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Methylene tetrahydrofolate reductase gene polymorphisms and their association with methotrexate toxicity: a meta-analysis

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Autor
Spyridopoulou, K. P.; Dimou, N. L.; Hamodrakas, S. J.; Bagos, P. G.
Fecha
2012
DOI
10.1097/FPC.0b013e32834ded2a
Materia
gene polymorphisms
meta-analysis
methotrexate toxicity
methylene
tetrahydrofolate reductase
ACUTE LYMPHOBLASTIC-LEUKEMIA
RHEUMATOID-ARTHRITIS PATIENTS
VERSUS-HOST-DISEASE
SINGLE-NUCLEOTIDE POLYMORPHISMS
STEM-CELL
TRANSPLANTATION
INFLAMMATORY-BOWEL-DISEASE
HIGH-DOSE METHOTREXATE
NEURAL-TUBE DEFECTS
METHYLENETETRAHYDROFOLATE REDUCTASE
THYMIDYLATE-SYNTHASE
Biotechnology & Applied Microbiology
Genetics & Heredity
Pharmacology
& Pharmacy
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Resumen
Objective A systematic review and a meta-analysis were conducted, to investigate the possible association of methylene tetrahydrofolate reductase (MTHFR) gene polymorphisms with adverse effects related to methotrexate (MTX). Methods A systematic literature search in PubMed retrieved a total of 44 studies (42 unique articles). Two polymorphisms were included in the meta-analysis: C677T and A1298C. Random effect models were used in the analysis. Odds ratios along with their 95% confidence intervals were computed to compare the distribution of alleles and genotypes between cases and controls. Results The analysis highlighted a significant association of C677T polymorphism with overall MTX toxicity, hepatotoxicity, hematological toxicity, and neurotoxicity. It also revealed an association with MTX toxicity in patients with rheumatoid arthritis. In contrast, a protective effect of C677T MTHFR polymorphism on acute graft-versus-host disease and on patients treated with hematopoietic cell transplantation was found. As for the A1298C polymorphism, a statistically significant association with overall MTX toxicity and a protective role of the polymorphism in rheumatoid arthritis patients was detected. Conclusion These results indicate the association of MTHFR polymorphisms with MTX toxicity. However, further studies are needed to reveal the underlying biological mechanism of the association. Pharmacogenetics and Genomics 22: 117-133 (C) 2012 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
URI
http://hdl.handle.net/11615/33310
Colecciones
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19743]
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