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Identification of biomarkers of hypertrophic cardiomyopathy development and progression in Dutch MYBPC3 founder mutation carriers

Identification of biomarkers of hypertrophic cardiomyopathy development and progression in Dutch MYBPC3 founder mutation carriers - BIO FOr CARe

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON47925
Enrollment
1000
Registered
2016-03-24
Start date
2017-01-12
Completion date
Unknown
Last updated
2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

hypertrophic cardiomyopathy / thick heart muscle

Interventions

None listed

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: MYBPC3 founder mutation carrier and 18 years or older

Exclusion criteria

Exclusion criteria: Cardiac transplant

Design outcomes

Primary

MeasureTime frame
Main study determinants/potential predictors - Age (at carrier diagnosis) - Gender - cMyBP-C protein content in exosomes isolated from plasma - creatine/guanidine acetic acid ratio in plasma - delta creatine/guanidine acetic acid ratio in plasma prior/after exercise test - acylcarnitine profile in plasma - delta acylcarnitine profile in plasma prior/after exercise test Dependent of the study question of the prospective cohort the endpoints are: 1) development of severe HCM 2) progression of HCM to severe HCM For the case-control study at baseline: a severe HCM phenotype. A severe cardiac phenotype will be defined as one or more of the following: septal thickness of >= 20 mm, cardiac arrest due to ventricular arrhythmia, LVEF

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)