Association Between High-Sensitivity C-Reactive Protein and Metabolic Syndrome Among Hispanic/Latino Participants of the Hispanic Community Health Study/Study of Latinos.

IF 1.3 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Metabolic syndrome and related disorders Pub Date : 2024-06-01 Epub Date: 2024-04-02 DOI:10.1089/met.2023.0298
Robert A Mesa, Oriana M Damas, Neil Schneiderman, Ana M Palacio, Linda C Gallo, Gregory A Talavera, Daniela Sotres-Alvarez, Martha L Daviglus, Amber Pirzada, Maria M Llabre, Tali Elfassy
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引用次数: 0

Abstract

Purpose: To determine whether high-sensitivity C-reactive protein (hsCRP) is associated with incident Metabolic Syndrome (MetS) among U.S. Hispanic/Latino adults. Patients and Methods: The Hispanic Community Health Study/Study of Latinos is a longitudinal observational cohort assessing cardiovascular health among diverse U.S. Hispanic/Latino adults. hsCRP was measured at visit 1 (2008-2011) and classified as low, moderate, or high, based on the Centers for Disease Control and Prevention and American Heart Association (CDC/AHA) guidelines. All MetS components [abdominal obesity, triglycerides, high-density lipoprotein (HDL) cholesterol, blood pressure, and fasting glucose] were measured at visit 1 and visit 2 (2014-2017). MetS was defined as the presence of three or more components based on the 2005 definition from the modified Third Report of the National Cholesterol Education Program Adult Treatment Panel (modified NCEP ATP III). Participants free of MetS at visit 1 and with complete data on hsCRP and all MetS components were included (n = 6121 participants). We used Poisson regression analysis to determine whether hsCRP was associated with incident MetS after adjusting for demographic, behavioral, and clinical factors. All analyses accounted for the complex survey design of the study. Results: In fully adjusted models, moderate versus low hsCRP was associated with a 33% increased risk of MetS [incidence rate ratio (IRR): 1.33, 95% confidence interval (CI): 1.10-1.61], while high versus low hsCRP was associated with a 89% increased risk of MetS (IRR: 1.89, 95% CI: 1.58-2.25). Conclusions: Greater levels of hsCRP were associated with new onset of MetS in a diverse sample of U.S. Hispanic/Latino adults. Results suggest that hsCRP may be an independent risk factor for MetS.

西班牙裔社区健康研究/拉美裔研究中西班牙裔/拉美裔参与者的高敏 C 反应蛋白与代谢综合征之间的关系。
目的:确定高敏 C 反应蛋白 (hsCRP) 是否与美国拉美裔成人代谢综合征 (MetS) 的发病有关。患者和方法:西班牙裔社区健康研究/拉美裔研究是一项纵向观察性队列研究,旨在评估美国不同的西班牙裔/拉美裔成年人的心血管健康状况。根据美国疾病控制与预防中心和美国心脏协会(CDC/AHA)的指南,在第 1 次就诊(2008-2011 年)时测量 hsCRP,并将其分为低、中、高三个等级。所有 MetS 成分[腹部肥胖、甘油三酯、高密度脂蛋白 (HDL) 胆固醇、血压和空腹血糖]均在 1 次就诊和 2 次就诊(2014-2017 年)时进行测量。根据 2005 年美国国家胆固醇教育计划成人治疗小组第三次报告(修订版 NCEP ATP III)中的定义,MetS 被定义为存在三个或三个以上的成分。我们纳入了第 1 次就诊时未患有 MetS 且 hsCRP 和所有 MetS 成分数据完整的参与者(n = 6121 人)。在对人口、行为和临床因素进行调整后,我们使用泊松回归分析来确定 hsCRP 是否与 MetS 事件相关。所有分析都考虑到了该研究的复杂调查设计。结果显示在完全调整模型中,中度 hsCRP 与低 hsCRP 相比,MetS 风险增加了 33%[发病率比 (IRR):1.33,95% 置信区间 (CI):1.10-1.61],而高 hsCRP 与低 hsCRP 相比,MetS 风险增加了 89%(IRR:1.89,95% 置信区间 (CI):1.58-2.25)。结论在美国西班牙裔/拉美裔成年人的不同样本中,hsCRP 水平升高与新发 MetS 相关。结果表明,hsCRP 可能是 MetS 的一个独立风险因素。
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来源期刊
Metabolic syndrome and related disorders
Metabolic syndrome and related disorders MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
3.40
自引率
0.00%
发文量
74
审稿时长
6-12 weeks
期刊介绍: Metabolic Syndrome and Related Disorders is the only peer-reviewed journal focusing solely on the pathophysiology, recognition, and treatment of this major health condition. The Journal meets the imperative for comprehensive research, data, and commentary on metabolic disorder as a suspected precursor to a wide range of diseases, including type 2 diabetes, cardiovascular disease, stroke, cancer, polycystic ovary syndrome, gout, and asthma. Metabolic Syndrome and Related Disorders coverage includes: -Insulin resistance- Central obesity- Glucose intolerance- Dyslipidemia with elevated triglycerides- Low HDL-cholesterol- Microalbuminuria- Predominance of small dense LDL-cholesterol particles- Hypertension- Endothelial dysfunction- Oxidative stress- Inflammation- Related disorders of polycystic ovarian syndrome, fatty liver disease (NASH), and gout
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