Polycystic Ovary Syndrome, Metabolic Syndrome, and Inflammation in the Hispanic Community Health Study/Study of Latinos

Author:

Rao Hridya C1ORCID,Meyer Michelle L2,Kominiarek Michelle A3,Daviglus Martha L4,Gallo Linda C5,Cordero Christina6ORCID,Syan Raveen7,Perreira Krista M8,Talavera Gregory A5,Fernández-Rhodes Lindsay1

Affiliation:

1. Department of Biobehavioral Health, The Pennsylvania State University , University Park, PA 16802 , USA

2. Department of Emergency Medicine, University of North Carolina at Chapel Hill , Chapel Hill, NC 27599 , USA

3. Department of Obstetrics and Gynecology, Northwestern University , Chicago, IL 60611 , USA

4. Institute of Minority Health Research, University of Illinois , Chicago, IL 60612 , USA

5. Department of Psychology, San Diego State University , San Diego, CA 92182 , USA

6. Department of Psychology, University of Miami , Miami, FL 33124 , USA

7. Department of Urology, University of Miami , Miami, FL 33136 , USA

8. Department of Social Medicine, HCHS/SOL Coordinating Center, University of North Carolina at Chapel Hill , Chapel Hill, NC 27599 , USA

Abstract

Abstract Context Polycystic ovary syndrome (PCOS) is a multifaceted endocrine disorder with reproductive and metabolic dysregulation. PCOS has been associated with inflammation and metabolic syndrome (MetS); however, the moderating effects of inflammation as measured by C-reactive protein (CRP) and menopause on the PCOS-MetS association have not been studied in Hispanic/Latinas with PCOS who have a higher metabolic burden. Objective We studied the cross-sectional association between PCOS and (1) MetS in 7316 females of the Hispanic Community Health Study/Study of Latinos (HCHS/SOL), (2) subcomponents of MetS including impaired fasting glucose (IFG) and elevated triglycerides (TGL), and (3) effect modification by menopausal status and CRP. Design The HCHS/SOL is a multicenter, longitudinal, and observational study of US Hispanic/Latinos. Our study sample included females from visit 2 with self-reported PCOS and MetS (ages 23-82 years). Results PCOS (prevalence = 18.8%) was significantly associated with MetS prevalence [odds ratio [odds ratio (OR) = 1.41 (95% confidence interval: 1.13-1.76)], IFG and TGL (OR = 1.42 (1.18-1.72), OR = 1.48 (1.20-1.83), respectively]. We observed effect modification by menopausal status (ORpre = 1.46, Pint  = .02; ORpost = 1.34, Pint  = .06) and CRP (ORelevated = 1.41, Pint  = .04; ORnormal = 1.26, Pint  = .16) on the PCOS-MetS association. We also observed a superadditive interaction between CRP and PCOS, adjusting for which resulted in an attenuated effect of PCOS on MetS (OR = 1.29 [0.93-1.78]). Conclusion Hispanic/Latino females with PCOS had higher odds of MetS, IFG, and elevated TGL than their peers without PCOS. Interaction analyses revealed that the odds of MetS are higher among PCOS females who have premenopausal status or high inflammation. Interventions in Hispanic/Latinas should target these outcomes for effective management of the disease.

Funder

National Heart, Lung, and Blood Institute

University of North Carolina

University of Miami

Albert Einstein College of Medicine

University of Illinois at Chicago

San Diego State University

National Institute on Minority Health and Health Disparities

National Institute on Deafness and Other Communication Disorders

National Institute of Dental and Craniofacial Research

National Institute of Diabetes and Digestive and Kidney Diseases

National Institute of Neurological Disorders and Stroke

Office of Dietary Supplements

National Center for Advancing Translational Sciences

American Heart Association

Publisher

The Endocrine Society

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