Genetic variants in the cytochrome P450 2D6 gene in the Sri Lankan population.

T D Praveen Tharanga, C M V Jinadasa, M F Risama, Priyadarshani Galappatthy, R L Jayakody, Vajira H W Dissanayake
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引用次数: 8

Abstract

Introduction: Cytochrome P450 2D6 (CYP2D6) enzymes are involved in the metabolism of a large number of commonly prescribed drugs such as antidepressants and cardiovascular drugs. The CYP2D6 *3, *4 and *14 variants associated with the loss of enzyme function; CYP2D6 *10 and *17 variants with reduced enzyme function; and CYP2D6 *2 variant with no effect on enzyme function. Establishing the frequency of these variant alleles in Sri Lankan population would be useful for optimizing pharmacotherapy with CYP2D6-substrate drugs.

Objective: The objective of this study was to determine the prevalence of CYP2D6 *2, *3, *4, *10, *14 and *17 variants in the main ethnic groups in the Sri Lankan population.

Materials and methods: A total of 90 deoxyribonucleic acid (DNA) samples (30 each from Sinhalese, Tamils and Moors) were selected from a DNA resource at the Human Genetic Unit, Faculty of Medicine, University of Colombo. This collection had been made for population genetic studies from a random population based volunteers. Genotyping was performed using published polymerase chain reaction/restriction fragment length polymorphism methods.

Results: The prevalence of the CYP2D6 variants in Sinhalese, Sri Lankan Tamils and Moors respectively were CYP2D6 *2: 37%, 41.6% and 37.9%; CYP2D6 *3: 60.3%, 45% and 30%; CYP2D6 *4: 21.6%, 6.6% and 8.3%; CYP2D6 *10: 40%, 35% and 44%. CYP2D6 *14 and *17 variants were not identified.

Conclusion: CYP2D6*3, *4 and *10 variants, which are associated with reduced or loss of CYP2D6 enzyme function were found in our population in significant frequencies. CYP2D6*4, which is reported to be a Caucasian variant was also found in all three ethnic groups.

Abstract Image

Abstract Image

斯里兰卡人群中细胞色素P450 2D6基因的遗传变异
细胞色素P450 2D6 (CYP2D6)酶参与了抗抑郁药、心血管药物等大量常用处方药的代谢。与酶功能丧失相关的CYP2D6 *3、*4和*14变异;酶功能降低的CYP2D6 *10和*17变体;CYP2D6 *2变异对酶功能无影响。在斯里兰卡人群中建立这些变异等位基因的频率将有助于优化cyp2d6底物药物的药物治疗。目的:本研究的目的是确定CYP2D6 *2、*3、*4、*10、*14和*17变异在斯里兰卡主要民族人群中的流行情况。材料和方法:从科伦坡大学医学院人类遗传单元的DNA资源中选择了90份脱氧核糖核酸(DNA)样本(僧伽罗人、泰米尔人和摩尔人各30份)。这些资料是从随机抽取的志愿者中收集的,用于群体遗传研究。采用已发表的聚合酶链反应/限制性片段长度多态性方法进行基因分型。结果:僧伽罗人、斯里兰卡泰米尔人和摩尔人CYP2D6 *2的患病率分别为37%、41.6%和37.9%;CYP2D6 *3: 60.3%、45%、30%;CYP2D6 *4: 21.6%、6.6%和8.3%;CYP2D6 *10: 40%、35%和44%。CYP2D6 *14和*17未被发现。结论:CYP2D6*3、*4和*10变异与CYP2D6酶功能降低或丧失相关,在我国人群中存在显著频率。据报道,CYP2D6*4是一种高加索变异,在所有三个种族中也发现了。
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