[Association of the -c.108C>T and c.192Q>R polymorphisms of the PON1 gene with preeclampsia among Chinese women].

Xinyuan Zhang, Ping Fan, Qingqing Liu, Xinghui Liu, Huai Bai, Yujie Wu, Suiyan Li
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引用次数: 0

Abstract

Objective: To assess the association of -c.108C>T and c.192Q>R polymorphisms of paraoxonase 1 (PON1) gene with preeclampsia (PE) and the influence of genotypes on the metabolic and oxidative stress indexes among Chinese women.

Methods: This case-control study has included 334 patients with PE and 1337 healthy pregnant women. The -c.108C>T and c.192Q>R genotypes were determined by PCR and restriction fragment length polymorphism method. Metabolic and oxidative stress parameters were also analyzed.

Results: No statistical difference in the genotypic and allelic frequencies for the -c.108C>T and c.192Q>R polymorphisms of the PON1 gene was found between the PE patients and the healthy controls (P > 0.05). Nevertheless, the 192Q-108T haplotype of these polymorphisms was associated with an increased risk of PE (P = 0.007). Total antioxidant capacity (TAC) and atherosderosis index were higher in patients with the -108TT genotype compared with those with a CT genotype (P < 0.05); whilst total oxidant status was lower in patients with a CT genotype compared with those with a CC genotype (P = 0.036). Malondialdehyde level was higher in patients with a 192RR genotype compared with those with a QQ genotype (P = 0.019). TAC level was higher in patients with a RR genotype compared with those with a QR genotype (P = 0.015).

Conclusion: The 192Q-108T haplotype of the PON1 gene is associated with the risk for PE. These polymorphisms may be associated with abnormal lipid metabolism and oxidative stress among Chinese PE patients.

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[PON1基因的-c.108C>T和c.192Q>R多态性与中国妇女子痫前期的关系]。
目的评估副氧合酶 1(PON1)基因-c.108C>T 和 c.192Q>R 多态性与子痫前期(PE)的相关性,以及基因型对中国女性代谢和氧化应激指标的影响:这项病例对照研究纳入了334名子痫前期患者和1337名健康孕妇。采用 PCR 和限制性片段长度多态性方法测定了-c.108C>T 和 c.192Q>R 基因型。同时还分析了代谢和氧化应激参数:结果:在 PE 患者和健康对照组之间,PON1 基因的 -c.108C>T 和 c.192Q>R 多态性的基因型和等位基因频率没有统计学差异(P > 0.05)。然而,这些多态性的 192Q-108T 单倍型与 PE 风险增加有关(P = 0.007)。与 CT 基因型患者相比,-108TT 基因型患者的总抗氧化能力(TAC)和动脉粥样硬化指数更高(P < 0.05);而与 CC 基因型患者相比,CT 基因型患者的总氧化状态更低(P = 0.036)。基因型为 192RR 的患者丙二醛水平高于基因型为 QQ 的患者(P = 0.019)。RR基因型患者的TAC水平高于QR基因型患者(P = 0.015):结论:PON1 基因的 192Q-108T 单倍型与 PE 风险有关。这些多态性可能与中国 PE 患者的脂质代谢异常和氧化应激有关。
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来源期刊
中华医学遗传学杂志
中华医学遗传学杂志 Medicine-Medicine (all)
CiteScore
0.50
自引率
0.00%
发文量
9521
期刊介绍: Chinese Journal of Medical Genetics is a medical journal, founded in 1984, under the supervision of the China Association for Science and Technology, sponsored by the Chinese Medical Association (hosted by Sichuan University), and is now a monthly magazine, which attaches importance to academic orientation, adheres to the scientific, scholarly, advanced, and innovative, and has a certain degree of influence in the industry. Chinese Journal of Medical Genetics is a journal of Peking University, and is now included in Peking University Journal (Chinese Journal of Humanities and Social Sciences), CSCD Source Journals of Chinese Science Citation Database (with extended version), Statistical Source Journals (China Science and Technology Dissertation Outstanding Journals), Zhi.com (in Chinese), Wipu (in Chinese), Wanfang (in Chinese), CA Chemical Abstracts (U.S.), JST (Japan Science and Technology Science and Technology), and JST (Japan Science and Technology Science and Technology Research Center). ), JST (Japan Science and Technology Agency), Pж (AJ) Abstracts Journal (Russia), Copernicus Index (Poland), Cambridge Scientific Abstracts, Abstracts and Citation Database, Abstracts Magazine, Medical Abstracts, and so on.
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