ReGistry of hypeRtrophic cArDIomyopathy: Regional fEatures, geNeTics and Course

This study is observational registry of patients with HCM in Russian Federation. The study seeks to elucidate disease progression, identify contributing clinical factors, and explore new as well as previously established associations between genetic and acquired determinants and clinical features of HCM.The Additional Objectives of the Study are:

• To evaluate the natural progression of HCM in non-operated patients who have indications for myectomy and in high-risk patients for SCD, who have not been implanted with an ICD.
• To clarify the relationship between pediatric and adult HCM by constructing large pedigrees, including clinically and genetically examined relatives.
• To evaluate real-world clinical practices, both surgical and therapeutic, in the management of LV obstruction.
• To investigate the impact of comorbidities on phenotypic expression of HCM.
• To establish a group of national HCM experts and centers of excellence. We plan to include 1400 patients with HCM in the study.The examination of patients includes the collection of clinical information, ECG, EchoCG, Holter ECG monitoring, etc.• During follow-up period, patients or their relatives will be contacted by phone at least once every 12 months
• At follow-up visits, information regarding the study endpoints, ant medical examinations, and interventions that have occurred since the time of enrollment will be collected. Investigators are encouraged to make every effort to obtain official medical records that document these endpoints and any interventions that have taken place.

The genetic study aims to identify the causative genetic variants associated with HCM in enrolled patients (probands). The genetic testing will be conducted using new-generation sequencing (NGS) with target gene panels. In the study cohort of patients, an analysis of the effect of common genetic variants, identified based on the literature or GWAS, on the course of HCM will be conducted. In the study cohort (partially or entirely), genome-wide sequencing might be performed to replicate the significance of existing variants and to identify new genetic determinants that define the development of the HCM phenotype.

A comparative analysis of different parameters will be performed across various subgroups, categorized by the following characteristics (but not limited to them):

• Sex
• Age at first diagnosis
• Proband or relative status
• Presence of LV obstruction
• Morphological type of HCM
• Presence of comorbidities
• Presence of mutations or VUSs in sarcomere genes

In addition to the clinical and genetic spectrum and endpoints, the rate and type of diagnostic and treatment procedures related to HCM will be assessed.

In cases where the diagnosis of HCM was reconsidered or declined based on the results of additional investigations after enrollment, such patients will not be included in the prognosis analysis. However, they will be described in the clinical and genetic profile of the study population.

Inclusion criteria

• Any age
• Signed informed consent form (ICF) for participation in the study, including genetic testing
• Meets the criteria for HCM HCM Criteria for Probands ≥ 18 Years Based on ECHO or CMR
• End-diastolic LV wall thickness ≥ 15mm in any segment of the LV HCM Criteria for Probands ≥ 18 Years with Arterial Hypertension
• 1st degree of AH: The same ECHO/CMR criteria as patients without AH
• 2nd and 3rd degrees of AH:
• Asymmetric LV hypertrophy: the ratio of septum / LV PW ≥ 1.5 or apical HCM
• If asymmetry < 1.5, the wall thickness must be ≥ 20mm
• For all patients with arterial hypertension, the presence of at least one of the following ECG changes is obligatory:
• Pathological "dagger" Q wave
• T-wave inversion ≥ 3mm in ≥ 2 adjacent leads
• Poor R progression / QS / RV1 > RV2 < RV3 in V1-V4

HCM Criteria for First-degree Relatives ≥ 18 Years Based on ECHO or CMR and ECG:

• End-diastolic LV wall thickness ≥ 13mm in any segment and/or ECG changes in the absence of CAD, such as (at least one of the following):
• Quantitative signs of LV hypertrophy* + repolarization changes
• T wave inversions in at least 2 adjacent leads: ≥ 3mm in V3-V6, I, aVL or ≥ 5mm in II, III, aVF
• Pathological Q waves (> 25% of R) in at least 2 adjacent leads: II, III, aVF (in the absence of left anterior hemiblock) or V1-V4, or I, aVL, V5-V6

*Presence at least one of the following:

• Sokolow-Lyon index (S in V1 + R in V5 or V6) > 35mm
• R or S in limb leads ≥ 20mm
• S in V1 or V2 ≥ 30mm
• R in V5 or V6 ≥ 30mm HCM Criteria for Children and Adolescents < 18 Years
• End-diastolic LV wall thickness in any segment > 2.5 standard deviations (> 2.5 z-score) above the norms for the index gender, age and weight (or body surface area) in asymptomatic children/adolescents without a family history of HCM
• End-diastolic LV wall thickness in any segment > 2.0 standard deviations (> 2.0 z-score) above the norms for the index gender, age and weight (or body surface area) in children/adolescents with a family history of HCM or a positive genetic test

Exclusion criteria

• Uncontrolled arterial hypertension of 2nd - 3rd degree with mild/moderate (&lt; 20mm) or symmetric LV hypertrophy or a "normal" ECG
• Hemodynamically significant congenital or acquired valve heart disease
• Established diagnosis of metabolic, infiltrative, endocrine, or other diseases known as "phenocopies of HCM"