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Evolution of imaging findings, laboratory and functional parameters in rheumatoid arthritis patients after one year of treatment with anti-TNF-α agents


1, 2, 3, 4, 5, 6, 7, 8

 

  1. Department of Radiology, University Hospital of Heraklion, Medical School, University of Crete, Heraklion, Crete, Greece. edetorakis@hotmail.com
  2. Department of Radiology, University Hospital of Heraklion, Medical School, University of Crete, Heraklion, Crete, Greece.
  3. Department of Thoracic Medicine and Laboratory of Molecular and Cellular Pneumonology, University Hospital of Heraklion, Medical School, University of Crete, Heraklion, Crete, Greece.
  4. Department of Rheumatology, University Hospital of Heraklion, Medical School, University of Crete, Heraklion, Crete, Greece.
  5. Department of Rheumatology, University Hospital of Heraklion, Medical School, University of Crete, Heraklion, Crete, Greece.
  6. Department of Radiology, University Hospital of Heraklion, Medical School, University of Crete, Heraklion, Crete, Greece.
  7. Department of Thoracic Medicine and Laboratory of Molecular and Cellular Pneumonology, University Hospital of Heraklion, Medical School, University of Crete, Heraklion, Crete, Greece.
  8. Department of Radiology, University Hospital of Heraklion, Medical School, University of Crete, Heraklion, Crete, Greece.

CER9147
2017 Vol.35, N°1
PI 0043, PF 0052
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PMID: 27908307 [PubMed]

Received: 26/11/2015
Accepted : 08/04/2016
In Press: 27/10/2016
Published: 26/01/2017

Abstract

OBJECTIVES:
To investigate the efficacy and safety of anti-TNF-α agent treatment compared to non-biologic DMARDs in rheumatoid arthritis patients.
METHODS:
82 consecutive patients, 29 males, 53 females, aged 42-79, diagnosed with RA and suitable for anti-TNF-α treatment composed two study groups: 42 with pre-existing rheumatoid arthritis-related interstitial lung disease (RA-ILD) and 40 without RA-ILD. Respective control groups consisted of 44 patients with pre-existing RA-ILD and 44 patients without RA-ILD, treated with non-biologic DMARDs. All patients underwent chest high resolution computed tomography (HRCT), pulmonary function tests (PFTs) and peripheral blood biomarkers at baseline and after one year of treatment.
RESULTS:
There was a significant decrease of air trapping extent and bronchial wall thickening after treatment in RA-ILD and RA-non ILD study groups (p<0.05). This was accompanied by a statistically significant improvement of maximum mid-expiratory flow (MMEF75-25), RV and RV/TLC in both study groups (p<0.05). In the RA-ILD study group ILD extent scores remained unchanged after anti-TNF-α treatment. None of the RA-non ILD group developed new-onset ILD. In both RA-ILD and RA-non ILD control groups, HRCT findings and PFTs did not differ significantly at the one-year follow-up study. Methotrexate (MTX) regression analysis showed in both RA-ILD study and control groups a negative correlation between MTX dose and ILD extent score at one-year and between MTX dose and air trapping extent at baseline and after one year of treatment.
CONCLUSIONS:
Anti-TNF-α treatment, in contrast to non-biologic DMARDs, there was an improvement of small airways disease. There was no new-onset ILD or exacerbation of preexisting-ILD, especially in patients treated with anti-TNF-α agents, supporting the efficacy and favourable safety profile of this treatment in RA patients.

Rheumatology Article