Huang Jichong, Zhu Tingting, Qu Yi, Mu Dezhi
Department of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, 610041, China.
Key Laboratory of Obstetric & Gynecologic and Pediatric Diseases and Birth Defects of Ministry of Education, Sichuan University, Chengdu, 610041, China.
PLoS One. 2016 Apr 25;11(4):e0153655. doi: 10.1371/journal.pone.0153655. eCollection 2016.
The etiology of non-genetic intellectual disability (ID) is not fully known, and we aimed to identify the prenatal, perinatal and neonatal risk factors for ID.
PubMed and Embase databases were searched for studies that examined the association between pre-, peri- and neonatal factors and ID risk (keywords "intellectual disability" or "mental retardation" or "ID" or "MR" in combination with "prenatal" or "pregnancy" or "obstetric" or "perinatal" or "neonatal". The last search was updated on September 15, 2015. Summary effect estimates (pooled odds ratios) were calculated for each risk factor using random effects models, with tests for heterogeneity and publication bias.
Seventeen studies with 55,344 patients and 5,723,749 control individuals were eligible for inclusion in our analysis, and 16 potential risk factors were analyzed. Ten prenatal factors (advanced maternal age, maternal black race, low maternal education, third or more parity, maternal alcohol use, maternal tobacco use, maternal diabetes, maternal hypertension, maternal epilepsy and maternal asthma), one perinatal factor (preterm birth) and two neonatal factors (male sex and low birth weight) were significantly associated with increased risk of ID.
This systemic review and meta-analysis provides a comprehensive evidence-based assessment of the risk factors for ID. Future studies are encouraged to focus on perinatal and neonatal risk factors and the combined effects of multiple factors.
非遗传性智力残疾(ID)的病因尚不完全清楚,我们旨在确定ID的产前、围产期和新生儿危险因素。
检索PubMed和Embase数据库,查找研究产前、围产期和新生儿因素与ID风险之间关联的研究(关键词为“智力残疾”或“精神发育迟缓”或“ID”或“MR”,并与“产前”或“妊娠”或“产科”或“围产期”或“新生儿”组合)。最后一次检索于2015年9月15日更新。使用随机效应模型计算每个危险因素的汇总效应估计值(合并比值比),并进行异质性检验和发表偏倚检验。
17项研究涉及55344例患者和5723749例对照个体,符合纳入我们分析的条件,共分析了16个潜在危险因素。10个产前因素(母亲年龄较大、母亲为黑人种族、母亲教育程度低、第三胎及以上、母亲饮酒、母亲吸烟、母亲患糖尿病、母亲患高血压、母亲患癫痫和母亲患哮喘)、1个围产期因素(早产)和2个新生儿因素(男性和低出生体重)与ID风险增加显著相关。
本系统评价和荟萃分析为ID危险因素提供了全面的循证评估。鼓励未来的研究关注围产期和新生儿危险因素以及多种因素的综合作用。