Charlotte H. W. Wijers, Iris A. L. M. van Rooij, Carlo L. M. Marcelis, Han G. Brunner, Ivo de Blaauw, Nel Roeleveld
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引用次数: 57
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Abstract
Congenital anorectal malformations (ARMs) are one of the most frequently observed birth defects of the digestive system. However, their etiology remains elusive. Therefore, we aim to summarize and critically appraise all existing literature on the genetic and nongenetic etiology of nonsyndromic ARM and to conclude with unifying hypotheses and directions for future research. A structured literature search on English language human studies was conducted in PubMed and Embase up to October 1, 2013, resulting in 112 included articles. Research on the identification of genes underlying nonsyndromic ARM is remarkably scarce. Most studies were focused on screening of candidate genes for mutations or single-nucleotide polymorphisms, which did not yield any substantial evidence. Nongenetic factors fairly consistently found to be associated with ARM are assisted reproductive techniques, multiple pregnancy, preterm delivery, low birth weight, maternal overweight or obesity, and preexisting diabetes. This review provides indications for the involvement of both genes and nongenetic risk factors in the etiology of ARM. In future studies, large cohorts of patients with ARM from national and international collaborations are needed to acquire new hypotheses and knowledge through hypothesis-generating approaches. Challenges for future studies may also lie in the investigation of gene–gene and gene–environment interactions. Birth Defects Research (Part C) 102:382–400, 2014. © 2014 Wiley Periodicals, Inc.
非综合征性肛肠畸形的遗传和非遗传病因:系统综述
先天性肛肠畸形(ARMs)是最常见的消化系统出生缺陷之一。然而,它们的病因仍然难以捉摸。因此,我们的目标是总结和批判性评价所有关于非综合征性ARM的遗传和非遗传病因的现有文献,并得出统一的假设和未来的研究方向。在PubMed和Embase中对英语人类研究进行结构化文献检索,截至2013年10月1日,共纳入112篇文章。对非综合征性ARM的基因鉴定的研究非常少。大多数研究都集中在候选基因突变或单核苷酸多态性的筛选上,没有产生任何实质性的证据。与ARM相关的非遗传因素有辅助生殖技术、多胎妊娠、早产、低出生体重、母亲超重或肥胖以及既往糖尿病。这篇综述提供了基因和非遗传危险因素在ARM病因学中的作用。在未来的研究中,需要来自国家和国际合作的大量ARM患者队列,通过假设生成方法获得新的假设和知识。未来研究的挑战还可能在于基因-基因和基因-环境相互作用的研究。出生缺陷研究(C辑)(2):382 - 394,2014。©2014 Wiley期刊公司
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