Efficacy of procalcitonin and pentraxin-3 as early biomarkers for differential diagnosis of pleural effusions

Author:

Sharma Anita1,Agrawal Apurva2,Sindhwani Girish3,Sharma Ashish4,Tomo Sojit5,Charan Jaykaran5,Yadav Dharmveer5,Sharma Praveen5ORCID

Affiliation:

1. Himalaya Institute of Medical Science, Swami Rama Himalaya University , Dehradun , Uttrakhand , India

2. RNT Medical College, Rajasthan University of Health Science , Udaipur , Rajasthan , India

3. All India Institute of Medical Sciences , Rishikesh , Uttrakhand , India

4. Geetanjali Medical College, Geetanjali University , Udaipur , Rajasthan , India

5. All India Institute of Medical Sciences , Jodhpur , Rajasthan , India

Abstract

Abstract Objectives Pleural effusion, defined as an abnormal accumulation of fluid in pleural space, can be of two types: transudative and exudative. The primary aim of the study was to assess the predictive accuracy of procalcitonin (PCT) and pentraxin-3 (PTX-3) in comparison to other biochemical markers such as C-reactive protein (CRP), and adenosine deaminase (ADA) in the differential diagnosis of pleural effusions. Methods A cross-sectional analytical study was conducted on patients with pleural effusion. Multiple comparisons and receiver-operating characteristics (ROC) analyses were made to evaluate the diagnostic significance of biochemical markers. Results Sixty-six patients with exudative pleural effusion classified as malignant, tuberculous, and parapneumonic effusions (malignant pleural effusion [MPE], tuberculous [TPE], and parapneumonic [PPE]) were included. Significant differences in pleural fluid levels in both PCT (p-value: 0.001) and PTX-3(p-value: 0.001), as well as serum levels of PCT (p-value: 0.001), were observed between the three groups. ROC analysis showed both PTX-3 and PCT having favorable discrimination ability with high sensitivity (≥90%) and specificity to predict PPE from TPE and MPE. Conclusions Evaluation of serum and pleural fluid PCT and levels of PTX-3 in the pleural fluid may be used as an early biomarker to differentiate the etiology of pleural effusion.

Publisher

Walter de Gruyter GmbH

Subject

Internal Medicine

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