Evidence map›Paper›PMID 25543971›Full record

Trial reportJACC. Heart failure2015

Diltiazem treatment for pre-clinical hypertrophic cardiomyopathy sarcomere mutation carriers: a pilot randomized trial to modify disease expression.

Carolyn Y Ho, Neal K Lakdawala, Allison L Cirino, Steven E Lipshultz, Elizabeth Sparks, Siddique A Abbasi, Raymond Y Kwong, Elliott M Antman, Christopher Semsarian, Arantxa González and 5 more

2 registry-linked trialsOpen access · greenAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in JACC. Heart failure, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 85 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed, 3 pooled it
10.7field-weighted citation impact, top 1% 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.

NCT00319982 phase2 / phase3completednot on this map

Treatment of Preclinical Hypertrophic Cardiomyopathy With Diltiazem

TypeinterventionalSponsorBrigham and Women's HospitalRan2006 to 2013Enrolled39ConditionsHypertrophic CardiomyopathyArmsDiltiazem, Placebo
NCT02948998 phase4unknown statusnot on this mapstarted 2018, after this paper: background citation

Evaluating the Effect of Spironolactone on Hypertrophic Cardiomyopathy-- a Multicenter Randomized Control Trial

TypeinterventionalSponsorXinhua Hospital, Shanghai Jiao Tong University School of MedicineRan2018 to 2020Enrolled260ConditionsHypertrophic Cardiomyopathy, FibrosisArmsSpironolactone
3 · Its place in the literature

Who cites it

85 citing papers in PubMed, 3 syntheses or guidelines pooled it, 158 citations in OpenAlex.

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  3. Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).Genetics in medicine : official journal of the American College of Medical Genetics · 2018
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25 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 6 institutions in 3 countries.

Carolyn Y HoCardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts. Electronic address: cho@partners.org.
Neal K LakdawalaCardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts.
Allison L CirinoCardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts.
Steven E LipshultzDepartment of Pediatrics, Wayne State University School of Medicine, and Department of Cardiology, Children's Hospital of Michigan, Detroit, Michigan.
Elizabeth SparksDepartment of Medicine, Johns Hopkins Hospital, Baltimore, Maryland.
Siddique A AbbasiCardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts.
Raymond Y KwongCardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts.
Elliott M AntmanCardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts.
Christopher SemsarianAgnes Ginges Centre for Molecular Cardiology, Centenary Institute; Sydney Medical School, University of Sydney and Department of Cardiology, Royal Prince Alfred Hospital, Sydney, Australia.
Arantxa GonzálezProgram of Cardiovascular Diseases, Centre for Applied Medical Research, University of Navarra, Pamplona, Spain.
Begoña LópezProgram of Cardiovascular Diseases, Centre for Applied Medical Research, University of Navarra, Pamplona, Spain.
Javier DiezProgram of Cardiovascular Diseases, Centre for Applied Medical Research, University of Navarra, Pamplona, Spain; Department of Cardiology and Cardiac Surgery, University of Navarra Clinic, Pamplona, Spain.
E John OravDepartment of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Steven D ColanBoston Children's Hospital, Boston, Massachusetts.
Christine E SeidmanCardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts; Howard Hughes Medical Institute, New York, New York.
Brigham and Women's Hospital · USUniversidad de Navarra · ESBoston Children's Hospital · USJohns Hopkins Hospital · USThe University of Sydney · AUWayne State University · US

Funding

Noninvasive Cardiovascular Imaging Research Training ProgramT32HL094301 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI Marcelo F DI CARLI · 2010 to 2026
$7.8M
Diagnostic and Treatment Strategies for Preclinical HCMK23HL078901 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI HO, CAROLYN Y · 2005 to 2009
$795k
NHLBI NIH HHS K23 HL078901NHLBI NIH HHS T32 HL094301
6 · The paper itself

Abstract

objectivesThe study sought to assess the safety, feasibility, and effect of diltiazem as disease-modifying therapy for at-risk hypertrophic cardiomyopathy (HCM) mutation carriers.

backgroundHCM is caused by sarcomere mutations and characterized by left ventricular hypertrophy (LVH) with increased risk of heart failure and sudden death. HCM typically cannot be diagnosed early in life, although subtle phenotypes are present. Animal studies indicate that intracellular calcium handling is altered before LVH develops. Furthermore, early treatment with diltiazem appeared to attenuate disease emergence.

methodsIn a pilot, double-blind trial, we randomly assigned 38 sarcomere mutation carriers without LVH (mean 15.8 years of age) to therapy with diltiazem 360 mg/day (or 5 mg/kg/day) or placebo. Treatment duration ranged from 12 to 42 months (median 25 months). Study procedures included electrocardiography, echocardiography, cardiac magnetic resonance imaging, and serum biomarker measurement.

resultsDiltiazem was not associated with serious adverse events. Heart rate and blood pressure did not differ significantly between groups. However, mean left ventricular (LV) end-diastolic diameter improved toward normal in the diltiazem group but decreased further in controls (change in z-scores, +0.6 vs. -0.5; p < 0.001). Mean LV thickness-to-dimension ratio was stable in the diltiazem group but increased in controls (-0.02 vs. +0.15; p = 0.04). Among MYBPC3 mutation carriers, LV wall thickness and mass, diastolic filling, and cardiac troponin I levels improved in those taking diltiazem compared with controls. Four participants developed overt HCM, 2 in each treatment group.

conclusionsPre-clinical administration of diltiazem is safe and may improve early LV remodeling in HCM. This novel strategy merits further exploration. (Treatment of Preclinical Hypertrophic Cardiomyopathy With Diltiazem; NCT00319982).

Indexed as

HeterozygoteAdolescentAdultCalcium Channel BlockersCardiomyopathy, HypertrophicCarrier ProteinsChildChild, PreschoolDiastoleDiltiazemDouble-Blind MethodEchocardiographyFemaleGenetic Predisposition to DiseaseHeart VentriclesHumansCalcium Channel BlockersCarrier ProteinsDiltiazemMyosin Binding Protein CTroponin Icardiomyopathygeneticshypertrophytranslational researchtreatmenttrials

Identifiers

PMID25543971
PMCPMC4323670
OpenAlexW2219899519

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.