Literature DB >> 9287046

rhIGF-I administration reduces insulin requirements, decreases growth hormone secretion, and improves the lipid profile in adults with IDDM.

P V Carroll1, M Umpleby, G S Ward, S Imuere, E Alexander, D Dunger, P H Sönksen, D L Russell-Jones.   

Abstract

IDDM is associated with elevated circulating levels of growth hormone (GH) and reduced insulin-like growth factor I (IGF-I). GH antagonizes the action of insulin-increasing insulin requirements in IDDM. The effects of subcutaneously administered rhIGF-I on glycemic control, insulin requirements, and GH secretion were studied in eight adults with IDDM. Patients received either placebo or rhIGF-I (50 microg/kg b.i.d.) for 19 days in a randomized, double-blind, parallel-design, placebo-controlled trial. Overnight GH, plasma glucose, free insulin, IGF-I, fructosamine, and lipid profiles were assessed during this period. rhIGF-I therapy increased IGF-I concentration from 117.1 +/- 14.2 (mean +/- SE) ng/ml (baseline) to 310.5 +/- 40.6 and 257.1 +/- 41.2 ng/ml on day 5 (P < 0.01 vs. baseline) and day 20 (P < 0.01 vs. baseline), respectively. After 19 days of rhIGF-I treatment, fructosamine concentrations were unchanged compared with baseline (439 +/- 32 vs. 429 +/- 35 micromol/l, day -1 vs. day 20, respectively), yet insulin requirements were decreased by approximately 45% (0.67 +/- 0.08 vs. 0.36 +/- 0.07 U x kg(-1) x day(-1), day -1 vs. day 19, respectively, P < 0.005). After 4 days of rhIGF-I therapy, there was a decrease in free insulin levels (8.38 +/- 1.47 vs. 4.98 +/- 0.84 mU/l, P < 0.05), mean overnight GH concentration (12.6 +/- 3.3 vs. 3.8 +/- 2.1 mU/l, P = 0.05), and total cholesterol and triglycerides (4.68 +/- 0.31 vs. 4.25 +/- 0.35 mmol/l, P < 0.05, 1.27 +/- 0.19 vs. 0.95 +/- 0.21 mmol/l, P < 0.001, respectively). There was no change in any variable in the placebo-treated patients. This study demonstrates that subcutaneous administration of rhIGF-I decreases insulin requirements and improves the plasma lipid profile while maintaining glycemic control in adults with IDDM. The excess nocturnal release of GH, characteristic of IDDM, is also decreased by rhIGF-I therapy.

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Year:  1997        PMID: 9287046     DOI: 10.2337/diab.46.9.1453

Source DB:  PubMed          Journal:  Diabetes        ISSN: 0012-1797            Impact factor:   9.461


  5 in total

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Journal:  Endocr Rev       Date:  2009-07-09       Impact factor: 19.871

2.  In vitro and in vivo effects of IGF-I on adiposity in HIV-associated metabolic disease: a pilot study.

Authors:  Roy J Kim; Sumit Vaghani; Larisa M Zifchak; Joseph H Quinn; Weimian He; Pablo Tebas; Ian Frank
Journal:  Arch Med Res       Date:  2013-07-16       Impact factor: 2.235

3.  Effects of physical training on serum and pituitary growth hormone contents in diabetic rats.

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Journal:  Pituitary       Date:  2009-04-16       Impact factor: 4.107

Review 4.  Growth hormone, IGF-I and insulin and their abuse in sport.

Authors:  R I G Holt; P H Sönksen
Journal:  Br J Pharmacol       Date:  2008-03-31       Impact factor: 8.739

5.  Study of insulin resistance in relation to serum IGF-I levels in subjects with different degrees of glucose tolerance.

Authors:  Srinivas Martha; Narayana Pantam; Surender Thungathurthi; Vummentala L N Rao; Krishna Devarakonda
Journal:  Int J Diabetes Dev Ctries       Date:  2008-04
  5 in total

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