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Updated: May 23, 2025

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
Diagnostic accuracy of interleukin 32γ for tuberculous pleural effusion
Qi Wang1,2, Li Ma3,4,5, Kan Zhai1,2
1Department of Respiratory and Critical Care Medicine, Beijing Institute of Respiratory Medicine and Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Background:
Accurate diagnosis of tuberculous pleural effusion (TPE) with biomarkers remains difficult. Interleukin 32gamma (IL-32γ) is a recently discovered proinflammatory cytokines which plays a vital role in the immune response to TPE. This study aimed to assess the diagnostic accuracy of IL-32γ for TPE, especially in different ages of patients.
Methods:
Patients with a confirmed diagnosis of pleural effusion were systematically recruited from Beijing Chao-Yang Hospital between June 2019 and May 2022. The concentration of IL-32γ and interferon-gamma (IFN-γ) were evaluated in the pleural effusions with different etiology from 188 patients using enzyme-linked immunosorbent assay method. Adenosine deaminase (ADA) was determined by peroxidase method.
Results:
At a threshold value of 181.56 ng/L, IL-32γ demonstrated an area under the curve (AUC) of 0.812 [95% confidence interval (CI): 0.748-0.865], with sensitivity, specificity, positive likelihood ratio (PLR), negative likelihood ratio (NLR), positive predictive value (PPV), and negative predictive value (NPV) of 70.2%, 86.0%, 5.0, 0.4, 92.0%, and 55.7%, respectively. In elderly patients (aged >65 years), IL-32γ demonstrated an AUC of 0.984 (95% CI: 0.891-1.000). Notably, the diagnostic accuracy of IL-32γ was significantly higher than that of ADA (P=0.03) and IFN-γ (P=0.02). Similarly, the AUCs for IL-32γ combined with ADA (0.981, 95% CI: 0.886-1.000) and IL-32γ combined with IFN-γ (1.000, 95% CI: 0.920-1.000) were significantly higher than those of ADA (P=0.04) or IFN-γ (P=0.01) alone in elderly patients.
Conclusions:
IL-32γ can be used as a valuable biomarker for identifying patients with TPE, especially in elderly patients aged >65 years.
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