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Association of peak C-reactive protein with long-term clinical outcomes in patients with ST-segment elevation myocardial infarction.

Authors :
Hori Y
Sakakura K
Jinnouchi H
Taniguchi Y
Tsukui T
Watanabe Y
Yamamoto K
Seguchi M
Wada H
Fujita H
Source :
Heart and vessels [Heart Vessels] 2023 Jun; Vol. 38 (6), pp. 764-772. Date of Electronic Publication: 2023 Feb 21.
Publication Year :
2023

Abstract

Peak C-reactive protein (CRP) levels following ST-segment elevation myocardial infarction (STEMI) are associated with left ventricular thrombus formation or cardiac rupture. However, the impact of peak CRP on long-term outcomes in patients with STEMI is not completely understood. The purpose of this retrospective study was to compare the long-term all-cause death after STEMI between patients with and without high peak CRP levels. We included 594 patients with STEMI, and divided them into the high CRP group (n = 119) and the low-moderate CRP group (n = 475) according to the quintile of peak CRP levels. The primary endpoint was all-cause death after the discharge of the index admission. The mean peak CRP level was 19.66 ± 5.14 mg/dL in the high CRP group, whereas that was 6.43 ± 3.86 mg/dL in the low-moderate CRP group (p < 0.001). During the median follow-up duration of 1045 days (Q1 284 days, Q3 1603 days), a total of 45 all-cause deaths were observed. The Kaplan-Meier curves showed that all-cause death was more frequently observed in the high CRP group than in the low-moderate CRP group (p = 0.002). The multivariate Cox hazard analysis revealed that high CRP was significantly associated with all-cause death (hazard ratio 2.325, 95% confidence interval 1.246-4.341, p = 0.008) after controlling for confounding factors. In conclusion, high peak CRP was significantly associated with all-cause death in patients with STEMI. Our results suggest that peak CRP may be useful to stratify patients with STEMI for the risk of future death.<br /> (© 2023. Springer Nature Japan KK, part of Springer Nature.)

Details

Language :
English
ISSN :
1615-2573
Volume :
38
Issue :
6
Database :
MEDLINE
Journal :
Heart and vessels
Publication Type :
Academic Journal
Accession number :
36809395
Full Text :
https://doi.org/10.1007/s00380-023-02250-z