Increased Rates of Meal Absorption Do Not Explain Elevated 1-Hour Glucose in Subjects With Normal Glucose Tolerance
Abstract Context In subjects with normal fasting glucose (NFG) and normal glucose tolerance (NGT), glucose concentrations >155 mg/dL 1 hour after 75 g of oral glucose predict increased risk of progression to diabetes. Recently, it has been suggested that the mechanism underlying this abnormality...
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Veröffentlicht in: | Journal of the Endocrine Society 2019-01, Vol.3 (1), p.135-145 |
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Sprache: | eng |
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Zusammenfassung: | Abstract
Context
In subjects with normal fasting glucose (NFG) and normal glucose tolerance (NGT), glucose concentrations >155 mg/dL 1 hour after 75 g of oral glucose predict increased risk of progression to diabetes. Recently, it has been suggested that the mechanism underlying this abnormality is increased gut absorption of glucose.
Objective
We sought to determine the rate of systemic appearance of meal-derived glucose in subjects classified by their 1-hour glucose after a 75-g oral glucose challenge.
Design
This was a cross-sectional study. Participating subjects underwent a 75-g oral glucose challenge and a labeled mixed meal test.
Setting
An inpatient clinical research unit at an academic medical center.
Participants
Thirty-six subjects with NFG/NGT participated in this study.
Interventions
Subjects underwent an oral glucose tolerance test. Subsequently, they underwent a labeled mixed meal to measure fasting and postprandial glucose metabolism.
Main Outcome Measures
We examined β-cell function and the rate of meal appearance (Meal Ra) in NFG/NGT subjects. Subsequently, we examined the relationship of peak postchallenge glucose with Meal Ra and indices of β-cell function.
Results
Peak glucose concentrations correlated inversely with β-cell function. No relationship of Meal Ra with peak postchallenge glucose concentrations was observed.
Conclusion
In subjects with NFG/NGT, elevated 1-hour peak postchallenge glucose concentrations reflect impaired β-cell function rather than increased systemic meal appearance. |
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ISSN: | 2472-1972 2472-1972 |
DOI: | 10.1210/js.2018-00222 |