← 返回

Genetic ancestry and risk of atrial fibrillation in individuals of Black ethnicity in the UK Biobank.

Genetic ancestry and risk of atrial fibrillation in individuals of Black ethnicity in the UK Biobank.

期刊: Open heart 日期: 2026-07-31 PMID: 42538060 DOI: 10.1136/openhrt-2026-004206 浏览: 19
作者: Liu C, Sun YV, Li L, Collin LJ, Shah AJ, Alonso A
C, L., YV, S., L, L., LJ, C., AJ, S., & A, A. (2026). Genetic ancestry and risk of atrial fibrillation in individuals of Black ethnicity in the UK Biobank.. Open heart. https://doi.org/10.1136/openhrt-2026-004206
C L, YV S, L L, LJ C, AJ S, A A. Genetic ancestry and risk of atrial fibrillation in individuals of Black ethnicity in the UK Biobank.. Open heart. 2026; doi: 10.1136/openhrt-2026-004206
C L, YV S, L L, et al. Genetic ancestry and risk of atrial fibrillation in individuals of Black ethnicity in the UK Biobank.[J]. Open heart. 2026. DOI: 10.1136/openhrt-2026-004206.
@article{c2026,
  author = {Liu C and Sun YV and Li L and Collin LJ and Shah AJ and Alonso A},
  title = {Genetic ancestry and risk of atrial fibrillation in individuals of Black ethnicity in the UK Biobank.},
  journal = {Open heart},
  year = {2026},
  doi = {10.1136/openhrt-2026-004206},
  note = {PMID: 42538060},
}
TY  - JOUR
AU  - Liu C
AU  - Sun YV
AU  - Li L
AU  - Collin LJ
AU  - Shah AJ
AU  - Alonso A
TI  - Genetic ancestry and risk of atrial fibrillation in individuals of Black ethnicity in the UK Biobank.
T2  - Open heart
PY  - 2026
DO  - 10.1136/openhrt-2026-004206
AN  - PMID:42538060
ER  - 

摘要

BACKGROUND: Black individuals have a lower incidence of atrial fibrillation (AF) than White individuals, despite a higher burden of traditional risk factors. Prior studies have suggested that European genetic ancestry may contribute to this paradox, but findings have been inconsistent. METHODS: We examined the association between European genetic ancestry and incident AF among 6920 UK Biobank (UKB) participants who self-identified as Black and were free of AF at baseline. European ancestry proportions were estimated by comparing participants to HapMap populations and were analysed both continuously and categorically using Cox proportional hazards models. Non-linear associations were evaluated using flexible spline curves. We then conducted a meta-analysis combining these results with those from the Atherosclerosis Risk in Communities Study, the Cardiovascular Health Study and the Women's Health Initiative. RESULTS: During a median follow-up of 13.7 years, 205 (3%) participants developed incident AF. Each 10% increase in European ancestry was non-significantly associated with increased AF risk (HR 1.07 (95% CI 0.95 to 1.20)), and individuals in the highest European ancestry category had a higher AF incidence rate compared with all other categories. Random-effects meta-analysis of all four cohorts yielded a pooled relative risk (RR) of 1.09 (95% CI 0.99 to 1.21), with substantial heterogeneity largely driven by the Women's Health Initiative (WHI) study. Excluding WHI resulted in a pooled estimate (RR 1.14 (95% CI 1.05 to 1.23)) without heterogeneity. CONCLUSION: In UKB, European ancestry proportion was not significantly linked to incident AF, and pooled cross-cohort results were heterogeneous. Excluding WHI in sensitivity analyses produced a modest positive pooled association with no heterogeneity.

AI 智能解读

相关文献

返回分类: 心律失常 查看原文 (DOI)
已选择 0 篇文献