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. Author manuscript; available in PMC: 2023 Oct 1.
Published in final edited form as: Circ Genom Precis Med. 2022 Sep 22;15(5):e003675. doi: 10.1161/CIRCGEN.121.003675

Table 3.

Phenotypes in Carriers of Pathogenic/Likely Pathogenic Variants Associated with Brugada Syndrome

Carriers (N=4) Noncarriers (N=20) P value
Demographics
 Age, years 66.5 ± 15.5 66.6 ± 13.7 NA
 Female 3 (75%) 15 (75%)
 Genetic ancestry
  European 3 (75%) 15 (75%)
  African 1 (25%) 5 (25%)
Electrocardiogram
 Individuals with electrocardiogram 3 (75%) 20 (100%) 0.2
  Type 1 Brugada pattern 0 0 NA
Other findings
 PR interval, ms 258 ± 69 162 ± 21 0.009
 1st degree atrioventricular block + left axis deviation 2 (67%) 1 (5%) 0.03
 QRS duration, ms 113 ± 3 97 ± 19 0.06
 Syncope 2 (50%) 4 (20%) 0.3
 Atrial fibrillation/flutter 2 (50%) 6 (30%) 0.6
 Nonsustained/sustained ventricular tachycardia 0 3 (15%) 1
 Permanent pacemaker 2 (50%) 2 (10%) 0.1
 Implantable cardioverter-defibrillator 0 1 (5%) 1
 Obstructive coronary artery disease 1 (25%) 12 (60%) 0.3

Continuous measures are described as mean ± standard deviation and are compared using the Wilcoxon rank-sum test. Categorical variables are described as N (%) and are compared using Fisher’s exact test. P values in bold indicate p <0.05. NA, not applicable.