Evidence map›Paper›PMID 20560006›Full record

ReviewJournal of cardiovascular translational research2009

Experimental therapies in hypertrophic cardiomyopathy.

Ali J Marian

Open access · greenAbstract readReview
In one paragraph

Review in Journal of cardiovascular translational research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

16 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. The Role of the NOD1/Rip2 Signaling Pathway in Myocardial Remodeling in Spontaneously Hypertensive Rats.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  3. Article
  4. Hypertrophic cardiomyopathy: genetics and clinical perspectives.Cardiovascular diagnosis and therapy · 2019
    Review
  5. Review
  6. Article
  7. I-1-deficiency negatively impacts survival in a cardiomyopathy mouse model.International journal of cardiology. Heart & vasculature · 2015
    Article
  8. Article
  9. Article
  10. Review
  11. Hypertrophic cardiomyopathy: The need for randomized trials.Global cardiology science & practice · 2013
    Review
  12. cAMP and Epac in the regulation of tissue fibrosis.British journal of pharmacology · 2012
    Review
  13. Article
  14. Article
  15. Mechanisms of disease: hypertrophic cardiomyopathy.Nature reviews. Cardiology · 2011
    Review
  16. Hypertrophic cardiomyopathy: from genetics to treatment.European journal of clinical investigation · 2010
    Review
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

1 author at 1 institution in 1 country.

Ali J MarianCenter for Cardiovascular Genetics, St. Luke's Episcopal Hospital and Texas Heart Institute, Brown Foundation Institute of Molecular Medicine, The Unversity of Texas Health Science Center, Houston, TX 77030, USA. Ali.J.Marian@uth.tmc.edu
Brown Foundation · US

Funding

Canonical Wnt Signaling in Pathogenesis and Rescue of ARVC PhenotypeR01HL088498 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MARIAN, ALI J · 2008 to 2017
$3.4M
Modifier Genes of Familial Hypertrophic CardiomyopathyR01HL068884 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI MARIAN, ALI J. · 2001 to 2005
$3.2M
NHLBI NIH HHS R01 HL068884NHLBI NIH HHS R01 HL088498
6 · The paper itself

Abstract

The quintessential clinical diagnostic phenotype of human hypertrophic cardiomyopathy (HCM) is primary cardiac hypertrophy. Cardiac hypertrophy is also a major determinant of mortality and morbidity including the risk of sudden cardiac death (SCD) in patients with HCM. Reversal and attenuation of cardiac hypertrophy and its accompanying fibrosis is expected to improve morbidity as well as decrease the risk of SCD in patients with HCM.The conventionally used pharmacological agents in treatment of patients with HCM have not been shown to reverse or attenuate established cardiac hypertrophy and fibrosis. An effective treatment of HCM has to target the molecular mechanisms that are involved in the pathogenesis of the phenotype. Mechanistic studies suggest that cardiac hypertrophy in HCM is secondary to activation of various hypertrophic signaling molecules and, hence, is potentially reversible. The hypothesis is supported by the results of genetic and pharmacological interventions in animal models. The results have shown potential beneficial effects of angiotensin II receptor blocker losartan, mineralocorticoid receptor blocker spironolactone, 3-hydroxy-3-methyglutaryl-coenzyme A reductase inhibitors simvastatin and atorvastatin, and most recently, N-acetylcysteine (NAC) on reversal or prevention of hypertrophy and fibrosis in HCM. The most promising results have been obtained with NAC, which through multiple thiol-responsive mechanisms completely reversed established cardiac hypertrophy and fibrosis in three independent studies. Pilot studies with losartan and statins in humans have established the feasibility of such studies. The results in animal models have firmly established the reversibility of established cardiac hypertrophy and fibrosis in HCM and have set the stage for advancing the findings in the animal models to human patients with HCM through conducting large-scale efficacy studies.

Indexed as

AnimalsCardiomyopathy, HypertrophicCardiovascular AgentsDeath, Sudden, CardiacDrugs, InvestigationalFibrosisGenetic Predisposition to DiseaseHumansMyocardiumPhenotypeTreatment OutcomeCardiovascular AgentsDrugs, Investigational

Identifiers

PMID20560006
PMCPMC2904688
OpenAlexW2070031931

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.