Ajmaline provocation in Brugada syndrome revealed that post-ajmaline right ventricular ejection fraction inversely correlated with electrical substrate extent (r=-0.830, P<0.001).
Case-Control (n=48)
Does ajmaline provocation reveal a correlation between electrical substrate extent and right ventricular mechanical abnormalities in high-risk patients with Brugada syndrome?
Brugada syndrome involves dynamic right ventricular electromechanical abnormalities, with functional impairment directly correlating with the extent of the electrical substrate unmasked by ajmaline.
Estimación del efecto: r = -0.830
valor p: p=<0.001
Background: Brugada syndrome (BrS) is considered a purely electrical disease with variable electrical substrates. Variable rates of mechanical abnormalities have been also reported. Whether exists a link between electrical and mechanical abnormalities has never been previously explored. This investigational physiopathological study aimed to determine the relationship between the substrate size/location, as exposed by ajmaline provocation, and the severity of mechanical abnormalities, as assessed by cardiac magnetic resonance in patients with BrS. Methods: Twenty-four consecutive high-risk patients with BrS (mean age, 38±11 years, 17 males), presenting with malignant syncope and documented polymorphic ventricular tachycardia/ventricular fibrillation, and candidate to implantable cardioverter defibrillator implantation, underwent cardiac magnetic resonance and electroanatomic maps. During each examination, ajmaline test (1 mg/kg over 5 minutes) was performed. Cardiac magnetic resonance findings were compared with 24 age, sex, and body surface area-matched controls. In patients with BrS, the correlation between the electrical substrate extent and right ventricular regional mechanical abnormalities before/after ajmaline challenge was analyzed. Results: After ajmaline, patients with BrS showed a reduction of right ventricular (RV) ejection fraction ( P <0.001), associated with decreased transversal displacement (U, P <0.001) and longitudinal strain (ε, P <0.001) localized at RV outflow tract. In patients with BrS significant preajmaline/postajmaline changes of transversal displacement (ΔU, P <0.001) and longitudinal strain (Δε, P <0.001) were found. In the control group, no mechanical changes were observed after ajmaline. The electrical substrate consistently increased after ajmaline from 1.7±2.8 cm 2 to 14.2±7.3 cm 2 ( P <0.001), extending from the RV outflow tract to the neighboring segments of the RV anterior wall. Postajmaline RV ejection fraction inversely correlated with postajmaline substrate extent ( r =−0.830, P <0.001). In patients with BrS and normal controls, cardiac magnetic resonance detected neither myocardial fibrosis nor RV outflow tract morphological abnormalities. Conclusions: BrS is a dynamic RV electromechanical disease, where functional abnormalities correlate with the maximal extent of the substrate size. These findings open new lights on the physiopathology of the disease. Registration: URL: https://clinicaltrial.gov ; Unique identifier: NCT03524079.
Pappone et al. (Mon,) conducted a case-control in Brugada syndrome (n=48). Ajmaline provocation vs. Matched controls was evaluated on Correlation between electrical substrate extent and right ventricular regional mechanical abnormalities before/after ajmaline challenge (r = -0.830, p=<0.001). Ajmaline provocation in Brugada syndrome revealed that post-ajmaline right ventricular ejection fraction inversely correlated with electrical substrate extent (r=-0.830, P<0.001).
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