Acquirement of Clinical and Genomic Data to Diagnose in Rare Inherited Cardiomyopathy

NCT ID: NCT06948344

Last Updated: 2025-05-13

Basic Information

• Recruitment Status: RECRUITING
• Total Enrollment: 560 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2023-10-10
• Study Completion Date: 2028-08-22

Brief Summary

"Background Information Cardiomyopathy is one of the leading causes of heart failure. In cases where cardiomyopathy does not respond to guideline-directed medical therapy for heart failure, the disease may progress to a stage where heart transplantation is the only viable treatment option. According to the 2022 Korean Organ Transplant Registry (KOTRY) report, cardiomyopathy accounted for approximately 65% of heart transplant indications in Korea, making it one of the most challenging unresolved issues in modern cardiology. Furthermore, cardiomyopathy is associated with a high risk of sudden cardiac death due to ventricular fibrillation or ventricular tachycardi and implantable cardioverter-defibrillators are often recommended as a preventive measure. Given that sudden cardiac death frequently occurs in young and middle-aged individuals, it is a major public health concern in developed countries such as North America and Western/Northern Europe, prompting ongoing societal and medical efforts to reduce its burden. The risk of sudden cardiac death imposes a persistent psychological burden on family members of patients with cardiomyopathy. Because sudden death can also occur in children and adolescents, current clinical guidelines recommend early cardiac evaluation and genetic counseling for family members of affected individuals.

This study seeks to overcome the current limitations in the genetic diagnosis of cardiomyopathy, including the low diagnostic yield of currently available gene panels. To date, most genetic data on cardiomyopathy have been derived from Western populations. There is a significant lack of population-specific genomic data for East Asians, particularly Koreans, making it difficult to interpret the results of genetic testing in Korean patients.

By developing bioinformatics algorithms that comprehensively analyze whole genome sequencing (WGS) data, including single nucleotide variants (SNVs), insertions/deletions (indels), and structural variations, this study aims to generate a reference dataset tailored to the Korean population. This will directly improve the genetic diagnosis of cardiomyopathy in Korean patients. Additionally, by identifying novel pathogenic variants through WGS, this study may elucidate new disease mechanisms underlying cardiomyopathy. These findings could provide a theoretical basis for developing novel diagnostic biomarkers, therapeutic targets, and even gene-based therapies. The present study is part of a multi-phase national research project supported by the Korea Disease Control and Prevention Agency and the Korea National Institute of Health, conducted as a registry cohort titled the ""Korean Cardiomyopathy Cohort (KCC)"".

Objectives This study aims to establish a diagnostic research framework to elucidate the genetic architecture of rare inherited cardiomyopathies through comprehensive analysis of whole genome sequencing data, with the goal of identifying novel diagnostic approaches

Detailed Description

"Study Design The investigator will collect data from patients diagnosed with cardiomyopathy and will utilize secondary, real-world patient data obtained from electronic medical records at participating institutions.

Study Methods

1. Blood samples will be collected after obtaining informed consent from eligible patients during outpatient visits or hospitalization. Informed consent will be obtained in a private setting to ensure patient confidentiality, with sufficient explanation provided. The study will follow standard diagnostic and treatment guidelines commonly applied to heart failure patients in Korea. Demographic information, clinical characteristics, imaging data (echocardiography, cardiac MRI), laboratory findings, and cardiovascular events will be documented separately using a case report form.

2. Following informed consent, approximately 5-10 mL of whole blood will be drawn on the same day or during the subsequent outpatient visit. The sample will be transported to SCL on the day of collection, where plasma and buffy coat will be separated and stored.

3. Genomic, laboratory, and imaging data will be integrated for comprehensive statistical analysis.

4. All study data will be stored on password-protected computers with restricted access. No personal identifiers will be included to ensure data confidentiality."

Conditions

Cardiomyopathy; Whole Genome Sequencing

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

WGS cohort

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

patients aged 19 years or older who have provided written consent for participation, have the capability to consent voluntarily and have been diagnosed with cardiomyopathy, as defined by one of the following criteria: -Ones with suspected genetic cardiomyopathy of unknown etiology, meeting at least one of the following conditions: i) Patients with idiopathic cardiomyopathy, for whom no clear secondary causes (e.g., history of hypertension, alcohol abuse, or chemotherapy) can be identified, and in whom a genetic etiology is strongly suspected.

ii) Patients who have previously undergone genetic testing using an NGS panel, but no pathogenic variants were identified, and further evaluation with whole genome sequencing (WGS) is warranted.

iii) Patients diagnosed with cardiomyopathy before the age of 50, without known contributing factors such as hypertension or excessive alcohol consumption, raising a strong suspicion of a genetic cause.

-Patients with a family history of genetic cardiomyopathy, defined as having at least one first-degree relative (parent, sibling, or child) diagnosed with the same type of cardiomyopathy, confirming a familial genetic pattern.

Exclusion Criteria

• Patients with confirmed ischemic cardiomyopathy (when stenosis of 75% or more of major coronary arteries is confirmed on coronary artery imaging or ischemic cardiomyopathy findings such as transmural LGE on cardiac MRI)
• Heart failure with other etiologies (e.g., valvular heart disease, endocrine disease)

• Minimum Eligible Age: 19 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Yonsei University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Byung-Su Yoo, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Wonju Severance Christian Hospital

Jin-Oh Choi, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Samsung Medical Center

Hyun-jai Cho, MD

Role: PRINCIPAL_INVESTIGATOR

Seoul National University Hospital

Jae Young Cho, MD

Role: PRINCIPAL_INVESTIGATOR

Chonnam National University Hospital

Soo Yong Lee, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Pusan National University Yangsan Hospital

Ju-Hee Lee, MD

Role: PRINCIPAL_INVESTIGATOR

Chungbuk National University

Junho Hyun, MD, MSc

Role: PRINCIPAL_INVESTIGATOR

Asan Medical Center

Minjae Yoon, MD

Role: PRINCIPAL_INVESTIGATOR

Seoul National University Bundang Hospital

Eui-Young Choi, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Gangnam Severance Hospital

Jung Hyun Choi, MD

Role: PRINCIPAL_INVESTIGATOR

Pusan National University Hospital

In-Cheol Kim, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Keimyung University Dongsan Medical Center

Wook-Jin Chung, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Gil Medical Center

Moon Seoung Soh, MD

Role: PRINCIPAL_INVESTIGATOR

Ajou University School of Medicine

Jin-Ok Jeong, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Chungnam National University Hospital

Locations

Division of Cardiology, Severance Cardiovascular hospital Department of Internal Medicine, Yonsei University College of Medicine

Seoul, , South Korea

Site Status: RECRUITING

Countries

South Korea

Central Contacts

Jaewon Oh, M.D. Ph.D.

Role: CONTACT

ericjcoh@yuhs.ac

Facility Contacts

Jaewon Oh, M.D., Ph.D.

Role: primary

ericjcoh@yuhs.ac

+82-10-6273-0615

Other Identifiers

4-2023-0855

Identifier Type: -

Identifier Source: org_study_id