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Response to methotrexate predicts long-term mortality of patients with rheumatoid arthritis independent of the degree of response: results of a re-evaluation 30 years after baseline
C. Krause1, G. Herborn2, J. Braun3, H. Rudolf4, S. Wassenberg5, R. Rau6, D. Krause7
- University of Münster, Germany.
- Department of Rheumatology, Evangelisches Fachkrankenhaus, Ratingen, Germany.
- Rheumazentrum Ruhrgebiet, Herne, Germany.
- Department of Medical Informatics, Biometry and Epidemiology, Ruhr-University, Bochum, Germany.
- Department of Rheumatology, Evangelisches Fachkrankenhaus, Ratingen, Germany.
- Department of Rheumatology, Evangelisches Fachkrankenhaus, Ratingen, Germany.
- Department of Medical Informatics, Biometry and Epidemiology, Ruhr-University, Bochum, Germany. gundi.krause@t-online.de
CER9681
2017 Vol.35, N°3
PI 0384, PF 0389
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PMID: 27974101 [PubMed]
Received: 25/06/2016
Accepted : 29/09/2016
In Press: 13/12/2016
Published: 07/06/2017
Abstract
OBJECTIVES:
To assess if there is a correlation between the degree of response to treatment with methotrexate (MTX) and long-term mortality in a cohort of patients with rheumatoid arthritis (RA) established in Germany in the early eighties.
METHODS:
RA patients who had started MTX treatment between 1980 and 1987 were included. One year after baseline, the treatment response was evaluated. Responders were defined as patients with at least 20% decline in the swollen joint count (out of 32 joints) and the ESR with a prednisone dosage <5 mg/day. Thereafter, assessments were performed at 10, 18, and 30 years after baseline. Standardised mortality ratios (SMR) were calculated, Cox regression and logistic regression were performed.
RESULTS:
The cohort comprised 271 patients. In 2015, about 30 years after the initiation of MTX therapy, 185 patients (68%) were deceased, 52 (19%) lost to follow-up and 34 alive. The response after the first year of MTX treatment was the strongest predictor of survival with a hazard ratio of 0.44 (95% confidence interval [CI]: 0.30-0.65). However, even responders still had an SMR of 1.37 (95% CI 1.31–1.65), but this was much worse for non-responders who had an SMR of 4.22 (95% CI 3.13–5.56). Using Cox regression analysis no difference was detected between responders with more than 50% improvement (38% of all patients) and those with 20–50% improvement (28%).
CONCLUSIONS:
The predictive value of a response to one year of MTX therapy for long-term mortality of RA patients is independent of the degree of response.