Frequent Conversion of Tuberculosis Screening Tests During Anti-tumour Necrosis Factor Therapy in Patients with Rheumatic Diseases
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Objectives: To determine the rate of tuberculosis (TB) screening test conversion during anti-tumour necrosis factor (TNF) therapy in rheumatic patients with negative baseline screening.
Methods: This was a prospective study of rheumatic patients with negative baseline TB screening (tuberculin skin test (TST): <5 mm, and negative T-SPOT.TB, QuantiFERON-TB Gold In Tube (QFT-GIT) and chest X-ray) treated with anti-TNF agents. All patients underwent re-screening for TB with all assays 1 year later. Factors associated with TB test conversion were analysed and compared between 'converters' and 'non-converters'.
Results: Seventy patients (mean age 50.6±15.5 years) with rheumatic disease (33 with rheumatoid arthritis, 33 with spondyloarthropathies and 4 with other conditions) were enrolled. Patients were treated with different anti-TNFs (27 with adalimumab, 14 etanercept, 16 infliximab, 8 golimumab, 5 certolizumab pegol) for 1 year. Twenty patients (29%) displayed conversion of at least one screening assay 12 months after anti-TNF therapy: conversion of TST occurred in 9 (13%), T-SPOT.TB in 7 (10%) and QFT-GIT in 5 (7%). Only one patient had concomitant conversion of more than one screening test. Univariate and multivariate analysis revealed that only infliximab was associated with a decreased rate of TB screening assay conversion (OR 0.048, 95% CI 0.004 to 0.606, p=0.017). No patient (40% received isoniazid therapy) developed active TB during follow-up (27±12 months).
Conclusions: Approximately one third of patients with negative baseline TB screening develop conversion of at least one screening test during anti-TNF treatment. These findings should be considered when designing re-screening strategies and contemplating latent TB therapy.
Magalhaes V, Bonfiglioli K, Gomes C, Bonfa E, de Medeiros-Ribeiro A, Saad C Adv Rheumatol. 2024; 64(1):70.
PMID: 39272122 DOI: 10.1186/s42358-024-00406-7.
Foppiano Palacios C, Chowdhary V, Hao R, Danve A, Malinis M PLoS One. 2024; 19(7):e0306337.
PMID: 38959249 PMC: 11221665. DOI: 10.1371/journal.pone.0306337.
Fragoulis G, Dey M, Zhao S, Schoones J, Courvoisier D, Galloway J RMD Open. 2022; 8(2).
PMID: 36323488 PMC: 9639159. DOI: 10.1136/rmdopen-2022-002726.
Alsukait S, Alsaad A, Alotaibi G, Alsaif F, Alotaibi H Indian J Dermatol. 2022; 67(1):1-4.
PMID: 35656235 PMC: 9154160. DOI: 10.4103/ijd.ijd_201_21.
Jalowska M, Gornowicz-Porowska J, Seraszek-Jaros A, Kaczmarek E, Bowszyc-Dmochowska M, Bartkiewicz P Postepy Dermatol Alergol. 2021; 38(4):611-614.
PMID: 34658703 PMC: 8501442. DOI: 10.5114/ada.2021.108904.