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Sleep Disorder Phenotypes and the Risk of Incident Heart Failure: A meta-analysis with Mendelian randomization validation.

Sleep Disorder Phenotypes and the Risk of Incident Heart Failure: A meta-analysis with Mendelian randomization validation.

期刊: Saudi medical journal 日期: 2026-03-01 PMID: 42238282 DOI: 10.15537/1658-3175.1035 浏览: 48
作者: Yan F, Fan L, Chen Y
F, Y., L, F., & Y, C. (2026). Sleep Disorder Phenotypes and the Risk of Incident Heart Failure: A meta-analysis with Mendelian randomization validation.. Saudi medical journal. https://doi.org/10.15537/1658-3175.1035
F Y, L F, Y C. Sleep Disorder Phenotypes and the Risk of Incident Heart Failure: A meta-analysis with Mendelian randomization validation.. Saudi medical journal. 2026; doi: 10.15537/1658-3175.1035
F Y, L F, Y C. Sleep Disorder Phenotypes and the Risk of Incident Heart Failure: A meta-analysis with Mendelian randomization validation.[J]. Saudi medical journal. 2026. DOI: 10.15537/1658-3175.1035.
@article{f2026,
  author = {Yan F and Fan L and Chen Y},
  title = {Sleep Disorder Phenotypes and the Risk of Incident Heart Failure: A meta-analysis with Mendelian randomization validation.},
  journal = {Saudi medical journal},
  year = {2026},
  doi = {10.15537/1658-3175.1035},
  note = {PMID: 42238282},
}
TY  - JOUR
AU  - Yan F
AU  - Fan L
AU  - Chen Y
TI  - Sleep Disorder Phenotypes and the Risk of Incident Heart Failure: A meta-analysis with Mendelian randomization validation.
T2  - Saudi medical journal
PY  - 2026
DO  - 10.15537/1658-3175.1035
AN  - PMID:42238282
ER  - 

摘要

OBJECTIVES: To quantify how specific sleep-disorder phenotypes are related to incident heart failure (HF) using a meta-analysis of cohort data and to probe causal relevance via 2-sample Mendelian randomization (MR). METHODS: Fourteen cohorts comprised of participants without HF at baseline were pooled (49,501 exposed; 337,317 controls). A random effects meta-analysis produced pooled hazard ratios (HRs) with 95% confidence intervals (CIs). A bidirectional two-sample MR was used to evaluate the causal effects of sleep phenotypes on HF. RESULTS: Overall, sleep disorders were linked to a higher incidence of HF (pooled HR 1.46; 95% CI 1.30-1.63; p<0.001). In terms of phenotype, obstructive sleep apnea (OSA) was significantly associated (pooled HR 1.39; 95% CI 1.18-1.64; p < 0.001), whereas insomnia was not independently associated with HF (pooled HR 1.11; 95% CI 0.75-1.62; p = 0.609). The MR analyses supported a causal effect of OSA on HF (inverse-variance weighted odds ratio 1.12; 95% CI 1.03-1.23; p = 0.007) and revealed no causal evidence for insomnia. CONCLUSIONS: Sleep disorders are associated with increased HF risk, which varies by phenotype. Convergent observational and genetic evidence implicates OSA in increased HF risk, whereas insomnia shows no independent or causal association. These findings prioritize OSA screening and targeted prevention in HF risk mitigation.

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