Metabolomic Changes Upon Conjugated Linoleic Acid Supplementation and Predictions of Body Composition Responsiveness

Author:

He Yafang1,Xu Kun1,Li Yunfeng1,Chang Huan2,Liao Xia3,Yu Hang4,Tian Tian5,Li Chao1,Shen Yuan1,Wu Qian1,Liu Xin1ORCID,Shi Lin67ORCID

Affiliation:

1. Key Laboratory for Disease Prevention and Control and Health Promotion of Shaanxi Province, Department of Epidemiology and Biostatistics, School of Public Health, Global Health Institute, Xi’an Jiaotong University Health Science Center , Xi’an, 710061 , China

2. Department of Clinical Nutrition, The Affiliated Hospital of Northwest University, Xi’an No.3 Hospital , Xi’an, 710032 China

3. Department of Nutrition, The First Affiliated Hospital, Xi’an Jiaotong University , Xi’an, 710061 , China

4. Department of Cardiovascular Medicine, The First Affiliated Hospital, Xi’an Jiaotong University , Xi’an, 710061 , China

5. Department of Nutrition, Xi’an Daxing Hospital , Xi’an, 710016 , China

6. School of Food Engineering and Nutritional Science, Shaanxi Normal University , Xi’an 710119 , China

7. Department of Biology and Biological Engineering, Food and Nutrition Science, Chalmers University of Technology , Gothenburg, SE-412 96 , Sweden

Abstract

Abstract Context Conjugated linoleic acid (CLA) may optimize body composition, yet mechanisms underlining its benefits are not clear in humans. Objective We aimed to reveal the CLA-induced changes in the plasma metabolome associated with body composition improvement and the predictive performance of baseline metabolome on intervention responsiveness. Methods Plasma metabolome from overnight fasted samples at pre- and post-intervention of 65 participants in a 12-week randomized, placebo-controlled trial (3.2 g/day CLA vs 3.2 g/day sunflower oil) were analyzed using untargeted LC-MS metabolomics. Mixed linear model and machine learning were applied to assess differential metabolites between treatments, and to identify optimal panel (based on baseline conventional variables vs metabolites) predicting responders of CLA-derived body composition improvement (increased muscle variables or decreased adiposity variables) based on dual-energy x-ray absorptiometry. Results Compared with placebo, CLA altered 57 metabolites (P < 0.10) enriched in lipids/lipid-like molecules including glycerophospholipids (n = 7), fatty acyls (n = 6), and sphingolipids (n = 3). CLA-upregulated cholic acid (or downregulated aminopyrrolnitrin) was inversely correlated with changes in muscle and adiposity variables. Inter-individual variability in response to CLA-derived body composition change. The areas under the curves of optimal metabolite panels were higher than those of optimal conventional panels in predicting favorable response of waist circumference (0.93 [0.82-1.00] vs 0.64 [0.43-0.85]), visceral adiposity index (0.95 [0.88-1.00] vs 0.58 [0.35-0.80]), total fat mass (0.94 [0.86-1.00] vs 0.69 [0.51-0.88]) and appendicular fat mass (0.97 [0.92-1.00] vs 0.73 [0.55-0.91]) upon CLA supplementation (all FDR P < 0.05). Conclusion Post-intervention metabolite alterations were identified, involving in lipid/energy metabolism, associated with body composition changes. Baseline metabolite profiling enhanced the prediction accuracy for responsiveness of CLA-induced body composition benefits.

Funder

National Natural Science Foundation of China

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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