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. 2022 Oct 26;4(1):vdac169. doi: 10.1093/noajnl/vdac169

Table 1.

Sociodemographic and clinical characteristics glioma cohort and longitudinal subgroup

Glioma cohort (N = 222) Longitudinal subgroup (n = 70)
Age, mean (SD) 45.6 (13.3) 41.0 (11.6)
Sex, n (%)
 Male 126 (56.8%) 42 (60.0%)
 Female 96 (43.2%) 28 (40.0%)
Level of education (Verhage), n (%)
 Low (1–4) 41 (18.5%) 11 (15.7%)
 Middle (5) 75 (33.8%) 26 (37.1%)
 High (6–7) 106 (47.7%) 32 (45.7%)
 Missing 1 (1.4%)
Tumor hemisphere, n (%)
 Left 137 (61.7%) 46 (65.7%)
 Right 81 (36.5%) 23 (32.9%)
 Both 4 (1.8%) 1 (1.4%)
Tumor location, n (%)
 Frontal 132 (59.5%) 41 (58.6%)
 Non-frontal 90 (40.5%) 29 (41.4%)
WHO grade, n (%)
 II 114 (51.4%) 47 (67.1%)
 III 60 (27.0%) 20 (28.6%)
 IV 48 (21.6%) 3 (4.3%)
Tumor type, n (%)
 Oligodendroglioma 74 (33.3%) 33 (47.1%)
 Astrocytoma, IDH mutated 67 (30.2%) 24 (34.3%)
 Astrocytoma, IDH wildtype 10 (4.5%) 3 (4.3%)
 Astrocytoma, IDH status unknown 14 (6.3%) 3 (4.3%)
 Oligoastrocytoma* 9 (4.1%) 4 (5.7%)
 Glioblastoma, IDH mutated 5 (2.3%) 1 (1.4%)
 Glioblastoma, IDH wildtype 21 (9.5%) 2 (2.9%)
 Glioblastoma, IDH status unknown 22 (9.9%) 0 (0%)
Using anti-epileptic drugs, n (%)
 No 5 (2.3%) 1 (1.4%)
 Yes 163 (73.4%) 52 (74.3%)
 Missing 54 (24.3%) 17 (24.3%)
Number of included assessments per patient, n (%)
 1 137 (61.7%)
 2 68 (30.3%) 70 (100%)
 3 10 (4.5%)
 4 6 (2.7%)
 6 1 (0.5%)

Abbreviations: SD, standard deviation; n, number.

*Histological diagnosis of these patients was based on the 2007 WHO classification of the central nervous system tumors, and could not be re-classified because molecular markers were not available50.