4.7 Article

Sleep patterns, genetic susceptibility, and incident cardiovascular disease: a prospective study of 385 292 UK biobank participants

Journal

EUROPEAN HEART JOURNAL
Volume 41, Issue 11, Pages 1182-+

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/eurheartj/ehz849

Keywords

Cardiovascular disease; Sleep behaviour; Genetic predisposition to disease

Funding

  1. National Heart, Lung, and Blood Institute [HL071981, HL034594, HL126024]
  2. National Institute of Diabetes and Digestive and Kidney Diseases [DK115679, DK091718, DK100383, DK078616]
  3. American Heart Association Scientist Development Award [0730094N]
  4. NIGMS [P20GM109036]
  5. China Scholarship Council [201706010313]
  6. National Key R&D Program of China [2016YFC0900500, 2016YFC0900501, 2016YFC0900504]
  7. MRC [MC_PC_12028] Funding Source: UKRI

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Aim To quantify the association of combined sleep behaviours and genetic susceptibility with the incidence of cardiovascular disease (CVD). Methods and results This study included 385 292 participants initially free of CVD from UK Biobank. We newly created a healthy sleep score according to five sleep factors and defined the low-risk groups as follows: early chronotype, sleep 7-8 h per day, never/rarely insomnia, no snoring, and no frequent excessive daytime sleepiness. Weighted genetic risk scores of coronary heart disease (CHD) or stroke were calculated. During a median of 8.5 years of follow-up, we documented 7280 incident CVD cases including 4667 CHD and 2650 stroke cases. Compared to those with a sleep score of 0-1, participants with a score of 5 had a 35% (19-48%), 34% (22-44%), and 34% (25-42%) reduced risk of CVD, CHD, and stroke, respectively. Nearly 10% of cardiovascular events in this cohort could be attributed to poor sleep pattern. Participants with poor steep pattern and high genetic risk showed the highest risk of CHD and stroke. Conclusion this large prospective study, a healthy sleep pattern was associated with reduced risks of CVD, CHD, and stroke among participants with low, intermediate, or high genetic risk.

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