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Association of 11 variants of the dopaminergic and cognitive pathways genes with major depression, schizophrenia and bipolar disorder in the Pakistani population.
Nasir Hashmi, Aisha; Sabina Raja, Merlyn; Taj, Rizwan; Ahmed Dharejo, Raees; Agha, Zehra; Qamar, Raheel; Azam, Maleeha.
  • Nasir Hashmi A; Translational Genomics Laboratory, COMSATS University Islamabad, Islamabad, Pakistan.
  • Sabina Raja M; Translational Genomics Laboratory, COMSATS University Islamabad, Islamabad, Pakistan.
  • Taj R; Department of Psychiatry, Pakistan Institute of Medical Sciences, Islamabad, Pakistan.
  • Ahmed Dharejo R; Department of Psychiatry, Pakistan Institute of Medical Sciences, Islamabad, Pakistan.
  • Agha Z; Translational Genomics Laboratory, COMSATS University Islamabad, Islamabad, Pakistan.
  • Qamar R; Science and Technology Sector, ICESCO, Rabat, Morocco.
  • Azam M; Pakistan Academy of Science, Islamabad, Pakistan.
Int J Neurosci ; : 1-13, 2023 Aug 29.
Article en En | MEDLINE | ID: mdl-37642370
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.
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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Año: 2023 Tipo del documento: Article