Evidence map›Paper›PMID 29177058›Full record

ArticleOpen heart

Biomarkers of cardiovascular stress and fibrosis in preclinical hypertrophic cardiomyopathy.

Jennifer E Ho, Ling Shi, Sharlene M Day, Steven D Colan, Mark W Russell, Jeffrey A Towbin, Mark V Sherrid, Charles E Canter, John Lynn Jefferies, Anne Murphy and 10 more

Open access · goldAbstract read
In one paragraph

Article in Open heart. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

25 citing papers in PubMed, 32 citations in OpenAlex.

  1. Trial
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  5. Article
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  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Circulating Biomarkers in Hypertrophic Cardiomyopathy.Journal of the American Heart Association · 2022
    Review
  14. The Impact of Mavacamten on the Pathophysiology of Hypertrophic Cardiomyopathy: A Narrative Review.American journal of cardiovascular drugs : drugs, devices, and other interventions · 2022
    Review
  15. Review
  16. Hypertrophic cardiomyopathy β-cardiac myosin mutation (P710R) leads to hypercontractility by disrupting super relaxed state.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  17. The Time Has Come to Explore Plasma Biomarkers in Genetic Cardiomyopathies.International journal of molecular sciences · 2021
    Review
  18. Article
  19. Observational
  20. Observational
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 at 11 institutions in 2 countries.

Jennifer E HoDivision of Cardiology, Department of Medicine, Cardiovascular Research Center, Massachusetts General Hospital, Ann Arbor, Michigan, USA.
Ling ShiNew England Research Institutes, Watertown, Massachusetts, USA.
Sharlene M DayDepartments of Internal Medicine and Pediatrics, University of Michigan, Ann Arbor, Michigan, USA.
Steven D ColanDepartment of Cardiology, Boston Children's Hospital, Boston, Massachusetts, USA.
Mark W RussellDepartments of Internal Medicine and Pediatrics, University of Michigan, Ann Arbor, Michigan, USA.
Jeffrey A TowbinThe Heart Institute and Pediatric Cardiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Mark V SherridDivision of Cardiology, Department of Medicine, New York University Langone Medical Center, New York, New York, USA.
Charles E CanterDepartment of Pediatrics, Washington University School of Medicine, St Louis, Missouri, USA.
John Lynn JefferiesThe Heart Institute and Pediatric Cardiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Anne MurphyDivision of Pediatric Cardiology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Matthew TaylorDepartment of Medicine, University of Colorado Denver CU-Cardiovascular Institute, Aurora, Colorado, USA.
Luisa MestroniDepartment of Medicine, University of Colorado Denver CU-Cardiovascular Institute, Aurora, Colorado, USA.
Allison L CirinoCardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Lynn A SleeperNew England Research Institutes, Watertown, Massachusetts, USA.
Peter JarolimDepartment of Pathology, Brigham and Women's Hospital, Boston, MA, USA.
Begoña LopezProgram of Cardiovascular Diseases, Center for Applied Medical Research, University of Navarra, Pamplona, Spain.
Arantxa GonzalezProgram of Cardiovascular Diseases, Center for Applied Medical Research, University of Navarra, Pamplona, Spain.
Javier DiezProgram of Cardiovascular Diseases, Center for Applied Medical Research, University of Navarra, Pamplona, Spain.
E John OravDepartment of Biostatistics, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Carolyn Y HoDivision of Cardiology, Department of Medicine, Cardiovascular Research Center, Massachusetts General Hospital, Ann Arbor, Michigan, USA.
Brigham and Women's Hospital · USUniversidad de Navarra · ESCincinnati Children's Hospital Medical Center · USMassachusetts General Hospital · USNew England Research Institutes · USUniversity of Colorado Denver · USUniversity of Michigan–Ann Arbor · USBoston Children's Hospital · USJohns Hopkins University · USNYU Langone Health · USWashington University in St. Louis · US

Funding

Using Genetics for Early Phenotyping & Prevention of Hypertrophic CardiomyopathyP20HL101408 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI HO, CAROLYN Y, SEIDMAN, CHRISTINE E · 2010 to 2011
$1.5M
The Role of Galectin-3 in Cardiac Remodeling and Heart FailureK23HL116780 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI HO, JENNIFER E · 2013 to 2017
$832k
NHLBI NIH HHS K23 HL116780NHLBI NIH HHS P20 HL101408
6 · The paper itself

Abstract

Objective: Sarcomeric gene mutation carriers without overt left ventricular hypertrophy (G+/LVH-) can harbour subclinical changes in cardiovascular structure and function that precede the development of hypertrophic cardiomyopathy (HCM). We sought to investigate if circulating biomarkers of cardiovascular stress and collagen metabolism among G+/LVH- individuals, measured at rest and following exercise provocation, yield further insights into the underlying biology of HCM. Methods: We studied 76 individuals with overt HCM, 50 G+/LVH- individuals and 41 genotype-negative related controls enrolled in a cross-sectional, multicentre observational study (HCMNet). Biomarkers of cardiac stress (N-terminal pro-B-type natriuretic peptide, NT-proBNP; high-sensitivity troponin I, hsTnI; soluble ST2) and fibrosis (carboxy-terminal propeptide of procollagen type I; C-terminal telopeptide of type I collagen; galectin-3; periostin) were measured. Results: Individuals with overt HCM had elevated NT-proBNP and hsTnI compared with G+/LVH- subjects and controls at rest, along with an exaggerated increase in NT-proBNP and hsTnI in response to exercise. We found no detectable differences in resting or exercise-provoked biomarker profiles of cardiovascular stress and fibrosis among G+/LVH- individuals compared with healthy controls despite subtle echocardiographic differences in cardiac structure and function. Conclusion: Dynamic exercise testing exaggerated resting differences in natriuretic peptides and troponin elevations among individuals with overt HCM. In contrast, we found no differences in biomarker profiles of cardiovascular stress and fibrosis among G+/LVH- individuals compared with controls even after maximal exercise provocation. Our findings highlight the need for continued investigation into early phenotypes of sarcomeric gene mutations and the evolution of HCM.

Indexed as

biomarkerechocardiographyhypertrophic cardiomyopathy

Identifiers

PMID29177058
PMCPMC5687543
OpenAlexW2765949756

What OpenQuestion holds

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LicenceCC BY-NC
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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.