Association between the variability of the ABCA13 gene and the risk of major depressive disorder and schizophrenia in the Han Chinese population

Jianhua Chen, Raja Amjad Waheed Khan, Meng Wang, Kuanjun He, Qingzhong Wang, Zhiqiang Li, Wenjin Li, Z. Wen, Zhijian Song, Jiawei Shen, Yifeng Xu, Yongyong Shi
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引用次数: 9

Abstract

Abstract Objectives: The ATP-binding cassette transporter superfamily is one of the largest membrane protein families, which is responsible for transportation of substances across the membranes by utilising energy. Some research has bridged the variations in ABCA13 with occurrence of psychiatric disorders. To investigate the overlapping risk conferred by ABCA13 for both major depressive disorder and schizophrenia, we analysed tag single nucleotide polymorphisms (tag SNPs). Methods: We used TaqMan® technology to genotype 1045 major depressive disorder patients, 1235 schizophrenia patients and 1235 healthy controls of Han Chinese origin. Results: We found that rs7789493 (Pallele = 7.23E-04, Pgenotype =.001) was associated with major depressive disorder, while rs17132388 (Pallele = 1.63E-04, Pgenotype = 7.50E-04) and rs6583476 (Pallele = 5.50E-04, Pgenotype =.002) showed statistically significant association with schizophrenia. Conclusions: Our results indicate that the ABCA13 gene may contain overlapping common genetic risk factors for both major depressive disorder and schizophrenia in the Han Chinese population. The study on variants conferring overlapping risk for multiple psychiatric disorders could be tangible pathogenesis support in clinical or diagnostic references.
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ABCA13基因变异与汉族人群重度抑郁症和精神分裂症风险之间的关系
摘要目的:atp结合盒转运蛋白超家族是最大的膜蛋白家族之一,它通过利用能量负责物质跨膜运输。一些研究将ABCA13的变异与精神疾病的发生联系起来。为了研究ABCA13对重度抑郁症和精神分裂症的重叠风险,我们分析了标签单核苷酸多态性(标签snp)。方法:采用TaqMan®技术对1045例重度抑郁症患者、1235例精神分裂症患者和1235例汉族健康对照进行基因分型。结果:我们发现rs7789493 (Pallele = 7.23E-04, Pgenotype =.001)与重度抑郁症相关,rs17132388 (Pallele = 1.63E-04, Pgenotype = 7.50E-04)和rs6583476 (Pallele = 5.50E-04, Pgenotype =.002)与精神分裂症相关有统计学意义。结论:我们的研究结果表明,ABCA13基因可能包含汉族人群重度抑郁症和精神分裂症的重叠共同遗传危险因素。对多种精神疾病重叠风险的变异的研究可以为临床或诊断参考提供切实的发病机制支持。
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