Association of Endocrine Disrupting Chemicals With the Metabolic Syndrome Among Women in the Multiethnic Cohort Study

Author:

Ihenacho Ugonna1ORCID,Guillermo Cherie2ORCID,Wilkens Lynne R2ORCID,Franke Adrian A3ORCID,Tseng Chiuchen1,Li Yuqing4,Sangaramoorthy Meera4,Derouen Mindy C4ORCID,Haiman Christopher A15ORCID,Stram Daniel O1ORCID,Le Marchand Loïc2ORCID,Cheng Iona4ORCID,Wu Anna H1ORCID

Affiliation:

1. Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California , Los Angeles, CA 90089 , USA

2. Population Sciences in the Pacific Program, University of Hawaii Cancer Center , Honolulu, HI 96813 , USA

3. Cancer Biology Program, University of Hawaii Cancer Center , Honolulu, HI 96813 , USA

4. Department of Epidemiology and Biostatistics, University of California San Francisco , San Francisco, CA 94158, USA

5. Center for Genetic Epidemiology, University of Southern California , Los Angeles, CA 90089 , USA

Abstract

Abstract Metabolic syndrome (MetS) is associated with a high risk of cardiovascular disease, a leading cause of death among women. MetS is a diagnosis of at least 3 of the following: high blood pressure, high fasting glucose, high triglycerides, high waist circumference, and low high-density lipoprotein cholesterol. Epidemiological studies suggest that endocrine disrupting chemical (EDC) exposure is positively associated with individual components of MetS, but evidence of an association between EDCs and MetS remains inconsistent. In a cross-sectional analysis within the Multiethnic Cohort Study, we evaluated the association between 4 classes of urinary EDCs (bisphenol A [BPA], triclosan, parabens, and phthalates) and MetS among 1728 women. Multivariable logistic regression was used to estimate odds ratios and 95% CI for the association between tertiles of each EDC and MetS adjusting for age, body mass index (BMI), racial and ethnic group, and breast cancer status. Stratified analyses by race and ethnicity and BMI were conducted. MetS was identified in 519 (30.0%) women. We did not detect statistically significant associations of MetS with BPA, triclosan, or phthalate metabolite excretion. MetS was inversely associated with total parabens (Ptrend = .002). Although there were suggestive inverse associations between EDCs and MetS among Latino and African American women, and women with BMI < 30 kg/m2, there was no statistically significant heterogeneity in associations by race and ethnicity or BMI. These findings suggest an inverse association between parabens and MetS in larger multiethnic studies. Prospective analyses to investigate suggested differences in associations by race, ethnicity, and BMI are warranted.

Funder

National Cancer Institute at the National Institutes of Health

California Breast Cancer Research Program

Hawaii Community Foundation

National Cancer Institute

University of Hawaii Cancer Center

National Institute of Environmental Health Sciences

Publisher

The Endocrine Society

Subject

Endocrinology, Diabetes and Metabolism

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