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日本精神分裂症患者中乙二醛酶I移码变异体p.P122fs的评估。

Assessment of a glyoxalase I frameshift variant, p.P122fs, in Japanese patients with schizophrenia.

作者信息

Ishizuka Kanako, Kimura Hiroki, Kushima Itaru, Inada Toshiya, Okahisa Yuko, Ikeda Masashi, Iwata Nakao, Mori Daisuke, Aleksic Branko, Ozaki Norio

机构信息

Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya.

Department of Neuropsychiatry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama.

出版信息

Psychiatr Genet. 2018 Oct;28(5):90-93. doi: 10.1097/YPG.0000000000000204.

Abstract

Enhanced carbonyl stress has been observed in a subgroup of patients with schizophrenia. Glyoxalase I, which is encoded by GLO1, is an enzyme that protects against carbonyl stress. In this study, we focused on the association between rare genetic variants of GLO1 and schizophrenia. First, we identified one heterozygous frameshift variant, p.P122fs, in 370 Japanese schizophrenia cases with allele frequencies of up to 1% by exon-targeted mutation screening of GLO1. We then performed an association analysis on 1282 cases and 1764 controls with this variant. The variant was found in three cases and eight controls. There was no statistically significant association between p.P122fs in GLO1 and schizophrenia (P=0.25). This frameshift variant in GLO1 might occur at near-polymorphic frequencies in the Japanese population, although further investigations using larger samples and biological analyses are needed to exclude the possibility of a low-penetrance genetic risk associated with this variant.

摘要

在一部分精神分裂症患者中观察到了增强的羰基应激。由GLO1编码的乙二醛酶I是一种抵御羰基应激的酶。在本研究中,我们聚焦于GLO1的罕见基因变异与精神分裂症之间的关联。首先,通过对GLO1进行外显子靶向突变筛查,我们在370例日本精神分裂症患者中鉴定出一个杂合移码变异p.P122fs,其等位基因频率高达1%。然后,我们对携带该变异的1282例病例和1764例对照进行了关联分析。在3例病例和8例对照中发现了该变异。GLO1中的p.P122fs与精神分裂症之间无统计学显著关联(P = 0.25)。GLO1中的这种移码变异在日本人群中可能以接近多态性的频率出现,不过需要使用更大样本进行进一步研究和生物学分析,以排除与该变异相关的低外显率遗传风险的可能性。

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