Evidence map›Paper›PMID 39630269›Full record

ArticleHeart and vessels2025

Prognostic value of combining cardiac myosin-binding protein C and N-terminal pro-B-type natriuretic peptide in patients without acute coronary syndrome treated at medical cardiac intensive care units.

Hideto Nishimura, Junnichi Ishii, Hiroshi Takahashi, Yuya Ishihara, Kazuhiro Nakamura, Fumihiko Kitagawa, Eirin Sakaguchi, Yuko Sasaki, Hideki Kawai, Takashi Muramatsu and 10 more

Abstract read
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Article in Heart and vessels, 2025. 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

20 authors.

Hideto NishimuraDepartment of Cardiology, Fujita Health University School of Medicine, 1-98 Kutsukake-cho, Dengakugakubo, Toyoake, 470-1192, Japan.
Junnichi IshiiDepartment of Cardiology, Fujita Health University School of Medicine, 1-98 Kutsukake-cho, Dengakugakubo, Toyoake, 470-1192, Japan. jishii@fujita-hu.ac.jp.ORCID http://orcid.org/0000-0003-2695-0461
Hiroshi TakahashiDepartment of Cardiology, Fujita Health University School of Medicine, 1-98 Kutsukake-cho, Dengakugakubo, Toyoake, 470-1192, Japan.
Yuya IshiharaDepartment of Laboratory of Clinical Medicine, Fujita Health University Hospital, Toyoake, Japan.
Kazuhiro NakamuraDepartment of Laboratory of Clinical Medicine, Fujita Health University Hospital, Toyoake, Japan.
Fumihiko KitagawaDepartment of Laboratory of Clinical Medicine, Fujita Health University Hospital, Toyoake, Japan.
Eirin SakaguchiFaculty of Medical Technology, School of Health Sciences, Fujita Health University, Toyoake, Japan.
Yuko SasakiSysmex R&D Center Europe GmbH, Hamburg, Germany.
Hideki KawaiDepartment of Cardiology, Fujita Health University School of Medicine, 1-98 Kutsukake-cho, Dengakugakubo, Toyoake, 470-1192, Japan.
Takashi MuramatsuDepartment of Cardiology, Fujita Health University School of Medicine, 1-98 Kutsukake-cho, Dengakugakubo, Toyoake, 470-1192, Japan.
Masahide HaradaDepartment of Cardiology, Fujita Health University School of Medicine, 1-98 Kutsukake-cho, Dengakugakubo, Toyoake, 470-1192, Japan.
Akira YamadaDepartment of Cardiology, Fujita Health University School of Medicine, 1-98 Kutsukake-cho, Dengakugakubo, Toyoake, 470-1192, Japan.
Sadako Tanizawa-MotoyamaDepartment of Cardiology, Fujita Health University School of Medicine, 1-98 Kutsukake-cho, Dengakugakubo, Toyoake, 470-1192, Japan.
Hiroyuki NaruseFaculty of Medical Technology, School of Health Sciences, Fujita Health University, Toyoake, Japan.
Masayoshi SaraiDepartment of Cardiology, Fujita Health University School of Medicine, 1-98 Kutsukake-cho, Dengakugakubo, Toyoake, 470-1192, Japan.
Masanobu YanaseDepartment of Cardiology, Fujita Health University School of Medicine, 1-98 Kutsukake-cho, Dengakugakubo, Toyoake, 470-1192, Japan.
Hideki IshiiDepartment of Cardiovascular Medicine, Gunma University Graduate School of Medicine, Maebashi, Japan.
Eiichi WatanabeDepartment of Cardiology, Fujita Health University School of Medicine, 1-98 Kutsukake-cho, Dengakugakubo, Toyoake, 470-1192, Japan.
Yukio OzakiDepartment of Cardiology, Fujita Health University School of Medicine, 1-98 Kutsukake-cho, Dengakugakubo, Toyoake, 470-1192, Japan.
Hideo IzawaDepartment of Cardiology, Fujita Health University School of Medicine, 1-98 Kutsukake-cho, Dengakugakubo, Toyoake, 470-1192, Japan.

Funding

JSPS KAKENHI 22K07487
6 · The paper itself

Abstract

We investigated the prognostic value of cardiac myosin-binding protein C (cMyC), a novel cardiospecific marker, both independently and in combination with N-terminal pro-B-type natriuretic peptide (NT-proBNP), for predicting 6-month all-cause mortality in patients without acute coronary syndrome (ACS) treated at medical (nonsurgical) cardiac intensive care units (CICUs). Admission levels of cMyC, high-sensitivity cardiac troponin T (hs-cTnT), and NT-proBNP were measured in 1032 consecutive patients (mean age; 70 years) without ACS hospitalized acutely in medical CICUs for the treatment of cardiovascular disease. Serum cMyC was closely correlated with hs-cTnT and moderately with NT-proBNP (r = 0.92 and r = 0.49, respectively, p < 0.0001). During the 6-month follow-up period after admission, there were 109 (10.6%) all-cause deaths, including 72 cardiovascular deaths. Both cMyC and NT-proBNP were independent predictors of 6-month all-cause mortality (all p < 0.05). Combining cMyC and NT-proBNP with a baseline model of established risk factors improved patient classification and discrimination beyond any single biomarker (all p < 0.05) or the baseline model alone (both p < 0.0001). Moreover, patients were divided into nine groups using cMyC and NT-proBNP tertiles, and the adjusted hazard ratio (95% confidence interval) for 6-month all-cause mortality in patients with both biomarkers in the highest vs. lowest tertile was 9.67 (2.65-35.2). When cMyC was replaced with hs-cTnT, similar results were observed for hs-cTnT. In addition, the C-indices for addition of cMyC or hs-cTnT to the baseline model were similar (0.798 vs. 0.800, p = 0.94). In conclusion, similar to hs-cTnT, cMyC at admission may be a potent, independent predictor of 6-month all-cause mortality in patients without ACS treated at medical CICUs, and their prognostic abilities may be comparable. Combining cMyC or hs-cTnT with NT-proBNP may substantially improve early risk stratification of this population.

Indexed as

Carrier ProteinsCoronary Care UnitsNatriuretic Peptide, BrainPeptide FragmentsAcute Coronary SyndromeAgedBiomarkersCause of DeathFemaleFollow-Up StudiesHumansMaleMiddle AgedMyosin Binding Protein CPredictive Value of TestsPrognosisBiomarkersCarrier ProteinsMyosin Binding Protein CNatriuretic Peptide, BrainPeptide Fragmentspro-brain natriuretic peptide (1-76)Troponin TAll-cause mortalityCardiac myosin-binding protein CHigh-sensitivity cardiac troponin TMedical cardiac intensive care unitsNon-acute coronary syndromeN-terminal pro-B-type natriuretic peptide

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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.