Tsai Hui-Ju, Liu Xin, Mestan Karen, Yu Yunxian, Zhang Shanchun, Fang Yaping, Pearson Colleen, Ortiz Katherin, Zuckerman Barry, Bauchner Howard, Cerda Sandra, Stubblefield Phillip G, Xu Xiping, Wang Xiaobin
Mary Ann and J. Milburn Smith Child Health Research Program, Children's Memorial Hospital and Children's Memorial Research Center, Department of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Hum Genet. 2008 May;123(4):359-69. doi: 10.1007/s00439-008-0485-9. Epub 2008 Mar 5.
Preterm delivery (PTD, <37 weeks of gestation) is a significant clinical and public health problem. Previously, we reported that maternal smoking and metabolic gene polymorphisms of CYP1A1 MspI and GSTT1 synergistically increase the risk of low birth weight. This study investigates the relationship between maternal smoking and metabolic gene polymorphisms of CYP1A1 MspI and GSTT1 with preterm delivery (PTD) as a whole and preterm subgroups. This case-control study included 1,749 multi-ethnic mothers (571 with PTD and 1,178 controls) enrolled at Boston Medical Center. After adjusting covariates, regression analyses were performed to identify individual and joint associations of maternal smoking, two functional variants of CYP1A1 and GSTT1 with PTD. We observed a moderate effect of maternal smoking on PTD (OR = 1.6; 95% CI: 1.1-2.2). We found that compared to non-smoking mothers with low-risk genotypes, there was a significant joint association of maternal smoking, CYP1A1 (Aa/aa) and GSTT1 (absent) genotypes with gestational age (beta = -3.37; SE = 0.86; P = 9 x 10(-5)) and with PTD (OR = 5.8; 95% CI: 2.0-21.1), respectively. Such joint association was particularly strong in certain preterm subgroups, including spontaneous PTD (OR = 8.3; 95% CI: 2.7-30.6), PTD < 32 weeks (OR = 11.1; 95% CI: 2.9-47.7), and PTD accompanied by histologic chorioamnionitis (OR = 15.6; 95% CI: 4.1-76.7). Similar patterns were observed across ethnic groups. Taken together, maternal smoking significantly increased the risk of PTD among women with high-risk CYP1A1 and GSTT1 genotypes. Such joint associations were strongest among PTD accompanied by histologic chorioamnionitis.
早产(PTD,妊娠<37周)是一个重大的临床和公共卫生问题。此前,我们报道孕妇吸烟以及CYP1A1 MspI和GSTT1的代谢基因多态性会协同增加低出生体重的风险。本研究调查孕妇吸烟与CYP1A1 MspI和GSTT1的代谢基因多态性与整体早产(PTD)及早产亚组之间的关系。这项病例对照研究纳入了在波士顿医疗中心登记的1749名多民族母亲(571名早产母亲和1178名对照)。在调整协变量后,进行回归分析以确定孕妇吸烟、CYP1A1和GSTT1的两个功能变体与早产之间的个体和联合关联。我们观察到孕妇吸烟对早产有中度影响(OR = 1.6;95% CI:1.1 - 2.2)。我们发现,与具有低风险基因型的非吸烟母亲相比,孕妇吸烟、CYP1A1(Aa/aa)和GSTT1(缺失)基因型与孕周(β = -3.37;SE = 0.86;P = 9×10⁻⁵)以及与早产(OR = 5.8;95% CI:2.0 - 21.1)之间分别存在显著的联合关联。这种联合关联在某些早产亚组中尤为强烈,包括自发性早产(OR = 8.3;95% CI:2.7 - 30.6)、孕周<32周的早产(OR = 11.1;95% CI:2.9 - 47.7)以及伴有组织学绒毛膜羊膜炎的早产(OR = 15.6;95% CI:4.1 - 76.7)。在不同种族群体中观察到类似模式。综上所述,孕妇吸烟显著增加了具有高风险CYP1A1和GSTT1基因型女性的早产风险。这种联合关联在伴有组织学绒毛膜羊膜炎的早产中最为强烈。