Severe Early-Onset Obesity Due to Bioinactive Leptin Caused by a p.N103K Mutation in the Leptin Gene

Martin Wabitsch, Jan‐Bernd Funcke, Julia von Schnurbein, Friederike Denzer, Georgia Lahr(University Medical Center), Inas Mazen(National Water Research Center), Mona El Gammal(National Water Research Center), Christian Denzer, Anja Moß, Klaus‐Michael Debatin(University Medical Center), Peter Gierschik(Universität Ulm), Vanisha Mistry(Addenbrooke's Hospital), Julia M. Keogh(University of Cambridge), I. Sadaf Farooqi(Wellcome Trust), Barbara Moepps(Universität Ulm), Pamela Fischer‐Posovszky
The Journal of Clinical Endocrinology & Metabolism
July 17, 2015
Cited by 104Open Access
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Abstract

CONTEXT: Congenital leptin deficiency is a very rare cause of severe early-onset obesity. We recently characterized a mutation in the leptin gene (p.D100Y), which was associated with detectable leptin levels and bioinactivity of the hormone. CASE DESCRIPTION: We now describe two siblings, a 9-year-old girl and a 6-year-old boy with severe early-onset obesity and hyperphagia, both homozygous for a c.309C>A substitution in the leptin gene leading to a p.N103K amino acid exchange in the protein and detectable circulating levels of leptin. In vitro experiments in a heterologous cell system demonstrated that the mutated protein was biologically inactive. Treatment with sc recombinant human leptin led to rapid improvement of eating behavior and weight loss. CONCLUSIONS: Sequencing of the leptin gene may need to be considered in hyperphagic, severely obese children with detectable levels of circulating leptin.


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