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Updated: Aug 19, 2026

Detection and Quantification of Calcitonin Gene-Related Peptide (CGRP) in Human Plasma Using a Modified Enzyme-Linked Immunosorbent Assay
Published on: June 16, 2023
What cardiologists do need to know about procalcitonin
Christian Mueller1, Mirjam Christ-Crain, Beat Müller
1Department of Internal Medicine, University Hospital Basel, Switzerland. chmueller@uhbs.ch
Insights
Procalcitonin aids in diagnosing infective endocarditis (IE) and reduces antibiotic use in lower respiratory tract infections (LRTI). This biomarker shows high sensitivity and specificity for IE and safely decreases antibiotic prescriptions for LRTI.
Area of Science:
- Biomarkers in Infectious Diseases
- Clinical Microbiology
- Cardiology
Background:
- Infective endocarditis (IE) diagnosis is challenging due to varied presentations.
- Lower respiratory tract infections (LRTI) are often overtreated with antibiotics, contributing to resistance.
- Procalcitonin is a novel marker for systemic bacterial infections.
Purpose of the Study:
- To evaluate procalcitonin's utility in diagnosing IE.
- To assess the impact of procalcitonin-guided therapy on antibiotic use in LRTI.
Main Methods:
- Prospective cohort study of patients with suspected IE, comparing procalcitonin levels with final diagnoses.
- Analysis of procalcitonin's diagnostic accuracy (ROC curve, sensitivity, specificity, predictive values).
- Evaluation of a procalcitonin-based strategy to guide antibiotic treatment in LRTI patients.
Main Results:
- Procalcitonin levels were significantly higher in IE patients (median 6.56 µg/L) vs. non-IE (median 0.44 µg/L).
- Procalcitonin demonstrated superior diagnostic accuracy for IE (AUC 0.856) compared to C-reactive protein (AUC 0.657).
- Procalcitonin-guided therapy reduced antibiotic exposure in LRTI by 51% (adjusted relative risk 0.49) without compromising outcomes.
Conclusions:
- Procalcitonin is a valuable biomarker for diagnosing IE, with a suggested cutoff of 2.3 µg/L for optimal predictive accuracy.
- Procalcitonin-guided management safely and substantially reduces antibiotic usage in LRTI, addressing concerns of antibiotic resistance.
Abstract:
This review will highlight the potential application of procalcitonin, a novel marker of systemic bacterial infection, in two clinical settings relevant to cardiologists: infective endocarditis (IE) and lower respiratory tract infections (LRTI): The variability in the clinical presentation of infective endocarditis (IE) makes the diagnosis a clinical challenge. However, rapid diagnosis and initiation of effective treatment are essential to good patient outcome. Serum calcitonin precursor levels, including procalcitonin, are elevated in systemic bacterial infections and seem to be helpful in the diagnosis of IE. The utility of procalcitonin in clinical practice was examined in a prospective cohort of patients with the suspicion of IE. Procalcitonin was significantly higher in patients with IE (median 6.56 microg/L) as compared with patients with other final diagnoses (median 0.44 microg/L, p < 0.001). The area under the ROC curve using procalcitonin to predict infective endocarditis was 0.856, as compared to 0.657 for C-reactive protein. The optimum concentration of procalcitonin for the calculation of positive and negative predictive accuracy as obtained from the ROC curve was 2.3 microg/L. Using this cut-off, the test characteristics of procalcitonin were as follows: sensitivity 81%, specificity 85%, negative predictive value 92%, positive predictive value 72%. Although most LRTIs are due to viral infections, they are very often treated with antibiotics. This excessive use of antibiotics is believed to be the main cause of the spread of antibiotic-resistant bacteria. A procalcitonin-based therapeutic strategy has shown to reduce antibiotic usage in LRTI. Based upon serum procalcitonin levels, the use of antibiotics was more or less discouraged (<0.1 or <0.25 microg/L) or encouraged (> or =0.5 or > or =0.25 microg/L), respectively. Final diagnoses included pneumonia (36%), acute exacerbation of COPD (25%), and acute bronchitis (24%). Clinical and laboratory outcome was similar in both groups and favourable in 96.7%. In the procalcitonin group, the adjusted relative risk of antibiotic exposure was 0.49 (p < 0.001), as compared to the standard group. Thus, using a sensitive assay, procalcitonin-guidance substantially and safely reduced antibiotic usage in LRTI.
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