Published May 17, 2021 | Version 1.0
Dataset Open

Metabolomic profiling identifies complex lipid species and amino acid analogues associated with response to weight loss interventions

  • 1. Duke Molecular Physiology Institute, Duke University, Durham, NC 27701, USA
  • 2. Metabolomics Platform, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA
  • 3. Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA
  • 4. Duke Clinical Research Institute, Duke University, Durham, NC 27701, USA
  • 5. Columbia University Irving Medical Center, New York, NY 10032, USA
  • 6. Department of Medicine, Duke University School of Medicine, Durham, NC 27710, USA

Description

Obesity is an epidemic internationally. While weight loss interventions are efficacious, they are compounded by heterogeneity with regards to clinically relevant metabolic responses. Thus, we sought to identify metabolic biomarkers that are associated with beneficial metabolic changes to weight loss and which distinguish individuals with obesity who would most benefit from a given type of intervention. Liquid chromatography mass spectrometry-based profiling was used to measure 765 metabolites in baseline plasma from three different weight loss studies: WLM (behavioral intervention, N=443), STRRIDE-PD (exercise intervention, N=163), and CBD (surgical cohort, N=125). The primary outcome was percent change in insulin resistance (as measured by the Homeostatic Model Assessment of Insulin Resistance [%∆HOMA-IR]) over the intervention. Overall, 92 individual metabolites were associated with %∆HOMA-IR after adjustment for multiple comparisons. Concordantly, the most significant metabolites were triacylglycerols (TAGs; p=2.3e-5) and diacylglycerols (DAGs; p=1.6e-4), with higher baseline TAG and DAG levels associated with a greater improvement in insulin resistance with weight loss. In tests of heterogeneity, 50 metabolites changed differently between weight loss interventions; we found amino acids, peptides, and their analogues to be most significant (4.7e-3) in this category. Our results highlight novel metabolic pathways associated with heterogeneity in response to weight loss interventions, and related biomarkers which could be used in future studies of personalized approaches to weight loss interventions.

Notes

NAB and SHS are funded by American Heart Association Strategically Focused Research Network 17SFRN33670990 and 17SFRN33700155. LCK, CBC, AAD, and SHS are funded by NHLBI 5R01HL127009. REG is funded by NIDDK 5R01DK081572.

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Additional details

Related works

Is supplement to
Preprint: 10.1101/2020.10.05.326025 (DOI)
Journal article: 10.1371/journal.pone.0240764 (DOI)