Shaikh Nuzhat, Dadachanji Roshan, Meherji Pervin, Shah Nalini, Mukherjee Srabani
Department of Molecular Endocrinology, National Institute for Research in Reproductive Health (ICMR), J.M. Street, Parel, Mumbai, India.
Department of Infertility, National Institute for Research in Reproductive Health (ICMR), Mumbai, India.
Gene. 2016 Feb 15;577(2):180-6. doi: 10.1016/j.gene.2015.11.033. Epub 2015 Nov 25.
Insulin-like factor 3 (INSL3), secreted by the ovarian theca cells is involved in androgen production, follicular growth and oocyte maturation. Both androgens and INSL3 levels are reported to be elevated in women with polycystic ovary syndrome (PCOS), indicating that INSL3 could contribute to PCOS etiology. This case-control association study explored the impact of INSL3 polymorphisms on PCOS susceptibility and its related traits.
Genotyping of exonic polymorphisms of INSL3 was performed in controls (n=333) and PCOS (n=405) women. Phenotyping (clinical, biochemical and hormonal parameters) was carried out in 205 controls and 301 PCOS women. Genotype, haplotype and genotype-phenotype associations were determined using statistical tests.
Three polymorphisms in exon 1-rs2286663 (G/A), rs1047233 (A/G), and rs6523 (A/G), and one in exon 3-rs1003887 (G/A), were present in our study subjects. The frequencies of rs6523 and AGAG haplotype were significantly increased in PCOS women. The rs6523 polymorphism showed significant association with increased cholesterol and HDL-C levels in PCOS women while in controls with decreased FBS, Bio-T and FAI, and increased SHBG levels. Significant association of, rs1047233 polymorphism with improved androgen related parameters in controls, rs2286663 polymorphism with decreased QUICKI in PCOS and rs1003887 polymorphism with increased insulin levels and HOMA-IR in controls were observed.
The rs6523 polymorphism and AGAG haplotype of INSL3 showed significant association with increased risk of PCOS. Additionally, INSL3 polymorphisms influenced metabolic and hyperandrogenemia related parameters in both controls and PCOS women. This is the first study to suggest that INSL3 may be a genetic predisposition factor in PCOS pathophysiology.
胰岛素样因子3(INSL3)由卵巢膜细胞分泌,参与雄激素生成、卵泡生长和卵母细胞成熟。据报道,多囊卵巢综合征(PCOS)女性的雄激素和INSL3水平均升高,这表明INSL3可能与PCOS的病因有关。这项病例对照关联研究探讨了INSL3基因多态性对PCOS易感性及其相关特征的影响。
对333名对照女性和405名PCOS女性进行INSL3外显子多态性基因分型。对205名对照女性和301名PCOS女性进行表型分析(临床、生化和激素参数)。使用统计检验确定基因型关联、单倍型关联和基因型-表型关联。
在我们的研究对象中,外显子1中有三个多态性——rs2286663(G/A)、rs1047233(A/G)和rs6523(A/G),外显子3中有一个多态性——rs1003887(G/A)。PCOS女性中rs6523和AGAG单倍型的频率显著增加。rs6523多态性与PCOS女性胆固醇和高密度脂蛋白胆固醇(HDL-C)水平升高显著相关,而在对照女性中与空腹血糖(FBS)、生物利用睾酮(Bio-T)和游离雄激素指数(FAI)降低以及性激素结合球蛋白(SHBG)水平升高相关。观察到rs1047XX3多态性与对照女性雄激素相关参数改善显著相关,rs2286663多态性与PCOS女性定量胰岛素敏感性检查指数(QUICKI)降低显著相关,rs1003887多态性与对照女性胰岛素水平和胰岛素抵抗稳态模型评估(HOMA-IR)升高显著相关。
INSL3的rs6523多态性和AGAG单倍型与PCOS风险增加显著相关。此外,INSL3多态性影响对照女性和PCOS女性的代谢及高雄激素血症相关参数。这是第一项表明INSL3可能是PCOS病理生理学中遗传易感性因素的研究。