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赞比亚接受抗逆转录病毒治疗的艾滋病毒感染者中的代谢综合征:患病率及相关因素。

Metabolic syndrome in Zambian adults with human immunodeficiency virus on antiretroviral therapy: Prevalence and associated factors.

机构信息

University of Zambia School of Public Health.

Mulungushi University School of Medicine and Health Sciences, Livingstone.

出版信息

Medicine (Baltimore). 2021 Apr 9;100(14):e25236. doi: 10.1097/MD.0000000000025236.

DOI:10.1097/MD.0000000000025236
PMID:33832083
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8036111/
Abstract

Metabolic syndrome (MetS) is a constellation of factors including hypertension, abdominal obesity, dyslipidemia, and insulin resistance that separately and together significantly increase risk for cardiovascular disease (CVD) and diabetes. In sub-Saharan Africa, with a substantial burden of human immunodeficiency virus (HIV) and increasing prevalence of CVD and diabetes, there is a paucity of epidemiological data on demographic, laboratory, and clinical characteristics associated with MetS among people with HIV (people with human [PWH]). Therefore, this study aimed to determine the burden and factors influencing MetS in antiretroviral therapy (ART)-experienced individuals in Zambia.We collected cross-sectional demographic, lifestyle, anthropometric, clinical, and laboratory data in a cohort of ART-experienced (on ART for ≥6 months) adults in 24 urban HIV treatment clinics of Zambia between August, 2016 and May, 2020. MetS was defined as having ≥3 of the following characteristics: low high density lipoprotein cholesterol (HDL-c) (<1.0 mmol/L for men, <1.3 for women), elevated waist circumference (≥94 cm for men, ≥80 cm for women), elevated triglycerides (≥1.7 mmol/L), elevated fasting blood glucose (≥5.6 mmol/L), and elevated blood pressure (BP) (systolic BP ≥130 or diastolic BP ≥85 mm Hg). Virological failure (VF) was defined as HIV viral load ≥1000 copies/mL. The following statistical methods were used: Chi-square test, Wilcoxon rank-sum test, and multivariable logistic regression.Among 1108 participants, the median age (interquartile range [IQR]) was 41 years (34, 49); 666 (60.1%) were females. The prevalence of MetS was 26.3% (95% confidence interval [CI] 23.9-29.1). Age (adjusted odds ratio [OR] 1.07; 95% CI 1.04-1.11), female sex (OR 3.02; 95% CI 1.55-5.91), VF (OR 1.98; 95% CI 1.01-3.87), dolutegravir (DTG)-based regimen (OR 2.10; 95% CI 1.05-4.20), hip-circumference (OR 1.03; 95% CI 1.01-1.05), T-lymphocyte count (OR 2.23; 95% CI 1.44-3.43), high-sensitivity C-reactive protein (hsCRP) (OR 1.14; 95% CI 1.01-1.29), and fasting insulin (OR 1.02; 95% CI 1.01-1.04) were significantly associated with MetS.Metabolic syndrome was highly prevalent among HIV+ adults receiving ART in Zambia and associated with demographic, clinical, anthropometric, and inflammatory characteristics. The association between MetS and dolutegravir requires further investigation, as does elucidation of the impact of MetS on ART outcomes in sub-Saharan African PWH.

摘要

代谢综合征(MetS)是一组因素的集合,包括高血压、腹部肥胖、血脂异常和胰岛素抵抗,这些因素单独或共同显著增加了心血管疾病(CVD)和糖尿病的风险。在撒哈拉以南非洲,艾滋病毒(HIV)负担沉重,心血管疾病和糖尿病的患病率不断上升,但有关 HIV 感染者(PWH)中与 MetS 相关的人口统计学、实验室和临床特征的流行病学数据很少。因此,本研究旨在确定赞比亚接受抗逆转录病毒治疗(ART)的个体中 MetS 的负担和影响因素。

我们在赞比亚 24 个城市 HIV 治疗诊所的接受 ART 治疗(≥6 个月)的成年人队列中收集了横断面的人口统计学、生活方式、人体测量、临床和实验室数据,从 2016 年 8 月至 2020 年 5 月。代谢综合征定义为具有以下 3 种或 3 种以上特征:低高密度脂蛋白胆固醇(男性<1.0mmol/L,女性<1.3mmol/L)、腰围升高(男性≥94cm,女性≥80cm)、甘油三酯升高(≥1.7mmol/L)、空腹血糖升高(≥5.6mmol/L)和血压升高(收缩压≥130mmHg 或舒张压≥85mmHg)。病毒学失败(VF)定义为 HIV 病毒载量≥1000copies/ml。采用卡方检验、Wilcoxon 秩和检验和多变量逻辑回归进行统计分析。

在 1108 名参与者中,中位年龄(四分位间距 [IQR])为 41 岁(34,49);666 名(60.1%)为女性。代谢综合征的患病率为 26.3%(95%置信区间 [CI] 23.9-29.1)。年龄(调整后的优势比 [OR] 1.07;95%CI 1.04-1.11)、女性(OR 3.02;95%CI 1.55-5.91)、VF(OR 1.98;95%CI 1.01-3.87)、多替拉韦(DTG)为基础的方案(OR 2.10;95%CI 1.05-4.20)、臀围(OR 1.03;95%CI 1.01-1.05)、T 淋巴细胞计数(OR 2.23;95%CI 1.44-3.43)、高敏 C 反应蛋白(hsCRP)(OR 1.14;95%CI 1.01-1.29)和空腹胰岛素(OR 1.02;95%CI 1.01-1.04)与 MetS 显著相关。

在赞比亚接受 ART 的 HIV 阳性成年人中,代谢综合征的患病率很高,与人口统计学、临床、人体测量和炎症特征有关。代谢综合征与多替拉韦的相关性需要进一步研究,阐明代谢综合征对撒哈拉以南非洲 HIV 感染者 ART 结局的影响也需要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4a4/8036111/11deb2a12793/medi-100-e25236-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4a4/8036111/11deb2a12793/medi-100-e25236-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4a4/8036111/11deb2a12793/medi-100-e25236-g001.jpg

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