Continuous subcutaneous IGF-1 therapy via insulin pump in a patient with Donohue syndrome

DR Weber, DE Stanescu, R Semple… - Journal of Pediatric …, 2014 - degruyter.com
DR Weber, DE Stanescu, R Semple, C Holland, SN Magge
Journal of Pediatric Endocrinology and Metabolism, 2014degruyter.com
Donohue syndrome (DS) is a severe form of congenital insulin resistance due to mutation (s)
in the insulin receptor (INSR) gene. Given the similarities between insulin and insulin-like
growth factor 1 (IGF-1) receptors, recombinant human IGF-1 (rhIGF-1) has been used to treat
severe insulin resistance due to INSR mutation (s). Traditional subcutaneous therapy may
be limited by the shortened IGF-1 half-life in these patients. We report the case of a female
with molecularly confirmed DS treated with continuous rhIGF-1 therapy via an insulin pump …
Abstract
Donohue syndrome (DS) is a severe form of congenital insulin resistance due to mutation(s) in the insulin receptor (INSR) gene. Given the similarities between insulin and insulin-like growth factor 1 (IGF-1) receptors, recombinant human IGF-1 (rhIGF-1) has been used to treat severe insulin resistance due to INSR mutation(s). Traditional subcutaneous therapy may be limited by the shortened IGF-1 half-life in these patients. We report the case of a female with molecularly confirmed DS treated with continuous rhIGF-1 therapy via an insulin pump. With treatment, the patient’s hemoglobin A1c decreased from 9.8% to 8.8%, and her weight increased by 0.8 kg. Development of an ovarian tumor complicated her course, but it was unclear whether this was related to rhIGF-1 therapy. Limited treatment options exist for patients with DS. The use of continuous rhIGF-1 via an insulin pump may be a viable option, although further experience is needed to establish safety and efficacy.
De Gruyter