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22号染色体缺失与精神分裂症中的自杀行为

Chromosome 22 Deletions and Suicidal Behavior in Schizophrenia.

作者信息

Bani-Fatemi Ali, Adanty Christopher, Dai Nasia, Graff Ariel, Gerretsen Philip, De Luca Vincenzo

机构信息

Centre for Addiction and Mental Health, Toronto, Ontario, Canada.

Centre for Addiction and Mental Health, Toronto, Ontario, Canada,

出版信息

Neuropsychobiology. 2021;80(5):393-400. doi: 10.1159/000513645. Epub 2021 Feb 18.

Abstract

BACKGROUND

Studies have shown that the overall copy number variant (CNV) load is associated with schizophrenia. Schizophrenia is a mental disorder that is frequently associated with suicidal behavior.

METHODS

We recruited 263 patients with schizophrenia from the Centre for Addiction and Mental Health. The Columbia Suicide Severity Rating Scale was used to assess the presence of lifetime suicide attempt. Genotyping was completed using the Illumina Omni 2.5 chip. We tested the association between deletion events on chromosome 22 with suicide attempt in our schizophrenia sample.

RESULTS

There was no significant difference between suicide attempters and non-attempters considering the presence/absence of deletion events on chromosome 22.

CONCLUSION

Although our results did not show a significant association between deletions on chromosome 22 and suicide attempt in schizophrenia, CNV studies may reveal important, novel insights and open further investigation for the treatment of neuropsychiatric diseases.

摘要

背景

研究表明,总体拷贝数变异(CNV)负荷与精神分裂症有关。精神分裂症是一种常与自杀行为相关的精神障碍。

方法

我们从成瘾与心理健康中心招募了263名精神分裂症患者。使用哥伦比亚自杀严重程度评定量表评估终生自杀未遂情况。使用Illumina Omni 2.5芯片完成基因分型。我们在精神分裂症样本中测试了22号染色体缺失事件与自杀未遂之间的关联。

结果

考虑22号染色体上缺失事件的有无,自杀未遂者和未未遂者之间没有显著差异。

结论

尽管我们的结果未显示22号染色体缺失与精神分裂症患者自杀未遂之间存在显著关联,但CNV研究可能会揭示重要的新见解,并为神经精神疾病的治疗开启进一步的研究。

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