Context: Traditional risk factors for type 2 diabetes mellitus are weak predictors of changes in glucose tolerance and insulin sensitivity in youth. Objective: To identify early metabolic features of insulin resistance (IR) in youth and whether they predict deterioration of glycemic control. Design and Setting: A cross-sectional and longitudinal study was conducted at the Yale Pediatric Obesity Clinic. Patients and Intervention: Concentrations of a-hydroxybutyrate, b-hydroxybutyrate, lactate, and branched-chain amino acids (BCAAs) were measured by nuclear magnetic resonance spectroscopy in 78 nondiabetic adolescents during an oral glucose tolerance test (OGTT). Associations between baseline metabolic alterations and longitudinal changes in glucose control were tested in 16 subjects after a mean follow-up of 2.3 years. Main Outcome Measures: The relationship between metabolite levels, parameters of IR, and glycemic control, and their progression over time. Results: Elevated fasting a-hydroxybutyrate levels were observed in adolescents with reduced insulin sensitivity after adjusting for age, sex, ethnicity, Tanner stage, and body mass index z-score (P = 0.014). Plasmaa-hydroxybutyrate and BCAAswere increased throughout the course of theOGTT in this group (P, 0.03). Notably, borderline IR was associated with a progressive a-hydroxybutyrate decrease from elevated baseline concentrations to normal levels (P = 0.02). Increased baseline a-hydroxybutyrate concentrations were further associated with progressive worsening of glucose tolerance and disposition index. Conclusion: a-HydroxybutyrateandBCAAconcentrationsduring anOGTTcharacterizeinsulin-resistant youth andpredict worseningofglycemic control. These findingsprovide potentialbiomarkers for risk assessment of type 2 diabetes and new insights into IR pathogenesis.

Elevated a-hydroxybutyrate and branched-chain amino acid levels predict deterioration of glycemic control in adolescents

Trico D.
Primo
;
2017-01-01

Abstract

Context: Traditional risk factors for type 2 diabetes mellitus are weak predictors of changes in glucose tolerance and insulin sensitivity in youth. Objective: To identify early metabolic features of insulin resistance (IR) in youth and whether they predict deterioration of glycemic control. Design and Setting: A cross-sectional and longitudinal study was conducted at the Yale Pediatric Obesity Clinic. Patients and Intervention: Concentrations of a-hydroxybutyrate, b-hydroxybutyrate, lactate, and branched-chain amino acids (BCAAs) were measured by nuclear magnetic resonance spectroscopy in 78 nondiabetic adolescents during an oral glucose tolerance test (OGTT). Associations between baseline metabolic alterations and longitudinal changes in glucose control were tested in 16 subjects after a mean follow-up of 2.3 years. Main Outcome Measures: The relationship between metabolite levels, parameters of IR, and glycemic control, and their progression over time. Results: Elevated fasting a-hydroxybutyrate levels were observed in adolescents with reduced insulin sensitivity after adjusting for age, sex, ethnicity, Tanner stage, and body mass index z-score (P = 0.014). Plasmaa-hydroxybutyrate and BCAAswere increased throughout the course of theOGTT in this group (P, 0.03). Notably, borderline IR was associated with a progressive a-hydroxybutyrate decrease from elevated baseline concentrations to normal levels (P = 0.02). Increased baseline a-hydroxybutyrate concentrations were further associated with progressive worsening of glucose tolerance and disposition index. Conclusion: a-HydroxybutyrateandBCAAconcentrationsduring anOGTTcharacterizeinsulin-resistant youth andpredict worseningofglycemic control. These findingsprovide potentialbiomarkers for risk assessment of type 2 diabetes and new insights into IR pathogenesis.
2017
Trico, D.; Prinsen, H.; Giannini, C.; De Graaf, R.; Juchem, C.; Li, F.; Caprio, S.; Santoro, N.; Herzog, R. I.
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/1033163
 Attenzione

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo

Citazioni
  • ???jsp.display-item.citation.pmc??? 26
  • Scopus 55
  • ???jsp.display-item.citation.isi??? 51
social impact