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Placebo-controlled trial reveals that suppressing nocturnal growth hormone improves insulin sensitivity in girls with type 1 diabetes, suggesting growth hormone directly causes morning resistance.
The aims of the present study were to compare nocturnal growth hormone (GH) secretion, insulin requirements and insulin sensitivity on two occasions in six adolescent girls with type 1 diabetes when the GH secretion was reduced one night by an oral dose of 100 mg of pirenzepine at bedtime. The mean nocturnal intravenous insulin infusion required to maintain a normal constant blood glucose concentration between 24:00 and 07:00 was 53% higher during the night on placebo (p = 0.0212). During the night on pirenzepine, the serum GH area under the curve (AUC) was reduced in all patients to a mean concentration which was 50.1% (15-78%) of that during the night without pirenzepine (p = 0.0036). The nocturnal urinary GH excretion was also reduced in all of the investigated patients (p = 0.0229). Insulin sensitivity in the morning, measured by the euglycaemic hyperinsulinaemic glucose clamp, increased significantly from 115 +/- 51 mg m-2 min-1 after the night on placebo to 205 +/- 67 mg m-2 min-1 after the night on pirenzepine (p = 0.0161). No side-effects were observed during the pirenzepine night. Negative correlations were found between the nocturnal serum GH AUC and the insulin-stimulated glucose metabolism (r = -0.65, p = 0.0241) and between the nocturnal urinary GH excretion and the insulin-stimulated glucose metabolism (r = -0.77, p = 0.0054). In conclusion, the present study shows a relation between GH secretion and insulin resistance in adolescent girls with type 1 diabetes. The administration of pirenzepine acutely reduces GH secretion and improves insulin sensitivity.
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Åman et al. (1996) studied this question.
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