Association between leptin receptor (LEPR) and brain-derived neurotrophic factor (BDNF) gene variants and obesity: a case-control study

被引:14
作者
Marti, A. [1 ]
Santos, J. L. [1 ,2 ]
Gratacos, M. [3 ,4 ]
Moreno-Aliaga, M. J. [1 ]
Maiz, A. [2 ]
Martinez, J. A. [1 ]
Estivill, X. [3 ,4 ,5 ,6 ]
机构
[1] Univ Navarra, Dept Nutr & Food Sci, Navarra 31080, Spain
[2] Pontificia Univ Catolica Chile, Sch Med, Dept Nutr Diabet & Metab, Santiago, Chile
[3] CIBERESP, Barcelona, Catalonia, Spain
[4] CRG UPF, Genes & Dis Program, Genet Causes Dis Grp, Barcelona, Catalonia, Spain
[5] CeGen CRG, Barcelona Genotyping Node, Barcelona, Catalonia, Spain
[6] UPF, Dept Hlth & Expt Life Sci, Barcelona, Catalonia, Spain
关键词
obesity; leptin receptor; brain-derived neurotrophic factor; case-control study; BODY-MASS INDEX; ANOREXIA-NERVOSA; WEIGHT; RISK; SPECTRUM; EXTREME; LINKAGE; GAIN;
D O I
10.1179/147683009X423355
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Introduction: Human and animal studies provide evidence for a relevant role of the leptin receptor (LEPR) and the brain-derived neurotrophic factor (BDNF) genes in energy homeostasis. Aim: To assess the association between human LEPR and BDNF genetic variants with adult obesity. Design and methods: Case-control study in Pamplona (Navarra, Spain) with adult obese subjects (n = 159) and normal weight controls (n = 154) Four common polymorphisms of the LEPR gene (Lys109Arg, Gln223Arg, Ser34Ser, Lys656Asn) and 17 variants of the BDNF gene, including the Val66Met variant, were genotyped. Results: No significant case-control differences were found in allele/genotype frequencies after adjusting for relevant co-variates. Haplotype analysis did not detect any significant association between LEPR or BDNF variants and obesity. No associations were found between LEPR variants and serum leptin levels. Conclusions: Our results do not support a major role of LEPR or BDNF common polymorphisms in multifactorial adult obesity.
引用
收藏
页码:183 / 188
页数:6
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