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Clinical value of plasma pentraxin 3 levels for predicting cardiac troponin elevation after percutaneous coronary intervention.

Authors :
Wang, Zheng
Sato, Akira
Akiyama, Daiki
Kimura, Taizo
Tajiri, Kazuko
Hoshi, Tomoya
Sakai, Satoshi
Koike, Akira
Miyauchi, Takashi
Aonuma, Kazutaka
Source :
Life Sciences. Jan2014, Vol. 95 Issue 1, p40-44. 5p.
Publication Year :
2014

Abstract

Aims: Post-procedural myocardial necrosis manifested by elevated cardiac troponin T (cTnT) often complicates percutaneous coronary intervention (PCI). Plasma pentraxin 3 (PTX3) levels are increased in patients with arterial inflammation and especially unstable angina pectoris (UAP). This study tested whether plasma PTX3 levels can predict post-PCI cTnT elevation. Main methods: We evaluated 94 consecutive patients with AP and normal pre-PCI cTnT levels who underwent PCI. Pre-PCI virtual histology-intravascular ultrasound was performed to assess culprit plaque composition. Plasma PTX3 and serum hs-CRP levels were measured pre-PCI. Patients were divided into 2 groups according to presence (Group I, n=34) or absence (Group II, n=60) of post-PCI cTnT elevation >3× the upper limit of normal at 24h after PCI. Key findings: Plasma PTX3 (4.06±2.05ng/ml vs 2.17±1.02ng/ml, p<0.001), serum hs-CRP levels (0.25±0.03 vs 0.16±0.03mg/dl, p=0.048), plaque burden (80.9±5.3 vs 75.4±10.6%, p=0.047), presence of positive remodeling (59 vs 25%, p=0.034), and percent necrotic core area (19.0±7.4 vs 14.0±5.9%, p=0.046) were significantly higher in Group I than in Group II. Receiver-operating characteristic curve analysis showed that with a best cut-off value of 2.83ng/ml, plasma PTX3 level (AUC 0.823) predicted post-PCI cardiac TnT elevation better than did serum hs-CRP level (AUC 0.618). Multiple logistic regression analysis showed that plasma PTX3 level was the most independent predictor of post-PCI cardiac cTnT elevation (OR: 2.65; 95% CI: 1.56–10.1; p=0.003). Significance: Plasma PTX3 level may be a useful marker for predicting post-PCI cardiac cTnT elevation, which is associated with inflammatory status of culprit lesions. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00243205
Volume :
95
Issue :
1
Database :
Academic Search Index
Journal :
Life Sciences
Publication Type :
Academic Journal
Accession number :
93585892
Full Text :
https://doi.org/10.1016/j.lfs.2013.11.021