Pre-, peri- and neonatal risk factors for autism

被引:174
作者
Guinchat, Vincent [1 ]
Thorsen, Poul [2 ]
Laurent, Claudine [1 ,3 ]
Cans, Christine [4 ]
Bodeau, Nicolas [1 ]
Cohen, David [1 ]
机构
[1] Pitie Salpetriere Univ Hosp, Dept Child & Adolescent Psychiat, Paris, France
[2] Lillebaelt Hosp, Dept Obstet & Gynecol, Kolding, Denmark
[3] Univ Paris 06, Pitie Salpetriere Hosp,UMR 7225, Biotechnol & Biotherapy Unit,UMR S 975, Res Ctr,Brain & Spinal Cord Inst,INSERM,CNRS, Paris, France
[4] Register Disabled Children & Isere Cty Perinatal, Grenoble, France
关键词
Autism; prenatal; perinatal; neonatal; pervasive developmental disorders; risk factor; pregnancy; MINOR PHYSICAL ANOMALIES; OBSTETRIC COMPLICATIONS; SPECTRUM DISORDERS; PATERNAL AGE; PERINATAL FACTORS; CHILDHOOD AUTISM; INFANTILE-AUTISM; BIRTH-WEIGHT; HEAD CIRCUMFERENCE; PARENTAL AGE;
D O I
10.1111/j.1600-0412.2011.01325.x
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective. To identify pre-, peri- and neonatal risk factors for pervasive developmental disorders (PDD). Methods. We searched the Medline database through March 2011 for relevant casecontrol and population-based studies on pre-, peri- and neonatal hazards related to PDD, including autism. We identified 85 studies for this review. Data were extracted systematically and organized according to risk factors related to family history, pregnancy, gestational age, delivery, birth milestones and the neonate's condition at birth. Results. During the prenatal period, risk factors for PDD were advanced maternal or paternal ages, being firstborn vs. third or later, maternal prenatal medication use and mother's status as foreign born. During the perinatal and neonatal periods, the risk factors for PDD were preterm birth, breech presentation, planned cesarean section, low Apgar scores, hyperbilirubinemia, birth defect and a birthweight small for gestational age. The influence of maternal pre-eclampsia, diabetes, vomiting, infections and stress during pregnancy requires further study in order to determine risk for PDD. Discussion. Despite evidence for the association of some pre-, peri- and neonatal risk factors associated with PDD, it remains unclear whether these risks are causal or play a secondary role in shaping clinical expression in individuals with genetic vulnerability. A plausible hypothsesis is that improvements in obstetric and neonatal management have led to an increased rate of survivors with pre-existing brain damage. Given the variety of risk factors, we propose that future studies should investigate combinations of multiple factors, rather than focusing on a single factor.
引用
收藏
页码:287 / 300
页数:14
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