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脂肪酸酰胺水解酶(FAAH)基因的突变筛查和关联研究与早发和成年肥胖有关。

Mutation screen and association studies for the fatty acid amide hydrolase (FAAH) gene and early onset and adult obesity.

机构信息

Department of Child and Adolescent Psychiatry and Psychotherapy, University of Duisburg-Essen, Essen, Germany.

出版信息

BMC Med Genet. 2010 Jan 1;11:2. doi: 10.1186/1471-2350-11-2.

Abstract

BACKGROUND

The orexigenic effects of cannabinoids are limited by activation of the endocannabinoid degrading enzyme fatty acid amide hydrolase (FAAH). The aim of this study was to analyse whether FAAH alleles are associated with early and late onset obesity.

METHODS

We initially assessed association of five single nucleotide polymorphisms (SNPs) in FAAH with early onset extreme obesity in up to 521 German obese children and both parents. SNPs with nominal p-values <or= 0.1 were subsequently analysed in 235 independent German obesity families. SNPs associated with childhood obesity (p-values <or2= 0.05) were further analysed in 8,491 adult individuals of a population-based cohort (KORA) for association with adult obesity. One SNP was further analysed in 985 German obese adults and 588 normal and underweight controls. In parallel, we screened the FAAH coding region for novel sequence variants in 92 extremely obese children using single-stranded-conformation-polymorphism-analysis and denaturing HPLC and assessed the implication of the identified new variants for childhood obesity.

RESULTS

The trio analysis revealed some evidence for an association of three SNPs in FAAH (rs324420 rs324419 and rs873978) with childhood obesity (two-sided p-values between 0.06 and 0.10). Although analyses of these variants in 235 independent obesity families did not result in statistically significant effects (two-sided p-values between 0.14 and 0.75), the combined analysis of all 603 obesity families supported the idea of an association of two SNPs in FAAH (rs324420 and rs2295632) with early onset extreme obesity (p-values between 0.02 and 0.03). No association was, however, found between these variants and adult obesity. The mutation screen revealed four novel variants, which were not associated with early onset obesity (p > 0.05).

CONCLUSIONS

As we observed some evidence for an association of the FAAH variants rs2295632 rs324420 with early onset but not adult obesity, we conclude that the FAAH variants analyzed here at least do not seem to play a major role in the etiology of obesity within our samples.

摘要

背景

大麻素的食欲促进作用受到内源性大麻素降解酶脂肪酸酰胺水解酶 (FAAH) 的激活限制。本研究的目的是分析 FAAH 等位基因是否与早发性和迟发性肥胖有关。

方法

我们最初评估了 FAAH 中的五个单核苷酸多态性 (SNP) 与多达 521 名德国肥胖儿童及其父母的早发性极度肥胖之间的关联。随后分析了与儿童肥胖相关的 SNP (p 值 <or= 0.1) 在 235 个独立的德国肥胖家庭中的情况。与儿童肥胖相关的 SNP (p 值 <or2= 0.05) 进一步在基于人群的队列 (KORA) 的 8491 名成年个体中进行分析,以与成人肥胖相关。一个 SNP 进一步在 985 名德国肥胖成年人和 588 名正常体重和体重不足的对照组中进行分析。同时,我们使用单链构象多态性分析和变性高效液相色谱法对 92 名极度肥胖的儿童进行 FAAH 编码区的新型序列变异筛查,并评估了鉴定的新变异对儿童肥胖的影响。

结果

三项分析结果显示,FAAH 中的三个 SNP(rs324420、rs324419 和 rs873978)与儿童肥胖有关(双侧 p 值在 0.06 和 0.10 之间)。尽管对 235 个独立肥胖家庭中的这些变体进行分析并未导致统计学上的显著效果(双侧 p 值在 0.14 和 0.75 之间),但对所有 603 个肥胖家庭的综合分析支持 FAAH 中两个 SNP(rs324420 和 rs2295632)与早发性极度肥胖有关的观点(双侧 p 值在 0.02 和 0.03 之间)。然而,这些变体与成人肥胖无关。突变筛查发现了四个新的变体,它们与早发性肥胖无关(p > 0.05)。

结论

由于我们观察到 FAAH 变体 rs2295632 和 rs324420 与早发性而非成人肥胖之间存在关联的一些证据,因此我们得出结论,我们分析的 FAAH 变体至少在我们的样本中似乎没有在肥胖的病因学中起主要作用。

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