Summary
The long pentraxin 3 (PTX3) is a recently identified member of the pentraxin protein
family that includes C-reactive protein. PTX3 is produced by the major cell types
involved in atherosclerotic lesions in response to inflammatory stimuli, and elevated
plasma levels are found in several conditions including acute coronary syndromes (ACS).
The aim of this study was to assess the value of PTX3 as a prognostic marker of mortality
and recurrent ischaemic events in a consecutive series of patients admitted with acute
chest pain and potential ACS.
The patients received follow-up for 24 months. Blood samples were taken on admission
for measurement of PTX3, high sensitive C-reactive protein (hsCRP), B-type natriuretic
peptide (BNP), and troponin T. All-cause mortality at 24 months in the study cohort
was 15.2%. Patients in the upper PTX3 quartiles had a significantly higher death risk
than those in the lowest quartile (Q3: hazard ratio [HR] 2.36; 95% CI 1.12–4.99; p=0.024,
and Q4: HR 3.60; 95% CI 1.68–7.72; p=0.001). Elevated BNP levels were also significantly
associated with a fatal outcome (Q3: HR 3.05; 95% CI 1.16–7.99; p=0.024; and Q4: HR
3.90; 95% CI 1.48–10.26; p=0.006). Elevation in hsCRP was not associated with increased
death risk. As PTX3 predicted mortality independently of BNP, the combination of these
two biomarkers showed an incremental prognostic value.
PTX3 is a new biomarker related to inflammation that, independently of BNP, strongly
predicts long-term all-cause mortality in patients with acute chest pain. The combination
of these two biomarkers enhances the prognostic value over either marker alone.
Keywords
PTX3 - chest pain - prognosis - clinical studies - atherothrombosis - inflammation