Literature DB >> 29684488

Association of CACNA1C with bipolar disorder among the Pakistani population.

Madiha Khalid1, Terri M Driessen2, Jong Seo Lee3, Leon Tejwani4, Asad Rasool5, Muhammad Saqlain5, Pakeeza Arzoo Shiaq5, Muhammad Hanif5, Amber Nawaz6, Andrew T DeWan7, Ghazala Kaukab Raja8, Janghoo Lim9.   

Abstract

Many single nucleotide polymorphisms (SNPs) have been identified for Bipolar disorder (BD), but association between SNPs and BD can vary depending on the population tested. SNPs rs10994336 and rs9804190 in ANK3 and rs1006737 in CACNA1C have emerged as the most highly replicated SNPs significantly associated with BD. The aim of the present study was to assess the association of these SNPs with BD in the Pakistani population, which has never before been examined. A total of 120 BD and 120 control individuals from Pakistan were examined in this analysis. Genotyping results indicated that rs1006737 in CACNA1C was significantly associated with BD, while rs10994336 or rs9804190 in ANK3 was not significant when examined individually. However, risk score assessment found that the presence of two or more risk alleles was significantly associated with disease, indicating that risk alleles from ANK3 and CACNA1C may additively contribute to BD. A protein-protein interaction network was generated using STRING to probe the relationship between ANK3 and CACNA1C interactors and their associations with BD. While none of the interactors are directly linked to BD, they play a role in pathways linked to BD, including oxytocin and dopamine signaling pathways. Collectively, these results reveal a significant association of CACNA1C with BD among the Pakistani population, extending results from other ethnic groups to the Pakistani population for the first time.
Copyright © 2018 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  ANK3; Bipolar disorder; CACNA1C; Pakistan

Mesh:

Substances:

Year:  2018        PMID: 29684488      PMCID: PMC5970093          DOI: 10.1016/j.gene.2018.04.061

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


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