Abstract

Evidence from populations at risk for type 1 diabetes, type 2 diabetes or gestational diabetes substantiates the 1-hour plasma glucose as a sensitive alternative marker for identifying high-risk individuals when ß-cell function is relatively more functional. An elevated 1-hour plasma glucose could therefore diagnose dysglycemia and risk for complications across the glycemic spectrum. Reducing the 2-hour oral glucose tolerance test to 1-hour would reduce the burden on patients, likely reduce costs, and enhance its accessibility in practice.

Highlights

  • The heterogeneity of diabetes has been the subject of considerable discussion given the complexity of classifying diabetes further mitigated by genetics and environmental factors [1, 2]

  • While type 1 diabetes is generally diagnosed based on the presence of antibodies and type 2 diabetes by obesity and insulin resistance, it has become increasingly evident that younger individuals with type 1 diabetes may be insulin resistant and overweight or obese adolescents can have type 2 diabetes and the metabolic syndrome [1]

  • In TrialNet Pathway to Prevention (TNPTP) as well, an Index60 value ≥2.00 identified more individuals with characteristics typical of type 1 diabetes than glucose criteria [25]. These findings suggest that the Index60 threshold ≥2.00 could diagnose type 1 diabetes earlier [24, 25]

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Summary

Michael Bergman*

Division of Endocrinology, Diabetes and Metabolism, VA New York Harbor Healthcare System, NYU Grossman School of Medicine, New York, NY, United States. Evidence from populations at risk for type 1 diabetes, type 2 diabetes or gestational diabetes substantiates the 1-hour plasma glucose as a sensitive alternative marker for identifying high-risk individuals when ß-cell function is relatively more functional. An elevated 1-hour plasma glucose could diagnose dysglycemia and risk for complications across the glycemic spectrum. Reducing the 2-hour oral glucose tolerance test to 1-hour would reduce the burden on patients, likely reduce costs, and enhance its accessibility in practice. Specialty section: This article was submitted to Clinical Diabetes, a section of the journal Frontiers in Endocrinology

INTRODUCTION
DISCUSSION

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