Obstetrics and Gynecology, Prosserman Center for Population Health Research, Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, University of Toronto, Toronto, ON, Canada.
Department of Obstetrics and Gynecology, Sainte-Justine Hospital Research Center, University of Montreal, Montreal, QC, Canada.
Int J Gynaecol Obstet. 2018 Aug;142(2):221-227. doi: 10.1002/ijgo.12528. Epub 2018 May 30.
To determine whether pre-eclampsia is associated with polymorphisms in superoxide dismutase (SOD) genes among mother-father-infant triads.
We did this follow-up cohort study at 17 urban hospitals in Canada between October 1, 2008, and September 30, 2010. We recruited Canadian participants who had participated in the International Trial of Antioxidant Supplementation for the Prevention of Pre-eclampsia. Saliva specimens were collected for DNA extraction. The SOD1 +35A/C (rs2234694) and SOD2 Ala16Val C/T (rs4880) single-nucleotide polymorphisms (SNPs) were genotyped.
Dual presence of the SOD2 Ala16Val TT variant among mother-father pairs (n=657) was associated with an increased risk of pre-eclampsia when compared with the absence of the TT variant among the mother-father pairs (7/48 [14.6%] vs 11/339 [3.2%]; adjusted odds ratio 6.80, 95% confidence interval 2.32-19.95; P<0.001). By contrast, presence of a single T variant in mother-father pairs (16/270 [5.9%]) or mother-infant pairs (8/179 [4.5%]) was not associated with pre-eclampsia. The SOD1 +35A/CSNP was not associated with pre-eclampsia.
The SOD2 Ala16Val SNP might be involved in paternal influence on the maternal predisposition to pre-eclampsia. Genotyping of mother-father pairs could be a promising strategy to identify pre-eclampsia genes.
确定母体-父体-婴儿三联体中超氧化物歧化酶(SOD)基因的多态性是否与先兆子痫有关。
我们在 2008 年 10 月 1 日至 2010 年 9 月 30 日期间在加拿大的 17 家城市医院进行了这项随访队列研究。我们招募了参加抗氧化剂补充预防先兆子痫国际试验的加拿大参与者。采集唾液样本用于 DNA 提取。对 SOD1+35A/C(rs2234694)和 SOD2Ala16ValC/T(rs4880)单核苷酸多态性(SNPs)进行基因分型。
与母亲-父亲对子中不存在 TT 变体的情况相比,母亲-父亲对子中存在 SOD2Ala16ValTT 变体的双重存在(n=657)与先兆子痫的风险增加相关(7/48[14.6%]与 11/339[3.2%];调整后的优势比 6.80,95%置信区间 2.32-19.95;P<0.001)。相比之下,母亲-父亲对子(16/270[5.9%])或母亲-婴儿对子(8/179[4.5%])中存在单个 T 变体与先兆子痫无关。SOD1+35A/C SNP 与先兆子痫无关。
SOD2Ala16Val SNP 可能参与了父亲对母亲易患先兆子痫的影响。对母亲-父亲对子进行基因分型可能是一种很有前途的识别先兆子痫基因的策略。