S Wiegand1, H Krude. 1. Sozialpädiatrisches Zentrum (SPZ), Charité-Universitätsmedizin Berlin, Berlin, Deutschland.
Abstract
BACKGROUND: Monogenic and syndromic obesity are rare diseases with variable manifestation. Therefore diagnosis is difficult and often delayed. OBJECTIVES: The purpose of this work was to develop a clinical diagnostic algorithm for earlier diagnosis. MATERIAL AND METHODS: Available publications for clinical symptoms and molecular defects of monogenic and syndromic obesity cases were evaluated. RESULTS: Monogenic and syndromic obesity can be expected in cases with early manifestation before the age of 5 years and a BMI above 40 or above the 99th percentile. Syndromic cases are mostly associated with a low IQ and dwarfism. Monogenic cases are associated with additional endocrine defects. Measurement of serum leptin proves the treatable leptin deficiency. Sequencing of the melanocortin-4 receptor gene (MC4R) allows diagnosis of the most frequent monogenic form of obesity. Treatment with a melanocyte-stimulating hormone (MSH) analog can be expected in the future. Early treatment of children with Prader-Willi syndrome can prevent severe obesity. CONCLUSION: Because in some cases treatment is available, monogenic and syndromic obesity should be diagnosed early. Based on the disease symptoms, serum leptin, and MC4R sequencing, a diagnostic algorithm is proposed, which can be used to diagnose cases of morbid obesity.
BACKGROUND: Monogenic and syndromic obesity are rare diseases with variable manifestation. Therefore diagnosis is difficult and often delayed. OBJECTIVES: The purpose of this work was to develop a clinical diagnostic algorithm for earlier diagnosis. MATERIAL AND METHODS: Available publications for clinical symptoms and molecular defects of monogenic and syndromic obesity cases were evaluated. RESULTS: Monogenic and syndromic obesity can be expected in cases with early manifestation before the age of 5 years and a BMI above 40 or above the 99th percentile. Syndromic cases are mostly associated with a low IQ and dwarfism. Monogenic cases are associated with additional endocrine defects. Measurement of serum leptin proves the treatable leptin deficiency. Sequencing of the melanocortin-4 receptor gene (MC4R) allows diagnosis of the most frequent monogenic form of obesity. Treatment with a melanocyte-stimulating hormone (MSH) analog can be expected in the future. Early treatment of children with Prader-Willi syndrome can prevent severe obesity. CONCLUSION: Because in some cases treatment is available, monogenic and syndromic obesity should be diagnosed early. Based on the disease symptoms, serum leptin, and MC4R sequencing, a diagnostic algorithm is proposed, which can be used to diagnose cases of morbid obesity.
Authors: R S Jackson; J W Creemers; S Ohagi; M L Raffin-Sanson; L Sanders; C T Montague; J C Hutton; S O'Rahilly Journal: Nat Genet Date: 1997-07 Impact factor: 38.330
Authors: Ida J Hatoum; Nicholas Stylopoulos; Amanda M Vanhoose; Kelli L Boyd; Deng Ping Yin; Kate L J Ellacott; Lian Li Ma; Kasia Blaszczyk; Julia M Keogh; Roger D Cone; I Sadaf Farooqi; Lee M Kaplan Journal: J Clin Endocrinol Metab Date: 2012-04-06 Impact factor: 5.958