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Metabolomic profiling identifies complex lipid species and amino acid analogues associated with response to weight loss interventions.
Bihlmeyer, Nathan A; Kwee, Lydia Coulter; Clish, Clary B; Deik, Amy Anderson; Gerszten, Robert E; Pagidipati, Neha J; Laferrère, Blandine; Svetkey, Laura P; Newgard, Christopher B; Kraus, William E; Shah, Svati H.
Affiliation
  • Bihlmeyer NA; Duke Molecular Physiology Institute, Duke University, Durham, North Carolina, United States of America.
  • Kwee LC; Duke Molecular Physiology Institute, Duke University, Durham, North Carolina, United States of America.
  • Clish CB; Metabolomics Platform, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, United States of America.
  • Deik AA; Metabolomics Platform, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, United States of America.
  • Gerszten RE; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, United States of America.
  • Pagidipati NJ; Duke Clinical Research Institute, Duke University, Durham, North Carolina, United States of America.
  • Laferrère B; Department of Medicine, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Svetkey LP; Columbia University Irving Medical Center, New York, New York, United States of America.
  • Newgard CB; Department of Medicine, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Kraus WE; Duke Molecular Physiology Institute, Duke University, Durham, North Carolina, United States of America.
  • Shah SH; Duke Molecular Physiology Institute, Duke University, Durham, North Carolina, United States of America.
PLoS One ; 16(5): e0240764, 2021.
Article in En | MEDLINE | ID: mdl-34043632
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 [%ΔHOMA-IR]) over the intervention. Overall, 92 individual metabolites were associated with %ΔHOMA-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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers / Weight Loss / Metabolomics / Obesity Type of study: Risk_factors_studies / Systematic_reviews Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2021 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers / Weight Loss / Metabolomics / Obesity Type of study: Risk_factors_studies / Systematic_reviews Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2021 Document type: Article Affiliation country: United States Country of publication: United States