Echocardiographic Strain Abnormalities Precede Left Ventricular Hypertrophy Development in Hypertrophic Cardiomyopathy Mutation Carriers

Int J Mol Sci. 2024 Jul 25;25(15):8128. doi: 10.3390/ijms25158128.

Abstract

Hypertrophic cardiomyopathy (HCM) is a genetic disease characterized by unexplained left ventricular hypertrophy (LVH), diastolic dysfunction, and increased sudden-death risk. Early detection of the phenotypic expression of the disease in genetic carriers without LVH (Gen+/Phen-) is crucial for emerging therapies. This clinical study aims to identify echocardiographic predictors of phenotypic development in Gen+/Phen-. Sixteen Gen+/Phen- (one subject with troponin T, six with myosin heavy chain-7, and nine with myosin-binding protein C3 mutations), represented the study population. At first and last visit we performed comprehensive 2D speckle-tracking strain echocardiography. During a follow-up of 8 ± 5 years, five carriers developed LVH (LVH+). At baseline, these patients were older than those who did not develop LVH (LVH-) (30 ± 8 vs. 15 ± 8 years, p = 0.005). LVH+ had reduced peak global strain rate during the isovolumic relaxation period (SRIVR) (0.28 ± 0.05 vs. 0.40 ± 0.11 1/s, p = 0.048) and lower global longitudinal strain (GLS) (-19.8 ± 0.4 vs. -22.3 ± 1.1%; p < 0.0001) than LVH- at baseline. SRIVR and GLS were not correlated with age (overall, p > 0.08). This is the first HCM study investigating subjects before they manifest clinically significant or relevant disease burden or symptomatology, comparing at baseline HCM Gen+/Phen- subjects who will develop LVH with those who will not. Furthermore, we identified highly sensitive, easily obtainable, age- and load-independent echocardiographic predictors of phenotype development in HCM gene carriers who may undergo early preventive treatment.

Keywords: diastolic strain rate; genetics; global longitudinal strain; hypertrophic cardiomyopathy; left ventricular hypertrophy; screening; strain echocardiography; subclinical detection.

MeSH terms

  • Adolescent
  • Adult
  • Cardiac Myosins / genetics
  • Cardiomyopathy, Hypertrophic* / diagnostic imaging
  • Cardiomyopathy, Hypertrophic* / genetics
  • Carrier Proteins / genetics
  • Echocardiography* / methods
  • Female
  • Heterozygote
  • Humans
  • Hypertrophy, Left Ventricular* / diagnostic imaging
  • Hypertrophy, Left Ventricular* / etiology
  • Hypertrophy, Left Ventricular* / genetics
  • Male
  • Middle Aged
  • Mutation*
  • Myosin Heavy Chains / genetics
  • Phenotype
  • Troponin T / genetics
  • Young Adult

Substances

  • Myosin Heavy Chains
  • Troponin T
  • Carrier Proteins
  • myosin-binding protein C
  • MYH7 protein, human
  • Cardiac Myosins