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[未提及具体基因名称]基因的表达与自闭症谱系障碍临床表现的关联

Association of , , , and Genes' Expression with the Clinical Presentation of Autism Spectrum Disorder.

作者信息

Wilczyński Krzysztof Maria, Auguściak-Duma Aleksandra, Stasik Aleksandra, Cichoń Lena, Kawalec Alicja, Janas-Kozik Małgorzata

机构信息

Department of Developmental Age Psychiatry and Psychotherapy, Medical University of Silesia, 40-061 Katowice, Poland.

John Paul II Children's and Family Health Center in Sosnowiec sp. z o.o., Gabrieli Zapolskiej 3, 41-218 Sosnowiec, Poland.

出版信息

Curr Issues Mol Biol. 2023 Oct 16;45(10):8359-8371. doi: 10.3390/cimb45100527.

Abstract

Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder that affects social interactions, communication, and behavior. Although the predominant genetic predisposition to ASD seems beyond doubt, its exact nature remains unclear. In the context of social cognition disorders and the basis of ASD, the oxytocinergic and vasopresynergic systems arouse great interest among researchers. The aim of the present study was to analyze gene expression levels for oxytocin and vasopressin receptors, as well as CD38 protein and oxytocinase, in the context of the clinical picture of autism spectrum disorders. The study included 90 people, of whom 63 were diagnosed with ASD based on anamnesis, mental status testing, and the ADOS-2 protocol. The results obtained in the presented study indicate that the balance between the levels of expression of the CD38 gene and the oxytocinase gene plays a key role in the risk and clinical presentation of ASD. In a hypothetical scenario, an imbalance in the expression of CD38 and LNPEP could potentially lead to alterations in the concentrations of oxytocin and vasopressin. At the same time, the most frequently studied genes-AVPR1a and OXTR-seem to be at best of marginal importance for the risk of ASD.

摘要

自闭症谱系障碍(ASD)是一种复杂的神经发育障碍,会影响社交互动、沟通和行为。尽管ASD的主要遗传易感性似乎毋庸置疑,但其确切性质仍不清楚。在社会认知障碍的背景下以及ASD的基础方面,催产素能和加压素能系统引起了研究人员的极大兴趣。本研究的目的是在自闭症谱系障碍的临床症状背景下,分析催产素和加压素受体、CD38蛋白和催产素酶的基因表达水平。该研究纳入了90人,其中63人根据病史、精神状态测试和ADOS-2协议被诊断为ASD。本研究获得的结果表明,CD38基因和催产素酶基因的表达水平之间的平衡在ASD的风险和临床表现中起关键作用。在一个假设的情景中,CD38和LNPEP表达的失衡可能会导致催产素和加压素浓度的改变。同时,研究最频繁的基因——AVPR1a和OXTR——对于ASD风险似乎至多只有边际重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6034/10604998/c78c65243b77/cimb-45-00527-g001.jpg

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