Evidence map›Paper›PMID 41272438›Full record

ArticleBMC cardiovascular disorders2025

Association between re-elevation of cardiac biomarkers and in-hospital MACE after primary PCI in STEMI patients.

Xiaodou Niu, Yuanji Ma, Xiaotong Cui, Wei Gao, Yan Xia, Shujing Wu, Meng Zhang, Yaolin Chen, Lihua Guan, Hongyi Wu

Abstract read
In one paragraph

Article in BMC cardiovascular disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Xiaodou Niu *Department of Cardiology, Zhongshan Hospital, Fudan University (Xiamen Branch), Xiamen, Fujian, China.
Yuanji Ma *Department of Cardiology, Zhongshan Hospital, Fudan University, Shanghai Institute of Cardiovascular Diseases, Shanghai, China.
Xiaotong Cui *Department of Cardiology, Zhongshan Hospital, Fudan University, Shanghai Institute of Cardiovascular Diseases, Shanghai, China.
Wei GaoDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai Institute of Cardiovascular Diseases, Shanghai, China.
Yan XiaDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai Institute of Cardiovascular Diseases, Shanghai, China.
Shujing WuDepartment of Cardiology, Zhongshan Hospital, Fudan University (Xiamen Branch), Xiamen, Fujian, China.
Meng ZhangDepartment of Cardiology, Zhongshan Hospital, Fudan University (Xiamen Branch), Xiamen, Fujian, China.
Yaolin ChenDepartment of Cardiology, Zhongshan Hospital, Fudan University (Xiamen Branch), Xiamen, Fujian, China.
Lihua GuanDepartment of Cardiology, Zhongshan Hospital, Fudan University (Xiamen Branch), Xiamen, Fujian, China. guan.lihua@zs-hospital.sh.cn.
Hongyi WuDepartment of Cardiology, Zhongshan Hospital, Fudan University (Xiamen Branch), Xiamen, Fujian, China. wu.hongyi@zs-hospital.sh.cn.

Funding

The General programs of the Natural Science Foundation of Fujian Province 2024J011435the Natural Science Foundation of Shanghai Grant 21ZR1412700
6 · The paper itself

Abstract

backgroundPrevious studies have indicated that after reperfusion therapy in patients with myocardial infarction, high-sensitivity cardiac troponin T (hs-cTnT) may exhibit a secondary increase following the initial peak decline, presenting a biphasic pattern. The clinical significance of this second peak remains controversial. Meanwhile, whether creatine kinase-MB (CK-MB) demonstrates a similar secondary increase and its clinical implications have been rarely investigated.

methodsThis retrospective study enrolled patients with ST-segment elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (PPCI). The associations of the second increase in the levels of myocardial markers including CK-MB and hs-cTnT and clinical outcomes were analyzed. The main study outcome was the rate of in-hospital major adverse cardiovascular events (MACE), including cardiac death, recurrent AMI, unplanned revascularization and stroke.

resultsA total of 264 patients were included in the study (220 males; average age of 63 ± 12 years). The phenomenon of a second increase in myocardial markers, including hs-cTnT and CK-MB, was observed in a significant subset of patients with STEMI following PPCI: the proportions of patients with isolated hs-cTnT secondary rise, isolated CK-MB secondary rise, and dual secondary rise were 29.9%, 11.7%, and 9.1%, respectively. The incidence of MACE in the isolated hs-cTnT secondary rise group (1.3%) was not significantly different from that in the no secondary rise group (1.5%). In contrast, both the isolated CK-MB secondary rise group (9.7%) and the dual secondary rise group (16.7%) showed higher MACE rates compared to the no secondary rise group.

conclusionsIn conclusion, a secondary rise in CK-MB, whether isolated or concurrent with hs-cTnT, is associated with a significantly higher risk of MACE. In contrast, an isolated secondary rise in hs-cTnT does not appear to confer an increased risk. These findings suggest that CK-MB, rather than hs-cTnT, is a more critical biomarker for identifying the biphasic pattern that predicts adverse outcomes in post-MI patients after reperfusion.

Indexed as

Creatine Kinase, MB FormPercutaneous Coronary InterventionST Elevation Myocardial InfarctionTroponin TAgedBiomarkersFemaleHospital MortalityHumansMaleMiddle AgedPredictive Value of TestsRecurrenceRetrospective StudiesRisk AssessmentRisk FactorsBiomarkersCreatine Kinase, MB FormTroponin TCardiac markersPrognosisSecond increaseSTEMI

Identifiers

PMID41272438
PMCPMC12639922

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.