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• W2890326470 abstract "Several case series of extreme early-onset obesity due to mutations in the human leptin receptor (LEPR) gene have been reported. In this review we summarize published functional and phenotypic data on mutations in the human LEPR gene causing severe early-onset obesity. Additionally, we included data on six new cases from our obesity center. Literature research was performed using PubMed and OMIM. Functional relevance of mutations was estimated based on reported functional analysis, mutation size, and location, as well as phenotypic characteristics of affected patients. We identified 57 cases with 38 distinct LEPR mutations. We found severe early-onset obesity, hyperphagia, and hypogonadotropic hypogonadism as cardinal features of a complete loss of LEPR function. Other features, for example, metabolic disorders and recurring infections, were variable in manifestation. Obesity degree or other manifestations did not aggregate by genotype. Few patients underwent bariatric surgery with variable success. Most mutations occurred in the fibronectin III and cytokine receptor homology II domains, whereas none was found in cytoplasmic domain. In silico data were available for 25 mutations and in vitro data were available for four mutations, revealing residual activity in one case. By assessing provided information on the clinical phenotype, functional analysis, and character of the 38 mutations, we assume residual LEPR activity for five additional mutations. Functional in vitro analysis is necessary to confirm this assumption." @default.
• W2890326470 created "2018-09-27" @default.
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• W2890326470 date "2018-09-17" @default.
• W2890326470 modified "2023-10-15" @default.
• W2890326470 title "Functional and Phenotypic Characteristics of Human Leptin Receptor Mutations" @default.
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• W2890326470 doi "https://doi.org/10.1210/js.2018-00123" @default.
• W2890326470 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6293235" @default.
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• W2890326470 hasPublicationYear "2018" @default.
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