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. 2021 Jul 22;36(5):1190–1203. doi: 10.3904/kjim.2020.634

Table 7.

Clinical features of primary myelofibrosis patients experiencing and not experiencing thrombotic events

Variable With TE (n = 4) Without TE (n = 26) p value
Age, yr 77.0 ± 3.3 63.1 ± 12.6 0.039
Male sex 3 (75.0) 17 (65.4) 0.704
Palpable splenomegaly 0 14 (53.8) 0.044
Laboratory findings
 WBC, × 109/L 10.8 ± 6.0 13.8 ± 11.6 0.626
 Monocytes, × 109/L 1.2 ± 1.3 0.9 ± 0.7 0.513
 Hemoglobin, g/dL 10.0 ± 1.4 10.3 ± 2.7 0.831
 Platelets, × 109/L 784.8 ± 565.8 357.5 ± 246.4 0.012
 LDH, × UNL 1.5 ± 0.2 2.2 ± 1.7 0.463
Driver gene mutation
JAK2V617F 3/4 (75.0) 11/18 (61.1) 0.362
CALR 0/4 (0.0) 5/18 (27.8) 0.562
IPSS 0.543
 Low 0 5 (19.2)
 Intermediate-1 2 (50.0) 6 (23.1)
 Intermediate-2 2 (50.0) 9 (34.6)
 High 0 6 (23.1)
Comorbidity
 Hypertension 3 (75.0) 7 (26.9) 0.058
 Diabetes mellitus 1 (25.0) 6 (23.1) 0.933
 Chronic kidney disease 0 3 (11.5) 0.474
 Smoking 0 3 (11.5) 0.474
Hemorrhagic event 0 1 (3.8) 0.867
Follow-up duration, yr 2.4 ± 2.2 4.5 ± 4. 4 0.365

Values are presented as mean ± SD or number (%).

TE, thrombotic event; WBC, white blood cell; LDH, lactate dehydrogenase; UNL, upper normal limit; JAK2, Janus kinase 2; CALR, calreticulin; IPSS, International Prognostic Scoring System.