Metabolite patterns link diet, obesity, and type 2 diabetes in a Hispanic population.


Journal

Metabolomics : Official journal of the Metabolomic Society
ISSN: 1573-3890
Titre abrégé: Metabolomics
Pays: United States
ID NLM: 101274889

Informations de publication

Date de publication:
22 09 2021
Historique:
received: 28 03 2021
accepted: 01 09 2021
entrez: 23 9 2021
pubmed: 24 9 2021
medline: 19 1 2022
Statut: epublish

Résumé

Obesity is a precursor of type 2 diabetes (T2D). Our aim was to identify metabolic signatures of T2D and dietary factors unique to obesity. We examined a subsample of the Boston Puerto Rican Health Study (BPRHS) population with a high prevalence of obesity and T2D at baseline (n = 806) and participants (without T2D at baseline) at 5-year follow-up (n = 412). We determined differences in metabolite profiles between T2D and non-T2D participants of the whole sample and according to abdominal obesity status. Enrichment analysis was performed to identify metabolic pathways that were over-represented by metabolites that differed between T2D and non-T2D participants. T2D-associated metabolites unique to obesity were examined for correlation with dietary food groups to understand metabolic links between dietary intake and T2D risk. False Discovery Rate method was used to correct for multiple testing. Of 526 targeted metabolites, 179 differed between T2D and non-T2D in the whole sample, 64 in non-obese participants and 120 unique to participants with abdominal obesity. Twenty-four of 120 metabolites were replicated and were associated with T2D incidence at 5-year follow-up. Enrichment analysis pointed to three metabolic pathways that were overrepresented in obesity-associated T2D: phosphatidylethanolamine (PE), long-chain fatty acids, and glutamate metabolism. Elevated intakes of three food groups, energy-dense takeout food, dairy intake and sugar-sweetened beverages, associated with 13 metabolites represented by the three pathways. Metabolic signatures of lipid and glutamate metabolism link obesity to T2D, in parallel with increased intake of dairy and sugar-sweetened beverages, thereby providing insight into the relationship between dietary habits and T2D risk.

Identifiants

pubmed: 34553271
doi: 10.1007/s11306-021-01835-x
pii: 10.1007/s11306-021-01835-x
pmc: PMC8458177
doi:

Substances chimiques

Glutamates 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

88

Subventions

Organisme : NIDDK NIH HHS
ID : K01 DK107804
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG055948
Pays : United States
Organisme : NIAMS NIH HHS
ID : K01 AR067894
Pays : United States
Organisme : NHLBI NIH HHS
ID : P50 HL105185
Pays : United States
Organisme : NIA NIH HHS
ID : P01 AG023394
Pays : United States

Informations de copyright

© 2021. This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply.

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Auteurs

Laurence D Parnell (LD)

USDA Agricultural Research Service, Nutrition and Genomics Laboratory, JM-USDA Human Nutrition Research Center on Aging at Tufts University, Boston, MA, USA.

Sabrina E Noel (SE)

Department of Biomedical and Nutritional Sciences, University of Massachusetts Lowell, Lowell, MA, USA.

Shilpa N Bhupathiraju (SN)

Channing Division of Network Medicine, Harvard Medical School and Brigham and Women's Hospital, Boston, MA, USA.
Department of Nutrition, Harvard T.H. Chan School of Public Health, Harvard University, Boston, MA, USA.

Caren E Smith (CE)

Nutrition and Genomics Laboratory, JM-USDA Human Nutrition Research Center On Aging at Tufts University, Boston, MA, USA.

Danielle E Haslam (DE)

Channing Division of Network Medicine, Harvard Medical School and Brigham and Women's Hospital, Boston, MA, USA.
Department of Nutrition, Harvard T.H. Chan School of Public Health, Harvard University, Boston, MA, USA.

Xiyuang Zhang (X)

Department of Biomedical and Nutritional Sciences, University of Massachusetts Lowell, Lowell, MA, USA.

Katherine L Tucker (KL)

Department of Biomedical and Nutritional Sciences, University of Massachusetts Lowell, Lowell, MA, USA.

Jose M Ordovas (JM)

Nutrition and Genomics Laboratory, JM-USDA Human Nutrition Research Center On Aging at Tufts University, Boston, MA, USA.
IMDEA Food Institute, CEI UAM + CSIC, Madrid, Spain.
Centro Nacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain.

Chao-Qiang Lai (CQ)

USDA Agricultural Research Service, Nutrition and Genomics Laboratory, JM-USDA Human Nutrition Research Center on Aging at Tufts University, Boston, MA, USA. chaoqiang.lai@usda.gov.

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Classifications MeSH