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. Author manuscript; available in PMC: 2022 Jul 20.
Published in final edited form as: Ann Neurol. 2021 Jun 3;90(1):159–169. doi: 10.1002/ana.26129

Table 4.

Biomarker Values, Stratified by Study Group

Biomarkera Cancer-Plus-Stroke
(n=50)
Stroke-Only
(n=50)
Cancer-Only
(n=50)
P-value Across Groupsb,c
Coagulation
 D-dimer 2,552 (830–6,640) 405 (204–740) 670 (400–1,730) <0.001
 TAT 20 (4–34) 6 (2–28) 4 (1–12) <0.001
Platelets
 P-selectin 40 (28–62) 26 (21–33) 34 (27–45) <0.001
Endothelium
 Thrombomodulin 5,310 (4,222–5,117) 3,712 (3,097–4,371) 4,081 (3,214–5,117) <0.001
 sICAM-1 244 (204–388) 176 (137–205) 224 (182–264) <0.001
 sVCAM-1 1,075 (803–1,564) 705 (585–933) 888 (611–1,053) <0.001
Embolic disease
 TCD HITS present 16 (32) 8 (16) 3 (6) 0.004

Abbreviations: TAT, thrombin-antithrombin; sICAM-1, soluble intercellular adhesion molecule-1; sVCAM-1, soluble vascular cell adhesion molecule-1; TCD, transcranial Doppler; HITS, high-intensity transient signals.

a

Data reported as number (%) for categorical variables and median (interquartile range) for continuous variables. Units of measure for hematological biomarkers are ng/ml, except thrombomodulin which is listed as pg/ml.

b

Kruskal-Wallis tests were used to determine whether median hematological biomarker levels were different between the three groups, while the Chi-square test was used to determine whether the proportion of participants with TCD HITS were different between the three groups. The listed p-values correspond to these analyses.

c

Between-group comparisons performed using the Wilcoxon Rank-Sum test for the hematological biomarkers and the Chi-square test for the embolic disease biomarker were also all significant except for TAT when comparing the cancer-plus-stroke group to the stroke-only group (p=0.063) and P-selectin when comparing the cancer-plus-stroke group to the cancer-only group (p=0.062). These analyses’ individual P-values are not provided in the Table.