Key result
Higher 24-hour post-PCI PTX3 linked to increased long-term MACE risk in stable CAD.
Cohort (n=596)
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Pentraxin-3 (PTX3) is an inflammatory marker thought to be more specific to cardiovascular inflammation than C-reactive protein (CRP). Our aim was to assess the prognostic value of PTX3 in patients with stable coronary artery disease (CAD) after drug eluting stent (DES) implantation. Plasma PTX3 levels were measured before percutaneous coronary intervention (PCI) and at 24 h post-PCI in 596 consecutive patients with stable CAD. Patients were followed up for a median of 3 years (range 1-5) for major adverse cardiovascular events (MACEs). We found that the post-PCI plasma PTX3 levels were significantly higher at 24 h after PCI than pre-PCI, patients with MACEs had higher post-PCI PTX3 levels compared with MACEs-free patients, patients with higher post-PCI PTX3 levels (median > 4.384 ng/mL) had a higher risk for MACEs than those with PTX3 < 4.384 ng/mL, and post-PCI PTX3, cTnI, multiple stents, and age but not high-sensitivity CRP (hsCRP) were independently associated with the prevalence of MACEs after DES implantation. The present study shows that post-PCI PTX3 may be a more reliable inflammatory predictor of long-term MACEs in patients with stable CAD undergoing DES implantation than CRP. Measurement of post-PCI PTX3 levels could provide a rationale for risk stratification of patients with stable CAD after DES implantation.
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Guo et al. (2014) conducted a cohort in Stable coronary artery disease undergoing drug-eluting stent implantation (n=596). Elevated 24-hour post-PCI plasma Pentraxin-3 (PTX3 > 4.384 ng/mL) vs. Lower 24-hour post-PCI plasma Pentraxin-3 (PTX3 < 4.384 ng/mL) was evaluated on Major adverse cardiovascular events (MACEs). Higher 24-hour post-PCI plasma PTX3 levels (>4.384 ng/mL) independently predicted a higher risk of long-term MACEs over a median 3-year follow-up in stable CAD patients after DES implantation.
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