Key result
Amyloid cardiomyopathy exhibits a higher VE/VCO2 slope and earlier anaerobic threshold versus matched heart failure.
Why the study?
It was unclear whether cardiac output reduction or ventilation inefficiency plays a predominant role in limiting exercise in patients with amyloid cardiomyopathy.
Does amyloid cardiomyopathy cause greater ventilation inefficiency and earlier anaerobic threshold during exercise compared to matched heart failure patients?
Cohort (n=518)
Yes
Does amyloid cardiomyopathy cause greater ventilation inefficiency and earlier anaerobic threshold during exercise compared to matched heart failure patients?
Absolute Event Rate: 37.4% vs 32.1%
p-value: p=<0.0001
Patients with amyloid cardiomyopathy exhibit more severe ventilation inefficiency and earlier anaerobic threshold during exercise compared to matched heart failure patients, with ATTR patients showing greater impairment than AL patients.
CPET abnormalities may aid amyloid cardiomyopathy evaluation; leaves open prognostic value and therapeutic implications in prospective studies.
Aims Amyloid cardiomyopathy is caused by the deposition of light chain (AL) or transthyretin amyloid (ATTR) fibrils, that leads to a restrictive cardiomyopathy, often resulting in heart failure (HF) with preserved or reduced ejection fraction. This study aimed to determine whether cardiac output reduction or ventilation inefficiency plays a predominant role in limiting exercise in patients with amyloid cardiomyopathy. Methods We conducted a multicentre prospective study in patients with AL or ATTR cardiomyopathy who underwent cardiopulmonary exercise testing across four centres. Patients were compared with a propensity-score matched HF cohort based on age, gender, left ventricular ejection fraction (LVEF), and peak oxygen consumption (VO2). Results Data from 267 amyloid patients aged 77 (72, 81) years, 86% male, with a median N-terminal pro B-type natriuretic peptide (NT-proBNP) of 2187 (1140, 4383) ng/L, exercise parameters of peak VO2 of 14.1 (11.6;16.9) mL/min/kg, a minute ventilation to carbon dioxide production (VE/VCO2) slope of 37.4 (32.5, 42.6) and a LVEF of 50% (44%, 59%) were analysed. We identified 251 amyloid cardiomyopathy–HF matches. Amyloid patients had a signifnicantly higher VE/VCO2 slope [37.4, inter quartile range (IQR): 32.7, 43.1 vs. 32.1, IQR: 28.7, 37.0, P < 0.0001], NT-proBNP (2249, IQR: 1187, 4420 vs. 718, IQR: 405, 2161 ng/L, P < 0.001), peak heart rate (121 ± 28 vs. 115 ± 27 beats/min, P = 0.007) and peak ventilation (51, IQR: 42, 62 vs. 43, IQR: 33, 53 L/min, P < 0.0001) with earlier anaerobic threshold (VO2 at AT: 8.9, IQR: 6.8, 10.8 vs. 10.8, IQR: 8.9, 12.7 mL/min/kg, P < 0.0001) compared with HF. Between amyloid patients, AL patients (n = 27) were younger (63, IQR: 58, 70 vs. 78, IQR: 72, 81 years, P < 0.0001), had lower VE/VCO2 slope (35.0, IQR: 30.0, 38.7 vs. 38.0, IQR: 32.8, 43.1, P = 0.019), higher end-tidal carbon dioxide partial pressure both at AT (35.1 ± 4.8 vs. 31.4 ± 4.7 mmHg, P < 0.001) and peak exercise (32, IQR: 28, 35 vs. 30, IQR: 26, 33 mmHg, P = 0.039) as compared with ATTR (n = 233). Conclusions A higher VE/VCO2 slope and an earlier AT, determining functional capacity impairment, was assessed in patients with amyloid cardiomyopathy compared with the matched HF cohort. Additionally, patients with ATTR might display more severe exercise limitations as compared with AL.
No takes yet. Share an insight, caveat, or question.
Willixhofer et al. (2024) conducted a cohort in Amyloid cardiomyopathy (n=518). Amyloid cardiomyopathy (exposure) vs. Propensity-score matched heart failure cohort was evaluated on VE/VCO2 slope (p=<0.0001). Patients with amyloid cardiomyopathy exhibited significantly higher ventilation inefficiency (VE/VCO2 slope 37.4 vs 32.1, P<0.0001) and earlier anaerobic threshold compared to matched heart failure.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: