美国育龄妇女多囊卵巢综合征特征与代谢综合征的关系

IF 1.6 Q3 OBSTETRICS & GYNECOLOGY
Women's health reports (New Rochelle, N.Y.) Pub Date : 2025-04-14 eCollection Date: 2025-01-01 DOI:10.1089/whr.2024.0143
Deepali K Ernest, Asha Collier, Aparajita Chandrasekhar, Luyu Xie, Shaghayegh Darraji, Jenil Patel, Jaime P Almandoz, Sarah E Messiah
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引用次数: 0

摘要

背景:多囊卵巢综合征(PCOS)与全球不同种族和民族女性的代谢健康相关,但在美国女性中,关于PCOS与代谢综合征(MetS)之间关系的研究有限。目的:研究美国不同种族/民族的育龄妇女多囊卵巢综合征(PCOS)特征与肿瘤转移的关系。方法:对2011-2016年全国健康与营养检查调查中2172名女性(12-49岁)的横断面数据进行分析。单变量logistic回归模型确定了未调整的MetS及其组成部分(中枢性肥胖、血糖、血压和甘油三酯升高以及低高密度脂蛋白胆固醇)与PCOS特征(对数转换总睾酮(LTT)、性激素结合球蛋白(LSHBG)、闭经和口服避孕药(OCP)的使用)之间的关联。多变量逻辑模型检验了按种族和民族分层的年龄调整关联。结果:分析样本(平均年龄为30.3岁,59%非西班牙裔白人,12.4%非西班牙裔黑人,18.7%西班牙裔/拉丁裔,6.2%非西班牙裔亚洲人,3.7%其他/多种族)的met患病率为14.5%。总体而言,MetS与年龄、体重指数、种族/民族、LTT和LSHBG浓度、闭经和OCP使用有关(所有p < 0.01),并且许多PCOS特征对个体MetS成分具有保护作用。随着LSHBG的增加,大多数种族/民族的MetS几率显著降低,但对个体MetS特征的影响不同。结论:研究结果表明,在美国不同种族和民族的育龄妇女中,PCOS特征与MetS之间存在显著关联。需要更多强有力的纵向研究来进一步了解PCOS和MetS之间的潜在机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of Polycystic Ovarian Syndrome Features and Metabolic Syndrome Among Reproductive-Aged Women in the United States.

Background: Polycystic ovarian syndrome (PCOS) is associated with the metabolic health of racially and ethnically diverse women globally, but limited research exists on the association of PCOS and metabolic syndrome (MetS) among women in the United States.

Objective: To examine the association of PCOS features and MetS in a racially/ethnically diverse population of reproductive-aged women in the United States.

Methods: Cross-sectional data from 2,172 women (12-49 years) from the 2011-2016 National Health and Nutrition Examination Survey were analyzed. Univariate logistic regression models determined unadjusted associations of MetS and its components (elevated central obesity, glucose, blood pressure and triglyceride, and low high-density lipoprotein cholesterol) with PCOS features (log-transformed total testosterone (LTT), sex-hormone binding globulin (LSHBG), amenorrhea, and oral contraceptive pills (OCP) use). Multivariable logistic models examined age-adjusted associations stratified by race and ethnicity.

Results: The analytical sample (mean age = 30.3 years, 59% non-Hispanic White, 12.4% non-Hispanic Black, 18.7% Hispanic/Latina, 6.2% non-Hispanic Asian, 3.7% Other/multi-race) had a MetS prevalence of 14.5%. Overall, MetS was associated with age, body mass index, race/ethnicity, LTT and LSHBG concentrations, amenorrhea, and OCP use (p < 0.01 for all), and many of the PCOS features were protective against individual MetS components. Most race/ethnicities showed significantly lower odds of MetS with an increase in LSHBG, with varying impacts on individual MetS features.

Conclusions: Findings suggest significant associations between PCOS features and MetS among a racially and ethnically diverse population of reproductive-aged women in the United States. More robust and longitudinal studies are needed to further understand the underlying mechanism linking PCOS and MetS.

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CiteScore
1.30
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