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非综合征性肛门直肠畸形的遗传和非遗传病因:一项系统综述。

Genetic and nongenetic etiology of nonsyndromic anorectal malformations: a systematic review.

作者信息

Wijers Charlotte H W, van Rooij Iris A L M, Marcelis Carlo L M, Brunner Han G, de Blaauw Ivo, Roeleveld Nel

机构信息

Department for Health Evidence, Radboud university medical center, Nijmegen, The Netherlands.

出版信息

Birth Defects Res C Embryo Today. 2014 Dec;102(4):382-400. doi: 10.1002/bdrc.21068.

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.

摘要

先天性肛门直肠畸形(ARMs)是消化系统中最常见的出生缺陷之一。然而,其病因仍不清楚。因此,我们旨在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研究方向。截至2013年10月1日,在PubMed和Embase上对英语语言的人体研究进行了结构化文献检索,共纳入112篇文章。关于鉴定非综合征性ARM潜在基因的研究非常稀少。大多数研究集中于筛选候选基因的突变或单核苷酸多态性,但未得出任何实质性证据。相当一致地发现与ARM相关的非遗传因素包括辅助生殖技术、多胎妊娠、早产、低出生体重、母亲超重或肥胖以及糖尿病史。本综述为基因和非遗传危险因素参与ARM病因提供了线索。在未来的研究中,需要来自国内和国际合作的大量ARM患者队列,通过产生假设的方法获得新的假设和知识。未来研究的挑战可能还在于基因-基因和基因-环境相互作用的研究。

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