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Analysis of Sex and Recurrence Ratios in Simplex and Multiplex Autism Spectrum Disorder Implicates Sex-Specific Alleles as Inheritance Mechanism

机译:单纯性和多重自闭症谱系障碍的性别和复发比分析暗示特定性别等位基因为遗传机制

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Autism spectrum disorder (ASD) has a strong male bias, with four times as many affected males as females. ASD is hypothesized to follow a polygenic disease model. While prior literature has linked several genes with the disorder, the specific genetic causes and inheritance methods underlying the condition are still widely unknown. Here, we investigate two popular theories of polygenic inheritance that could account for the male preponderance of ASD: a multiple-threshold model in which females must have a higher genetic burden in order to be affected, and a sex-specific allele model in which variants in genes and regulatory regions have sex-specific effects. We use phenotypic information from the Simons Simplex Collection of families with simplex ASD and the iHART collection of families with multiplex ASD to compare ratios of affected males and females and sex-specific recurrence rates with predictions from each of the inheritance mechanisms. Our results suggest that a sex-specific allele model can be used to explain the male bias behind ASD inheritance.
机译:自闭症谱系障碍(ASD)具有强烈的男性偏见,受影响的男性是女性的四倍。假设ASD遵循多基因疾病模型。尽管现有文献已经将几种基因与该疾病联系在一起,但仍普遍未知导致该病的具体遗传原因和遗传方法。在这里,我们研究了两种流行的多基因遗传理论,这些理论可以解释男性自发症的优势:多阈值模型(其中女性必须承受更高的遗传负担才能受到影响)和性别特定的等位基因模型(其中变体在基因和调节区域有性别特异性作用。我们使用来自单纯性ASD的家庭的Simons单纯形收藏和具有多重ASD的家庭的iHART收藏的表型信息,将受影响男性和女性的比例以及特定性别的复发率与每种继承机制的预测进行比较。我们的结果表明,可以使用性别特定的等位基因模型来解释ASD遗传背后的男性偏见。

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