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Platelet PIA1/PIA2 polymorphism and the risk of periprocedural myocardial infarction in patients with acute coronary syndromes undergoing coronary angioplasty

Authors :
Gioel Gabrio Secco
Fabiola Sinigaglia
Alon Schaffer
Ettore Cassetti
Lucia Barbieri
Harry Suryapranata
Paolo Marino
Monica Verdoia
Pasquale Perrone-Filardi
Giuseppe De Luca
Verdoia, Monica
Secco, Gioel G.
Cassetti, Ettore
Schaffer, Alon
Barbieri, Lucia
PERRONE FILARDI, Pasquale
Marino, Paolo
Suryapranata, Harry
Sinigaglia, Fabiola
De Luca, Giuseppe
Source :
Blood Coagulation & Fibrinolysis, 25, 107-13, Blood Coagulation & Fibrinolysis, 25, 2, pp. 107-13
Publication Year :
2014

Abstract

Item does not contain fulltext Acute coronary syndromes (ACSs) represent a high-risk condition, as enhanced platelet reactivity importantly influences myocardial perfusion and procedural results after percutaneous coronary intervention (PCI). In fact, higher rate of periprocedural myocardial infarction (PMI) and reduced event-free survival have been reported in these patients. The single nucleotide polymorphism Leu33Pro of platelet glycoprotein IIIa has been related to an increased platelet reactivity, a lower response to antiplatelet agents and higher risk of stent restenosis. Therefore, our aim was to evaluate the impact of this polymorphism on PMI in patients undergoing PCI for non-ST-segment elevation MI (NSTEMI). Our population is represented by 478 consecutive patients undergoing coronary angioplasty for NSTEMI. Cardiac biomarkers were monitored at intervals from 8 to 48 h after the procedure. Genetic analysis was performed to assess the presence of Leu33Pro polymorphism. A total of 156 patients (32.6%) were polymorphic. Clinical features did not differ according to genetic status, neither pharmacological treatment pre and during angioplasty. PlA carriers had lower rate of calcifications (P = 0.01) and higher coronary tortuosity (P = 0.03) at angiography and underwent more frequently to thrombectomy (P = 0.05). PCI-related complications did not differ according to genotype. Leu33Pro polymorphism was not associated with increased risk of periprocedural myonecrosis and PMI even after correction for baseline differences, [odds ratio (OR) (95% confidence interval (CI) = 0.70 (0.44-1.13), P = 0.15 for PMI and OR (95% CI) = 0.77 (0.53-1.11), P = 0.17 for myonecrosis, respectively]. Results were confirmed in high-risk subgroups of patients. In conclusion, among patients undergoing PCI for ACS, the polymorphism Leu33Pro of platelet glycoprotein IIIa is not associated with increased risk of PMI.

Details

ISSN :
14735733 and 09575235
Volume :
25
Issue :
2
Database :
OpenAIRE
Journal :
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis
Accession number :
edsair.doi.dedup.....089fe5bfb07033f6fed1d7927191f5e7