4.2 Article

Folate metabolic pathway single nucleotide polymorphisms: a predictive pharmacogenetic marker of methotrexate response in Indian (Asian) patients with rheumatoid arthritis

Journal

PHARMACOGENOMICS
Volume 16, Issue 18, Pages 2019-2034

Publisher

FUTURE MEDICINE LTD
DOI: 10.2217/pgs.15.145

Keywords

folate metabolism; homocysteine; Indians; methotrexate; pharmacogenomics; pharmacokinetics

Funding

  1. Council for Scientific and Industrial Research, New Delhi, India
  2. Lady Tata Memorial Trust, Mumbai, India
  3. NIH [R01CA132946, R21CA155524, AR060861, AR057781, AR065964, AI071651]
  4. Rheumatology Research Foundation
  5. Cure JM Foundation
  6. Mayo Clinic Foundation
  7. Foundation of Minnesota

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Aim: We evaluated the pharmacogenetic influence of genetic polymorphisms in folate pathway genes in Indian rheumatoid arthritis patients receiving methotrexate (MTX). Patients & methods: Twelve polymorphisms within nine folate pathway genes were analyzed for association with MTX response in 322 Indian rheumatoid arthritis (RA) patients and MTX pharmacokinetics in 94 RA patients. Results: Polymorphisms in GGH, SHMT1 and TS were associated with MTX-related adverse events while SNPs in MTHFR and RFC1/SLC19A1 were associated with MTX efficacy. TS5' UTR and SHMT1 polymorphisms were associated with higher plasma levels of MTX. Conclusion: Polymorphisms in folate-MTX pathway genes contribute to MTX response and affect MTX concentrations in Indian RA patients. A toxicogenetic index could identify patients who develop adverse events to MTX.

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