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. 2018 May 20;16(6):1121–1127. doi: 10.1111/jth.14129

Table 1.

Baseline characteristics including podoplanin expression, IDH1 mutation status and peripheral blood parameters in our patient cohort

Demographics Patients studied n (% miss.) Podoplanin +, ++ and +++ (n = 151) Podoplanin – (n = 62) P‐value IDH1 mutant (n = 42) IDH1 wild‐type (n = 171) P‐value
Median age at study entry 213 (0%) 55 [44–66] 60 [48–68] 46 [37–56] <0.0001 42 [36–50] 60 [48–67] <0.0001
Female sex 213 (0%) 79 (37%) 54 (36%) 25 (40%) 0.53 17 (40%) 62 (36%) 0.61
Body mass index (BMI, kg/m²) 213 (0%) 25 [23–28] 26 [23–28] 25 [23–27] 0.53 24 [23–27] 26 [23–28] 0.25
Newly‐diagnosed malignancy 213 (0%) 185 (87%) 136 (90%) 49 (79%) 0.03 35 (83%) 150 (88%) 0.45
Brain tumor types 213 (0%) / / / <0.0001 / / <0.0001
Glioblastoma/sarcoma (WHO IV) / 152 (71%) 124 (82%) 28 (18%) / 18 (12%) 134 (88%) /
Anaplastic glioma (WHO III) / 38 (18%) 14 (37%) 24 (63%) / 18 (47%) 20 (53%) /
Low‐grade glioma (WHO II) / 10 (5%) 3 (30%) 7 (70%) / 4 (40%) 6 (60%) /
Other 13 (6%) 10 (77%) 3 (23%) / 2 (15%) 11 (85%) /
Laboratory parameters
Platelet count (G L−1) 213 (0%) 240 [194–311] 227 [186–285] 286 [241–355] <0.0001 297 [244–338] 232 [190–289] 0.0004
D‐dimer μg mL−1 190 (11%) 0.7 [0.3–1.4] 0.8 [0.5–1.9] 0.4 [0.2–0.8] <0.0001 0.4 [0.3–0.8] 0.7 [0.4–1.7] 0.008
Soluble P‐selectin, ng mL−1 197 (8%) 37 [29–49] 37 [29–48] 39 [29–51] 0.51 37 [29–49] 38 [29–50] 0.91
Peak thrombin generation, nm 212 (0%) 347 [184–543] 374 [198–552] 284 [167–493] 0.12 280 [163–490] 363 [190–551] 0.23
Serum calcium (total), mmol L−1 124 (42%) 2.37 [2.27–2.46] 2.36 [2.25–2.44] 2.37 [2.31–2.50] 0.05 2.40 [2.31–2.50] 2.36 [2.26–2.44] 0.09
Serum calcium (albumin corrected), mmol L−1 124 (42%) 2.31 [2.27–2.38] 2.32 [2.27–2.39] 2.30 [2.23–2.36] 0.15 2.28 [2.22–2.37] 2.32 [2.27–2.39] 0.06

Median levels [25th–75th percentile] are given for continuous data and absolute frequencies (%) for count data. P‐values for the comparison between podoplanin‐positive and podoplanin‐negative tumors, as well as between IDH1 wild‐type and IDH1 mutation, are reported.