Key result
Impaired glucose tolerance linked to ~3-fold faster annual decline in first-phase insulin secretion.
Observational (n=396)
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Reveals that aging accelerates beta-cell secretion decline in impaired glucose tolerance without affecting insulin sensitivity, indicating secretion loss drives age-related glucose deterioration.
OBJECTIVE: To examine the effect of aging on insulin secretion (first- and second-phase insulin release) and insulin sensitivity in people with normal glucose tolerance (NGT) or impaired glucose tolerance (IGT). RESEARCH DESIGN AND METHODS: First- and second-phase insulin secretion and insulin sensitivity were assessed in hyperglycemic clamp experiments in 266 individuals with NGT and 130 individuals with IGT, ranging in age from approximately 20 to approximately 70 years. Changes in beta-cell function were compared using the disposition index to adjust for differences in insulin sensitivity. RESULTS: As expected, both phases of insulin release and insulin sensitivity were reduced in individuals with IGT (all P < 0.01). Insulin sensitivity was not independently correlated with age in either group. In people with NGT, the disposition index for first- and second-phase insulin release decreased similarly at a rate of approximately 0.7% per year. In people with IGT, the disposition indexes for first- and second-phase insulin release decreased at greater rates ( approximately 2.2 and 1.4% per year, P = 0.002 and 0.009, respectively, vs. NGT), with the decrease in first phase being greater than that of second phase (P = 0.025). CONCLUSIONS: Insulin secretion (both first and second phase) normally decreases at a rate of approximately 0.7% per year with aging; this decrease in beta-cell function is accelerated about two-fold in people with impaired glucose tolerance-first phase to a greater extent than second phase. Finally, aging per se has no effect on insulin sensitivity independent of changes in body composition.
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Szoke et al. (2008) conducted an observational in Normal and impaired glucose tolerance (n=396). Impaired glucose tolerance (IGT) vs. Normal glucose tolerance (NGT) was evaluated on Annual decrease in disposition index for first-phase insulin release (p=0.002). Aging-related decline in first-phase insulin secretion was significantly accelerated in individuals with impaired glucose tolerance compared to those with normal glucose tolerance (2.2% vs 0.7% per year; P=0.002).
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