Prevalence of ABCB1 3435C>T polymorphism in the Cuban population.

Q2 Pharmacology, Toxicology and Pharmaceutics Drug metabolism and personalized therapy Pub Date : 2021-12-06 DOI:10.1515/dmpt-2020-0156
Idania Rodeiro Guerra, Jose Herrea, Elizabeth Cuétara, Gabino Garrido, Elizabeth Reyes, Ioanna Martínez, Carlos L Pérez, Gisselle Fernández, Ivones Hernández-Balmaseda, René Delgado, Julia C Stingl, Wim Vanden Berghe
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Abstract

Objectives: ABCB1 gene polymorphisms can modify P-glycoprotein function with clinical consequences.

Methods: The 3435C>T polymorphism prevalence was analyzed using oligonucleotide probes and next-generation sequencing in 421 unrelated healthy individuals living in Cuba. Data were stratified by gender, ethnic background and residence. The genotype and allelic frequencies were determined.

Results: The genotype distribution met the Hardy-Weinberg equilibrium assumption. The allelic frequency was 63.5% for the 3435C variant. The genotype frequencies were 41.1% for CC, 44.9% for CT and 14.0% for TT. The allele and genotype distributions differed between individuals living in La Habana and Santiago de Cuba (p<0.05) when ethnic background was analyzed. The allelic distribution was similar among Admixed and Black subjects, and they differed from Caucasians. The CC genotype was equally distributed among Admixed and Black subjects, and they differed from Caucasians. The TT genotype frequency differed between Caucasians and Admixed. The CT genotype was distributed differently among the three groups. Similar distribution was obtained in Brazilians, whereas some similarities were observed in African, Spanish and Chinese populations, consistent with the mixed Cuban ethnic origin.

Conclusions: This is the first report on allele and genotype frequencies of the 3435C>T polymorphism in Cuba, which may support personalized medicine programs.

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ABCB1 3435C>T多态性在古巴人群中的流行
目的:ABCB1基因多态性可改变p -糖蛋白功能并产生临床后果。方法:采用寡核苷酸探针和新一代测序技术,分析421例古巴无亲缘关系健康人群3435C>T多态性的流行情况。数据按性别、种族背景和居住地分层。测定基因型和等位基因频率。结果:基因型分布符合Hardy-Weinberg平衡假设。3435C变异的等位基因频率为63.5%。CC基因型频率为41.1%,CT为44.9%,TT为14.0%。结论:本文首次报道了古巴3435C>T多态性的等位基因和基因型频率,为个性化医疗方案提供了依据。
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来源期刊
Drug metabolism and personalized therapy
Drug metabolism and personalized therapy Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
2.30
自引率
0.00%
发文量
35
期刊介绍: Drug Metabolism and Personalized Therapy (DMPT) is a peer-reviewed journal, and is abstracted/indexed in relevant major Abstracting Services. It provides up-to-date research articles, reviews and opinion papers in the wide field of drug metabolism research, covering established, new and potential drugs, environmentally toxic chemicals, the mechanisms by which drugs may interact with each other and with biological systems, and the pharmacological and toxicological consequences of these interactions and drug metabolism and excretion. Topics: drug metabolizing enzymes, pharmacogenetics and pharmacogenomics, biochemical pharmacology, molecular pathology, clinical pharmacology, pharmacokinetics and drug-drug interactions, immunopharmacology, neuropsychopharmacology.
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