An Association Study Between Educational Attainment-related Genes and Cognitive Functions in Japanese Patients with Schizophrenia Based on Full Pleiotropy.

Juntendo Iji Zasshi Pub Date : 2024-02-10 eCollection Date: 2024-01-01 DOI:10.14789/jmj.JMJ23-0009-OA
Narihiro Orimo, Narimasa Katsuta, Wanyi Mao, Eriko Fukushima, Kaori Kawahara, Ken Nakayama, Hitoki Hirose, Hiroki Yamashita, Shohei Nishimon
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Abstract

Objectives: This study presents the multifaceted effects of candidate loci identified by genome-wide association studies on parameters such as educational background and the clinical symptoms of Japanese patients with schizophrenia along with detailed psychological measurements. This study aimed to investigate whether gene mutations that affect cognitive dysfunction are (1) related to the onset of schizophrenia and (2) also affect cognitive dysfunction in patients with schizophrenia.

Design: Case-control study.

Methods: This study evaluated 12 single-nucleotide polymorphisms (SNPs) (rs10189857, rs2175263, rs9398171, rs12670234, rs6466056, rs11156875, rs2018916, rs11663602, rs11885093, rs9404453, rs2473938, and rs4275659) that are common in Japanese individuals and demonstrated a relationship with schizophrenia and educational attainment in a previous genome-wide study. We included 640 Japanese patients (schizophrenia group) and 640 healthy participants (control group). Both groups were investigated for the relationship between the SNPs and educational attainment as well as psychometric evaluations of cognitive function.

Results: The 12 SNPs were not identified as genetic risk factors for schizophrenia. However, rs9404453 was associated with a decline in educational achievement, educational performance, Japanese Adult Reading Test (JART100) score, and Wechsler Adult Intelligence Scale-Revised (WAIS-R) (full-scale intelligence quotient [FSIQ]) score in patients with schizophrenia, SNP rs6466056 was associated with a decline in the WAIS-R (FSIQ) score, and SNP rs11663602 was associated with a decline in the JART100 score.

Conclusion: The SNPs rs9404453, rs6466056, and rs11663602 may be associated with academic performance or cognitive decline in patients with schizophrenia, although the overall findings from psychological tests did not show the expected consistency.

基于全多态性的日本精神分裂症患者教育成就相关基因与认知功能的关联研究
研究目的本研究介绍了全基因组关联研究发现的候选位点对日本精神分裂症患者的教育背景和临床症状等参数的多方面影响,以及详细的心理测量结果。本研究旨在探讨影响认知功能障碍的基因突变是否(1)与精神分裂症的发病有关,以及(2)是否也会影响精神分裂症患者的认知功能障碍:设计:病例对照研究:本研究评估了 12 个单核苷酸多态性(SNPs)(rs10189857、rs2175263、rs9398171、rs12670234、rs6466056、rs11156875、rs2018916、rs11663602、rs11885093、rs9404453、rs2473938和rs4275659),这些基因在日本人中很常见,并且在之前的一项全基因组研究中被证明与精神分裂症和教育程度有关。我们纳入了 640 名日本患者(精神分裂症组)和 640 名健康参与者(对照组)。我们对这两组人的 SNPs 与教育程度之间的关系以及认知功能的心理测量进行了调查:结果:12 个 SNPs 未被确定为精神分裂症的遗传风险因素。然而,rs9404453 与精神分裂症患者的教育成就、教育表现、日本成人阅读测试(JART100)得分和韦氏成人智力量表-修订版(WAIS-R)(全量表智商 [FSIQ])得分的下降有关,SNP rs6466056 与 WAIS-R (FSIQ) 分数的下降有关,SNP rs11663602 与 JART100 分数的下降有关:结论:尽管心理测试的总体结果未显示出预期的一致性,但SNPs rs9404453、rs6466056和rs11663602可能与精神分裂症患者的学习成绩或认知能力下降有关。
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