High-sensitivity C-reactive protein predicts adverse outcomes after non-ST-segment elevation acute coronary syndrome regardless of GRACE risk score, but not after ST-segment elevation myocardial infarction

Autor: José Ramón González-Juanatey, Sergio Raposeiras Roubín, Pablo Aguiar Souto, Isabel Arufe, Michel Jacquet Hervet, Belén Outes, Ezequiel Álvarez Castro, José María García-Acuña, María V. Reino-Maceiras, Beatriz Paradela Dobarro, Filomena Roubín-Camiña, Maria José Castromán, Cristina Barreiro Pardal, Raymundo Ocaranza Sánchez, Emad Abu Assi
Jazyk: angličtina
Rok vydání: 2013
Předmět:
Zdroj: Revista Portuguesa de Cardiologia, Vol 32, Iss 2, Pp 117-122 (2013)
Revista Portuguesa de Cardiologia (English Edition), Vol 32, Iss 2, Pp 117-122 (2013)
ISSN: 0870-2551
Popis: Introduction: Atherosclerosis is an active process and the inflammatory component appears to be particularly correlated with the development of acute coronary syndromes (ACS). C-reactive protein (CRP) is an acute phase protein that appears in the circulation in response to inflammatory cytokines. The present study investigated the association between high-sensitivity C-reactive protein (hsCRP) on admission and follow-up prognosis after an ACS. Methods: We included 151 consecutive patients admitted to the coronary care unit with a diagnosis of ACS (47% ST-segment elevation myocardial infarction [STEMI]). The primary endpoint was the combination of cardiac death and myocardial reinfarction during the follow-up period (median 19.8 months, interquartile range 16.3–23.7 months). Results: The occurrence of follow-up events was significantly related to admission hsCRP level, which was an excellent predictor of cardiac death and reinfarction during follow-up (HR 1.091, 95% CI 1.014–1.174; p=0.019). Stratifying the population based on type of ACS, adjusted by variables associated with cardiac events in univariate analysis (hsCRP, diabetes, depressed ejection fraction and GRACE risk score), hsCRP proved to be an independent predictor of follow-up outcomes only in non-STEMI patients (HR 1.217, 95% CI: 1.093–1.356, p
Databáze: OpenAIRE