EARLY-MYO-HHD: Differentiating Hypertrophic Cardiomyopathy From Hypertensive Heart Disease

Sponsor
RenJi Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT03271385
Collaborator
Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University (Other), Ruijin Hospital (Other), LanZhou University (Other), Kunming Medical University (Other), Beijing Anzhen Hospital (Other), West China Hospital (Other)
230
1
48
4.8

Study Details

Study Description

Brief Summary

Differentiating hypertrophic cardiomyopathy (HCM) from hypertensive heart disease (HHD) unavoidably encounters diagnostic challenges especially in patient of suspected HCM with history of hypertension. Diverse and overlapping forms of HCM can often lead to ambiguity when diagnosis is based on a single genetic or morphological index.

The investigators have deduced a integrated formula based on cardiac magnetic resonance (CMR) imaging and established a differentiating flow-chart between HCM and HHD, the investigators aim to identify their method in the current multi-center trial.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: evaluated by the predetermined differentiating formula

Detailed Description

Both hypertrophic cardiomyopathy (HCM) and hypertensive heart disease (HHD) present left ventricular hypertrophy (LVH), but the prognosis varies. Nevertheless, the feasibility of distinguishing these two conditions is limited by the fact that overlapping LVH and diverse forms of HCM can often lead to diagnostic ambiguity when diagnosis is based on a single morphological index. Diagnosis is more difficult in a patient with a history of hypertension and with left ventricular wall thickness between 11 and 15 mm. It also puzzles the situation when hypertrophy without outflow-track obstruction was found in hypertensive subjects which might not be explained solely by the history of hypertension.

The investigators have deduced an integrated formula based on cardiac magnetic resonance (CMR) imaging and established a differentiating flow-chart between HCM and HHD. In this study, the investigators aim to explore the applicability of the quantifying scheme for distinguishing HCM from HHD in the multi-center trial.

Study Design

Study Type:
Observational
Actual Enrollment :
230 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
EARLY Differentiation of MYOcardial Hypertrophy From Hypertensive Heart Disease: a Multi-center, Prospective, Controlled Clinical Trial
Actual Study Start Date :
Jul 1, 2017
Anticipated Primary Completion Date :
Jun 30, 2021
Anticipated Study Completion Date :
Jul 1, 2021

Arms and Interventions

Arm Intervention/Treatment
hypertrophic cardiomyopathy group

The hypertrophic cardiomyopathy was diagnosed by left ventricular hypertrophy via echocardiography (wall thickness >15 mm) with either genetic determination of a pathogenic mutation or ) left ventricular hypertrophy (LVH) (end-diastolic wall thickness >15 mm) with resting left ventricular outflow tract obstruction or hypertrophy in a recognisable pattern, i.e., ventricular bulge in apical-variant HCM. And then patients with hypertrophic cardiomyopathy were evaluated by the predetermined differentiating formula.

Diagnostic Test: evaluated by the predetermined differentiating formula
After recruiting patients, collecting the baseline data, a CMR scan will be carried out and post-processed, a predetermined differentiating formula (including left ventricular morphology, ejection fraction, presence of late gadolinium enhancement, T1 value and strain data) will be used to produce a cardiac values, which is to be input into our differentiating flow.

hypertensive heart disease group

The diagnosis of hypertensive heart disease was based on medical history and conventional echocardiography. Long durations of uncontrolled hypertension for at least 5 years with systolic blood pressure [BP] ≥150 mm Hg or diastolic BP ≥90 mm Hg or both in the absence of other cardiac or systemic diseases were used as criteria. And then patients with hypertensive heart disease were evaluated by the predetermined differentiating formula.

Diagnostic Test: evaluated by the predetermined differentiating formula
After recruiting patients, collecting the baseline data, a CMR scan will be carried out and post-processed, a predetermined differentiating formula (including left ventricular morphology, ejection fraction, presence of late gadolinium enhancement, T1 value and strain data) will be used to produce a cardiac values, which is to be input into our differentiating flow.

control group

The healthy age-matched controls were generally volunteers with a normal electrocardiogram, normal echocardiographic examination, and overall normal CMR findings. And then patients with normal findings were were evaluated by the predetermined differentiating formula.

Diagnostic Test: evaluated by the predetermined differentiating formula
After recruiting patients, collecting the baseline data, a CMR scan will be carried out and post-processed, a predetermined differentiating formula (including left ventricular morphology, ejection fraction, presence of late gadolinium enhancement, T1 value and strain data) will be used to produce a cardiac values, which is to be input into our differentiating flow.

Outcome Measures

Primary Outcome Measures

  1. validation of the algorithm in all patients [after post-procession and complete the flow chart within 24 hours]

    Evaluate the area under the curve of our algorithm compared with single parameter (wall thickness, strain) in all patients

Secondary Outcome Measures

  1. validation of the algorithm in subgroup patients [after post-procession and complete the flow chart within 24 hours]

    Evaluate the area under the curve of our algorithm compared with single parameter (wall thickness, strain) in subgroup patients (HHD and HCM/HBP-; HHD and HCM/HBP+; HHD and HCM/OBSR-; HHD and HCM/HBP+/OBSR-)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Control group: (1) Absence of known systemic diseases; (2)Normal examinations(normal findings in both echocardiography and CMR).

  2. Hypertrophic cardiomyopathy: 1) genetic determination of a pathogenic mutation or 2) left ventricular hypertrophy (LVH) (end-diastolic wall thickness >15 mm) with resting left ventricular outflow tract obstruction or 3) hypertrophy in a recognizable pattern, i.e., ventricular bulge in apical-variant HCM; Of note, patients with documented HCM were divided into subgroups based on whether concomitant with hypertension or left ventricular outflow tract (LVOT) obstruction.

  3. Hypertensive Heart Disease: (1) Long durations of uncontrolled hypertension (systolic blood pressure≥150 mm Hg or diastolic blood pressure ≥90 mm Hg); Echocardiography: left ventricular wall thickness in diastolic >11mm; Absence of other cardiac or systemic diseases; (2) left ventricular mass/body surface area >81 g/m2 (Male) or >61 g/m2 (Female).

Exclusion Criteria:
  1. Documented coronary artery disease: previous history or CAG>50%;

  2. NYHA Ⅳ level;

  3. Severe aortic valve stenosis;

  4. Standard metallic contraindications to CMR;

  5. Systemic diseases or Infiltrative cardiomyopathy;

  6. Septal ablation for drug-refractory hypertrophic obstructive cardiomyopathy.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Renji Hospital Shanghai China 200127

Sponsors and Collaborators

  • RenJi Hospital
  • Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University
  • Ruijin Hospital
  • LanZhou University
  • Kunming Medical University
  • Beijing Anzhen Hospital
  • West China Hospital

Investigators

  • Study Chair: Meng Jiang, MD, RenJi Hospital, School of Medicine, Shanghai Jiaotong University
  • Study Director: Lianming Wu, MD, RenJi Hospital, School of Medicine, Shanghai Jiaotong University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
RenJi Hospital
ClinicalTrials.gov Identifier:
NCT03271385
Other Study ID Numbers:
  • 20170406J
First Posted:
Sep 5, 2017
Last Update Posted:
Dec 8, 2020
Last Verified:
Mar 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by RenJi Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 8, 2020