Genetic polymorphisms of PIP5K2A and course of schizophrenia.

4区 医学 Q4 Medicine
Evgeniya G Poltavskaya, Olga Yu Fedorenko, Natalya M Vyalova, Elena G Kornetova, Nikolay A Bokhan, Anton J M Loonen, Svetlana A Ivanova
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引用次数: 5

Abstract

Background: Schizophrenia is a severe highly heritable mental disorder. The clinical heterogeneity of schizophrenia is expressed in the difference in the leading symptoms and course of the disease. Identifying the genetic variants that affect clinical heterogeneity may ultimately reveal the genetic basis of the features of schizophrenia and suggest novel treatment targets. PIP5K2A (Phosphatidylinositol-4-Phosphate 5-Kinase Type II Alpha) has been investigated as a potential susceptibility gene for schizophrenia.

Methods: In this work, we studied the possible association between eleven polymorphic variants of PIP5K2A and the clinical features of schizophrenia in a population of 384 white Siberian patients with schizophrenia. Genotyping was carried out on QuantStudio 5 Real-Time PCR System with a TaqMan Validate SNP Genotyping Assay (Applied Biosystems, USA).

Results: PIP5K2A rs8341 (χ2 = 6.559, p = 0.038) and rs946961 (χ2 = 5.976, p = 0.049) showed significant association with course of schizophrenia (continuous or episodic). The rs8341*CT (OR = 1.63, 95% CI: 1.04-2.54) and rs946961*CC (OR = 5.17, 95% CI: 1.20-22.21) genotypes were associated with a continuous type of course, while the rs8341*TT genotype (OR = 0.53, 95% CI: 0.29-0.97) was associated with an episodic type of course of schizophrenia. Therefore rs8341*TT genotype presumably has protective effect against the more severe continuous course of schizophrenia compared to the episodic one.

Conclusions: Our experimental data confirm that PIP5K2A is a genetic factor influencing the type of course of schizophrenia in Siberian population. Disturbances in the phosphatidylinositol pathways may be a possible reason for the transition to a more severe continuous course of schizophrenia.

Abstract Image

Abstract Image

PIP5K2A基因多态性与精神分裂症病程的关系。
背景:精神分裂症是一种严重的高度遗传性精神障碍。精神分裂症的临床异质性表现在主要症状和病程的差异上。识别影响临床异质性的遗传变异可能最终揭示精神分裂症特征的遗传基础,并提出新的治疗靶点。PIP5K2A(磷脂酰肌醇-4-磷酸5激酶II型α)已被研究为精神分裂症的潜在易感基因。方法:研究了384例西伯利亚白种精神分裂症患者PIP5K2A的11个多态性变异与精神分裂症临床特征之间的可能关联。基因分型采用QuantStudio 5 Real-Time PCR系统,采用TaqMan Validate SNP基因分型试验(Applied Biosystems, USA)。结果:PIP5K2A rs8341 (χ2 = 6.559, p = 0.038)和rs946961 (χ2 = 5.976, p = 0.049)与精神分裂症病程(连续性或发作性)有显著相关性。rs8341*CT (OR = 1.63, 95% CI: 1.04-2.54)和rs946961*CC (OR = 5.17, 95% CI: 1.20-22.21)基因型与连续型病程相关,而rs8341*TT基因型(OR = 0.53, 95% CI: 0.29-0.97)与发作型病程相关。因此,rs8341*TT基因型可能对更严重的精神分裂症持续病程具有保护作用。结论:我们的实验数据证实PIP5K2A是影响西伯利亚人群精神分裂症病程类型的遗传因素。磷脂酰肌醇通路的紊乱可能是精神分裂症向更严重的持续性病程过渡的一个可能原因。
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来源期刊
BMC Medical Genetics
BMC Medical Genetics 医学-遗传学
自引率
0.00%
发文量
0
审稿时长
12 months
期刊介绍: BMC Medical Genetics is an open access journal publishing original peer-reviewed research articles in the effects of genetic variation in individuals, families and among populations in relation to human health and disease. Note: BMC Medical Genetics is now closed. This journal has merged with BMC Medical Genomics, a broad-scope, open access community journal for all medical genetics and genomics research.
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