Glycemia and inflammatory markers in acute coronary syndrome: Association with late post-hospital outcomes

被引:2
作者
Maciel, Patrfcia Tolledo
Pellanda, Lucia Campos
Portal, Vera Lucia
Schaan, Beatriz D'Agord
机构
[1] Unidade Pesquisa IC FUC, BR-90620001 Porto Alegre, RS, Brazil
[2] Mae de Deus Hosp, Porto Alegre, RS, Brazil
[3] Fed Sch Med Sci Porto Alegre, Porto Alegre, RS, Brazil
[4] Univ Fed Rio Grande do Sul, Hosp Clin Porto Alegre, Div Internal Med, BR-90046900 Porto Alegre, RS, Brazil
关键词
acute coronary syndromes; glycemia; inflammatory markers; major cardiovascular events; mortality;
D O I
10.1016/j.diabres.2007.04.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Glycemia and inflammatory markers were associated with clinical outcomes in patients with acute coronary syndrome (ACS). Objectives: To evaluate the role of glycemia and inflammatory markers as predictors of late cardiovascular outcomes after ACS. Methods: One hundred and ninety-nine ACS patients of a Coronary Care Unit were included, from March to November 2002. They were reassessed clinically after ∼3 years. Clinical variables, glycemia, CRP and fibrinogen were evaluated as event and mortality predictors. Statistical analyses included Cox multivariate analysis and survival curves (Kaplan-Meier). Results: At admission, 16.7% had normal glycemia. After 3 years, this proportion increased to 55.2%; the 40.6% who belonged to the borderline category decreased to 27.1%; the 42.7% with elevated glycemia decreased to 17.7%. Glycemia was not associated with the development of major cardiovascular events (MACE) and mortality at follow-up (∼3 years). Considering MACE, CRP (p < 0.001), but not fibrinogen, was predictive in bivariate analysis. Regarding mortality, both fibrinogen (p = 0.020) and CRP (p = 0.008) were predictive in bivariate analysis. Conclusion: Glycemia was not associated with late mortality after ACS, but inflammatory markers were, suggesting that these are more sensitive markers to predict events in long-term. Moreover, glucose intolerance prevalence is lower in the follow-up after the ACS episode. © 2007 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:263 / 269
页数:7
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