Metabolic Contrasts Between Youth and Adults With Impaired Glucose Tolerance or Recently Diagnosed Type 2 Diabetes: I. Observations Using the Hyperglycemic Clamp
To compare insulin sensitivity (M/I) and β-cell responses in youth versus adults with impaired glucose tolerance (IGT) or drug-naïve, recently diagnosed type 2 diabetes. In 66 youth (80.3% with IGT) and 355 adults (70.7% IGT), hyperglycemic clamps were used to measure ) M/I, ) acute (0-10 min [first...
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Veröffentlicht in: | Diabetes care 2018-08, Vol.41 (8), p.1696-1706 |
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Sprache: | eng |
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Zusammenfassung: | To compare insulin sensitivity (M/I) and β-cell responses in youth versus adults with impaired glucose tolerance (IGT) or drug-naïve, recently diagnosed type 2 diabetes.
In 66 youth (80.3% with IGT) and 355 adults (70.7% IGT), hyperglycemic clamps were used to measure
) M/I,
) acute (0-10 min [first phase]) C-peptide (ACPR
) and insulin (AIR
) responses to glucose,
) steady-state C-peptide and insulin concentrations at plasma glucose of 11.1 mmol/L, and
) arginine-stimulated maximum C-peptide (ACPR
) and insulin (AIR
) responses at plasma glucose >25 mmol/L. The fasting C-peptide-to-insulin ratio was used as an estimate of insulin clearance.
Insulin sensitivity was 46% lower in youth compared with adults (
< 0.001), and youth had greater acute and steady-state C-peptide (2.3- and 1.3-fold, respectively; each
< 0.001) and insulin responses to glucose (AIR
3.0-fold and steady state 2.2-fold; each
< 0.001). Arginine-stimulated C-peptide and insulin responses were also greater in youth (1.6- and 1.7-fold, respectively; each
< 0.001). After adjustment for insulin sensitivity, all β-cell responses remained significantly greater in youth. Insulin clearance was reduced in youth (
< 0.001). Participants with diabetes had greater insulin sensitivity (
= 0.026), with lesser C-peptide and insulin responses than those with IGT (all
< 0.001) but similar insulin clearance (
= 0.109).
In people with IGT or recently diagnosed diabetes, youth have lower insulin sensitivity, hyperresponsive β-cells, and reduced insulin clearance compared with adults. Whether these age-related differences contribute to declining β-cell function and/or impact responses to glucose-lowering interventions remains to be determined. |
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ISSN: | 0149-5992 1935-5548 |
DOI: | 10.2337/dc18-0244 |