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TPMT gene polymorphisms (c.238G>C, c.460G>A and c.719A>G) in a healthy Venezuelan population.
Mora, Yuselin; Villegas, Cecilia; Mora, Yamile M; Moreno, Nancy.
Afiliação
  • Mora Y; Instituto de Investigaciones Biomédicas 'Dr. Francisco J. Triana Alonso' (BIOMED) - Sección de Polimorfismos Genómicos, Facultad de Ciencias de la Salud, Universidad de Carabobo, Sede Aragua, Maracay, 2102, Venezuela.
  • Villegas C; Instituto de Investigaciones Biomédicas 'Dr. Francisco J. Triana Alonso' (BIOMED) - Sección de Polimorfismos Genómicos, Facultad de Ciencias de la Salud, Universidad de Carabobo, Sede Aragua, Maracay, 2102, Venezuela.
  • Mora YM; Instituto de Investigaciones Biomédicas 'Dr. Francisco J. Triana Alonso' (BIOMED) - Sección de Polimorfismos Genómicos, Facultad de Ciencias de la Salud, Universidad de Carabobo, Sede Aragua, Maracay, 2102, Venezuela.
  • Moreno N; Instituto de Investigaciones Biomédicas 'Dr. Francisco J. Triana Alonso' (BIOMED) - Sección de Polimorfismos Genómicos, Facultad de Ciencias de la Salud, Universidad de Carabobo, Sede Aragua, Maracay, 2102, Venezuela.
Pharmacogenomics ; 24(4): 219-225, 2023 03.
Article em En | MEDLINE | ID: mdl-36946340
ABSTRACT

Background:

The presence of polymorphisms in the TPMT gene is associated with adverse effects in patients treated with standard doses of thiopurine drugs. Scientific evidence recognizes significant ethnic differences in their frequencies and how their early identification can prevent clinical complications.

Methods:

150 healthy residents of Aragua, Venezuela were enrolled. The SNPs c.460G>A and c.719A>G were detected by PCR-restriction fragment length polymorphism assay and c.238G>C by allele-specific PCR.

Results:

All genotype polymorphisms were heterozygous. TPMT*1/*3A, TPMT*1/*3C and TPMT*1/*2 genotypes were found in 4.0, 2.0 and 0.7%, respectively.

Conclusion:

6.7% of individuals have an intermediate TPMT activity. These findings support the importance of prior genotyping of TPMT in Venezuelan patients who require thiopurine drug therapy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Metiltransferases Tipo de estudo: Prognostic_studies Limite: Humans País/Região como assunto: America do sul / Venezuela Idioma: En Revista: Pharmacogenomics Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Metiltransferases Tipo de estudo: Prognostic_studies Limite: Humans País/Região como assunto: America do sul / Venezuela Idioma: En Revista: Pharmacogenomics Ano de publicação: 2023 Tipo de documento: Article