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过氧化物酶体增殖物激活受体γ基因多态性对精神分裂症风险的影响:一项病例对照研究及计算分析

Impact of Proliferator-Activated Receptor γ Gene Polymorphisms on Risk of Schizophrenia: A Case-Control Study and Computational Analyses.

作者信息

Sargazi Saman, Mirani Sargazi Fariba, Moudi Mahdiyeh, Heidari Nia Milad, Saravani Ramin, Mirinejad Shekoufeh, Shahraki Sheida, Shakiba Mansoor

机构信息

Cellular and Molecular Research Center, Resistant Tuberculosis Institute, Zahedan University of Medical Sciences, Zahedan, Iran.

Genetics of Noncommunicable Disease Research Center, Resistant Tuberculosis Institute, Zahedan University of Medical Sciences, Zahedan, Iran.

出版信息

Iran J Psychiatry. 2020 Oct;15(4):286-296. doi: 10.18502/ijps.v15i4.4294.

Abstract

Schizophrenia (SCZ) is a common psychiatric disorder characterized by a complex mode of inheritance. Peroxisome proliferator-activated receptor-γ (PPARG) mainly regulates lipid and glucose metabolisms while it is constitutively expressed in rat primary microglial cultures. This preliminary study was aimed to investigate the relationship of two polymorphisms in the gene, rs1801282 C/G, and rs3856806 C/T, to the risk of SCZ in the southeast Iranian population. A total of 300 participants (150 patients with SCZ and 150 healthy controls) were enrolled. Genotyping was done using the amplification refractory mutation system polymerase chain reaction (ARMS-PCR) technique. Computational analyses were carried out to predict the potential effects of the studied polymorphisms. A significant link was found between genotypes of rs1801282 and SCZ susceptibility. The G allele of rs1801282 in CG and GG form of the codominant model increased the risk of SCZ by 2.49 and 2.64 folds, respectively. With regards to rs3856806, enhanced risk of SCZ was also observed under different inheritance models except for the overdominant model. Also, the T allele of rs3856806 enhanced the risk of SCZ by 3.19 fold. Computational analyses predicted that rs1801282 polymorphism might alter the secondary structure of -mRNA and protein function. At the same time, the other variant created the binding sites for some enhancer and silencer motifs. Our findings showed that rs1821282 and rs3856806 polymorphisms associate with SCZ susceptibility. Replication studies in different ethnicities with a larger population are needed to validate our findings.

摘要

精神分裂症(SCZ)是一种常见的精神障碍,具有复杂的遗传模式。过氧化物酶体增殖物激活受体γ(PPARG)主要调节脂质和葡萄糖代谢,在大鼠原代小胶质细胞培养物中组成性表达。这项初步研究旨在调查该基因中两个多态性位点rs1801282 C/G和rs3856806 C/T与伊朗东南部人群SCZ风险的关系。共招募了300名参与者(150名SCZ患者和150名健康对照)。使用扩增阻滞突变系统聚合酶链反应(ARMS-PCR)技术进行基因分型。进行了计算分析以预测所研究多态性的潜在影响。发现rs1801282的基因型与SCZ易感性之间存在显著关联。在共显性模型的CG和GG形式中,rs1801282的G等位基因分别使SCZ风险增加2.49倍和2.64倍。关于rs3856806,除了超显性模型外,在不同遗传模型下也观察到SCZ风险增加。此外,rs3856806的T等位基因使SCZ风险增加3.19倍。计算分析预测rs1801282多态性可能会改变mRNA的二级结构和蛋白质功能。同时,另一个变体为一些增强子和沉默子基序创造了结合位点。我们的研究结果表明,rs1821282和rs3856806多态性与SCZ易感性相关。需要在不同种族的更大人群中进行重复研究以验证我们的发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b60/7610076/efe99ad16fee/IJPS-15-286-g001.jpg

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