Association between sleep deficiency and cardiometabolic disease: implications for health disparities

Vittobai Rashika Rangaraj1, Kristen L Knutson1

  • 1Department of Medicine, University of Chicago, Chicago, IL, USA.

Sleep Medicine
|October 4, 2015
PubMed

Insights

Suboptimal sleep is linked to increased cardiometabolic disease risk. This review explores how poor sleep duration and quality may contribute to disparities in conditions like obesity and diabetes.

Area of Science:

  • Sleep science
  • Cardiometabolic health
  • Health disparities

Background:

  • Cardiometabolic diseases (obesity, diabetes, hypertension, cardiovascular disease) reduce quality and expectancy of life.
  • Minority populations and lower socioeconomic groups bear a disproportionate burden of cardiometabolic diseases.
  • Disparities in sleep duration and quality mirror those observed in cardiometabolic disease prevalence.

Purpose of the Study:

  • To review the association between sleep and cardiometabolic disease risk.
  • To investigate the potential role of suboptimal sleep in mediating cardiometabolic disease disparities.

Main Methods:

  • Reviewed experimental studies on sleep restriction/impairment and cardiometabolic biomarkers (glucose metabolism, insulin sensitivity, appetite regulation, immune function).
  • Reviewed observational studies on habitual sleep duration/quality and cardiometabolic disease prevalence/risk (obesity, diabetes, hypertension, cardiovascular disease).

Main Results:

  • Experimental studies demonstrate that restricted sleep duration and impaired sleep quality negatively impact biomarkers of cardiometabolic risk.
  • Observational studies consistently show an association between poor sleep and increased prevalence or risk of obesity, diabetes, hypertension, and cardiovascular disease.

Conclusions:

  • Suboptimal sleep, including insufficient duration and poor quality, is significantly associated with increased cardiometabolic disease risk.
  • Evidence supports the hypothesis that poor sleep may partially explain disparities in cardiometabolic disease burden among different populations.
Abstract

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