TY - JOUR
T1 - Rheumatoid arthritis with nontuberculous mycobacterial pulmonary disease
T2 - A retrospective, single-centre cohort study
AU - Takei, Hiroshi
AU - Nishina, Naoshi
AU - Namkoong, Ho
AU - Suzuki, Katsuya
AU - Uwamino, Yoshifumi
AU - Hasegawa, Naoki
AU - Takeuchi, Tsutomu
N1 - Publisher Copyright:
© 2021 Japan College of Rheumatology. Published by Oxford University Press. All rights reserved.
PY - 2022/5/1
Y1 - 2022/5/1
N2 - Objectives: Nontuberculous mycobacterial pulmonary disease (NTM-PD) is a rare but important comorbidity of rheumatoid arthritis (RA). Our objective was to investigate the association between NTM-PD and RA, especially regarding the immunosuppressive treatment of RA such as biological disease-modifying antirheumatic drugs (bDMARDs). Methods: We conducted a retrospective, single-centre cohort study. All RA patients regularly followed up at our rheumatology division in December 2012 were included in the study, and followed for 5 years. Results: At baseline, 26 of 1639 RA patients had NTM-PD. During the observation period, 14 were newly diagnosed with NTM-PD. For new diagnosis of NTM-PD, bDMARD use at baseline was not a significant risk factor. Among the 40 patients with NTM-PD, 16 were treated with a total of 27 bDMARDs after NTM-PD diagnosis. They did not present with a greater exacerbation of NTM-PD than those not treated with bDMARDs (25 vs. 17%, p =. 52). A total of 55 patients died, but nobody died of NTM-PD. NTM-PD was not associated with worse mortality in multivariate analysis (hazard ratio, 2.0; 95% CI, 0.6-6.4; p =. 26). Conclusions: Biological DMARD was not associated with worse prognosis of NTM-PD. Careful use of bDMARDs could be tolerated in RA patients with NTM-PD.
AB - Objectives: Nontuberculous mycobacterial pulmonary disease (NTM-PD) is a rare but important comorbidity of rheumatoid arthritis (RA). Our objective was to investigate the association between NTM-PD and RA, especially regarding the immunosuppressive treatment of RA such as biological disease-modifying antirheumatic drugs (bDMARDs). Methods: We conducted a retrospective, single-centre cohort study. All RA patients regularly followed up at our rheumatology division in December 2012 were included in the study, and followed for 5 years. Results: At baseline, 26 of 1639 RA patients had NTM-PD. During the observation period, 14 were newly diagnosed with NTM-PD. For new diagnosis of NTM-PD, bDMARD use at baseline was not a significant risk factor. Among the 40 patients with NTM-PD, 16 were treated with a total of 27 bDMARDs after NTM-PD diagnosis. They did not present with a greater exacerbation of NTM-PD than those not treated with bDMARDs (25 vs. 17%, p =. 52). A total of 55 patients died, but nobody died of NTM-PD. NTM-PD was not associated with worse mortality in multivariate analysis (hazard ratio, 2.0; 95% CI, 0.6-6.4; p =. 26). Conclusions: Biological DMARD was not associated with worse prognosis of NTM-PD. Careful use of bDMARDs could be tolerated in RA patients with NTM-PD.
KW - Biological DMARDs
KW - nontuberculous mycobacterium
KW - prognostic factors
KW - rheumatoid arthritis
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U2 - 10.1093/mr/roab032
DO - 10.1093/mr/roab032
M3 - Article
C2 - 34910202
AN - SCOPUS:85124357989
SN - 1439-7595
VL - 32
SP - 534
EP - 540
JO - Japanese Journal of Rheumatology
JF - Japanese Journal of Rheumatology
IS - 3
ER -