Thromboinflammation is associated with clinical outcome after ST-elevation myocardial infarction

被引:2
作者
Benkhoff, Marcel [1 ,2 ]
Alde, Karin [1 ]
Ehreiser, Vincent [3 ,4 ,5 ]
Dahlmanns, Jana [1 ]
Metzen, Daniel [1 ]
Haurand, Jean M. [1 ]
Duse, Dragos Andrei [1 ]
Jung, Christian [1 ,6 ]
Kelm, Malte [1 ,6 ]
Petzold, Tobias [3 ,5 ]
Polzin, Amin [1 ,6 ,7 ]
机构
[1] Heinrich Heine Univ Dusseldorf, Univ Hosp Dusseldorf, Med Fac, Dept Cardiol Pulmonol & Vasc Med, Dusseldorf, Germany
[2] Univ Vienna, Inst Analyt Chem, Vienna, Austria
[3] Charite, Deutsch Herzzentrum, Angiol & Intens Care Med, Campus Benjamin Franklin,Dept Cardiol, Berlin, Germany
[4] German Ctr Cardiovasc Res, Partner Site Berlin, Berlin, Germany
[5] Charite Univ Med Berlin, Friede Springer Ctr Cardiovasc Prevent Charite, Berlin, Germany
[6] Cardiovasc Res Inst Dusseldorf, Dusseldorf, Germany
[7] Imperial Coll London, Natl Heart & Lung Inst, London, England
关键词
NEUTROPHIL EXTRACELLULAR TRAPS; DUAL ANTIPLATELET THERAPY; TISSUE FACTOR; ARTERY; ACTIVATION; PREVENTION; THROMBOSIS;
D O I
10.1182/bloodadvances.2024014273
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Platelets are crucial in thrombus formation during ST-elevation myocardial infarction (STEMI). In addition, they also play an important role in postischemic thromboinflammation, which is determined by the interplay between activated platelets and neutrophils. The latter form neutrophil extracellular traps, which are detectable in plasma as citrullinated histone H3-deoxyribonucleic acid-DNA complexes. Prediction of the risk of recurrent events is important in precision medicine. Therefore, we investigated whether circulating thromboinflammatory markers predict clinical outcome after STEMI. We performed a prospective, multicentric, observational, all-comer study of patients with STEMI (n = 361). Thromboinflammation, measured as H3Cit-DNA complexes, was assessed on day 1 after presentation with STEMI as well as 5 days and 6 months after STEMI by enzyme-linked immunosorbent assay. Twelve months of clinical follow-up was conducted. Multivariate analysis was performed investigating which variables were independently associated with major adverse cardiac events (MACEs). Patients were aged 64 +/- 12 years; 80% were male; and 40% had diabetes mellitus. Thromboinflammation was enhanced during index hospitalization compared with 6-months follow-up (137.4 +/- 100.0 mu g/L vs 53.7 +/- 54.7 mu g/L; P < .001). Additionally, patients within the highest tertile of thromboinflammation at day 1 after STEMI showed worse outcome during follow-up (hazard ratio, 2.57; 95% confidence interval, 1.72-3.85; P < .001). Receiver operating characteristic analysis revealed a cutoff value of 219.3 mu g/L. In multivariate logistic regression analysis, thromboinflammation was independently associated with outcome after STEMI. To sum it up, thromboinflammation is enhanced in STEMI. It identifies patients at high risk of MACE. Therefore, thromboinflammation might be a promising target and marker in precision medicine. The trial was registered at www.clinicaltrials.gov as #NCT03539133.
引用
收藏
页码:5581 / 5589
页数:9
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