Abstract

We compared the results and differences of indeterminate rates between the QuantiFERON-TB Gold In-Tube (QFT-GIT) and QuantiFERON-TB Gold PLUS (QFT-PLUS) tests in patients with rheumatic diseases and analyzed the associated factors. Data of patients with rheumatic diseases who had undergone the QFT-GIT or QFT-PLUS test were used, and information regarding patient demographics, primary diagnosis, laboratory results, and medications was collected. Furthermore, indeterminate result rates of the patient cohort and healthy controls were also compared. A total of 177 (43.4%) and 231 (56.6%) patients had undergone QFT-GIT and QFT-PLUS tests, respectively. Among them, four (2.3%) and seven (3.0%) patients had indeterminate results, which did not differ between the QFT-GIT and QFT-PLUS groups. Indeterminate results were significantly higher among patients with rheumatic diseases than in healthy controls (2.7% vs. 0.2%, p < 0.001). Multivariate logistic regression revealed that the lymphocyte count (hazard ratio (HR) 0.998, 95% confidence interval (CI) 0.997, 1.000; p = 0.012) and albumin level (HR 0.366, 95% CI 0.150, 0.890; p = 0.027) were predictive of indeterminate results. A lymphocyte count of ≤810/mm3 and an albumin level of ≤3.7 mg/dL were capable of discriminating between indeterminate and determinate results. The QFT-GIT and QFT-PLUS tests have comparable diagnostic performances in patients with rheumatic diseases. Decreased lymphocyte and albumin levels contribute to indeterminate results.

Highlights

  • Tuberculosis (TB) is a highly contagious disease caused by Mycobacterium tuberculosis (MTB) infection and is a substantial public health burden

  • The frequency of males was higher in the QFT-PLUS group than in the QuantiFERONTB Gold In-Tube (QFT-GIT) group (39.4% vs. 29.4%, p = 0.036)

  • The results of the interferongamma release assay (IGRA) were similar between the QFT-GIT and QFT-PLUS groups; indeterminate results were found in 2.3% (4/177 patients) and 3.0% (7/231 patients) of patients in the QFT-GIT

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Summary

Introduction

Tuberculosis (TB) is a highly contagious disease caused by Mycobacterium tuberculosis (MTB) infection and is a substantial public health burden. Given that more than 10 million people are affected with TB annually, it stands as one of the leading causes of death worldwide [1]. Latent tuberculosis infection (LTBI) is defined as being infected with MTB in the absence of active signs and symptoms of TB. This is considered a major risk factor for developing active TB [2]; appropriate screening of LTBI in high-risk individuals is considered crucial in preventing the community transmission of TB. After the first approval of TSPOT.TB as a commercially available

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