Background: Sudden death is the leading cause of mortality in medically refractory epilepsy. Middle-aged persons with epilepsy (PWE) are under investigated regarding their mortality risk and burden of cardiovascular disease (CVD). Methods: Using UK Biobank, we identified 7,786 (1.6%) participants with a diagnosis of epilepsy and 6,171,803 person-years of follow-up (mean 12.30 years, SD 1.74); 566 individuals with prior history of stroke were excluded. The 7,220 PWE comprised the study cohort with the remaining 494,676 without epilepsy as the comparator group. Prevalence of CVD was determined using validated diagnostic codes. Cox proportional hazards regression were used to assess all-cause mortality and sudden death risk. Results: Hypertension, coronary artery disease, heart failure, valvular heart disease, and congenital heart disease were more prevalent in PWE. Arrhythmias including atrial fibrillation/flutter (12.2% vs 6.9%; p<0.01), bradyarrhythmias (7.7% vs 3.5%; p<0.01), conduction defects (6.1% vs 2.6%; p<0.01), and ventricular arrhythmias (2.3% vs 1.0%; p<0.01), as well as cardiac implantable electric devices (4.6% vs 2.0%; p<0.01) were more prevalent in PWE. PWE had higher adjusted all-cause mortality (HR 3.9 [95% CI, 3.01-3.39]), and sudden death-specific mortality (HR 6.65 [95% CI, 4.53-9.77]); and were almost 2 years younger at death [68.1 vs 69.8; p<0.001]. Conclusions: Middle-aged PWE have increased all-cause and sudden death specific mortality, and higher burden of CVD including arrhythmias and heart failure. Further work is required to elucidate mechanisms underlying all-cause mortality and sudden death risk in PWE of middle age, to identify prognostic biomarkers and develop preventative therapies in PWE.

Cardiovascular Disease Burden, Mortality and Sudden Death Risk in Epilepsy: a UK Biobank study

Ricci, Fabrizio;
2024-01-01

Abstract

Background: Sudden death is the leading cause of mortality in medically refractory epilepsy. Middle-aged persons with epilepsy (PWE) are under investigated regarding their mortality risk and burden of cardiovascular disease (CVD). Methods: Using UK Biobank, we identified 7,786 (1.6%) participants with a diagnosis of epilepsy and 6,171,803 person-years of follow-up (mean 12.30 years, SD 1.74); 566 individuals with prior history of stroke were excluded. The 7,220 PWE comprised the study cohort with the remaining 494,676 without epilepsy as the comparator group. Prevalence of CVD was determined using validated diagnostic codes. Cox proportional hazards regression were used to assess all-cause mortality and sudden death risk. Results: Hypertension, coronary artery disease, heart failure, valvular heart disease, and congenital heart disease were more prevalent in PWE. Arrhythmias including atrial fibrillation/flutter (12.2% vs 6.9%; p<0.01), bradyarrhythmias (7.7% vs 3.5%; p<0.01), conduction defects (6.1% vs 2.6%; p<0.01), and ventricular arrhythmias (2.3% vs 1.0%; p<0.01), as well as cardiac implantable electric devices (4.6% vs 2.0%; p<0.01) were more prevalent in PWE. PWE had higher adjusted all-cause mortality (HR 3.9 [95% CI, 3.01-3.39]), and sudden death-specific mortality (HR 6.65 [95% CI, 4.53-9.77]); and were almost 2 years younger at death [68.1 vs 69.8; p<0.001]. Conclusions: Middle-aged PWE have increased all-cause and sudden death specific mortality, and higher burden of CVD including arrhythmias and heart failure. Further work is required to elucidate mechanisms underlying all-cause mortality and sudden death risk in PWE of middle age, to identify prognostic biomarkers and develop preventative therapies in PWE.
File in questo prodotto:
File Dimensione Formato  
Can J Cardiol 2024 Shah.pdf

Solo gestori archivio

Tipologia: PDF editoriale
Dimensione 1.07 MB
Formato Adobe PDF
1.07 MB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11564/823645
Citazioni
  • ???jsp.display-item.citation.pmc??? 2
  • Scopus 4
  • ???jsp.display-item.citation.isi??? 4
social impact