Evaluation of a Role for NPY and NPY2R in the Pathogenesis of Obesity by Mutation and Copy Number Variation Analysis in Obese Children and Adolescents. (31st August 2017)

• Record Type: Journal Article
• Authors: Aerts, Evi; Geets, Ellen; Sorber, Laure; Beckers, Sigri; Verrijken, An; Massa, Guy; Van Hoorenbeeck, Kim; Verhulst, Stijn L; Van Gaal, Luc F; Van Hul, Wim
• Is Part Of: Annals of human genetics. Volume 82:Number 1(2018:Jan.)
• Page Start: 1
• Page End: 10
• Publication Date: 2017-08-31
• Subjects: NPY -- NPY2R -- Obesity -- Children -- CNV analysis -- Mutation analysis; Human genetics -- Periodicals; 599.935
• DOI: 10.1111/ahg.12211
• Languages: English
• ISSNs: 0003-4800

Abstract

Summary: Neuropeptide Y (NPY) and its G protein–coupled NPY Y2 Receptor (NPY2R) are highly expressed in orexigenic NPY/Agouti‐related peptide neurons within the arcuate nucleus, a major integrator of appetite control in the hypothalamus. As NPY and NPY2R are interesting candidate genes for obesity, we hypothesized that a genetic variation in these genes might be implicated in the pathogenesis of obesity. In the first part of this study, we performed a mutation analysis of the coding region of NPY and NPY2R with high‐resolution melting curve analysis. For the highly conserved NPY gene, an extended population of 436 obese children and adolescents was screened, while for NPY2R, a smaller subset of 306 patients was used. A control population of 300 healthy individuals was screened for NPY2R to determine the general prevalence of the variants found among patients. Direct sequencing was performed for samples with melting patterns deviating from wild‐type. In the second part of this study, Multiplex Amplicon Quantification (MAQ) analysis was performed in 308 obese children and adolescents to detect copy number variation (CNV) in the NPY2R region. Mutation analysis of the NPY gene led to the identification of one common missense variant (L7P; MAF 0.04), while the screening of the NPY2R gene resulted in the identification of one rare missense variant F87I in the patient population. In our CNV analysis, we could not identify copy number variation in the NPY2R region among obese children and adolescents. In summary, this study clearly indicates that genetic variation in NPY and NPY2R is at low frequency and thus does not make a major contribution to the obese phenotype in the general population.