阿尔茨海默病相关基因变异与自闭症谱系障碍的关联:伊拉克队列的病例对照研究

IF 2.8 4区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Wisam H. Hoidy, Mohammed H. Al-Saadi, Simon Clegg, Doaa H. Chyad
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引用次数: 0

摘要

自闭症谱系障碍(ASD)是一种神经发育障碍,表现为社会沟通困难和限制和重复行为的存在。病因尚不清楚,尽管有越来越多的证据表明共享的神经发育和神经退行性疾病途径。本研究旨在确定先前与阿尔茨海默病(AD)相关的基因变异是否在ASD易感性中起作用。在病例对照框架内,我们研究了270名伊拉克儿童的样本,其中135名患有ASD, 135名年龄匹配的6-12岁对照。采用T-ARMS PCR技术对5个与AD相关的多态性NECTIN2 (rs6859)、CR1 (rs670173)、CLU (rs7982)、ABCA7 (rs3764650)和BIN1 (rs744373)进行基因型分析。多态性基因型和等位基因频率分析采用卡方检验,优势比分析采用95%置信区间。除了生化分析外,还进行了年龄和性别分层分析。3个多态性与ASD显著相关:CR1 rs670173 (p = 0.007)、CLU rs7982 (p = 0.010)和BIN1 rs744373 (p = 0.013)。男性对女性的影响比强于女性对男性的影响。有趣的是,年龄在6 - 9岁的小男孩显示出CLU rs7982最显著的效果(OR = 1.92, 95% CI: 1.25-2.94, p = 0.003)。NECTIN2 rs6859 (p = 0.543)和ABCA7 rs3764650 (p = 0.102)无显著相关性。各组间生化指标无显著差异。我们的研究结果表明,一些ad相关的基因变异,特别是那些与神经炎症和突触活性相关的基因变异,可能会增加患ASD的风险。这加强了神经发育和神经退行性疾病之间共享遗传风险因素的概念,可能涉及神经回路形成和维持的共同机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of Alzheimer’s-Related Gene Variants with Autism Spectrum Disorder: A Case–Control Study in an Iraqi Cohort

Autism spectrum disorder (ASD) is a neurodevelopmental disorder that manifests as difficulties in social communication and the presence of restricted and repetitive behaviors. The etiology remains obscure, although there is increasing evidence of shared neurodevelopmental and neurodegenerative disorder pathways. This study aimed to determine whether gene variants previously linked to Alzheimer’s disease (AD) have a role in ASD susceptibility. Within a case–control framework, we studied a sample of 270 Iraqi children, 135 with ASD and 135 age-matched controls aged 6–12 years. T-ARMS PCR was used to determine the genotypes of five selected polymorphisms NECTIN2 (rs6859), CR1 (rs670173), CLU (rs7982), ABCA7 (rs3764650), and BIN1 (rs744373) that have been associated with AD. The polymorphism genotype and allele frequencies were analyzed using the chi-square test, and odds ratio analysis with 95% confidence intervals was conducted. Age and sex-stratified analyses in addition to biochemical profiling were also conducted. Significant associations with ASD were found for three polymorphisms: CR1 rs670173 (p = 0.007), CLU rs7982 (p = 0.010), and BIN1 rs744373 (p = 0.013). The male-to-female effect ratio was stronger than the female-to-male. Interestingly, younger boys aged 6 to 9 years demonstrated the most pronounced effect of CLU rs7982 (OR = 1.92, 95% CI: 1.25–2.94, p = 0.003). NECTIN2 rs6859 (p = 0.543) and ABCA7 rs3764650 (p = 0.102) did not yield significant associations. Biochemical parameters showed no significant differences among the groups. Our results imply that some AD-associated gene variants, especially those related to neuroinflammation and synaptic activity, could elevate the risk for ASD. This reinforces the notion of shared genetic risk factors between neurodevelopmental and neurodegenerative disorders, likely involving common mechanisms for the formation and maintenance of neural circuits.

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来源期刊
Journal of Molecular Neuroscience
Journal of Molecular Neuroscience 医学-神经科学
CiteScore
6.60
自引率
3.20%
发文量
142
审稿时长
1 months
期刊介绍: The Journal of Molecular Neuroscience is committed to the rapid publication of original findings that increase our understanding of the molecular structure, function, and development of the nervous system. The criteria for acceptance of manuscripts will be scientific excellence, originality, and relevance to the field of molecular neuroscience. Manuscripts with clinical relevance are especially encouraged since the journal seeks to provide a means for accelerating the progression of basic research findings toward clinical utilization. All experiments described in the Journal of Molecular Neuroscience that involve the use of animal or human subjects must have been approved by the appropriate institutional review committee and conform to accepted ethical standards.
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