Kidney Failure, Chronic Clinical Trial
Official title:
Insulin-like Growth Factor (IGF-I) in Hemodialysis Patients
The purpose of this study is to investigate whether the anabolic potentials of insulin may be used to reverse the catabolic effects of hemodialysis in non-diabetic patients with end-stage renal failure.
Nutritional markers such as lean body mass and serum albumin are strong predictors of the
mortality and morbidity in patients with end-stage renal failure (ESRF) on maintenance
hemodialysis (HD). Maintenance HD is considered to contribute to the malnutrition of
patients with ESRF, but the exact mechanism has remained unknown. However, we have recently
shown that the bioactivity of insulin-like growth factor-I (IGF-I) is reduced by 50% during
HD. Furthermore, we showed that the reduction in the bioactivity of IGF-I is directly linked
to an up-regulation of IGF-binding protein-1 (IGFBP-1), the only acutely regulated IGFBP,
which increased by 6-fold during HD. IGFBP-1 is produced in the liver, primarily under the
control of insulin, which promptly inhibits the hepatic production of IGFBP-1. As plasma
insulin remains fairly low during a maintenance HD, the increase in IGFBP-1 may be explained
by the absence of insulin.
The finding that HD acutely down-regulates the bioactivity of IGF-I by an up-regulation of
IGFBP-1 may not only explain the catabolic mechanisms of HD per se, it also opens for a new
treatment strategy of ESRF patients undergoing maintenance HD. Thus, on the basis of our
previous study we hypothesize that treatment of ERSF patients with high doses of insulin
during maintenance HD may counter-act the HD-induced stimulation of IGFBP-1, making it
possible to preserve the bioactivity of IGF-I, and thereby abolishing the catabolic impact
of HD.
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Allocation: Randomized, Endpoint Classification: Bio-availability Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Basic Science
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