肿瘤坏死因子- α (TNF-a)多态性与精神分裂症之间的关系:一项最新的荟萃分析

IF 2.9 4区 医学 Q2 PSYCHIATRY International Journal of Psychiatry in Clinical Practice Pub Date : 2022-09-01 Epub Date: 2022-02-21 DOI:10.1080/13651501.2021.2009879
Sidi He, Lei Zhang, Shunying Yu, Wenjuan Yu, Yimin Yu, Jingjing Huang, Huafang Li
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引用次数: 1

摘要

背景:先前的研究已经探索了肿瘤坏死因子- α (TNF-a)多态性与精神分裂症之间的关系。他们的结果是有争议的。我们进行了一项荟萃分析,以阐明TNF-a - 308 G/ a (rs1800629)、- 1031t /C(rs1799964)、- 863c / a (rs1800630)和-857 C/T (rs1799724)多态性与精神分裂症之间的关系。方法:纳入2020年10月15日之前发表的所有研究TNF-a多态性与精神分裂症之间关系的研究。在2个英文数据库和2个中文数据库中进行文献检索和鉴定。计算比值比(ORs)和95%置信区间(95% ci)。结果:对于-1031 T/C多态性,在整体分析中,等位基因模型中T等位基因显著降低精神分裂症风险(p = 0.006, OR = 0.88),显性模型中TC + CC基因型精神分裂症风险增加(p = 0.005, OR = 1.17)。同样,将合并分析纳入高质量研究时也得到相同的结果(等位基因模型:p = 0.005, OR = 0.86;优势模型:p = 0.007, OR = 1.20)。此外,当按种族分层时,结果显示,在等位基因模型中,T等位基因降低了东亚人患精神分裂症的风险(p = 0.031, OR = 0.90)。结论:TNF-a - 1031 T/C多态性与精神分裂症风险之间的关联可能是不可信的,而不是真正的关联或生物学因素。对于-1031T/C多态性,在整体分析中,等位基因模型中T等位基因显著降低精神分裂症风险,显性模型中TC + CC基因型精神分裂症风险增加。在等位基因模型中,按种族分层,T等位基因降低了东亚人的精神分裂症风险,在显性模型中,TC + CC基因型增加了东亚人的精神分裂症风险。
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Association between Tumor Necrosis factor-Alpha(TNF-a) polymorphisms and Schizophrenia: an updated meta-analysis.

Background: Previous studies have explored associations between Tumour Necrosis factor-Alpha (TNF-a) polymorphisms and Schizophrenia. Their results were controversial. We conducted a meta-analysis to clarify the association between TNF-a - 308 G/A(rs1800629), -1031T/C(rs1799964), -863C/A(rs1800630) and -857 C/T (rs1799724) polymorphisms and Schizophrenia.

Methods: All the studies that investigated the association between TNF-a polymorphisms and Schizophrenia published before 15 October 2020 were included in. The literature were comprehensively searched and identified in 2 English databases and 2 Chinese databases. The odds ratios (ORs) and 95% confidence intervals (95% CIs) were calculated.

Results: For -1031 T/C polymorphism, at the overall analysis, significantly decreased Schizophrenia risk was found in T allele in the allele model (p = 0.006, OR = 0.88) and increased Schizophrenia risk was found in TC + CC genotype in the dominant model (p = 0.005, OR = 1.17). Similarly, the same results were obtained when pooled analyses were included in high-quality studies (allele model: p = 0.005, OR = 0.86; dominant model: p = 0.007, OR = 1.20). In addition, when stratified by ethnicity, the results showed that in allele model, the T allele decreased Schizophrenia risk in East Asian (p = 0.031, OR = 0.90).

Conclusion: The association may most likely result from less-credible, rather than from true associations or biological factors on the TNF-a - 1031 T/C polymorphism with Schizophrenia risk.KeypointsFor -1031T/C polymorphism, at the overall analysis, significantly decreased schizophrenia risk was found in T allele in the allele model, and increased schizophrenia risk was found in TC + CC genotype in the dominant model.In allele model, the T allele decreased schizophrenia risk in East Asian when stratified by ethnicity, and in the dominant model, TC + CC genotype increased schizophrenia risk in East Asian.

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来源期刊
CiteScore
6.00
自引率
3.30%
发文量
42
审稿时长
>12 weeks
期刊介绍: International Journal of Psychiatry in Clinical Practice provides an international forum for communication among health professionals with clinical, academic and research interests in psychiatry. The journal gives particular emphasis to papers that integrate the findings of academic research into realities of clinical practice. Focus on the practical aspects of managing and treating patients. Essential reading for the busy psychiatrist, trainee and interested physician. Includes original research papers, comprehensive review articles and short communications. Key words: Psychiatry, Neuropsychopharmacology, Mental health, Neuropsychiatry, Clinical Neurophysiology, Psychophysiology, Psychotherapy, Addiction, Schizophrenia, Depression, Bipolar Disorders and Anxiety.
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