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中国汉族女性 GCLC rs17883901 多态性与子痫前期的遗传易感性分析。

Genetic susceptibility analysis of GCLC rs17883901 polymorphism to preeclampsia in Chinese Han women.

机构信息

Obstetrical Department, Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.

Clinical Laboratory, Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.

出版信息

Gynecol Endocrinol. 2020 Sep;36(9):781-785. doi: 10.1080/09513590.2020.1725970. Epub 2020 Feb 14.

Abstract

Preeclampsia (PE) is a specific obstetric disorder that may result in maternal and neonatal morbidity and mortality. Increasing evidence has been indicated that some candidate genes related to oxidative stress, such as glutamate-cysteine ligase, catalytic subunit (GCLC), glutamate-cysteine ligase, modifier subunit (GCLM), involve in the pathogenesis of PE. After the genetic contribution of GCLC rs17883901 polymorphism was analyzed by TaqMan allelic discrimination real-time PCR in 1001 PE patients and 1182 normal pregnant women, a case-control association analysis was performed. Although no statistical difference was found in genetic distribution of rs17883901 in GCLC between PE and control group ( = 2.201,  = .333 by genotypic,  = 0.524,  = .469, OR = 0.932, 95%CI = 0.771-1.128 by allelic), significant differences in the genotypic frequencies were investigated between mild PE group ( = 6.999,  = .030) or late-onset PE group ( = 6.197,  = .045) and control group. Furthermore, when dividing the mild PE patients, the late-onset PE patients and the controls into TT/CT + CC, TT + CT/CC, and TT/CC subgroups, we found statistical differences between mild PE and controls (TT/CT + CC: = 5.132,  = .023, OR = 2.948, 95%CI = 1.107-7.854; TT/CC: = 4.564,  = .033, OR = 2.793, 95%CI = 1.046-7.460) as well as late-onset PE and controls (TT/CT + CC: = 4.043,  = .044, OR = 2.248, 95%CI = 1.000-5.055). This is the first study to indicate GCLC rs17883901 polymorphism may be associated with a risk of mild PE and late-onset PE in Chinese Han women. However, additional well-designed studies with multi-ethnic and large-scale samples should be performed to validate our results.

摘要

子痫前期(PE)是一种特定的产科疾病,可能导致母婴发病率和死亡率升高。越来越多的证据表明,一些与氧化应激相关的候选基因,如谷氨酸-半胱氨酸连接酶,催化亚基(GCLC)、谷氨酸-半胱氨酸连接酶,调节亚基(GCLM),参与了 PE 的发病机制。在对 1001 例 PE 患者和 1182 例正常孕妇进行 TaqMan 等位基因鉴别实时 PCR 分析 GCLC rs17883901 的遗传贡献后,进行了病例对照关联分析。尽管在 PE 组和对照组之间,GCLC rs17883901 的遗传分布没有统计学差异(基因型 = 2.201, = .333,等位基因 = 0.524, = 0.469,OR = 0.932,95%CI = 0.771-1.128),但在轻度 PE 组( = 6.999, = .030)或晚发型 PE 组( = 6.197, = .045)与对照组之间,基因型频率存在显著差异。此外,当将轻度 PE 患者、晚发型 PE 患者和对照组分为 TT/CT+CC、TT+CT/CC 和 TT/CC 亚组时,我们发现轻度 PE 与对照组之间存在统计学差异(TT/CT+CC: = 5.132, = .023,OR = 2.948,95%CI = 1.107-7.854;TT/CC: = 4.564, = .033,OR = 2.793,95%CI = 1.046-7.460)以及晚发型 PE 与对照组之间(TT/CT+CC: = 4.043, = .044,OR = 2.248,95%CI = 1.000-5.055)。这是第一项表明 GCLC rs17883901 多态性可能与中国汉族妇女轻度 PE 和晚发型 PE 发病风险相关的研究。然而,应该进行更多设计良好的、具有多民族和大规模样本的研究来验证我们的结果。

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