Clinical Features, Genetic Findings, and Risk Stratification in Arrhythmogenic Right Ventricular Cardiomyopathy: Data From a Brazilian Cohort. (31st January 2023)
- Record Type:
- Journal Article
- Title:
- Clinical Features, Genetic Findings, and Risk Stratification in Arrhythmogenic Right Ventricular Cardiomyopathy: Data From a Brazilian Cohort. (31st January 2023)
- Main Title:
- Clinical Features, Genetic Findings, and Risk Stratification in Arrhythmogenic Right Ventricular Cardiomyopathy: Data From a Brazilian Cohort
- Authors:
- Quintella Sangiorgi Olivetti, Natália
Sacilotto, Luciana
Wulkan, Fanny
D'Arezzo Pessente, Gabrielle
Lombardi Peres de Carvalho, Mariana
Moleta, Danilo
Tessariol Hachul, Denise
Veronese, Pedro
Hardy, Carina
Pisani, Cristiano
Wu, Tan Chen
Vieira, Marcelo Luiz Campos
de França, Lucas Arraes
de Souza Freitas, Matheus
Rochitte, Carlos Eduardo
Bueno, Sávia Christina
Bastos Lovisi, Vitor
Krieger, José Eduardo
Scanavacca, Maurício
da Costa Pereira, Alexandre
da Costa Darrieux, Francisco - Abstract:
- Abstract : Background: Arrhythmogenic right ventricular cardiomyopathy (ARVC), a rare inherited disease, causes ventricular tachycardia, sudden cardiac death, and heart failure (HF). We investigated ARVC clinical features, genetic findings, natural history, and the occurrence of life-threatening arrhythmic events (LTAEs), HF death, or heart transplantation (HF-death/HTx) to identify risk factors. Methods: The clinical course of 111 consecutive patients with definite ARVC, predictors of LTAE, HF-death/HTx, and combined events were analyzed in the entire cohort and in a subgroup of 40 patients without sustained ventricular arrhythmia before diagnosis. Results: The 5-year cumulative probability of LTAE was 30% and HF-death/HTx was 10%. Predictors of HF-death/HTx were reduced right ventricle ejection fraction (HR: 0.93; P =0.010), HF symptoms (HR: 4.37; P =0.010), epsilon wave (HR: 4.99; P =0.015), and number of leads with low QRS voltage (HR: 1.28; P =0.001). Each additional lead with low QRS voltage increased the risk of HF-death/HTx by 28%. Predictors of LTAE were prior syncope (HR: 1.81; P =0.040), number of leads with T wave inversion (HR: 1.17; P =0.039), low QRS voltage (HR: 1.12; P =0.021), younger age (HR: 0.97; P =0.006), and prior ventricular arrhythmia/ventricular fibrillation (HR: 2.45; P =0.012). Each additional lead with low QRS voltage increased the risk of LTAE by 17%. In patients without ventricular arrhythmia before clinical diagnosis of ARVC, the number ofAbstract : Background: Arrhythmogenic right ventricular cardiomyopathy (ARVC), a rare inherited disease, causes ventricular tachycardia, sudden cardiac death, and heart failure (HF). We investigated ARVC clinical features, genetic findings, natural history, and the occurrence of life-threatening arrhythmic events (LTAEs), HF death, or heart transplantation (HF-death/HTx) to identify risk factors. Methods: The clinical course of 111 consecutive patients with definite ARVC, predictors of LTAE, HF-death/HTx, and combined events were analyzed in the entire cohort and in a subgroup of 40 patients without sustained ventricular arrhythmia before diagnosis. Results: The 5-year cumulative probability of LTAE was 30% and HF-death/HTx was 10%. Predictors of HF-death/HTx were reduced right ventricle ejection fraction (HR: 0.93; P =0.010), HF symptoms (HR: 4.37; P =0.010), epsilon wave (HR: 4.99; P =0.015), and number of leads with low QRS voltage (HR: 1.28; P =0.001). Each additional lead with low QRS voltage increased the risk of HF-death/HTx by 28%. Predictors of LTAE were prior syncope (HR: 1.81; P =0.040), number of leads with T wave inversion (HR: 1.17; P =0.039), low QRS voltage (HR: 1.12; P =0.021), younger age (HR: 0.97; P =0.006), and prior ventricular arrhythmia/ventricular fibrillation (HR: 2.45; P =0.012). Each additional lead with low QRS voltage increased the risk of LTAE by 17%. In patients without ventricular arrhythmia before clinical diagnosis of ARVC, the number of leads with low QRS voltage (HR: 1.68; P =0.023) was independently associated with HF-death/HTx. Conclusions: Our study demonstrated the characteristics of a specific cohort with a high prevalence of arrhythmic burden at presentation, male predominance, younger age and HF severe outcomes. Our main results suggest that the presence and extension of low QRS voltage can be a risk predictor for HF-death/HTx in ARVC patients, regardless of the arrhythmic risk. This study can contribute to the global ARVC risk stratification, adding new insights to the international current scientific knowledge. … (more)
- Is Part Of:
- Circulation. Volume 16:Number 2(2023)
- Journal:
- Circulation
- Issue:
- Volume 16:Number 2(2023)
- Issue Display:
- Volume 16, Issue 2 (2023)
- Year:
- 2023
- Volume:
- 16
- Issue:
- 2
- Issue Sort Value:
- 2023-0016-0002-0000
- Page Start:
- e011391
- Page End:
- Publication Date:
- 2023-01-31
- Subjects:
- arrhythmogenic right ventricular cardiomyopathy -- genetics -- heart failure -- heart transplantation -- risk assessment -- sudden cardiac death
Arrhythmia -- Periodicals
Heart -- Electric properties -- Periodicals
616.128 - Journal URLs:
- http://gateway.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&NEWS=n&PAGE=toc&D=ovft&AN=01337493-000000000-00000 ↗
http://circep.ahajournals.org/ ↗
http://journals.lww.com ↗ - DOI:
- 10.1161/CIRCEP.122.011391 ↗
- Languages:
- English
- ISSNs:
- 1941-3149
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3265.262500
British Library DSC - BLDSS-3PM
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