Mary Maniraja Jesintha, Saravanan Lakshmanan, Deecaraman Munuswamy, Vijayalakshmi Melantharu, Umashankar Vetrivel, Sailaja Jaigopal
Dr. MGR Educational and Research Institute, Maduravoyal, Chennai.
ARC International Fertility Research Center, Perambur, Chennai.
Bioinformation. 2017 May 31;13(5):149-153. doi: 10.6026/97320630013149. eCollection 2017.
Polycystic Ovary syndrome (PCOS) is the most common endocrine disorder affecting 5 - 10% of all women of reproductive age group. The present research was carried out to study the impact of Plasminogen Activator Inhibitor (PAI-1) 4G/5G polymorphism (rs1799889) in PCOS, and the risk of developing PCOS in South Indian Population. The study was carried out in 60 subjects of South Indian population (30 PCOS and 30 Non PCOS) recruited from ARC Research and Fertility Centre, Chennai, India. Genotype and Allelic frequencies were compared by Fisher exact test, Hardy Weinberg equilibrium. p<0.05 was considered statistically significant. The Genotype frequency difference between PCOS and non-PCOS was observed as statistically non-significant (p=0.4647, OR=1.3077, 95% CI 0.63-2.68). The allelic frequency distribution in Spontaneous Abortion (SAB) cases in total subjects is not found to be statistically significant (p=0. 29), however the PCOS women carrying mutant homozygous and heterozygous genotype are more prone to recurrent pregnancy loss. Out of 17 Implantation failure cases, 23.52% were found to carry mutant homozygous (4G/4G), and 66.66% carried mutant heterozygous (4G/5G), and 5.88% carried wild type homozygous (5G/5G), the allelic difference was highly significant with 4G (62.5%), and 5G (37.5%). P value is highly significant and recorded at p=0.0164. The positive correlation between PAI-1 4G/5G polymorphism and PCOS risk was not observed in this study, however, the correlation between Recurrent Pregnancy Loss (RPL) and Implantation failures were observed in PCOS cases.
多囊卵巢综合征(PCOS)是最常见的内分泌紊乱疾病,影响着5%至10%的育龄女性。本研究旨在探讨纤溶酶原激活物抑制剂(PAI-1)4G/5G多态性(rs1799889)对PCOS的影响以及印度南部人群患PCOS的风险。该研究在印度钦奈ARC研究与生育中心招募的60名印度南部人群受试者中进行(30名PCOS患者和30名非PCOS患者)。通过Fisher精确检验、哈迪-温伯格平衡比较基因型和等位基因频率。p<0.05被认为具有统计学意义。PCOS组与非PCOS组之间的基因型频率差异无统计学意义(p=0.4647,OR=1.3077,95%CI 0.63 - 2.68)。在所有受试者的自然流产(SAB)病例中,等位基因频率分布无统计学意义(p=0.29),然而携带突变纯合子和杂合子基因型的PCOS女性更容易反复流产。在17例植入失败病例中,发现23.52%携带突变纯合子(4G/4G),66.66%携带突变杂合子(4G/5G),5.88%携带野生型纯合子(5G/5G),4G(62.5%)和5G(37.5%)的等位基因差异高度显著。P值高度显著,记录为p=0.0164。本研究未观察到PAI-1 4G/5G多态性与PCOS风险之间的正相关,然而,在PCOS病例中观察到反复流产(RPL)与植入失败之间的相关性。