阻塞性睡眠呼吸暂停介导西班牙裔和拉丁裔社区糖尿病的遗传风险。

IF 5.4 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Yana Hrytsenko, Brian W Spitzer, Heming Wang, Suzanne M Bertisch, Kent D Taylor, Olga Garcia-Bedoya, Alberto R Ramos, Martha L Daviglus, Linda C Gallo, Carmen R Isasi, Jianwen Cai, Qibin Qi, Carmela Alcántara, Susan Redline, Tamar Sofer
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引用次数: 0

摘要

背景:阻塞性睡眠呼吸暂停(OSA)和其他睡眠障碍与患糖尿病(DM)的风险增加有关。我们研究了睡眠障碍是否会影响西班牙裔/拉丁裔个体患糖尿病的遗传风险。方法:我们开发了适用于西班牙裔/拉丁裔混合人群的2型糖尿病(T2D)多基因风险评分(T2D- prs)。我们在西班牙裔社区健康研究/拉丁裔研究(18-76岁,50.9%为女性)中估计了T2D-PRS与横断面DM (n = 12,342)和事件DM (n = 6965)的关联。我们进行了一项中介分析,其中T2D-PRS作为暴露,事件DM作为结果,OSA作为中介。此外,我们还进行了孟德尔随机化(MR)分析,以评估T2D和OSA之间的因果关系。结果:在这里,我们发现T2D-PRS每增加1个标准差,DM校正优势比(OR) = 2.67, 95% CI [2.40;2.97]和较高的DM发生率(事故率比(IRR) = 2.02, 95% CI [1.75;2.33])。在一项基于OSA严重程度分类的分层分析中,与中度至重度OSA患者相比,轻度OSA患者的相关性更强。中介分析表明,OSA介导了T2D- prs与DM的关联。在双样本MR分析中,T2D对OSA有因果影响,OR = 1.03, 95% CI [1.01;1.05], OSA与T2D有因果关系,OR = 2.34, 95% CI [1.59;3.44]。结论:这些结果支持OSA与DM之间的因果关系,其中OSA介导高达4.7%的DM遗传风险。OSA治疗可降低DM患病率。
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 in Hispanic and Latino communities.

Background: Obstructive sleep apnea (OSA), and other sleep disorders, are associated with increased risk of developing diabetes mellitus (DM). We examined whether sleep disorders influence the genetic risk of developing diabetes in Hispanic/Latino individuals.

Methods: We developed Type 2 Diabetes (T2D) polygenic risk score (T2D-PRS) useful in admixed Hispanic/Latino individuals. We estimated the association of the T2D-PRS with cross-sectional (n = 12,342) and incident (n = 6965) DM in the Hispanic Community Health Study/Study of Latinos (ages 18-76, 50.9% female). We conducted a mediation analysis with T2D-PRS 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: Here, we show that a 1 standard deviation increase in T2D-PRS has 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 are stronger in individuals with mild OSA compared to those with moderate to severe OSA. Mediation analysis suggests that OSA mediates the T2D-PRS association with DM. In two-sample MR analysis, T2D has a causal effect on OSA, OR = 1.03, 95% CI [1.01; 1.05], and OSA has a causal effect on T2D, with OR = 2.34, 95% CI [1.59; 3.44].

Conclusions: These results support a causal association between OSA and DM, with OSA mediating up to 4.7% of the genetic risk for DM. OSA treatment may reduce DM prevalence.

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