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Previously reported PDE3A-SLCO1C1 genetic variant does not correlate with anti-TNF response in a large UK rheumatoid arthritis cohort.
Smith, Samantha Louise; Plant, Darren; Lee, Xiu Hue; Massey, Jonathan; Hyrich, Kimme; Morgan, Ann W; Wilson, Anthony G; Isaacs, John; Barton, Anne.
Afiliação
  • Smith SL; Arthritis Research UK, Centre for Genetics & Genomics, Centre for Musculoskeletal Research, Manchester Academic Health Sciences Centre, The University of Manchester, Manchester, UK.
  • Plant D; NIHR Manchester Musculoskeletal BRU, Central Manchester Foundation Trust & University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
  • Lee XH; Arthritis Research UK, Centre for Genetics & Genomics, Centre for Musculoskeletal Research, Manchester Academic Health Sciences Centre, The University of Manchester, Manchester, UK.
  • Massey J; Arthritis Research UK, Centre for Genetics & Genomics, Centre for Musculoskeletal Research, Manchester Academic Health Sciences Centre, The University of Manchester, Manchester, UK.
  • Hyrich K; Arthritis Research UK, Centre for Epidemiology, Centre for Musculoskeletal Research, Manchester Academic Health Sciences Centre, The University of Manchester, Manchester, UK.
  • Morgan AW; Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds & NIHR Leeds Musculoskeletal Biomedical Research Unit, Leeds Teaching Hospitals NHS Trust, UK.
  • Wilson AG; UCD School of Medicine & Medical Science, Conway Institute, University College Dublin, Dublin, Ireland.
  • Isaacs J; NIHR Newcastle Biomedical Research Centre, Newcastle upon Tyne NHS Foundation Trust & Newcastle University, Newcastle-upon-Tyne, UK.
  • Barton A; Arthritis Research UK, Centre for Genetics & Genomics, Centre for Musculoskeletal Research, Manchester Academic Health Sciences Centre, The University of Manchester, Manchester, UK.
Pharmacogenomics ; 17(7): 715-20, 2016 05.
Article em En | MEDLINE | ID: mdl-27180831
AIM: A genetic variant has recently reached genome-wide significance for association with TNF-inhibitor response in rheumatoid arthritis patients. Here we undertake a replication study in a UK Caucasian population to test for association with TNF-inhibitor response. MATERIALS & METHODS: The genetic variant, rs3794271, located within the PDE3A-SLCO1C1 locus was analyzed for correlation with treatment response using both the EULAR classification criteria and absolute change in (Δ)DAS28 scores as outcome measures. RESULTS: Genotype data were available from 1750 TNF-inhibitor treated individuals. However, no evidence for association was observed (EULAR: p = 0.91 and ΔDAS28: p = 0.93). Furthermore, no significant associations were observed upon stratification by the anti-TNF received (p > 0.05). CONCLUSION: In the largest replication cohort conducted to date, no evidence for association was observed.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Artrite Reumatoide / Fator de Necrose Tumoral alfa / Antirreumáticos / Transportadores de Ânions Orgânicos / Nucleotídeo Cíclico Fosfodiesterase do Tipo 3 / Variantes Farmacogenômicos Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Pharmacogenomics Assunto da revista: FARMACOLOGIA / GENETICA MEDICA Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Artrite Reumatoide / Fator de Necrose Tumoral alfa / Antirreumáticos / Transportadores de Ânions Orgânicos / Nucleotídeo Cíclico Fosfodiesterase do Tipo 3 / Variantes Farmacogenômicos Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Pharmacogenomics Assunto da revista: FARMACOLOGIA / GENETICA MEDICA Ano de publicação: 2016 Tipo de documento: Article