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. 2019 Jan 24;27(3):117–126. doi: 10.1007/s12471-019-1226-5

Table 1.

Clinical characteristics of the study population

Mutation carriers (n = 120) Controls (n = 110) p-value
Age (years)  41 ± 13  44 ± 13  0.15
Female gender, n (%)  83 (69)  66 (60)  0.15
Body surface area (m2)   1.9 ± 0.2   1.9 ± 0.2  0.89
Systolic BP (mm Hg) 124 ± 18 125 ± 13  0.43
Diastolic BP (mm Hg)  76 ± 9  79 ± 8  0.02
Mean arterial pressure (mm Hg)  92 ± 11  94 ± 9  0.07
Medical history
– Arterial hypertension, n (%)   9 (8)   0 (0)  0.003
– Atrial fibrillation, n (%)   0 (0)   0 (0)  0.50
– Diabetes mellitus, n (%)   2 (2)   0 (0)  0.17
– Hypercholesterolaemia, n (%)   1 (1)   0 (0)  0.34
Medication
– Antihypertensive, n (%)a   8 (7)   0 (0)  0.01
– Statin, n (%)   4 (3)   0 (0)  0.05
– Antidiabetic, n (%)   2 (2)   0 (0)  0.17
– Antiplatelet, n (%)   2 (2)   0 (0)  0.17
– Oral anticoagulation, n (%)   1 (1)   0 (0)  0.34
Electrocardiography
– Sinus rhythm, n (%) 120 (100) 110 (100)  0.50
– Heart rate (beats/min)  67 ± 13  59 ± 9 <0.001
– Romhilt Estes ≥4, n (%)  11 (9)   2 (2)  0.02
– Pathological Q wave, n (%)   3 (3)   0 (0)  0.10
– T-wave inversion, n (%)   1 (0.8)   0 (0)  0.34

Data are expressed as mean ± standard deviation or as absolute and %

aIncludes diuretic (n = 3), beta-blocker (n = 3), ACE inhibitor (n = 2), angiotensin II antagonist (n = 2), calcium antagonist (n = 2)