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Genetic susceptibility analysis of GCLC rs17883901 polymorphism to preeclampsia in Chinese Han women.
Li, Jing; Yin, Fanglian; Lin, Yan; Gao, Ming; Wang, Ling; Liu, Shiguo; Song, Weiqing; Ye, Yuanhua.
Afiliação
  • Li J; Obstetrical Department, Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
  • Yin F; Obstetrical Department, Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
  • Lin Y; Clinical Laboratory, Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
  • Gao M; Transfusion Department, Lanzhou general hospital of Lanzhou Command, Lanzhou, Gansu, China.
  • Wang L; Department of Nephrology, Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
  • Liu S; Prenatal Diagnosis Center, Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
  • Song W; Clinical Laboratory, Municipal Hospital of Qingdao, Qingdao, Shandong, China.
  • Ye Y; Prenatal Diagnosis Center, Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Gynecol Endocrinol ; 36(9): 781-785, 2020 Sep.
Article em En | MEDLINE | ID: mdl-32054366
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 (χ2 = 2.201, p = .333 by genotypic, χ2 = 0.524, p = .469, OR = 0.932, 95%CI = 0.771-1.128 by allelic), significant differences in the genotypic frequencies were investigated between mild PE group (χ2 = 6.999, p = .030) or late-onset PE group (χ2 = 6.197, p = .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:χ2 = 5.132, p = .023, OR = 2.948, 95%CI = 1.107-7.854; TT/CC:χ2 = 4.564, p = .033, OR = 2.793, 95%CI = 1.046-7.460) as well as late-onset PE and controls (TT/CT + CC:χ2 = 4.043, p = .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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pré-Eclâmpsia / Polimorfismo de Nucleotídeo Único / Glutamato-Cisteína Ligase Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Pregnancy País/Região como assunto: Asia Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pré-Eclâmpsia / Polimorfismo de Nucleotídeo Único / Glutamato-Cisteína Ligase Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Pregnancy País/Região como assunto: Asia Idioma: En Ano de publicação: 2020 Tipo de documento: Article