Renu Singh, Tripti Grover, Ranjan Gupta, A. Ambekar, R. Jain, Arundhati Sharma
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Aim: To identify association of single nucleotide polymorphisms (SNPs) in COMT (rs4680 and rs2075507) and GABAA receptor genes (rs13172914 and rs211014) with AD. Method: A total of 100 AD patients diagnosed on the basis of DSM IV criteria from the outpatient clinic of the National Drug Dependence Treatment Centre (NDDTC) of All India Institute of Medical Sciences (AIIMS), and 100 healthy individuals from the general population were recruited. A detailed history including pattern of drug use and demographic details with pedigree information was noted. Genomic DNA from peripheral blood samples was processed for PCR amplification followed by restriction digestion to screen for the presence of polymorphisms. Genotype and allele frequencies were evaluated and correlated with alcohol use parameters including duration of alcohol use, age at onset of alcohol use, quantity of alcohol consumed (gms/day) and WHO ASSIST score and levels of liver function enzymes (SGPT and SGOT). Statistical analysis was performed using SPSS v21.0. Results: Genetic analysis of the study group revealed COMT rs4680 to be significantly associated with AD (p=0.03), while the other COMT SNP rs2075507 showed an association with increased levels of SGPT in the patients. GABAA receptor gene polymorphisms showed no association with AD. Conclusion: The study suggests a role of COMT gene polymorphism rs4680 in conferring susceptibility to AD.","PeriodicalId":14828,"journal":{"name":"Journal of Addiction Research and Therapy","volume":"41 1 1","pages":"1-6"},"PeriodicalIF":0.0000,"publicationDate":"2017-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"An Association Study of the COMT and GABA Gene Variants with Alcohol Dependence\",\"authors\":\"Renu Singh, Tripti Grover, Ranjan Gupta, A. Ambekar, R. Jain, Arundhati Sharma\",\"doi\":\"10.4172/2155-6105.1000350\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Alcohol dependence (AD), associated with high mortality and morbidity is caused due to involvement of both environmental and genetic factors. Behavioral effects of alcohol including cognitive impairment, motor incoordination, tolerance and dependence are likely due to its effect on the multiple brain proteins including neurotransmitters. Dysfunction in these neurotransmitter systems may be at the level of enzymes involved in metabolic degradation, or receptors involved in neurotransmission like dopamine, Gamma-amino butyric acid (GABA), serotonin etc. Genetic polymorphisms in these neurotransmitter systems are implicated in conferring susceptibility to AD. Aim: To identify association of single nucleotide polymorphisms (SNPs) in COMT (rs4680 and rs2075507) and GABAA receptor genes (rs13172914 and rs211014) with AD. Method: A total of 100 AD patients diagnosed on the basis of DSM IV criteria from the outpatient clinic of the National Drug Dependence Treatment Centre (NDDTC) of All India Institute of Medical Sciences (AIIMS), and 100 healthy individuals from the general population were recruited. A detailed history including pattern of drug use and demographic details with pedigree information was noted. Genomic DNA from peripheral blood samples was processed for PCR amplification followed by restriction digestion to screen for the presence of polymorphisms. Genotype and allele frequencies were evaluated and correlated with alcohol use parameters including duration of alcohol use, age at onset of alcohol use, quantity of alcohol consumed (gms/day) and WHO ASSIST score and levels of liver function enzymes (SGPT and SGOT). Statistical analysis was performed using SPSS v21.0. Results: Genetic analysis of the study group revealed COMT rs4680 to be significantly associated with AD (p=0.03), while the other COMT SNP rs2075507 showed an association with increased levels of SGPT in the patients. GABAA receptor gene polymorphisms showed no association with AD. 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引用次数: 1
摘要
酒精依赖(AD)与高死亡率和发病率相关,是由环境和遗传因素共同引起的。酒精对认知障碍、运动不协调、耐受性和依赖性等行为的影响可能是由于酒精对包括神经递质在内的多种脑蛋白的影响。这些神经递质系统的功能障碍可能与参与代谢降解的酶或参与神经传递的受体(如多巴胺、γ -氨基丁酸(GABA)、血清素等)有关。这些神经递质系统的遗传多态性与AD易感性有关。目的:探讨COMT基因(rs4680和rs2075507)和GABAA受体基因(rs13172914和rs211014)的单核苷酸多态性与AD的关系。方法:招募全印度医学科学研究所(AIIMS)国家药物依赖治疗中心(NDDTC)门诊根据DSM IV标准诊断的AD患者100例,以及来自普通人群的健康个体100例。记录了详细的病史,包括药物使用模式和人口统计细节以及家谱信息。来自外周血样本的基因组DNA进行PCR扩增处理,然后进行限制性酶切以筛选多态性的存在。对基因型和等位基因频率进行评估,并将其与酒精使用参数(包括饮酒持续时间、开始饮酒年龄、饮酒量(克/天)、WHO ASSIST评分和肝功能酶(SGPT和SGOT)水平相关联。采用SPSS v21.0进行统计学分析。结果:研究组的遗传分析显示COMT rs4680与AD显著相关(p=0.03),而另一个COMT SNP rs2075507与患者SGPT水平升高相关。GABAA受体基因多态性与AD无相关性。结论:COMT基因多态性rs4680在AD易感性中的作用。
An Association Study of the COMT and GABA Gene Variants with Alcohol Dependence
Alcohol dependence (AD), associated with high mortality and morbidity is caused due to involvement of both environmental and genetic factors. Behavioral effects of alcohol including cognitive impairment, motor incoordination, tolerance and dependence are likely due to its effect on the multiple brain proteins including neurotransmitters. Dysfunction in these neurotransmitter systems may be at the level of enzymes involved in metabolic degradation, or receptors involved in neurotransmission like dopamine, Gamma-amino butyric acid (GABA), serotonin etc. Genetic polymorphisms in these neurotransmitter systems are implicated in conferring susceptibility to AD. Aim: To identify association of single nucleotide polymorphisms (SNPs) in COMT (rs4680 and rs2075507) and GABAA receptor genes (rs13172914 and rs211014) with AD. Method: A total of 100 AD patients diagnosed on the basis of DSM IV criteria from the outpatient clinic of the National Drug Dependence Treatment Centre (NDDTC) of All India Institute of Medical Sciences (AIIMS), and 100 healthy individuals from the general population were recruited. A detailed history including pattern of drug use and demographic details with pedigree information was noted. Genomic DNA from peripheral blood samples was processed for PCR amplification followed by restriction digestion to screen for the presence of polymorphisms. Genotype and allele frequencies were evaluated and correlated with alcohol use parameters including duration of alcohol use, age at onset of alcohol use, quantity of alcohol consumed (gms/day) and WHO ASSIST score and levels of liver function enzymes (SGPT and SGOT). Statistical analysis was performed using SPSS v21.0. Results: Genetic analysis of the study group revealed COMT rs4680 to be significantly associated with AD (p=0.03), while the other COMT SNP rs2075507 showed an association with increased levels of SGPT in the patients. GABAA receptor gene polymorphisms showed no association with AD. Conclusion: The study suggests a role of COMT gene polymorphism rs4680 in conferring susceptibility to AD.