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Postprandial Metabolite Profiles and Risk of Prediabetes in Young People: A Longitudinal Multicohort Study.
Goodrich, Jesse A; Wang, Hongxu; Walker, Douglas I; Lin, Xiangping; Hu, Xin; Alderete, Tanya L; Chen, Zhanghua; Valvi, Damaskini; Baumert, Brittney O; Rock, Sarah; Berhane, Kiros; Gilliland, Frank D; Goran, Michael I; Jones, Dean P; Conti, David V; Chatzi, Leda.
Affiliation
  • Goodrich JA; Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles, CA.
  • Wang H; Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles, CA.
  • Walker DI; Gangarosa Department of Environmental Health, Rollins School of Public Health, Emory University, Atlanta, GA.
  • Lin X; Department of Environmental Medicine and Public Health, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Hu X; Clinical Biomarkers Laboratory, Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, Emory University, Atlanta, GA.
  • Alderete TL; Department of Integrative Physiology, University of Colorado Boulder, Boulder, CO.
  • Chen Z; Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles, CA.
  • Valvi D; Department of Environmental Medicine and Public Health, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Baumert BO; Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles, CA.
  • Rock S; Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles, CA.
  • Berhane K; Department of Biostatistics, Columbia University, New York, NY.
  • Gilliland FD; Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles, CA.
  • Goran MI; Division of Endocrinology, Department of Pediatrics, Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, CA.
  • Jones DP; Department of Pediatrics, Keck School of Medicine, Los Angeles, CA.
  • Conti DV; Clinical Biomarkers Laboratory, Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, Emory University, Atlanta, GA.
  • Chatzi L; Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles, CA.
Diabetes Care ; 47(1): 151-159, 2024 Jan 01.
Article in En | MEDLINE | ID: mdl-37971952
ABSTRACT

OBJECTIVE:

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. RESEARCH DESIGN AND

METHODS:

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.

RESULTS:

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]).

CONCLUSIONS:

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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prediabetic State / Diabetes Mellitus, Type 2 Limits: Adolescent / Adult / Humans Language: En Journal: Diabetes Care Year: 2024 Type: Article Affiliation country: Canada

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prediabetic State / Diabetes Mellitus, Type 2 Limits: Adolescent / Adult / Humans Language: En Journal: Diabetes Care Year: 2024 Type: Article Affiliation country: Canada