Santos Tayssia Beatriz Dos, Paula Helena Korres de, Balarin Marly Aparecida Spadotto, Silva-Grecco Roseane Lopes, Lima Marco Fábio Prata, Resende Elisabete Aparecida Mantovani Rodrigues de, Gomes Mariana Kefalas Oliveira, Cintra Mariangela Torreglosa Ruiz
Universidade Federal do Triângulo Mineiro (UFTM), Uberaba, MG, Brasil.
Arch Endocrinol Metab. 2019 Sep 2;63(5):501-508. doi: 10.20945/2359-3997000000167. eCollection 2019.
To investigate the association of the genetic variants of the folate metabolism genes (MTHFR C677T; MTHFR A1298C; MTR A2756G; MTRR A66G and RFC-1 A80G) with the development of polycystic ovary syndrome (PCOS).
This study included 203 women (99 women with PCOS and 104 controls). The genotyping was performed by PCR-RFLP. Chi-squared test and multiple logistic regression were used in the statistical analysis. Haplotype analysis was conducted using the SNPstat program. The results were presented in odds ratio (OR) and confidence interval of 95% (CI-95%), with a significance level of 5% (p ≤ 0.05).
The genotypic distribution of the RFC-1 A80G polymorphism showed significant difference between the two groups, showing that the heterozygous genotype (AG genotype) was most frequent in controls. The polymorphic homozygous (GG genotype) of MTRR A66G polymorphism were most frequent in controls. The T-C haplotype MTHFR C677T and A1298C polymorphisms were more frequent in the control group (OR = 0.19; CI 95% - 0.04 to 0.93 e p = 0.042). The multivariate analysis evidenced that family history of PCOS was more frequent in the PCOS group (OR = 3.29; CI 95% - 1.48 to 7.31; p = 0.003).
In our casuistry, the polymorphic homozygous of MTRR A66G polymorphism gene and heterozygous of RFC-1 A80G polymorphism gene, the haplotype T-C C677T and A1298C polymorphisms of MTHFR gene, can be associated with protective factors for the disease.
探讨叶酸代谢基因(MTHFR C677T;MTHFR A1298C;MTR A2756G;MTRR A66G和RFC-1 A80G)的基因变异与多囊卵巢综合征(PCOS)发生发展的关联。
本研究纳入203名女性(99名PCOS患者和104名对照)。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)进行基因分型。统计分析采用卡方检验和多元逻辑回归。使用SNPstat程序进行单倍型分析。结果以比值比(OR)和95%置信区间(CI-95%)表示,显著性水平为5%(p≤0.05)。
RFC-1 A80G多态性的基因型分布在两组间存在显著差异,表明杂合基因型(AG基因型)在对照组中最为常见。MTRR A66G多态性的纯合多态性(GG基因型)在对照组中最为常见。MTHFR C677T和A1298C多态性的T-C单倍型在对照组中更为常见(OR = 0.19;CI 95% - 0.04至0.93;p = 0.042)。多因素分析表明,PCOS家族史在PCOS组中更为常见(OR = 3.29;CI 95% - 1.48至7.31;p = 0.003)。
在我们的病例中,MTRR A66G多态性基因的纯合多态性、RFC-1 A80G多态性基因的杂合性、MTHFR基因的T-C C677T和A1298C多态性单倍型可能与该疾病的保护因素相关。