性会调节有和没有艾滋病毒的老年乌干达成年人中炎症与冠状动脉粥样硬化之间的关联。
Sex modulates the association between inflammation and coronary atherosclerosis among older Ugandan adults with and without HIV.
机构信息
Department of Medicine, Division of Cardiology, and.
Department of Global Health, University of Washington, Seattle, Washington, USA.
出版信息
AIDS. 2023 Mar 15;37(4):579-586. doi: 10.1097/QAD.0000000000003451. Epub 2022 Nov 29.
OBJECTIVE
Inflammation is key in the pathogenesis of atherosclerotic coronary artery disease (CAD). Distinct sex-specific inflammatory mechanisms may contribute to CAD in sub-Saharan Africa (SSA), where environmental and biological determinants of systemic inflammation may differ from those in high-income settings.
APPROACH AND RESULTS
We investigated sex differences in inflammatory markers and CAD in a 2-year prospective cohort of Ugandan adults enriched for cardiometabolic risk factors (RFs) and HIV. Seven plasma biomarkers were quantified at the baseline visit among 125 females and 75 males (50% with HIV) at least 45 years old at enrollment with one or more major cardiovascular RF. In year 2, coronary CT angiography (CCTA) was performed in 82 females and 50 males returning for follow-up (52% with HIV). In sex-specific models adjusted for cardiovascular RFs and HIV, tumor necrosis factor-alpha (TNF-α) RII and sCD163 predicted subsequent CAD in females, while only fibrinogen was predictive in males ( P < 0.05). Interleukin-6 (IL-6) and sCD14 were inversely associated with CAD in males ( P < 0.05). Sex modified the associations of TNF-α RII, sCD14, and sCD163 with CAD ( P < 0.05 for interaction). In multivariable multiple imputation models applied to missing year 2 CCTA data to test associations between serum biomarkers in the baseline cohort ( n = 200) and subsequent CAD, higher sCD163 was predictive in females only ( P < 0.05).
CONCLUSIONS
The positive link between inflammation and subclinical CAD was stronger among females than males in Uganda. Mechanisms by which sex modulates the relationship between inflammation and CAD should be further investigated in SSA.
目的
炎症是动脉粥样硬化性冠心病(CAD)发病机制中的关键因素。在撒哈拉以南非洲(SSA),特定于性别的炎症机制可能导致 CAD,其中系统性炎症的环境和生物学决定因素可能与高收入环境中的决定因素不同。
方法和结果
我们在乌干达成年人中进行了一项为期 2 年的前瞻性队列研究,该队列研究针对心血管代谢危险因素(RFs)和 HIV 进行了富集,研究了炎症标志物和 CAD 中的性别差异。在至少 45 岁的人群中,有 125 名女性和 75 名男性(50%携带 HIV)患有一个或多个主要心血管 RF,在基线时检测了 7 种血浆生物标志物。在第二年,有 82 名女性和 50 名男性(52%携带 HIV)返回进行随访,进行了冠状动脉 CT 血管造影(CCTA)。在按心血管 RF 和 HIV 调整的性别特异性模型中,肿瘤坏死因子-α(TNF-α)RII 和 sCD163 预测了女性的后续 CAD,而仅纤维蛋白原在男性中具有预测性(P<0.05)。白细胞介素-6(IL-6)和 sCD14 与男性的 CAD 呈负相关(P<0.05)。性别改变了 TNF-αRII、sCD14 和 sCD163 与 CAD 的关联(P<0.05 用于交互作用)。在多元缺失数据多重插补模型中,应用于缺失的第二年 CCTA 数据,以测试基线队列(n=200)中血清生物标志物与随后 CAD 之间的关联,仅在女性中 sCD163 升高具有预测性(P<0.05)。
结论
在乌干达,炎症与亚临床 CAD 之间的正相关关系在女性中比男性更强。SSA 中应进一步研究性别调节炎症与 CAD 之间关系的机制。
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