Environmental Health Investigations Branch, California Department of Public Health, Richmond, California 94804, USA.
Autism Res. 2011 Dec;4(6):456-63. doi: 10.1002/aur.219. Epub 2011 Aug 31.
Thyroid hormones substantially influence central nervous system development during gestation. We hypothesized that perturbations of early thyroid profiles may contribute to the development of autism spectrum disorders (ASD). Thyroid pathways could provide a mechanism by which environmental factors that affect the thyroid system may impact autism occurrence or phenotypic expression. We investigated whether thyroxine (T4) levels at birth are associated with subsequent ASD, using two existing California study groups in multivariate analysis. One study group included children born in the San Francisco Bay Area in 1994, with cases identified through the California Department of Developmental Services (DDS) and/or the Kaiser Permanente Medical Care Program of Northern California (244 cases, 266 controls); the other included children born in California in 1995, with cases identified through DDS (310 cases, 518 controls). Matched controls were selected from birth certificate records. This exploratory analysis suggested that infants with very low T4 (<3rd percentile) may have higher ASD risk, although results reached statistical significance only for the 1995 study group (1995: OR = 2.74 (95% CI 1.30-5.75; 1994: OR = 1.71 (95% CI 0.57-5.19). A variety of alternate analyses were conducted with available data, without further resolution of the difference between the two study groups. The results of our study indicate that further studies are warranted to investigate whether thyroid hormone perturbations play a role in the development of ASD by evaluating additional potential confounders and genotype or phenotype in larger studies.
甲状腺激素在妊娠期间对中枢神经系统发育有重要影响。我们假设早期甲状腺参数的紊乱可能导致自闭症谱系障碍(ASD)的发展。甲状腺途径可能提供了一种机制,即影响甲状腺系统的环境因素可能会影响自闭症的发生或表型表达。我们通过多元分析,调查了出生时甲状腺素(T4)水平是否与随后的 ASD 有关,使用了两个现有的加利福尼亚研究组。一个研究组包括 1994 年在旧金山湾区出生的儿童,病例通过加利福尼亚发育服务部(DDS)和/或北加利福尼亚凯撒永久医疗保健计划(244 例,266 例对照)确定;另一个研究组包括 1995 年在加利福尼亚出生的儿童,病例通过 DDS 确定(310 例,518 例对照)。匹配对照从出生证明记录中选择。这项探索性分析表明,甲状腺素非常低(<第 3 个百分位)的婴儿可能有更高的 ASD 风险,尽管结果仅在 1995 年研究组中达到统计学意义(1995:OR = 2.74(95% CI 1.30-5.75;1994:OR = 1.71(95% CI 0.57-5.19)。对可用数据进行了各种替代分析,但未能进一步解决两个研究组之间的差异。我们的研究结果表明,有必要进行进一步的研究,以评估其他潜在的混杂因素和基因型或表型,在更大的研究中,进一步探讨甲状腺激素紊乱是否在 ASD 的发展中起作用。