Anum Emmanuel A, Springel Edward H, Shriver Mark D, Strauss Jerome F
Department of Obstetrics and Gynecology, Virginia Commonwealth University, Richmond, Virginia 23298, USA.
Pediatr Res. 2009 Jan;65(1):1-9. doi: 10.1203/PDR.0b013e31818912e7.
Ethnic disparity in preterm delivery between African Americans and European Americans has existed for decades, and is likely the consequence of multiple factors, including socioeconomic status, environment, and genetics. This review summarizes existing information on genetic variation and its association with preterm birth in African Americans. Candidate gene-based association studies, in which investigators have evaluated particular genes selected primarily because of their potential roles in the process of normal and pathologic parturition, provide evidence that genetic contributions from both mother and fetus account for some of the disparity in preterm births. To date, most attention has been focused on genetic variation in pro- and anti-inflammatory cytokine genes and their respective receptors. These genes, particularly the pro-inflammatory cytokine genes and their receptors, are linked to matrix metabolism because these cytokines increase expression of matrix degrading metalloproteinases. However, the role that genetic variants that are different between populations play in preterm birth (e.g. the SERPINH1 - G56 SNP) cannot yet be quantified. Future studies based on genome wide association or admixture mapping may reveal other genes that contribute to disparity in prematurity.
非裔美国人和欧裔美国人在早产方面的种族差异已经存在了几十年,这可能是多种因素造成的,包括社会经济地位、环境和基因。这篇综述总结了非裔美国人中基因变异及其与早产关联的现有信息。基于候选基因的关联研究中,研究人员主要评估那些因其在正常和病理分娩过程中的潜在作用而被选择的特定基因,这些研究提供了证据表明母亲和胎儿的基因因素导致了部分早产差异。迄今为止,大多数关注都集中在促炎和抗炎细胞因子基因及其各自受体的基因变异上。这些基因,特别是促炎细胞因子基因及其受体,与基质代谢有关,因为这些细胞因子会增加基质降解金属蛋白酶的表达。然而,不同人群之间存在差异的基因变异在早产中所起的作用(例如SERPINH1 - G56单核苷酸多态性)尚无法量化。未来基于全基因组关联或混合映射的研究可能会揭示其他导致早产差异的基因。