Evidence map›Paper›PMID 42701926›Full record

ArticleThe international journal of cardiovascular imaging2026

Redefining NSTE-ACS risk assessment: The synergistic power of CT-enhanced GRACE 2.0 score for advanced prognosis.

Jing-Wen Ma, Shan Muhammad, U Joseph Schoepf, Chuang-Shi Wang, Zhi-Hui Hou, Yun-Qiang An, Er-Li Zhang, Yan Liang, Zhou Zhou, Ya-Hui Lin and 2 more

Abstract read
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In one paragraph

Article in The international journal of cardiovascular imaging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Jing-Wen MaDepartment of Radiology, Beijing Anzhen Hospital, Capital Medical University, Beijing, 100029, China.
Shan MuhammadDepartment of Thoracic Surgery, National Clinical Research Center for Cancer/Cancer Hospital, National Cancer Center, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China.
U Joseph SchoepfDivision of Cardiovascular Imaging, Department of Radiology and Radiological Science, Department of Medicine, Medical University of South Carolina, SC (U.J.S.,S.A.), Charleston, USA.
Chuang-Shi WangMedical Research and Biometrics Center, Peking Union Medical College, State Key Lab and National Center for Cardiovascular Diseases, Fuwai Hospital, Chinese Academy of Medical Sciences, #167 Bei-Li-Shi Street, Beijing, 100037, People's Republic of China.
Zhi-Hui HouDepartment of Radiology, Peking Union Medical College, State Key Lab and National Center for Cardiovascular Diseases, Fuwai Hospital, Chinese Academy of Medical Sciences, #167 Bei- Li-Shi Street, Beijing, 100037, People's Republic of China.
Yun-Qiang AnDepartment of Radiology, Peking Union Medical College, State Key Lab and National Center for Cardiovascular Diseases, Fuwai Hospital, Chinese Academy of Medical Sciences, #167 Bei- Li-Shi Street, Beijing, 100037, People's Republic of China.
Er-Li ZhangDepartment of Cardiology, Peking Union Medical College, State Key Lab and National Center for Cardiovascular Diseases, Fuwai Hospital, Chinese Academy of Medical Sciences, #167 Bei-Li-Shi Street, Beijing, 100037, People's Republic of China.
Yan LiangEmergency Center, Peking Union Medical College, State Key Lab and National Center for Cardiovascular Diseases, Fuwai Hospital, Chinese Academy of Medical Sciences, #167 Bei-Li-Shi Street, Beijing, 100037, People's Republic of China.
Zhou ZhouCenter of Laboratory Medicine, Peking Union Medical College, State Key Lab and National Center for Cardiovascular Diseases, Fuwai Hospital, Chinese Academy of Medical Sciences, #167 Bei-Li-Shi Street, Beijing, 100037, People's Republic of China.
Ya-Hui LinCenter of Laboratory Medicine, Peking Union Medical College, State Key Lab and National Center for Cardiovascular Diseases, Fuwai Hospital, Chinese Academy of Medical Sciences, #167 Bei-Li-Shi Street, Beijing, 100037, People's Republic of China.
Wei-Hua YinDepartment of Radiology, Peking Union Medical College, State Key Lab and National Center for Cardiovascular Diseases, Fuwai Hospital, Chinese Academy of Medical Sciences, #167 Bei- Li-Shi Street, Beijing, 100037, People's Republic of China.
Bin LuDepartment of Radiology, Peking Union Medical College, State Key Lab and National Center for Cardiovascular Diseases, Fuwai Hospital, Chinese Academy of Medical Sciences, #167 Bei- Li-Shi Street, Beijing, 100037, People's Republic of China. blu@vip.sina.com.

Funding

he National Natural Science Foundation of China Grant No.: 82102036the Ministry of Science and Technology of China, the National Key Research and Development Project Grant No.: 2016YFC1300403
6 · The paper itself

Abstract

The Global Registry of Acute Coronary Events (GRACE) 2.0 risk score has been recommended in guidelines to orient therapeutic strategy and risk assessment for non-ST-segment elevation acute coronary syndrome (NSTE-ACS). To evaluate the incremental value of computed tomography (CT)-based coronary atherosclerosis plaque burden to GRACE 2.0 score in refining the intermediate-term prognostic accuracy and risk stratification for emergency NSTE-ACS. In this prospective cohort study, from January 2017 to January 2021, NSTE-ACS individuals were enrolled and randomly divided into a developing and validation sets by 7:3. We estimated the correlations between GRACE 2.0 score and CT findings. The primary outcomes are the incremental prognostic value of CT for the GRACE 2.0 score's efficacy in predicting 3-year mortality or myocardial infarction (MI). A total of 1248 consecutive NSTE-ACS patients undergoing CT scans were prospectively included. The risk of 3-year mortality or MI was greater in the higher CACS category (HR, 2.31 [95% CI, 1.45-3.67]), SIS category (HR, 3.37 [95% CI, 2.36-4.82]) and luminal stenosis degree (HR, 1.69 [95% CI, 1.15-2.48]) stratified by CAD-RADS (coronary artery disease reporting and Data System) 2.0 than in the lower ones. The CT-GRACE model integrating CACS category, SSS and GRACE 2.0 risk score was compared with the GRACE 2.0 risk score to evaluate their discrimination and reclassification ability in predicting 3-year mortality or MI. The C-statistics were 0.889 (0.842, 0.937) and 0.742 (0.659, 0.826) in the validation set, respectively (ΔAUC=0.147, P < 0.001). Coronary atherosclerosis plaque burden features could provide more meaningful information for GRACE 2.0 risk score to evaluate the intermediate-term prognosis for emergency NSTE-ACS.

Indexed as

Computed tomographyGlobal Registry of Acute Coronary Events 2.0 risk scoreNon-ST-segment elevation acute coronary syndromeSemi-quantitative plaque burden

Identifiers

PMID42701926

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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.