Louwers Yvonne V, Rayner Nigel W, Herrera Blanca M, Stolk Lisette, Groves Christopher J, Barber Thomas M, Uitterlinden Andre G, Franks Stephen, Laven Joop S E, McCarthy Mark I
Department of Obstetrics and Gynecology, Subdivision of Reproductive Medicine, Erasmus MC University Medical Center, Rotterdam, the Netherlands.
Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom ; Oxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Oxford, United Kingdom.
PLoS One. 2014 Jan 31;9(1):e87335. doi: 10.1371/journal.pone.0087335. eCollection 2014.
Polycystic Ovary Syndrome (PCOS) has a strong genetic background and the majority of patients with PCOS have elevated BMI levels. The aim of this study was to determine to which extent BMI-increasing alleles contribute to risk of PCOS when contemporaneous BMI is taken into consideration.
Patients with PCOS and controls were recruited from the United Kingdom (563 cases and 791 controls) and The Netherlands (510 cases and 2720 controls). Cases and controls were of similar BMI. SNPs mapping to 12 BMI-associated loci which have been extensively replicated across different ethnicities, i.e., BDNF, FAIM2, ETV5, FTO, GNPDA2, KCTD15, MC4R, MTCH2, NEGR1, SEC16B, SH2B1, and TMEM18, were studied in association with PCOS within each cohort using the additive genetic model followed by a combined analysis. A genetic allelic count risk score model was used to determine the risk of PCOS for individuals carrying increasing numbers of BMI-increasing alleles.
None of the genetic variants, including FTO and MC4R, was associated with PCOS independently of BMI in the meta-analysis. Moreover, no differences were observed between cases and controls in the number of BMI-risk alleles present and no overall trend across the risk score groups was observed.
In this combined analysis of over 4,000 BMI-matched individuals from the United Kingdom and the Netherlands, we observed no association of BMI risk alleles with PCOS independent of BMI.
多囊卵巢综合征(PCOS)具有强大的遗传背景,大多数PCOS患者的BMI水平升高。本研究的目的是确定在考虑同期BMI的情况下,增加BMI的等位基因在多大程度上会增加PCOS的风险。
从英国(563例患者和791名对照)和荷兰(510例患者和2720名对照)招募PCOS患者和对照。病例和对照的BMI相似。使用加性遗传模型并进行联合分析,研究了映射到12个BMI相关基因座的单核苷酸多态性(SNP)与每个队列中的PCOS的相关性,这些基因座已在不同种族中广泛复制,即脑源性神经营养因子(BDNF)、FAIM2、ETS变异体5(ETV5)、脂肪量和肥胖相关基因(FTO)、6-磷酸葡萄糖脱氢酶(GNPDA2)、钾通道四聚体化结构域包含15(KCTD15)、促黑素细胞激素4受体(MC4R)、线粒体载体同源物2(MTCH2)、神经生长相关蛋白1(NEGR1)、分泌蛋白16B(SEC16B)、含SH2结构域的接头蛋白1(SH2B1)和跨膜蛋白18(TMEM18)。使用遗传等位基因计数风险评分模型来确定携带越来越多增加BMI的等位基因的个体患PCOS的风险。
在荟萃分析中,包括FTO和MC4R在内的所有遗传变异均独立于BMI与PCOS无关。此外,病例组和对照组在存在的BMI风险等位基因数量上没有差异,并且在风险评分组中未观察到总体趋势。
在对来自英国和荷兰的4000多名BMI匹配个体的联合分析中,我们观察到BMI风险等位基因与独立于BMI的PCOS之间没有关联。