Prenatal Exercise Training Alters Plasma Metabolite Responses To Acute Exercise In Pregnant Women With Obesity

PURPOSE:This study investigates how exercise training impacts post-exercise metabolites in sedentary, pregnant women with obesity. METHODS:This secondary analysis of participants included 119 sedentary pregnant women with obesity (age: 28 ± 5 yrs), assigned to an exercise (EX, N = 66, aerobic/resistance 3x/wk from ~13 wks to birth) or control (CON, N = 53, standard of care) group (RCT, NCT02125149). Participants underwent submaximal fitness tests at 12- and 24-wks with a workload increase to 15 RPE. Fingerstick blood samples post-exercise were analyzed using untargeted metabolomics (LC-MS/MS). Linear mixed models assessed the effects of gestation and exercise-by-gestation interaction (FDR < 0.1). RESULTS:A total of 401 metabolites were annotated. Four metabolites exhibited an exercise-by-gestation interaction: nicotinamide and cis-13,14-methylene heptadecanoic acid increased in CON over time and remained stable in EX. 2-hydroxy-3-methylbutyric acid was reduced in EX over time but remained unchanged in CON. Sarcosine was reduced in CON over time but remained unchanged in EX. A time effect was observed in 125 metabolites. For instance, in both groups throughout gestation, there was a reduction in post-exercise metabolites related to lipid/macronutrient metabolism/transport (e.g., D-carnitine, acetyl-L-carnitine, decanoylcarnitine), amino acid and betaine/homocysteine metabolism (e.g., 4-methyl-2-oxovaleric acid, dimethylglycine), and microbe-associated xenometabolism (e.g., α-hydroxyisobutyric acid, crotonobetaine). Additionally, throughout gestation, there was an increase in post-exercise metabolites related to sex hormone production and stress response (e.g., estriol 17-sulfate, cortisone), complex lipid and bile metabolism (e.g., palmitoyl sphingomyelin, tauro-α-muricholic acid), nucleotide metabolism (e.g., β-pseudouridine, N6-me-adenosine), and adaptations to oxidative stress (e.g., kynurenine metabolite 2,3-pyridinedicarboxylic acid, 3-aminobenzamide) in both groups. CONCLUSION:In conclusion, prenatal exercise training alters post-exercise metabolites related to energy production, inflammation, and hormonal regulation. Other metabolites change during pregnancy, reflecting the adaptation to gestation regardless of exercise training. Supported by: USDA-ARS# 6026-10700-001-000D (Arkansas Children’s Nutrition Center)

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Journal
Medicine & Science in Sports & Exercise
Published
2025-09-16
DOI
https://doi.org/10.1249/01.mss.0001161580.66921.da
Primary Topic
Birth, Development, and Health
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article
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article

Prenatal Exercise Training Alters Plasma Metabolite Responses To Acute Exercise In Pregnant Women With Obesity

Aline Andres, Renny S. Lan, Hailemariam Abrha Assress, Brian D. Piccolo et al.
Medicine & Science in Sports & Exercise
Birth, Development, and Health
article

Prenatal Exercise Training Alters Plasma Metabolite Responses To Acute Exercise In Pregnant Women With Obesity

Aline Andres, Renny S. Lan, Hailemariam Abrha Assress, Brian D. Piccolo, Elisabet Børsheim, Sean H. Adams, Brittany R. Allman-Tucker
article en

Abstract

PURPOSE:This study investigates how exercise training impacts post-exercise metabolites in sedentary, pregnant women with obesity. METHODS:This secondary analysis of participants included 119 sedentary pregnant women with obesity (age: 28 ± 5 yrs), assigned to an exercise (EX, N = 66, aerobic/resistance 3x/wk from ~13 wks to birth) or control (CON, N = 53, standard of care) group (RCT, NCT02125149). Participants underwent submaximal fitness tests at 12- and 24-wks with a workload increase to 15 RPE. Fingerstick blood samples post-exercise were analyzed using untargeted metabolomics (LC-MS/MS). Linear mixed models assessed the effects of gestation and exercise-by-gestation interaction (FDR < 0.1). RESULTS:A total of 401 metabolites were annotated. Four metabolites exhibited an exercise-by-gestation interaction: nicotinamide and cis-13,14-methylene heptadecanoic acid increased in CON over time and remained stable in EX. 2-hydroxy-3-methylbutyric acid was reduced in EX over time but remained unchanged in CON. Sarcosine was reduced in CON over time but remained unchanged in EX. A time effect was observed in 125 metabolites. For instance, in both groups throughout gestation, there was a reduction in post-exercise metabolites related to lipid/macronutrient metabolism/transport (e.g., D-carnitine, acetyl-L-carnitine, decanoylcarnitine), amino acid and betaine/homocysteine metabolism (e.g., 4-methyl-2-oxovaleric acid, dimethylglycine), and microbe-associated xenometabolism (e.g., α-hydroxyisobutyric acid, crotonobetaine). Additionally, throughout gestation, there was an increase in post-exercise metabolites related to sex hormone production and stress response (e.g., estriol 17-sulfate, cortisone), complex lipid and bile metabolism (e.g., palmitoyl sphingomyelin, tauro-α-muricholic acid), nucleotide metabolism (e.g., β-pseudouridine, N6-me-adenosine), and adaptations to oxidative stress (e.g., kynurenine metabolite 2,3-pyridinedicarboxylic acid, 3-aminobenzamide) in both groups. CONCLUSION:In conclusion, prenatal exercise training alters post-exercise metabolites related to energy production, inflammation, and hormonal regulation. Other metabolites change during pregnancy, reflecting the adaptation to gestation regardless of exercise training. Supported by: USDA-ARS# 6026-10700-001-000D (Arkansas Children’s Nutrition Center)

Medicine & Science in Sports & ExerciseVol. 57(10S)
University of Central Arkansas (US), Arkansas Children's Nutrition Center (US), Conway School of Landscape Design (US), University of Arkansas for Medical Sciences (US), University of California, Davis (US)
Openalex Percentile: Top 65%
Birth, Development, and Health
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