Abstract P2109: Sex Differences in the Plasma Metabolome Before and After Exercise Training

E Eric Leszczynski (Michigan State University, East Lansing, Michigan, United States) J Jacob Barber (Beth Israel Deaconess Medical Ctr, Boston, Massachusetts, United States) P Prashant Rao (Beth Israel Deaconess Medical Ctr, Boston, Massachusetts, United States) K Kiani Jacobs (University of South Carolina, Columbia, South Carolina, United States) M Michael Mi (Beth Israel Deaconess Medical Ctr, Boston, Massachusetts, United States) P Prasun Dev (University of South Carolina, Columbia, South Carolina, United States) C Charles Schwartz (University of South Carolina, Columbia, South Carolina, United States) S Sujoy Ghosh C Claude Bouchard (PENNINGTON BIOMEDICAL RESEARCH CTR, Baton Rouge, Louisiana, United States) C Clary Clish J Jeremy Robbins R Robert Gerszten M Mark Sarzynski (University of South Carolina, Columbia, South Carolina, United States)

Abstract

Background: Sex differences in metabolites, particularly their changes with exercise training, are largely unknown. We hypothesized that metabolites would not largely differ between males and females at baseline, but that most of the exercised-induced changes in metabolites would be sex-specific. Methods: Plasma metabolites were measured using untargeted LC-MS methods before and after a 20-week exercise intervention in participants from the HERITAGE Family Study (n=671, 56% Female, 35% Black, 17-65 yrs). A total of 810 metabolites were included. Sex differences at baseline were examined using Student t-tests. Paired t-tests were used to examine changes in metabolites with exercise training by sex. Significance was defined as FDR<0.05. Results: At baseline, the levels of 398 plasma metabolites were higher in males, while 155 were higher in females. The most significant sex differences were found for creatine, uric acid, and androsterone 3-glucuronide. Most exercise training changes in the plasma metabolome were sex-specific (74%, Fig 1A ). A majority of the female-specific metabolite changes were in carnitines and LPCs, with the highest individual changes in DG 30:1, CAR 10:2, and ectoine. Most of training changes observed only in males were in TGs, DGs, and PCs, with the greatest individual changes in PE 40:6, adenosine, and TG 54:9 ( Fig 1B ). Conclusions: Most of the plasma metabolites were different between sex groups at baseline, but importantly, a majority of the exercise-induced changes occurred in only males or females. The differential sex response of the plasma metabolome to exercise training observed in this study could represent important sex-specific metabolic pathway responses to an exercise intervention.

Article Details

Journal Circulation
Volume / Issue Vol. 151, Issue Suppl_1
Published March 11, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (13)

E

Eric Leszczynski

Michigan State University, East Lansing, Michigan, United States

J

Jacob Barber

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

P

Prashant Rao

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

K

Kiani Jacobs

University of South Carolina, Columbia, South Carolina, United States

M

Michael Mi

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

P

Prasun Dev

University of South Carolina, Columbia, South Carolina, United States

C

Charles Schwartz

University of South Carolina, Columbia, South Carolina, United States

S

Sujoy Ghosh

C

Claude Bouchard

PENNINGTON BIOMEDICAL RESEARCH CTR, Baton Rouge, Louisiana, United States

C

Clary Clish

J

Jeremy Robbins

R

Robert Gerszten

M

Mark Sarzynski

University of South Carolina, Columbia, South Carolina, United States