Association of 11 variants of the dopaminergic and cognitive pathways genes with major depression, schizophrenia and bipolar disorder in the Pakistani population.

IF 1.7 4区 医学 Q4 NEUROSCIENCES
International Journal of Neuroscience Pub Date : 2024-11-01 Epub Date: 2023-12-04 DOI:10.1080/00207454.2023.2251661
Aisha Nasir Hashmi, Merlyn Sabina Raja, Rizwan Taj, Raees Ahmed Dharejo, Zehra Agha, Raheel Qamar, Maleeha Azam
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引用次数: 0

Abstract

Background: The dopaminergic pathways control neural signals that modulate mood and behaviour along and have a vital role in the aetiology of major depression (MDD), schizophrenia (SHZ) and bipolar disorder (BD). Genome-wide association studies (GWAS) have reported several dopaminergic and cognitive pathway genes association with these disorders however, no such comprehensive data was available regarding the Pakistani population.Objective: The present study was conducted to analyse the 11 genetic variants of dopaminergic and cognitive system genes in MDD, SHZ, and BD in the Pakistani population.Methods: A total of 1237 subjects [MDD n = 479; BD n = 222; SHZ n = 146; and controls n = 390], were screened for 11 genetic variants through polymerase chain reaction (PCR) techniques. Univariant followed by multivariant logistic regression analysis was applied to determine the genetic association.Results: Significant risk associations were observed for rs4532 and rs1799732 with MDD; and rs1006737 and rs2238056 with BD. However, after applying multiple test corrections rs4532 and rs1799732 association did not remain significant for MDD. Moreover, a protective association was found for three variants; DRD4-120bp, rs10033951 and rs2388334 in the current cohort.Conclusions: The present study revealed the risk association of single nucleotide polymorphisms (SNPs) rs1006737 and rs2238056 with BD and the protective effect of the DRD4-120bp variant in MDD and BD, of rs2388334 in BD and of rs10033951 in MDD, BD, and SHZ in the current Pakistani cohort. Thus, the study is valuable in understanding the genetic basis of MDD, BD and SHZ in the Pakistani population, which may pave the way for future functional studies.

巴基斯坦人群中11种多巴胺能和认知途径基因变异与重度抑郁症、精神分裂症和双相情感障碍的关联
背景:多巴胺能通路控制调节情绪和行为的神经信号,并在重度抑郁症(MDD)、精神分裂症(SHZ)和双相情感障碍(BD)的病因学中起重要作用。全基因组关联研究(GWAS)已经报道了几种与这些疾病相关的多巴胺能和认知途径基因,然而,没有关于巴基斯坦人群的全面数据。目的:分析巴基斯坦人群中MDD、SHZ和BD患者多巴胺能和认知系统基因的11个遗传变异。方法:共1237例受试者[MDD n = 479;BD n = 222;SHZ n = 146;和对照组n = 390],通过聚合酶链反应(PCR)技术筛选11种遗传变异。采用单变量和多变量logistic回归分析确定遗传关联。结果:rs4532和rs1799732与MDD存在显著的风险关联;rs1006737和rs2238056与BD的相关性。然而,经过多次测试校正后,rs4532和rs1799732与MDD的相关性不再显著。此外,发现了三种变体的保护性关联;当前队列中的DRD4-120bp, rs10033951和rs2388334。结论:本研究揭示了单核苷酸多态性rs1006737和rs2238056与BD的风险关联,以及MDD和BD中DRD4-120bp变异、BD中rs2388334变异和MDD、BD和SHZ中rs10033951变异的保护作用。因此,该研究对了解巴基斯坦人群中MDD、BD和SHZ的遗传基础具有重要意义,为今后的功能研究铺平道路。
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来源期刊
CiteScore
5.10
自引率
0.00%
发文量
132
审稿时长
2 months
期刊介绍: The International Journal of Neuroscience publishes original research articles, reviews, brief scientific reports, case studies, letters to the editor and book reviews concerned with problems of the nervous system and related clinical studies, epidemiology, neuropathology, medical and surgical treatment options and outcomes, neuropsychology and other topics related to the research and care of persons with neurologic disorders.  The focus of the journal is clinical and transitional research. Topics covered include but are not limited to: ALS, ataxia, autism, brain tumors, child neurology, demyelinating diseases, epilepsy, genetics, headache, lysosomal storage disease, mitochondrial dysfunction, movement disorders, multiple sclerosis, myopathy, neurodegenerative diseases, neuromuscular disorders, neuropharmacology, neuropsychiatry, neuropsychology, pain, sleep disorders, stroke, and other areas related to the neurosciences.
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