Cheslack-Postava Keely, Susser Ezra, Liu Kayuet, Bearman Peter S
Department of Psychiatry, Columbia University, New York, New York, United States of America.
Department of Epidemiology, Columbia University, New York, New York, United States of America; New York State Psychiatric Institute, New York, New York, United States of America.
PLoS One. 2015 Oct 23;10(10):e0141338. doi: 10.1371/journal.pone.0141338. eCollection 2015.
Sibling sex ratios have been applied as an indirect test of a hypothesized association between prenatal testosterone levels and risk for autism, a developmental disorder disproportionately affecting males. Differences in sibling sex ratios between those with and without autism would provide evidence of a shared risk factor for autism and offspring sex. Conclusions related to prenatal testosterone, however, require additional assumptions. Here, we used directed acyclic graphs (DAGs) to clarify the elements required for a valid test of the hypothesis that sibling sex ratios differ between children with and without autism. We then conducted such a test using a large, population-based sample of children.
Over 1.1 million subjects, born in California from 1992-2007, and identified through birth records, were included. The association between autism diagnosis, determined using the administrative database of the California Department of Developmental Services, and the sex of the subsequent sibling was examined using generalized estimating equations. Sources of potential bias identified using DAGs were addressed.
Among male children with autism, 52.2% of next-born siblings were brothers, versus 51.0% for unaffected males. For females with autism, 50.2% of following siblings were brothers versus 51.2% among control females. The relative risk of a subsequent male sibling associated with autism diagnosis was 1.02 (95% confidence interval: 0.99, 1.04).
In a large, population-based sample we failed to find evidence suggesting an excess of brothers among children with autism while controlling for several threats to validity. This test cannot rule out a role of any given exposure, including prenatal testosterone, in either risk of autism or offspring sex ratio, but suggests against a common cause of both.
兄弟姐妹的性别比例已被用作一种间接测试,以检验产前睾酮水平与自闭症风险之间的假设关联。自闭症是一种发育障碍,男性受影响的比例过高。自闭症患者与非自闭症患者的兄弟姐妹性别比例差异,将为自闭症和后代性别提供共同风险因素的证据。然而,与产前睾酮相关的结论需要额外的假设。在此,我们使用有向无环图(DAGs)来阐明对自闭症患儿与非自闭症患儿的兄弟姐妹性别比例存在差异这一假设进行有效检验所需的要素。然后,我们使用一个基于人群的大型儿童样本进行了这样的检验。
纳入了1992年至2007年在加利福尼亚州出生、通过出生记录识别的超过110万名受试者。使用加利福尼亚州发展服务部的行政数据库确定自闭症诊断,并使用广义估计方程检验后续兄弟姐妹的性别之间的关联。解决了使用DAGs识别出的潜在偏倚来源。
在患有自闭症的男性儿童中,52.2%的次出生兄弟姐妹是兄弟,而未受影响的男性为51.0%。对于患有自闭症的女性,50.2%的后续兄弟姐妹是兄弟,而对照女性中这一比例为51.2%。与自闭症诊断相关的后续男性兄弟姐妹的相对风险为1.02(95%置信区间:0.99,1.04)。
在一个基于人群的大样本中,我们未能找到证据表明在控制了几个有效性威胁的情况下,自闭症患儿中有过多的兄弟。这项检验不能排除任何特定暴露因素(包括产前睾酮)在自闭症风险或后代性别比例中的作用,但表明两者不存在共同原因。