Choice of treatment affects plasma levels of insulin-like growth factor-binding protein-1 in noninsulin-dependent diabetes mellitus

J. Martin Gibson, Melissa Westwood, Steven R. Crosby, Christopher Gordon, Jeffrey M P Holly, William Fraser, Chris Anderson, Anne White, Robert J. Young

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Insulin-like growth factor (IGF)-binding protein-1 (IGFBP-1) modulates the metabolic and mitogenic effects of IGFs. Although IGFBP-1 levels are abnormally high in insulin-dependent diabetes (IDDM), relatively little is known in NIDDM; conflicting data have suggested both high and low levels. We investigated whether treatment modifies IGFBP-1 levels in two groups of NIDDM patients. Study 1 examined fasting concentrations in groups of patients with NIDDM, comparable except for treatment type (sulfonylurea, n = 23; once daily insulin, n = 15; sulfonylurea plus once daily insulin, n = 14; multiple insulin injections, n = 9) and 25 nondiabetic subjects. In sulfonylurea-treated patients there were markedly reduced plasma IGFBP-1 concentrations (median, interquartile range in parentheses): control, 61.0 (36-96) μg/L; sulfonylureas alone, 31.5 (21-61) μg/L (P <0.01); and sulfonylureas plus insulin, 31.5 (9-53) μg/L (P <0.01). Once daily insulin was associated with values similar to those in the control group [62.0 (27-103) μg/L; P = NS], whereas IGFBP-1 levels were higher with multiple insulin injection therapy [156.0 (71-184) μg/L; P <0.05]. Proinsulin levels were higher in sulfonylurea-treated patients, but there was no significant correlation between IGFBP-1 and proinsulin within any individual group. Study 2 examined the effects of treatment on the dynamics of IGFBP-1 levels between 0800-1900 h. In control subjects (n = 8), levels fell from 0800 h (mean ± SEM, 22.4 ± 5.2 μg/L) to 1000 h (14 ± 5.2 μg/L), followed by a rise, more rapid after food, to a peak at 1240 h (20.6 ± 3.7; μg/L). Levels then declined until 1500 h (10.7 ± 2.9 μg/L), with a further postprandial peak at 1840 h (23.1 ± 3.2 μg/L). Sulfonylurea therapy (n = 6) resulted in a complete loss of this pattern, with a marked fall in IGFBP-1 from 0800 h (22 ± 2.7 μg/L) to less than 7 μg/L for the remainder of the study (area under the curve, 1150-1400 h, P <0.001 vs. control). By contrast, in metformin-treated patients (n = 7), neither IGFBP-1 levels nor postprandial peaks were significantly different from those in the control group. Our findings suggest that in patients with NIDDM, the regulation of IGFBP-1 is markedly influenced by the choice of treatment.
    Original languageEnglish
    Pages (from-to)1369-1375
    Number of pages6
    JournalJournal of Clinical Endocrinology and Metabolism
    Volume80
    Issue number4
    Publication statusPublished - Apr 1995

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