Evidence map›Paper›PMID 36650606›Full record

ArticleEuropean journal of medical research2023

Declined plasma microfibrillar-associated protein 4 levels in acute coronary syndrome.

Chunming Han, Yuanshu Peng, Xiaoyan Yang, Zongsheng Guo, Xinchun Yang, Pixiong Su, Shubin Guo, Lei Zhao

Open access · goldAbstract read
In one paragraph

Article in European journal of medical research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.6field-weighted citation impact, top 16% of its field
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

3 citing papers in PubMed, 5 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

Chunming Han *Emergency Medicine Clinical Research Center, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Yuanshu Peng *Heart Center, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, 100020, China.
Xiaoyan Yang *Heart Center, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, 100020, China.
Zongsheng GuoHeart Center, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, 100020, China.
Xinchun YangHeart Center, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, 100020, China.
Pixiong SuHeart Center, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, 100020, China. supixiong1130@163.com.
Shubin GuoEmergency Medicine Clinical Research Center, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China. guoshubin@bjcyh.com.
Lei ZhaoHeart Center, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, 100020, China. lily885300@sina.com.
Capital Medical University · CNBeijing Chao-Yang Hospital · CNBeijing Administration Institute · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMicrofibrillar-associated protein (MFAP4), initially identified as an extracellular matrix protein, has been demonstrated in multiple human disorders, but it is yet to be discovered following acute coronary syndrome (ACS) in clinical practice. Therefore, this study aimed to investigate the relationship between circulating MFAP4 levels and coronary stenosis in ACS.

methodsWe performed the study in 148 ACS subjects, including 75 ST-segment elevation myocardial infarction (STEMI), 27 non-ST-segment elevation myocardial infarction (non-STEMI) and 46 unstable angina (UA). Clinical variables were collected and Gensini and Syntax stenosis scoring systems were applied to assess the severity of coronary stenosis. Kaplan-Meier and logistic regression analysis were used to analyze the relationship between MFAP4 and the severity of coronary stenosis or ACS outcomes. Spearman analysis was used to describe the correlation between MFAP4 and clinical parameters.

resultsCirculating MFAP4 levels were significantly decreased in the STEMI group (0.008 ng/ml) compared with the non-STEMI group (0.014 ng/ml) and UA group (0.019 ng/ml) (p < 0.001). After adjusting for confounding factors, we found that MFAP4 was an independent risk factor for STEMI (odds ratio = 0.395, 95% CI 0.174-0.895, p = 0.026). MFAP4 level was negatively correlated with Gensini score and Syntax score (r = - 0.311 and - 0.211, p < 0.001 and 0.01, respectively). Based on the MFAP4 level of 0.117 ng/ml, ACS patients were divided into two groups: the low-MFAP4 group (< 0.117 ng/ml, n = 60) and the high-MFAP4 group (≥ 0.117 ng/ml, n = 88). After the median follow-up of 165 days, Kaplan-Meier survival analysis revealed that the MACE-free rate was significantly lower in ACS patients with lower MFAP4 levels (p = 0.009).

conclusionsMFAP4 has a potential as a biomarker for the degree of coronary stenosis in ACS. Confirmation of observations in larger cohorts and longer follow-up periods is warranted.

Indexed as

Acute Coronary SyndromeCoronary StenosisST Elevation Myocardial InfarctionAngina, UnstableBiomarkersCarrier ProteinsExtracellular Matrix ProteinsGlycoproteinsHumansBiomarkersCarrier ProteinsExtracellular Matrix ProteinsGlycoproteinsMFAP4 protein, humanAcute coronary syndromeBiomarkerCoronary stenosisMicrofibrillar-associated protein 4Myocardial infarction

Identifiers

PMID36650606
PMCPMC9847181
OpenAlexW4317360646

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Registered trials

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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.