need to reexamine this association in a more comprehensive manner

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