Evidence map›Paper›PMID 28847594›Full record

ArticleThe American journal of cardiology2017

Usefulness of Released Cardiac Myosin Binding Protein-C as a Predictor of Cardiovascular Events.

Carl W Tong, Giuseppina F Dusio, Suresh Govindan, Dustin W Johnson, David T Kidwell, Lisa M De La Rosa, Paola C Rosas, Yang Liu, Elizabeth Ebert, M Karen Newell-Rogers and 3 more

Abstract read
In one paragraph

Article in The American journal of cardiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  5. Article
  6. Review
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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

13 authors.

Carl W TongDepartment of Medical Physiology, Texas A&M University Health Science Center College of Medicine, Temple, Texas; Baylor Scott & White Health-Central Texas, Internal Medicine/Cardiology Division, Temple, Texas.
Giuseppina F DusioUniversity of Arkansas for Medical Sciences, Little Rock, Arkansas.
Suresh GovindanDepartment of Cell and Molecular Physiology, Health Sciences Division, Loyola University Chicago, Maywood, Illinois.
Dustin W JohnsonBaylor Scott & White Health-Central Texas, Internal Medicine/Cardiology Division, Temple, Texas.
David T KidwellBaylor Scott & White Health-Central Texas, Internal Medicine/Cardiology Division, Temple, Texas.
Lisa M De La RosaBaylor Scott & White Health-Central Texas, Internal Medicine/Cardiology Division, Temple, Texas.
Paola C RosasDepartment of Medical Physiology, Texas A&M University Health Science Center College of Medicine, Temple, Texas.
Yang LiuDepartment of Medical Physiology, Texas A&M University Health Science Center College of Medicine, Temple, Texas.
Elizabeth EbertBaylor Scott & White Health-Central Texas, Internal Medicine/Cardiology Division, Temple, Texas.
M Karen Newell-RogersDepartment of Medical Physiology, Texas A&M University Health Science Center College of Medicine, Temple, Texas.
Jeffrey B MichelBaylor Scott & White Health-Central Texas, Internal Medicine/Cardiology Division, Temple, Texas.
Jerome P TrzeciakowskiDepartment of Medical Physiology, Texas A&M University Health Science Center College of Medicine, Temple, Texas.
Sakthivel SadayappanDepartment of Cell and Molecular Physiology, Health Sciences Division, Loyola University Chicago, Maywood, Illinois; Department of Internal Medicine, Heart, Lung and Vascular Institute, Cardiovascular Center, University of Cincinnati College of Medicine, Cincinnati, Ohio. Electronic address: sadayasl@ucmail.uc.edu.

Funding

Fast myosin binding protein-C and cardiac contractility in heart failureR01HL105826 · NHLBI · UNIVERSITY OF CINCINNATI · PI SADAYAPPAN, SAKTHIVEL · 2011 to 2025
$4.5M
Molecular mechanism of hypertrophic cardiomyopathy in populations of South Asian descendantsR01HL130356 · NHLBI · UNIVERSITY OF CINCINNATI · PI SADAYAPPAN, SAKTHIVEL · 2016 to 2019
$1.6M
Contributions of Cardiac Myosin Binding Protein-C to Healthy and Failing HeartsK08HL114877 · NHLBI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI TONG, CARL WEI-CHAN · 2012 to 2016
$656k
Proteomic approaches to validate novel cardiac biomarkers for myocardial infarctiK02HL114749 · NHLBI · UNIVERSITY OF CINCINNATI · PI SADAYAPPAN, SAKTHIVEL · 2012 to 2016
$498k
Cardiac Myosin Binding Protein-C Modulates Immune Response to Protect the HeartR03HL140266 · NHLBI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI TONG, CARL WEI-CHAN · 2017 to 2018
$149k
NHLBI NIH HHS K02 HL114749NHLBI NIH HHS K08 HL114877NHLBI NIH HHS R01 HL105826NHLBI NIH HHS R01 HL130356NHLBI NIH HHS R03 HL140266
6 · The paper itself

Abstract

Cardiac myosin binding protein-C (cMyBP-C) is a heart muscle-specific thick filament protein. Elevated level of serum cMyBP-C is an indicator of early myocardial infarction (MI), but its value as a predictor of future cardiovascular disease is unknown. Based on the presence of significant amount of cMyBP-C in the serum of previous study subjects independent of MI, we hypothesized that circulating cMyBP-C is a sensitive indicator of ongoing cardiovascular stress and disease. To test this hypothesis, 75 men and 83 women of similar ages were recruited for a prospective study. They underwent exercise stress echocardiography to provide pre- and poststress blood samples for subsequent determination of serum cMyBP-C levels. The subjects were followed for 1 to 1.5 years. Exercise stress increased serum cMyBP-C in all subjects. Twenty-seven primary events (such as death, MI, revascularization, invasive cardiovascular procedure, or cardiovascular-related hospitalization) and 7 critical events (CE; such as death, MI, stroke, or pulmonary embolism) occurred. After adjusting for sex and cardiovascular risk factors with multivariate Cox regression, a 96% sensitive prestress cMyBP-C threshold carried a hazard ratio of 8.1 with p = 0.041 for primary events. Most subjects (6 of 7) who had CE showed normal ejection fraction on echocardiography. Prestress cMyBP-C demonstrated area under receiver operating curve of 0.91 and multivariate Cox regression hazard ratio of 13.8 (p = 0.000472) for CE. Thus, basal cMyBP-C levels reflected susceptibility for a variety of cardiovascular diseases. Together with its high sensitivity, cMyBP-C holds potential as a screening biomarker for the existence of severe cardiovascular diseases.

Indexed as

AgedCardiovascular DiseasesCarrier ProteinsExercise TestFemaleHumansMaleMiddle AgedMyosin Binding Protein CPredictive Value of TestsProspective StudiesROC CurveStroke VolumeCarrier ProteinsMyosin Binding Protein C

Identifiers

PMID28847594
PMCPMC6034604

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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.