Department of Endocrinology, Diabetology and Isotope Treatment, Wroclaw Medical University, Wroclaw, Poland.
Int J Obes (Lond). 2011 Mar;35(3):373-7. doi: 10.1038/ijo.2010.145. Epub 2010 Sep 14.
The aim of this study was to determine whether genetic variation at the cannabinoid receptor-1 (CNR1) locus could have an effect on adiposity, fat distribution and obesity-related metabolic disorders in Polish postmenopausal women.
The A3813G (rs12720071), G1422A (rs1049353), A4895G (rs806368) and rs806381, rs10485170, rs6454674 and rs2023239 single-nucleotide polymorphisms of CNR1 were genotyped in 348 randomly selected postmenopausal women aged 50-60 years recruited from the Wroclaw city population.
CNR1 genotypes, anthropometric measures (body mass index (BMI), waist circumference (WC) and body fat distribution by dual energy X-ray absorptiometry) and metabolic parameters (glucose, lipid profile and Fasting Insulin Resistance Index for insulin resistance) were determined.
The 3813G allele was not significantly associated with higher body mass, BMI, WC, total fat or fat percentage, but was associated with higher android fat deposit (2971.78±1655.08 vs 2472.64±1300.53, P=0.007) and percentage of android fat (37.59±8.45 vs 35.66±7.63, P=0.062). No associations for the G1422A, A4895G, rs806381, rs10485170, rs6454674 and rs2023239 variants were observed.
There is an association of the variants of CNR1 with obesity-related phenotypes in Polish postmenopausal women. As cannabinoid receptor type 1 is a drug target for obesity, pharmacogenetic receptor gene analysis of obesity treatment by endocannabinoid blockade may be of interest to identify the best responders.
本研究旨在探讨大麻素受体 1(CNR1)基因座的遗传变异是否会影响波兰绝经后妇女的肥胖、脂肪分布和肥胖相关代谢紊乱。
本研究共纳入 348 名年龄在 50-60 岁的随机选取的绝经后女性,均来自弗罗茨瓦夫市人群。对其 CNR1 的 A3813G(rs12720071)、G1422A(rs1049353)、A4895G(rs806368)和 rs806381、rs10485170、rs6454674 和 rs2023239 单核苷酸多态性进行基因分型。
测定 CNR1 基因型、人体测量学指标(体重指数(BMI)、腰围(WC)和双能 X 射线吸收法测定的体脂分布)和代谢参数(血糖、血脂谱和胰岛素抵抗指数)。
3813G 等位基因与较高的体重、BMI、WC、总脂肪或脂肪百分比无显著相关性,但与较高的男性型脂肪沉积(2971.78±1655.08 比 2472.64±1300.53,P=0.007)和男性型脂肪百分比(37.59±8.45 比 35.66±7.63,P=0.062)相关。G1422A、A4895G、rs806381、rs10485170、rs6454674 和 rs2023239 变体之间没有相关性。
CNR1 变体与波兰绝经后妇女肥胖相关表型相关。由于大麻素受体 1 是肥胖的药物靶点,因此通过内源性大麻素阻断治疗肥胖的受体基因分析可能有助于识别最佳应答者。