阻塞性睡眠呼吸暂停介导糖尿病遗传风险:西班牙裔社区健康研究/拉丁裔研究

Yana Hrytsenko, Brian W. Spitzer, Heming Wang, Suzanne M. Bertisch, Kent Taylor, Olga Garcia-Bedoya, Alberto R. Ramos, Martha L. Daviglus, Linda C. Gallo, Carmen R. Isasi, Jianwen Cai, Qibin Qi, Carmela Alcantara, Susan Redline, Tamar Sofer
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引用次数: 0

摘要

研究目的我们试图评估阻塞性睡眠呼吸暂停(OSA)和其他睡眠障碍是否会增加糖尿病(DM)的遗传风险。研究设计与方法:利用 DIAGRAM 联盟和 "百万退伍军人计划"(Million Veteran Program)的 GWAS 统计摘要,我们开发出了适用于西班牙裔/拉美裔混血个体的多种族 2 型糖尿病(T2D)多基因风险评分(T2D-PRS)。我们估算了西班牙裔社区健康研究/拉美裔研究(HCHS/SOL)中 T2D-PRS 与横断面糖尿病和偶发性糖尿病的关系。我们进行了一项中介分析,将 T2D-PRS 作为暴露因子,将糖尿病事件作为结果,将 OSA 作为中介因子。此外,我们还进行了孟德尔随机化(MR)分析,以评估 T2D 与 OSA 之间的因果关系。结果:在 12342 名 HCHS/SOL 参与者中,基线血糖正常者占 48.4%,血糖过高者占 36.6%,糖尿病患者占 15%,女性占 50.9%。平均年龄为 41.5 岁,平均体重指数为 29.4。T2D-PRSs 与糖尿病基线和糖尿病事件密切相关。在基线时,主要 T2D-PRS 每增加 1 SD,DM 调整赔率 (OR) = 2.67,95% CI [2.40; 2.97],DM 发生率更高(发生率比 (IRR) = 2.02,95% CI [1.75; 2.33])。在基于OSA严重程度的分层分析中,轻度OSA患者与中重度OSA患者的相关性更强。中介分析表明,OSA 是 T2D-PRS 与 DM 关联的中介。在双样本 MR 分析中,T2D-PRS 对 OSA 有因果效应,OR = 1.03,95% CI [1.01; 1.05];OSA 对 T2D 有因果效应,OR = 2.34,95% CI [1.59; 3.44]。结论是OSA可能介导了T2D的遗传效应。关键词糖尿病;2型糖尿病;阻塞性睡眠呼吸暂停;多基因风险评分;西班牙裔或拉丁裔
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Obstructive sleep apnea mediates genetic risk of Diabetes Mellitus: The Hispanic Community Health Study/Study of Latinos
Objective: We sought to evaluate whether obstructive sleep apnea (OSA), and other sleep disorders, increase genetic risk of developing diabetes mellitus (DM). Research Design and Methods: Using GWAS summary statistics from the DIAGRAM consortium and Million Veteran Program, we developed multi-ancestry Type 2 Diabetes (T2D) polygenic risk scores (T2D-PRSs) useful in admixed Hispanic/Latino individuals. We estimated the association of the T2D-PRS with cross-sectional and incident DM in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL). We conducted a mediation analysis with T2D-PRSs as an exposure, incident DM as an outcome, and OSA as a mediator. Additionally, we performed Mendelian randomization (MR) analysis to assess the causal relationship between T2D and OSA. Results: Of 12,342 HCHS/SOL participants, at baseline, 48.4% were normoglycemic, 36.6% were hyperglycemic, and 15% had diabetes, and 50.9% identified as female. Mean age was 41.5, and mean BMI was 29.4. T2D-PRSs was strongly associated with baseline DM and with incident DM. At baseline, a 1 SD increase in the primary T2D-PRS had DM adjusted odds ratio (OR) = 2.67, 95% CI [2.40; 2.97] and a higher incident DM rate (incident rate ratio (IRR) = 2.02, 95% CI [1.75; 2.33]). In a stratified analysis based on OSA severity categories the associations were stronger in individuals with mild OSA compared to those with moderate to severe OSA. Mediation analysis suggested that OSA mediates the T2D-PRS association with DM. In two-sample MR analysis, T2D-PRS had a causal effect on OSA, OR = 1.03, 95% CI [1.01; 1.05], and OSA had a causal effect on T2D, with OR = 2.34, 95% CI [1.59; 3.44]. Conclusions: OSA likely mediates genetic effects on T2D. Keywords: Diabetes; Type 2 diabetes; Obstructive sleep apnea; Polygenic risk score; Hispanic or Latino
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