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. Author manuscript; available in PMC: 2022 Jun 24.
Published in final edited form as: Ann Hematol. 2020 Feb 19;99(4):781–789. doi: 10.1007/s00277-020-03962-2

Table 1.

Patient characteristics

Without PH With PH P value

n= 123 (%) n=20 (%)
Age (years) 0.019
 Mean ± SD 66.8 ± 9.7 71.8 ± 6.7
 Median (range) 68 (18–86) 73.5 (61–83)

Gender 0.048
 Male 63 (51) 15 (75)
 Female 60 (49) 5 (25)

Time (days) from MF diagnosis to ECHO 0.518
 Mean ± SD 1547.5 + 1120.3 1836.7 ± 1578.1
 Median (range) 1294 (21 – 6092) 1760 (251 – 7311)

MF type 0.470
 PMF 72 (59) 12 (60)
 Post-ET MF 21 (17) 5 (25)
 Post-PV MF 30 (24) 3 (15)

JAK2 mutation present 67 (54) 11(55) 0.965

WHO grading myelofibrosis* 0.932
 MF-1 16 (14) 2 (13)
 MF-2 49 (43) 8 (50)
 MF-3 50 (44) 6 (38)

DIPSS^ 0.731
 Low risk (0) 5 (4) -
 Intermediate-1 risk (1 to 2) 49 (40) 8 (40)
 Intermediate-2 risk (3 to 4) 53 (43) 8 (40)
 High risk (5 to 6) 15 (12) 4 (20)

Active therapy for MF 51 (41) 8 (40) 0.902

Co-morbid conditions

 Hypertension 65 (53) 16 (80) 0.028

 Hyperlipidemia 25 (20) 9 (45) 0.016

 Coronary artery disease 10 (8) 6 (30) 0.004

 Atrial fibrillation 5 (4) 1 (5) ≥0.999

 Hypothyroidism 28 (23) 7 (35) 0.238

 Diabetes Mellitus 11 (9) 1 (5) ≥0.999

 COPD 5 (4) 1 (5) ≥0.999

Clinical

 Dyspnea 13 (11) 7 (35) 0.003

 ECOG performance status 0.845
  0 48 (39) 6 (30)
  1 65 (53) 13 (65)
  2 8 (7) 1 (5)
  ≥3 2 (2) -

 Splenomegaly 76 (62) 16 (80) 0.137

 Hepatomegaly 19 (15) 6 (30) 0.112

Active treatment 51 (41) 8 (40) 0.902
*

Data not available in *10 and

^

1 patient

PH, pulmonary hypertension; MF, myelofibrosis; ECHO, echocardiogram; PMF, primary myelofibrosis; Post-ET, myelofibrosis post-essential thrombocytopenia; Post-PV, myelofibrosis post-polycythemia vera; WHO, World Health Organization; DIPSS, dynamic international prognostic scoring system; COPD, chronic obstructive pulmonary disease; ECOG, Eastern Cooperative Oncology Group