Autism-related routines and rituals associated with a mitochondrial aspartate/glutamate carrier SLC25A12 polymorphism.

Jeremy M Silverman, Joseph D Buxbaum, Nicolas Ramoz, James Schmeidler, Abraham Reichenberg, Eric Hollander, Gary Angelo, Christopher J Smith, Lauren A Kryzak
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引用次数: 60

Abstract

Evidence for a genetic association between autism and two single nucleotide polymorphisms (SNPs), rs2056202 and rs2292813, in the mitochondrial aspartate/glutamate carrier (SLC25A12) gene led us to ask whether any of the four previously identified familial traits in autism spectrum disorders (ASD) varied by these SNPs. In 355 ASD cases from 170 sibships we examined levels of the four traits in these SNPs using ANCOVA models. The primary models selected unrelated affected cases and used age and sex as covariates. An ancillary set of models used all affected siblings and included "sibship" as a random effects independent variable. We found significantly lower levels of routines and rituals associated with the presence of the less frequent A allele in rs2056206. No other significant differences were observed. The rs2056202 polymorphism may be associated with levels of routines and rituals in autism and related disorders.

自闭症相关的常规和仪式与线粒体天冬氨酸/谷氨酸载体SLC25A12多态性相关。
自闭症与线粒体天冬氨酸/谷氨酸载体(SLC25A12)基因中rs2056202和rs2292813两个单核苷酸多态性(snp)之间存在遗传关联的证据使我们想知道,自闭症谱系障碍(ASD)中先前确定的四种家族性特征中是否有任何一种与这些snp有关。在来自170个兄弟姐妹的355个ASD病例中,我们使用ANCOVA模型检查了这些snp中四个特征的水平。主要模型选择不相关的受影响病例,并使用年龄和性别作为协变量。一组辅助模型使用了所有受影响的兄弟姐妹,并将“兄弟姐妹关系”作为随机效应的独立变量。我们发现,在rs2056206中,与频率较低的A等位基因存在相关的常规和仪式水平明显较低。未观察到其他显著差异。rs2056202多态性可能与自闭症及相关疾病的常规和仪式水平有关。
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