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. Author manuscript; available in PMC: 2011 Jul 12.
Published in final edited form as: J Am Coll Cardiol. 2005 Feb 1;45(3):400–408. doi: 10.1016/j.jacc.2004.08.068

Table 2.

Demographic Data and Method of Risk Determination of ARVC in 48 Subjects at High Risk Who Received an ICD and 58 Matched Control Subjects From 11 Families With ARVC Linked to 3p25

Demographic
Parameters
ICD Cohort
Control Cohort
ICD Cohort M+F 48 Control Cohort M+F 58 p Value*
Males (n = 30)
Females (n = 18)
Males (n = 36)
Females (n = 22)
n % n % n % n %
Born <1950 2 6 1 5 25 69 19 86 3 44 <0.0001
Born ≥1950 28 93 17 95 11 31 3 14 45 14
Methods of diagnosis
 Obligate carrier (OC) 4 13 4 50 18 51 17 49 8 35 <0.0001
 DNA haplotype 22 74 14 39 5 50 5 50 36 10 <0.0001
 Clinical event (SCD or VT) 4 13 0 0 13 10 0 0 4 13 <0.05
Mean age at entry (yrs) 33.3 40.3 32.2 40 ns
Median age at entry (yrs) 32.9 42 32.7 39.2 ns
Standard deviation (yrs) 9.8 9.0 9.6 9.5 ns
*

Chi-square with 1 df for ICD M+F vs. control M+F.

ARVC = arrhythmogenic right ventricular cardiomyopathy; ICD = implantable cardioverter-defibrillator; SCD = sudden cardiac death; VT = ventricular tachycardia.