Abstract 4369515: Sex Differences in the Association of Obesity and Adiposity with Eicosanoid Metabolites

A Amanda Grundmann (Beth Israel Deaconess Medical Center at Harvard Medical School, Boston, Massachusetts, United States) J Juhi Parekh (Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States) M Mandana Chitsazan (Beth Israel Deaconess Medical Center at Harvard Medical School, Boston, Massachusetts, United States) E Emily Lau (Massachusetts General Hospital, Chestnut Hill, Massachusetts, United States) N Norrina Allen (NORTHWESTERN UNIVERSITY, Chicago, Illinois, United States) C Chiadi Ndumele (JOHNS HOPKINS HOSPITAL, Silver Spring, Maryland, United States) F Faye Norby (University of Minnesota, Minneapolis, Minnesota, United States) M Mohit Jain S Susan Cheng J Jennifer Ho (Harvard Medical School, Newton, Massachusetts, United States)

Abstract

Introduction: Sex differences in obesity-related cardiovascular disease (CVD) are widely recognized, but the underlying inflammatory pathways driving these differences remain poorly understood. Eicosanoids are bioactive lipids that govern the upstream initiation of inflammatory activity and may mediate obesity-related cardiovascular risk. Objective: We examined sex differences in the associations of obesity and adiposity measures, including body mass index (BMI), waist circumference (WC), waist-to-hip ratio (WHR), and waist-to-height ratio (WHtR), with over 800 eicosanoid metabolites. Methods: We studied Multi-Ethnic Study of Atherosclerosis (MESA) participants at exam 2 with available samples for eicosanoid analysis. Eicosanoids were assessed using a directed, non-targeted mass spectrometry-based platform. We examined the cross-sectional association of adiposity measures with eicosanoids using multivariable linear regression models. To assess sex differences, we included interaction terms (obesity measure × sex) and performed sex-stratified analyses. Analyses were considered significant at FDR q-value <0.05. Results: We included 5064 adults (age 63 ± 10 years; 53% women, BMI 28.3 ± 5.4 kg/m 2 ). Among 811 eicosanoids and related metabolites assayed, 61 displayed significant sex differences for at least one obesity measure ( Figure , FDR q <0.05 for sex interaction term). For example, lower BMI and other adiposity measures were associated with higher levels of linoleic acid derivatives (HpODE), with stronger associations in men vs women (men: β BMI ≈ -0.20, SE = 0.03, p ≈ 1.3×10 -6 ; women: β BMI ≈ -0.09, SE = 0.02, p ≈ 8.8×10 -7 ). Conversely, higher BMI and worse adiposity measures were associated with higher levels of prostaglandin A1, with stronger associations in men vs women (men: β BMI ≈ 0.28, SE = 0.02, p < 1×10 -12 ; women: β BMI ≈ 0.15, SE = 0.02, p < 1×10 -8 ). Conclusions: We found that sex modified the associations of obesity and adipose traits with pro- and anti-inflammatory eicosanoids. Lower levels of obesity measures were associated with higher levels of pro-inflammatory octadecadienoic acid derivatives (e.g., 13-HpODE), more pronounced in men, while higher levels of obesity measures were associated with higher levels of anti-inflammatory prostaglandin derivatives (e.g., PGA1), again more pronounced in men. These findings may reflect inflammatory pathways that contribute to sex differences in obesity-related cardiovascular disease.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (10)

A

Amanda Grundmann

Beth Israel Deaconess Medical Center at Harvard Medical School, Boston, Massachusetts, United States

J

Juhi Parekh

Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States

M

Mandana Chitsazan

Beth Israel Deaconess Medical Center at Harvard Medical School, Boston, Massachusetts, United States

E

Emily Lau

Massachusetts General Hospital, Chestnut Hill, Massachusetts, United States

N

Norrina Allen

NORTHWESTERN UNIVERSITY, Chicago, Illinois, United States

C

Chiadi Ndumele

JOHNS HOPKINS HOSPITAL, Silver Spring, Maryland, United States

F

Faye Norby

University of Minnesota, Minneapolis, Minnesota, United States

M

Mohit Jain

S

Susan Cheng

J

Jennifer Ho

Harvard Medical School, Newton, Massachusetts, United States