The role of selected polymorphisms in regulation of gene CD38 expression and their effect on the clinical picture of autism spectrum disorders - preliminary study.

IF 0.9 4区 医学 Q4 PSYCHIATRY
Krzysztof Maria Wilczyński, Aleksandra Auguściak-Duma, Lena Cichoń, Aleksandra Stasik, Małgorzata Janas-Kozik
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引用次数: 0

Abstract

Objectives: Clinical effects observed in cases of oxytocin deficiency can also manifest themselves in disorders of mechanisms responsible, for example, for its secretion. For oxytocin, this function is played by - among others - the cluster of differentiation antigen 38 (CD38). Existing literature along with the correlation between protein CD38 and oxytocin secretion raise interest in the context of their possible relation to the clinical picture and development of the autism spectrum disorders (ASD). The aim of the study was to analyze the correlations between polymorphisms rs3796863 and rs6449197 in gene CD38, the level of gene expression and the clinical picture and the risk of ASD diagnosis.

Methods: The study included 59 individuals with the mean age of 15.05 years with IQ > 90. The participants were divided into two groups: the studied group consisting of 37 persons with confirmed ASD diagnoses and the control group including 22 neurotypical individuals. Diagnosis verification was carried out via the ADOS-2 protocol.

Results: The comparative analysis with the standardized population based on the 1000Genomes database with the presence of clinically significant intensification of ASD traits showed the correlation of alleles "T" of polymorphisms rs3796863 and rs6449197, which are more frequent in the general population and are treated as "wild". In the inter-group analysis, this type of dependency was weaker, and the genotype of the control group was somehow intermediate between the studied group and the standardized population. In the ΔΔCt analysis, the normalized value of the relative expression level of gene CD38 showed that in the studied group the expression level was around 1.1-1.2 times higher than in the control group.

Conclusions: The obtained results show that a significant correlation with the severity of autism spectrum disorder traits is mainly observed in the carriers of wild variants of the studied polymorphisms, in which the related increase in the expression level of gene CD38 is also observed.

某些多态性在调控 CD38 基因表达中的作用及其对自闭症谱系障碍临床表现的影响--初步研究。
目的:在催产素缺乏症病例中观察到的临床效应也可能表现为催产素分泌等机制的紊乱。催产素的这一功能主要由分化抗原集群 38(CD38)发挥。现有文献以及 CD38 蛋白和催产素分泌之间的相关性引起了人们对它们与自闭症谱系障碍(ASD)的临床表现和发展可能存在的关系的兴趣。本研究旨在分析 CD38 基因多态性 rs3796863 和 rs6449197、基因表达水平与临床表现及 ASD 诊断风险之间的相关性:研究对象包括 59 名智商大于 90 的个体,平均年龄为 15.05 岁。参与者分为两组:研究组包括 37 名确诊为 ASD 的患者,对照组包括 22 名神经典型患者。诊断验证通过 ADOS-2 协议进行:与基于 1000Genomes 数据库的标准化人群的比较分析显示,多态性 rs3796863 和 rs6449197 的等位基因 "T "与 ASD 临床特征明显增强相关,而这两种多态性在普通人群中更为常见,并被视为 "野生"。在组间分析中,这种依赖性较弱,对照组的基因型在某种程度上介于研究组和标准化人群之间。在ΔΔCt分析中,CD38基因相对表达水平的归一化值显示,研究组的表达水平约为对照组的1.1-1.2倍:结论:研究结果表明,自闭症谱系障碍特征的严重程度与所研究多态性野生变异的携带者有明显的相关性,其中也观察到基因 CD38 表达水平的相关升高。
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来源期刊
Psychiatria polska
Psychiatria polska 医学-精神病学
CiteScore
2.30
自引率
23.50%
发文量
92
审稿时长
6-12 weeks
期刊介绍: Information not localized
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