Circulating Acylcarnitines Associated with Hypertrophic Cardiomyopathy Severity: an Exploratory Cross-Sectional Study in MYBPC3 Founder Variant Carriers.
Mark JansenA F SchmidtJ J M JansI ChristiaansS N van der CrabbenY M HoedemaekersD DooijesJ D H JongbloedL G BovenR H Lekanne DeprezA A M WildeJ van der VeldenR A de BoerJ P van TintelenF W AsselbergsA F BaasPublished in: Journal of cardiovascular translational research (2023)
Hypertrophic cardiomyopathy (HCM) is a relatively common genetic heart disease characterised by myocardial hypertrophy. HCM can cause outflow tract obstruction, sudden cardiac death and heart failure, but severity is highly variable. In this exploratory cross-sectional study, circulating acylcarnitines were assessed as potential biomarkers in 124 MYBPC3 founder variant carriers (59 with severe HCM, 26 with mild HCM and 39 phenotype-negative [G + P-]). Elastic net logistic regression identified eight acylcarnitines associated with HCM severity. C3, C4, C6-DC, C8:1, C16, C18 and C18:2 were significantly increased in severe HCM compared to G + P-, and C3, C6-DC, C8:1 and C18 in mild HCM compared to G + P-. In multivariable linear regression, C6-DC and C8:1 correlated to log-transformed maximum wall thickness (coefficient 5.01, p = 0.005 and coefficient 0.803, p = 0.007, respectively), and C6-DC to log-transformed ejection fraction (coefficient -2.50, p = 0.004). Acylcarnitines seem promising biomarkers for HCM severity, however prospective studies are required to determine their prognostic value.
Keyphrases
- hypertrophic cardiomyopathy
- left ventricular
- heart failure
- ejection fraction
- dendritic cells
- aortic stenosis
- cardiac resynchronization therapy
- diffusion weighted imaging
- pulmonary hypertension
- dna methylation
- genome wide
- optical coherence tomography
- atrial fibrillation
- coronary artery disease
- magnetic resonance
- gene expression
- immune response
- case control