Background: Genetic factors play an important role in susceptibility to methamphetamine. In this line, protein that interact with C-kinase-1 (PICK1) and brain-derived neurotrophic factor (BDNF) genes are linked to methamphetamine dependence (substance use disorder). Thus, in a case-control study, we investigated the association between polymorphisms of PICK1 and BDNF genes and methamphetamine dependence in an Iranian population from 2015 to 2018.
Methods: Total of 235 cases and 204 controls were recruited. The PICK1-rs713729, -rs2076369 and BDNF-rs6265 genotypes were determined via ARMS-PCR assay. Statistical analysis was performed, using SPSS 20.0, PHASE 2.1.1 program as well as SNP Analyzer 2.0.
Results: In the present study, two polymorphisms including PICK1-rs713729 (OR: 1.38 (CI: 1.08-1.52; P-value: 0.004) in multiplicative and dominant models, and PICK1-rs2076369 (OR: 1.31 (CI: 1.10-1.56; P-value: 0.002) in multiplicative, dominant and co-dominant models were associated with the risk of methamphetamine abuse. Moreover, haplotype analysis methods showed a significant association between haplotype AG (OR: 2.50 (CI: 1.50-4.16; P-value: 0.0002) in dominant, recessive and co-dominant models, and haplotype TT (OR: 0.67 (CI: 0.50-0.91; P-value: 0.009) in dominant model and co-dominant model with the risk of methamphetamine abuse. None of the polymorphisms in this study had a high level of linkage disequilibrium.
Conclusion: Our findings indicate that the PICK1 gene might be linked to methamphetamine dependence. Therefore, it can be stated that PICK1 might play a significant role in the pathophysiology of methamphetamine dependence in an Iranian population.
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Posted 20 Jul, 2020
Posted 20 Jul, 2020
Background: Genetic factors play an important role in susceptibility to methamphetamine. In this line, protein that interact with C-kinase-1 (PICK1) and brain-derived neurotrophic factor (BDNF) genes are linked to methamphetamine dependence (substance use disorder). Thus, in a case-control study, we investigated the association between polymorphisms of PICK1 and BDNF genes and methamphetamine dependence in an Iranian population from 2015 to 2018.
Methods: Total of 235 cases and 204 controls were recruited. The PICK1-rs713729, -rs2076369 and BDNF-rs6265 genotypes were determined via ARMS-PCR assay. Statistical analysis was performed, using SPSS 20.0, PHASE 2.1.1 program as well as SNP Analyzer 2.0.
Results: In the present study, two polymorphisms including PICK1-rs713729 (OR: 1.38 (CI: 1.08-1.52; P-value: 0.004) in multiplicative and dominant models, and PICK1-rs2076369 (OR: 1.31 (CI: 1.10-1.56; P-value: 0.002) in multiplicative, dominant and co-dominant models were associated with the risk of methamphetamine abuse. Moreover, haplotype analysis methods showed a significant association between haplotype AG (OR: 2.50 (CI: 1.50-4.16; P-value: 0.0002) in dominant, recessive and co-dominant models, and haplotype TT (OR: 0.67 (CI: 0.50-0.91; P-value: 0.009) in dominant model and co-dominant model with the risk of methamphetamine abuse. None of the polymorphisms in this study had a high level of linkage disequilibrium.
Conclusion: Our findings indicate that the PICK1 gene might be linked to methamphetamine dependence. Therefore, it can be stated that PICK1 might play a significant role in the pathophysiology of methamphetamine dependence in an Iranian population.
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