Postprandial Metabolite Profiles and Risk of Prediabetes in Young People: A Longitudinal Multicohort Study.


Journal

Diabetes care
ISSN: 1935-5548
Titre abrégé: Diabetes Care
Pays: United States
ID NLM: 7805975

Informations de publication

Date de publication:
16 Nov 2023
Historique:
received: 22 02 2023
accepted: 22 10 2023
medline: 17 11 2023
pubmed: 17 11 2023
entrez: 16 11 2023
Statut: aheadofprint

Résumé

Prediabetes in young people is an emerging epidemic that disproportionately impacts Hispanic populations. We aimed to develop a metabolite-based prediction model for prediabetes in young people with overweight/obesity at risk for type 2 diabetes. In independent, prospective cohorts of Hispanic youth (discovery; n = 143 without baseline prediabetes) and predominately Hispanic young adults (validation; n = 56 without baseline prediabetes), we assessed prediabetes via 2-h oral glucose tolerance tests. Baseline metabolite levels were measured in plasma from a 2-h postglucose challenge. In the discovery cohort, least absolute shrinkage and selection operator regression with a stability selection procedure was used to identify robust predictive metabolites for prediabetes. Predictive performance was evaluated in the discovery and validation cohorts using logistic regression. Two metabolites (allylphenol sulfate and caprylic acid) were found to predict prediabetes beyond known risk factors, including sex, BMI, age, ethnicity, fasting/2-h glucose, total cholesterol, and triglycerides. In the discovery cohort, the area under the receiver operator characteristic curve (AUC) of the model with metabolites and known risk factors was 0.80 (95% CI 0.72-0.87), which was higher than the risk factor-only model (AUC 0.63 [0.53-0.73]; P = 0.001). When the predictive models developed in the discovery cohort were applied to the replication cohort, the model with metabolites and risk factors predicted prediabetes more accurately (AUC 0.70 [95% CI 40.55-0.86]) than the same model without metabolites (AUC 0.62 [0.46-0.79]). Metabolite profiles may help improve prediabetes prediction compared with traditional risk factors. Findings suggest that medium-chain fatty acids and phytochemicals are early indicators of prediabetes in high-risk youth.

Identifiants

pubmed: 37971952
pii: 153865
doi: 10.2337/dc23-0327
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NCI NIH HHS
ID : P01CA196569
Pays : United States
Organisme : NIEHS NIH HHS
ID : K12ES033594
Pays : United States
Organisme : NIGMS NIH HHS
ID : R25GM143298
Pays : United States
Organisme : NHGRI NIH HHS
ID : U01HG013288
Pays : United States
Organisme : NIEHS NIH HHS
ID : R01 ES029944
Pays : United States
Organisme : NIEHS NIH HHS
ID : P30 ES007048
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01DK59211
Pays : United States
Organisme : NIMHD NIH HHS
ID : P50MD017344
Pays : United States

Informations de copyright

© 2023 by the American Diabetes Association.

Auteurs

Jesse A Goodrich (JA)

Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles, CA.

Hongxu Wang (H)

Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles, CA.

Douglas I Walker (DI)

Gangarosa Department of Environmental Health, Rollins School of Public Health, Emory University, Atlanta, GA.

Xiangping Lin (X)

Department of Environmental Medicine and Public Health, Icahn School of Medicine at Mount Sinai, New York, NY.

Xin Hu (X)

Clinical Biomarkers Laboratory, Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, Emory University, Atlanta, GA.

Tanya L Alderete (TL)

Department of Integrative Physiology, University of Colorado Boulder, Boulder, CO.

Zhanghua Chen (Z)

Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles, CA.

Damaskini Valvi (D)

Department of Environmental Medicine and Public Health, Icahn School of Medicine at Mount Sinai, New York, NY.

Brittney O Baumert (BO)

Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles, CA.

Sarah Rock (S)

Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles, CA.

Kiros Berhane (K)

Department of Biostatistics, Columbia University, New York, NY.

Frank D Gilliland (FD)

Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles, CA.

Michael I Goran (MI)

Division of Endocrinology, Department of Pediatrics, Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, CA.
Department of Pediatrics, Keck School of Medicine, Los Angeles, CA.

Dean P Jones (DP)

Clinical Biomarkers Laboratory, Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, Emory University, Atlanta, GA.

David V Conti (DV)

Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles, CA.

Leda Chatzi (L)

Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles, CA.

Classifications MeSH