伊拉克妇女维生素 D 受体 ApaI 基因的遗传多态性与多囊卵巢综合征生理参数的多样性

Safa F. Ali, Shiva Khezri, Ilham A. Khalaf, Dalia J. Mahmood
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摘要

多囊卵巢综合症(PCOS)是育龄妇女中普遍存在的一种荷尔蒙失调症,需要采取不同的管理策略。这项研究于 2023 年 1 月至 3 月在巴格达 Kamal Al-Samarrai 医院不孕不育中心进行,研究对象包括 80 名年龄在 18-45 岁之间的伊拉克妇女,其中包括 40 名多囊卵巢综合症患者和 40 名健康对照者。采用 PCR-RFLP 系统评估了激素指标(FSH、LH、T、PRL、Ca2+ 和维生素 D3)以及全血基因组 DNA 中的 Apa1 基因多态性。与对照组相比,多囊卵巢综合征患者的 LH、LH/FSH、T 和 PRL 水平明显升高(P < 0.01),维生素 D 和钙水平较低(P < 0.05)。对 VDR 基因 Apa1 多态性的研究发现,在多囊卵巢综合征患者中,"Aa "和 "aa "基因型的发病率很高,分别占 65.00% 和 25.00%,而对照组为 17.50%,对照组为 0.00%。aa "等位基因在多囊卵巢综合症中更为常见,成为该病的潜在风险因素。这项研究确定了 VDR 基因(Apa1)多态性与多囊卵巢综合症之间的密切联系,强调了 "aa "等位基因的重要性。该研究强调了同源变异基因型 "aa "是多囊卵巢综合症的一个重要风险因素,为了解多囊卵巢综合症的遗传基础提供了见解。
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Genetic Polymorphisms of the Vitamin D Receptor ApaI Gene and Physiological Parameters Diversity of Polycystic Ovary Syndrome in Iraqi Women
Polycystic ovary syndrome (PCOS) is a prevalent hormonal disorder among women of reproductive age, requiring diverse management strategies. This study, conducted at Kamal Al-Samarrai Hospital Fertility Center/Baghdad from January to March 2023, included 80 Iraqi women aged 18-45, comprising 40 with PCOS and 40 healthy controls. Hormonal markers (FSH, LH, T, PRL, Ca2+, and Vitamin D3) were systematically assessed, along with Apa1 gene polymorphisms in whole blood genomic DNA using PCR-RFLP. PCOS patients showed significantly elevated LH, LH/FSH, T, and PRL levels (p < 0.01) and lower Vitamin D and calcium levels (p < 0.05) compared to controls. The scrutiny of VDR gene Apa1 polymorphism uncovered a notable prevalence of "Aa" and "aa" genotypes among PCOS patients, constituting 65.00% and 25.00%, respectively, in contrast to the control group's 17.50% and 0.00% in controls. The "aa" allele, more frequent in PCOS, emerged as a potential risk factor for the condition. This study establishes a strong association between VDR gene (Apa1) polymorphism and PCOS, highlighting the significance of the "aa" allele. It emphasizes the homozygous variant genotype "aa" as a substantial risk factor for PCOS, providing insights into its genetic basis.
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