Dilated Cardiomyopathy-Cardiac Magnetic Resonance (DCM-CMR) Ancillary Study

Description

The Dilated Cardiomyopathy-Cardiac Magnetic Resonance (DCM-CMR) Study is an ancillary study from the parent study, DCM Precision Medicine Study. The rationale for the DCM-CMR study is to leverage cardiac magnetic resonance (CMR) imaging to detect earliest findings of DCM in the at-risk family members enrolled into the parent study.

Conditions

Dilated Cardiomyopathy

Study Overview

Study Details

Study overview

The Dilated Cardiomyopathy-Cardiac Magnetic Resonance (DCM-CMR) Study is an ancillary study from the parent study, DCM Precision Medicine Study. The rationale for the DCM-CMR study is to leverage cardiac magnetic resonance (CMR) imaging to detect earliest findings of DCM in the at-risk family members enrolled into the parent study.

Precision Medicine for Dilated Cardiomyopathy-Cardiac Magnetic Resonance to Identify Early Family Phenotypes

Dilated Cardiomyopathy-Cardiac Magnetic Resonance (DCM-CMR) Ancillary Study

Condition
Dilated Cardiomyopathy
Intervention / Treatment

-

Contacts and Locations

Columbus

The Ohio State University, Columbus, Ohio, United States, 43210

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. The FDR's proband was enrolled in the DCM Precision Medicine Study at 1 of 9 participating sites, or exceptions granted by study PI.
  • 2. The FDR's proband has had one or more variants identified, including P, LP and VUS.
  • 3. The FDR is able report to one of the participating sites for study enrollment.
  • 4. The FDR has no current contraindication for CMR (glomerular filtration rate (GFR) \<30 mL/min/1.73 m2, non-compatible device implant, or allergy to gadolinium contrast).
  • 5. The FDR has had no prior heart transplant.
  • 6. The FDR is ≥18 years of age.
  • 7. All races/ethnicity
  • 8. Ability to give informed consent.
  • 9. Ability to communicate in English.
  • 10. Subject is not pregnant (CMR may be conducted 3-6 months post delivery)
  • 11. Willingness to participate in a family-based study (subject willing to interact with OSU).
  • 1. Coronary artery disease (CAD) causing ischemic cardiomyopathy (\> 50% narrowing, any major epicardial coronary artery).
  • 2. Primary valvular disease.
  • 3. Adriamycin or other cardiotoxic drug exposure.
  • 4. Other forms of cardiomyopathy: Hypertrophic, Restrictive, or Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy.
  • 5. Congenital heart disease.
  • 6. Other detectable causes of dilated cardiomyopathy, including sarcoid and hemochromatosis.
  • 7. Other active multisystem disease, even if very rare, that may plausibly cause DCM (e.g., hypereosinophilic syndrome, cardiac involvement with connective tissue disease, Loeffler's endocarditis, endomyocardial fibrosis, etc) are excluded. Please call the PI to discuss if uncertain or not clear.
  • 8. Severe and untreated or untreatable hypertension (systolic blood pressures routinely greater than 180 mm Hg and/or diastolic blood pressures greater than 120 mm Hg, and if resistant to multidrug treatment). This includes profound hypertension associated with other multisystem disease (e.g., scleroderma, other vasculitides, etc).

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Ohio State University,

Ray Hershberger, MD, PRINCIPAL_INVESTIGATOR, Ohio State University

Karolina Zareba, MD, PRINCIPAL_INVESTIGATOR, Ohio State University

Daniel Kinnamon, PhD, PRINCIPAL_INVESTIGATOR, Ohio State University

Study Record Dates

2026-04