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. 2023 Nov 27;11(2):278–290. doi: 10.1002/acn3.51950

Table 1.

Participant characteristics.

Category Variable Value Overall, n = 97
Demographic and medical characteristics Female sex 40 (41%)
Mother's education High school or less/other 14 (14%)
Some college/college graduate 55 (57%)
Postgraduate degree 28 (29%)
Congenital heart disease diagnosis Single ventricle with arch obstruction 4 (4%)
Single ventricle without arch obstruction 20 (21%)
Biventricular with arch obstruction 7 (7%)
Biventricular without arch obstruction 66 (68%)
MRI model General electric MR750 5 (5%)
Siemens Prisma 65 (68%)
Siemens Prisma fit 25 (26%)
Cortical thickness 2.66 ± 0.15
MRI infarct number 0 86 (90%)
1–5 10 (10%)
Genetic characteristics ApoE ε2/ε4 genotype 29 (40%)
Chromatin LoF variant 9 (9%)
HBE LoF variant 61 (63%)
NDD LoF variant 8 (8%)
Total sulcal similarity measures Left hemisphere 0.7503 ± 0.0069
Left frontal 0.7626 ± 0.0076
Left temporal 0.7481 ± 0.0124
Left parietal 0.7331 ± 0.0148
Left occipital 0.7432 ± 0.0145
Right hemisphere 0.7379 ± 0.0228
Right frontal 0.7530 ± 0.0198
Right temporal 0.7379 ± 0.0271
Right parietal 0.7190 ± 0.0224
Right occipital 0.7389 ± 0.0222
Executive function testing Age at testing (years) 16.2 [9.8–22.4]
Category switching accuracy 10.6 ± 3.3
Number–letter switching 9.3 ± 3.6
Tower total achievement 9.8 ± 2.5

Values are mean ± SD, number (%), or median [interquartile range]. Data complete except for MRI model (n = 95), cortical thickness (n = 95), MRI infarct number (n = 96), ApoE ε2/ε4 genotype (n = 73), and total sulcal similarity measures (n = 92).

Abbreviations: ApoE, Apolipoprotein E; CHD, congenital heart disease; HBE, high brain expression; LoF, loss‐of‐function; MRI, magnetic resonance imaging; NDD, neurodevelopmental disability.