TMX2-CTNND1多态性对精神分裂症患者及其未受影响的兄弟姐妹皮层厚度的影响:基于靶区测序的探索性研究。

IF 3.6 3区 医学 Q1 PSYCHIATRY
Revista Brasileira de Psiquiatria Pub Date : 2024-01-01 Epub Date: 2024-01-12 DOI:10.47626/1516-4446-2023-3322
Wenjian Tan, Yixin Cheng, Danqing Huang, Dayi Liu, Jiamei Zhang, Jinyue Li, Zhening Liu, Yunzhi Pan
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引用次数: 0

摘要

目的:神经影像学和遗传学研究的发展揭示了形态异常和众多风险基因的存在及其关联:神经影像学和遗传学研究的发展揭示了精神分裂症的形态异常和众多风险基因及其关联:方法:测量了 129 名精神分裂症患者、42 名患者未受影响的兄弟姐妹和 112 名健康对照者的皮层厚度,并对候选基因进行了测序。比较了三组患者的皮层厚度(包括德西坎-基利安尼图谱中的 68 个区域)和基因变异(108 个精神分裂症风险基因中的变异),并对皮层厚度、临床症状、N 回和逻辑记忆测试等认知测试与基因变异之间的相关性进行了分析:研究发现,与健康对照组和未受影响的兄弟姐妹相比,精神分裂症患者的双侧额回、颞回和顶回明显变薄。此外,目标基因的关联分析发现,4个SNV与精神分裂症诊断有显著关联,包括TMX2-CTNND1(SNV20673)(PFDR = 0.008)和CENPM(rs35542507、rs41277477、rs73165153)(PFDR = 0.030)。此外,与非携带者相比,SNV20673 变异携带者右三角旁的皮质厚度更薄(PFDR = 0.048)。最后,研究发现精神分裂症患者右三角旁皮层厚度与逻辑记忆之间存在正相关(r = 0.199,P = 0.032):本研究发现了精神分裂症的区域形态异常,包括布洛卡区的右侧同源区,这与影响δ-1 catenin的风险变异有关,并影响逻辑记忆。这些发现表明候选基因位点、皮层厚度与精神分裂症之间存在潜在联系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Influence of TMX2-CTNND1 polymorphism on cortical thickness in schizophrenia patients and unaffected siblings: an exploratory study based on target region sequencing.

Objective: The advancement of neuroimaging and genetic research has revealed the presence of morphological abnormalities and numerous risk genes, along with their associations. We aimed to estimate magnetic resonance imaging-derived cortical thickness across multiple brain regions.

Methods: The cortical thickness of 129 schizophrenia patients, 42 of their unaffected siblings, and 112 healthy controls was measured and the candidate genes were sequenced. Comparisons were made of cortical thickness (including 68 regions of the Desikan-Killiany Atlas) and genetic variants (in 108 risk genes for schizophrenia) among the three groups, and correlation analyses were performed regarding cortical thickness, clinical symptoms, cognitive tests (such as the N-back task and the logical memory test), and genetic variants.

Results: Schizophrenia patients had significantly thinner bilateral frontal, temporal, and parietal gyri than healthy controls and unaffected siblings. Association analyses in target genes showed that four single nucleotide variants (SNVs) were significantly associated with schizophrenia, including thioredoxin-related transmembrane protein 2-catenin, cadherin-associated protein, delta 1 (SNV20673) (positive false discovery rate [PFDR] = 0.008) and centromere protein M (rs35542507, rs41277477, rs73165153) (PFDR = 0.030). Additionally, cortical thickness in the right pars triangularis was lower in carriers of the SNV20673 variant than in non-carriers (PFDR = 0.048). Finally, a positive correlation was found between right pars triangularis cortical thickness and logical memory in schizophrenia patients (r = 0.199, p = 0.032).

Conclusions: This study identified regional morphological abnormalities in schizophrenia, including the right homologue of Broca's area, which was associated with a risk variant that affected delta-1 catenin and logical memory. These findings suggest a potential association between candidate gene loci, cortical thickness, and schizophrenia.

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来源期刊
Revista Brasileira de Psiquiatria
Revista Brasileira de Psiquiatria 医学-精神病学
CiteScore
6.60
自引率
0.00%
发文量
83
审稿时长
6-12 weeks
期刊介绍: The Revista Brasileira de Psiquiatria (RBP) is the official organ of the Associação Brasileira de Psiquiatria (ABP - Brazilian Association of Psychiatry). The Brazilian Journal of Psychiatry is a bimonthly publication that aims to publish original manuscripts in all areas of psychiatry, including public health, clinical epidemiology, basic science, and mental health problems. The journal is fully open access, and there are no article processing or publication fees. Articles must be written in English.
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