Why the study?
The study was conducted to evaluate the combined prognostic value of genotype and late gadolinium enhancement in hypertrophic cardiomyopathy patients, including those with preserved left ventricular ejection fraction.
Does the combined presence of pathogenic genetic variants and late gadolinium enhancement predict major adverse cardiovascular and cerebrovascular events in patients with hypertrophic cardiomyopathy?
Does the combined presence of pathogenic genetic variants and late gadolinium enhancement predict major adverse cardiovascular and cerebrovascular events in patients with hypertrophic cardiomyopathy?
The combined assessment of genotype and late gadolinium enhancement significantly enhances risk stratification for major adverse cardiovascular and cerebrovascular events in patients with hypertrophic cardiomyopathy.
Aims To assess the combined prognostic value of genotype and late gadolinium enhancement (LGE) in hypertrophic cardiomyopathy (HCM) patients, including those with preserved left ventricular ejection fraction (LVEF). Methods In 135 HCM patients (age 52.43 ± 11.35 years, 79.26% male), whole-exome sequencing, echocardiography, and cardiac magnetic resonance (CMR) were performed. Major adverse cardiovascular and cerebrovascular events (MACCEs, e.g., cardiac death, progressive heart failure, sustained ventricular tachycardia/ventricular fibrillation, ICDs implantation, stroke, syncope, and atrial fibrillation) were analyzed over a median 15-month follow-up (IQR 9–36 months). Results Pathogenic/likely pathogenic variants (G+) were identified in 50 (37%) patients, and LGE (L+) in 54 (40%). L+ patients exhibited worse clinical profiles: higher NYHA III–IV class (37% vs. 11%, P < 0.001), increased heart failure hospitalization (26% vs. 7%, P = 0.003), larger LV end-diastolic volume (median: 135, IQR: 125.25–213.00 vs. median: 126, IQR: 106.00–155.50, P = 0.004), lower LVEF (median: 55%, IQR: 39.75%–62% vs. median: 58%, IQR: 48%–65.5%, P = 0.012), and higher G+ prevalence (52% vs. 28%, P = 0.004). Both L+ (HR = 2.237, 95% CI: 1.178–4.247; P = 0.014) and G+ (HR = 1.872, 95% CI: 1.040–3.371; P = 0.037) independently predicted MACCEs after adjusting for age, NYHA class III–IV, LVOT obstruction and LVEF, adjusting for age, NYHA class III–IV, LVOT obstruction and LVEF. MACCE rates escalated across subgroups: G−/L− (22%), G+/L− (39%), G−/L+ (41%), and G+/L+ (63%) ( P = 0.004). Among 89 patients with LVEF ≥150%, G+/L+ had the highest MACCE incidence (80% vs. 17% in G−/L−, P < 0.001). Conclusion The combined assessment of genotype and late gadolinium enhancement significantly enhances risk stratification and prognosis prediction in hypertrophic cardiomyopathy patients, including those with preserved left ventricular ejection fraction, providing valuable insights for clinical decision-making.
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Su et al. (2025) studied this question.
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