Advertisement






Click here for more guidelines.
CME Topic Collections Past Issues Search Current Issue Home
     

J Am Coll Cardiol, 2006; 48:1560-1566, doi:10.1016/j.jacc.2006.06.061 (Published online 25 September 2006).
© 2006 by the American College of Cardiology Foundation
This Article
Right arrow Abstract Freely available
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Patti, G.
Right arrow Articles by Di Sciascio, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Patti, G.
Right arrow Articles by Di Sciascio, G.

Protection From Procedural Myocardial Injury by Atorvastatin Is Associated With Lower Levels of Adhesion Molecules After Percutaneous Coronary Intervention

Results From the ARMYDA-CAMs (Atorvastatin for Reduction of MYocardial Damage during Angioplasty-Cell Adhesion Molecules) Substudy

Giuseppe Patti, MD*, Massimo Chello, MD*, Vincenzo Pasceri, MD, PhD, FACC{dagger}, Diego Colonna, MD{ddagger}, Annunziata Nusca, MD*, Marco Miglionico, MD*, Andrea D'Ambrosio, MD*, Elvio Covino, MD* and Germano Di Sciascio, MD, FACC*,*

* Department of Cardiovascular Sciences, Campus Bio-Medico University, Rome, Rome, Italy
{dagger} Interventional Cardiology Unit, San Filippo Neri Hospital of Rome, Rome, Italy
{ddagger} Second University of Naples, Naples, Italy


Figure 1
View larger version (18K):

[in a new window]
 
Figure 1 Design of the ARMYDA-CAMs (Atorvastatin for Reduction of MYocardial Damage during Angioplasty-Cell Adhesion Molecules) substudy. CAMs = cell adhesion molecules; CK-MB = creatine kinase-MB; CRP = C-reactive protein; ICAM-1 = intercellular cell adhesion molecule-1; PCI = percutaneous coronary intervention; VCAM-1 = vascular cell adhesion molecule-1.

 

Figure 2
View larger version (25K):

[in a new window]
 
Figure 2 Soluble intercellular cell adhesion molecule-1 (ICAM-1, top), E-selectin (middle), and vascular cell adhesion molecule-1 (VCAM-1, bottom) levels in the 2 arms at randomization (i.e., 7 days before intervention), at the time of intervention, after 8 and 24 h. The Wilcoxon signed rank test with Bonferroni's correction for the comparisons between time points in both arms showed a significant rise from baseline of ICAM-1, E-selectin, and VCAM-1 levels (p < 0.01) in all post-procedural determinations. This increase was significantly lower in the atorvastatin versus placebo arm at 8 and 24 h for E-selectin and at 24 h for ICAM-1. Data are mean ± SEM. PCI = percutaneous coronary intervention. White bars = atorvastatin; black bars = placebo.

 

Figure 3
View larger version (15K):

[in a new window]
 
Figure 3 Post-procedural 24-h percent increase from baseline of adhesion molecule levels. ICAM-1 = intercellular cell adhesion molecule-1; VCAM-1 = vascular cell adhesion molecule-1. White bars = atorvastatin; black bars = placebo.

 

Figure 4
View larger version (12K):

[in a new window]
 
Figure 4 (A) Incidence of procedural myocardial damage in patients of both arms according to post-procedural E-selectin peak levels. (Low E-selectin: <67 ng/ml, median value; high E-selectin: ≥67 ng/ml). (B) Post-procedural E-selectin peak levels (mean ± SEM) in patients with or without procedural myocardial damage (defined as post-procedural troponin-I elevation above normal limits). White bars = atorvastatin; black bars = placebo.

 




 
  CME Topic Collections Past Issues Search Current Issue Home

Advertisement