Literature DB >> 18551113

Further evidence for the role of ENPP1 in obesity: association with morbid obesity in Finns.

Kaisa Valli-Jaakola1, Elina Suviolahti, Camilla Schalin-Jäntti, Samuli Ripatti, Kaisa Silander, Laura Oksanen, Veikko Salomaa, Leena Peltonen, Kimmo Kontula.   

Abstract

The aim of this study was to investigate a series of single-nucleotide polymorphisms (SNPs) in the genes MC2R, MC3R, MC4R, MC5R, POMC, and ENPP1 for association with obesity. Twenty-five SNPs (2-7 SNPs/gene) were genotyped in 246 Finns with extreme obesity (BMI > or = 40 kg/m2) and in 481 lean subjects (BMI 20-25 kg/m2). Of the obese subjects, 23% had concomitant type 2 diabetes. SNPs and SNP haplotypes were tested for association with obesity and type 2 diabetes. Allele frequencies differed between obese and lean subjects for two SNPs in the ENPP1 gene, rs1800949 (P = 0.006) and rs943003 (P = 0.0009). These SNPs are part of a haplotype (rs1800949 C-rs943003 A), which was observed more frequently in lean subjects compared to obese subjects (P = 0.0007). Weaker associations were detected between the SNPs rs1541276 in the MC5R, rs1926065 in the MC3R genes and obesity (P = 0.04 and P = 0.03, respectively), and between SNPs rs2236700 in the MC5R, rs2118404 in the POMC, rs943003 in the ENPP1 genes and type 2 diabetes (P = 0.03, P = 0.02 and P = 0.02, respectively); these associations did not, however, remain significant after correction for multiple testing. In conclusion, a previously unexplored ENPP1 haplotype composed of SNPs rs1800949 and rs943003 showed suggestive evidence for association with adult-onset morbid obesity in Finns. In this study, we did not find association between the frequently studied ENPP1 K121Q variant, nor SNPs in the MCR or POMC genes and obesity or type 2 diabetes.

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Year:  2008        PMID: 18551113     DOI: 10.1038/oby.2008.313

Source DB:  PubMed          Journal:  Obesity (Silver Spring)        ISSN: 1930-7381            Impact factor:   5.002


  12 in total

1.  Possible role for ENPP1 polymorphism in obesity but not for INSIG2 and PLIN variants.

Authors:  Armand Peeters; Sigri Beckers; An Verrijken; Ilse Mertens; Luc Van Gaal; Wim Van Hul
Journal:  Endocrine       Date:  2009-04-28       Impact factor: 3.633

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Authors:  M Switonski; M Mankowska; S Salamon
Journal:  J Appl Genet       Date:  2013-08-31       Impact factor: 3.240

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Authors:  Robert P Lisak; Joyce A Benjamins
Journal:  Brain Sci       Date:  2017-08-14

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7.  The association between ANKH promoter polymorphism and chondrocalcinosis is independent of age and osteoarthritis: results of a case-control study.

Authors:  Abhishek Abhishek; Sally Doherty; Rose Maciewicz; Kenneth Muir; Weiya Zhang; Michael Doherty; Anna M Valdes
Journal:  Arthritis Res Ther       Date:  2014-01-27       Impact factor: 5.156

8.  Common genetic variation in and near the melanocortin 4 receptor gene (MC4R) is associated with body mass index in American Indian adults and children.

Authors:  Yunhua L Muller; Marie S Thearle; Paolo Piaggi; Robert L Hanson; Duncan Hoffman; Brittany Gene; Darin Mahkee; Ke Huang; Sayuko Kobes; Susanne Votruba; William C Knowler; Clifton Bogardus; Leslie J Baier
Journal:  Hum Genet       Date:  2014-08-08       Impact factor: 4.132

Review 9.  Hypothesis of the neuroendocrine cortisol pathway gene role in the comorbidity of depression, type 2 diabetes, and metabolic syndrome.

Authors:  Claudia Gragnoli
Journal:  Appl Clin Genet       Date:  2014-04-01

10.  α-Melanocyte stimulating hormone promotes muscle glucose uptake via melanocortin 5 receptors.

Authors:  Pablo J Enriori; Weiyi Chen; Maria C Garcia-Rudaz; Bernadette E Grayson; Anne E Evans; Sarah M Comstock; Ursel Gebhardt; Hermann L Müller; Thomas Reinehr; Belinda A Henry; Russell D Brown; Clinton R Bruce; Stephanie E Simonds; Sara A Litwak; Sean L McGee; Serge Luquet; Sarah Martinez; Martin Jastroch; Matthias H Tschöp; Matthew J Watt; Iain J Clarke; Christian L Roth; Kevin L Grove; Michael A Cowley
Journal:  Mol Metab       Date:  2016-08-05       Impact factor: 7.422

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