Article Text

PDF
Concise report
Influence of age on the outcome of antitumour necrosis factor alpha therapy in rheumatoid arthritis
  1. B J Radovits1,
  2. W Kievit1,
  3. J Fransen1,
  4. M A F J van de Laar2,
  5. T L Jansen3,
  6. P L C M van Riel1,
  7. R F J M Laan1
  1. 1
    Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
  2. 2
    Medisch Spectrum Twente and University Twente, Enschede, The Netherlands
  3. 3
    Medisch Centrum, Leeuwarden, The Netherlands
  1. Correspondence to Dr B J Radovits, Radboud University Nijmegen Medical Centre, Department of Rheumatology, PO Box 9101, Hp 470, 6500 HB Nijmegen, The Netherlands; B.Radovits{at}reuma.umcn.nl

Abstract

Objective: To investigate the influence of age on the effectiveness and tolerance of antitumour necrosis factor alpha (TNFα) therapy in rheumatoid arthritis (RA).

Methods: 730 patients of the Dutch Rheumatoid Arthritis Monitoring (DREAM) register were categorised into three groups according to their age at initiation of anti-TNFα therapy (<45, 45–65 and >65 years). Effectiveness of anti-TNFα therapy was primarily assessed by longitudinal analysis of the DAS28 during the first 12 months of treatment.

Results: Improvement in disease activity and physical functioning was significantly less in elderly patients, correcting for relevant confounders. Elderly patients reached the EULAR categories of good responders and remission less often than younger patients. Drug survival, co-medication use and tolerance were comparable between the three age groups.

Conclusion: Anti-TNFα therapy significantly reduced disease activity in all age groups of patients; however, it appeared less effective in elderly compared with younger RA patients.

Statistics from Altmetric.com

Footnotes

  • ▸ Additional supplemental table 2 is published online only athttp://ard.bmj.com/content/vol68/issue9

  • Funding Funding from the Dutch National Health Insurance Board and the Dutch affiliations of Wyeth Pharmaceuticals, Abbott Pharmaceuticals and Roche Pharmaceuticals enabled the data collection for the DREAM study.

  • Competing interests None.

  • Ethics approval The study protocol was approved by the local Ethics Committee.

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.