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Does Sex Modify an Association of Electrophysiological Substrate with Sudden Cardiac Death? The Atherosclerosis Risk in Communities (ARIC) Study.
Howell, Stacey J; German, David; Bender, Aron; Phan, Francis; Mukundan, Srini V; Perez-Alday, Erick A; Rogovoy, Nichole M; Haq, Kazi T; Yang, Katherine; Wirth, Ashley; Jensen, Kelly; Tereshchenko, Larisa G.
Afiliação
  • Howell SJ; Knight Cardiovascular Institute, Oregon Health & Science University, Portland, OR.
  • German D; Knight Cardiovascular Institute, Oregon Health & Science University, Portland, OR.
  • Bender A; Knight Cardiovascular Institute, Oregon Health & Science University, Portland, OR.
  • Phan F; Knight Cardiovascular Institute, Oregon Health & Science University, Portland, OR.
  • Mukundan SV; Knight Cardiovascular Institute, Oregon Health & Science University, Portland, OR.
  • Perez-Alday EA; Rush University Medical Center, Chicago, IL.
  • Rogovoy NM; Knight Cardiovascular Institute, Oregon Health & Science University, Portland, OR.
  • Haq KT; Knight Cardiovascular Institute, Oregon Health & Science University, Portland, OR.
  • Yang K; Knight Cardiovascular Institute, Oregon Health & Science University, Portland, OR.
  • Wirth A; Knight Cardiovascular Institute, Oregon Health & Science University, Portland, OR.
  • Jensen K; Sidney Kimmel Medical College, Philadelphia, PA.
  • Tereshchenko LG; Knight Cardiovascular Institute, Oregon Health & Science University, Portland, OR.
Cardiovasc Digit Health J ; 1(2): 80-88, 2020.
Article em En | MEDLINE | ID: mdl-34308405
ABSTRACT
BACKGROUND­ Sex is a well-recognized risk factor for sudden cardiac death (SCD). We hypothesized that sex modifies the association of electrophysiological (EP) substrate with SCD. METHODS­ Participants from the Atherosclerosis Risk in Communities study with analyzable ECGs (n=14,725; age, 54.2±5.8 yrs; 55% female, 74% white) were included. EP substrate was characterized by heart rate, QRS, QTc, Cornell voltage, spatial ventricular gradient (SVG), and sum absolute QRST integral (SAI QRST) ECG metrics. Two competing outcomes were adjudicated SCD and nonSCD. Interaction of ECG metrics with sex was studied in Cox proportional hazards and Fine-Gray competing risk models. Model 1 was adjusted for prevalent cardiovascular disease (CVD) and risk factors. Time-updated model 2 was additionally adjusted for incident non-fatal CVD. Relative hazard ratio (RHR) and relative sub-hazard ratio (RSHR) with a 95% confidence interval for SCD and nonSCD risk for women relative to men was calculated. Model 1 was adjusted for prevalent CVD and risk factors. Time-updated model 2 was additionally adjusted for incident non-fatal CVD. RESULTS­ Over a median follow-up of 24.4 years, there were 530 SCDs (incidence 1.72 (1.58-1.88)/1000 person-years). Women as compared to men experienced a greater risk of SCD associated with Cornell voltage (RHR 1.18(1.06-1.32); P=0.003), SAI QRST (RHR 1.16(1.04-1.30); P=0.007), and SVG magnitude (RHR 1.24(1.05-1.45); P=0.009), independently from incident CVD. CONCLUSION­ In women, the global EP substrate is associated with up to 24% greater risk of SCD than in men, suggesting differences in underlying mechanisms and the need for sex-specific SCD risk stratification.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Cardiovasc Digit Health J Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Cardiovasc Digit Health J Ano de publicação: 2020 Tipo de documento: Article