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Table 1 Clinical characteristics

From: Serum biomarker for diagnostic evaluation of pulmonary arterial hypertension in systemic sclerosis

Baseline demographics

Discovery cohort

Validation cohort 1

Validation cohort 2

lcSSc-PAH

lcSSc-no PAH

lcSSc-PAH

lcSSc-no PAH

lcSSc-PAH

lcSSc-no PAH

Age (year)

n = 13

n = 16

n = 23

n = 12

n = 11

n = 18

 Mean (SD)

65 (7.4)

50 (14)

66 (8.6)

54 (17.8)

66 (9.4)

62 (8.5)

  Median (range)

65 (56–81)

57 (25–70)

64 (52–85)

52 (26–76)

66 (52–81)

63 (46–79)

Sex

 Female, % (n)

92% (12)

87.5% (14)

83% (19)

92% (11)

100% (11)

83% (15)

  Male,% (n)

8% (1)

12.5% (2)

17% (4)

8% (1)

0% (0)

17% (3)

mPAP (mmHg)

 Mean (SD)

46 (9.1)

42 (12.3)

40 (10.8)

 Median (range)

45 (34–68)

43 (26–69)

42 (25–54)

mPCWP (mmHg)

 Mean (SD)

10 (2.7)

10 (4.3)

10 (3.2)

 Median (range)

11 (4–14)

11 (1–15)

9 (5–15)

PVR (Woods units)

 Mean (SD)

9 (4.9)

8 (5.3)

8 (4.1)a

 Median (range)

8 (5–24)

6 (3–27)

7 (3–13)a

ILD (Dx by HRCT)

 Positive, % (n)

7% (1)

13% (3)

0% (0)

 Negative, % (n)

83% (12)

87% (20)

100% (11)

Treatment

 Treated, % (n)

0% (0)

48% (11)

100% (11)

 Untreated, % (n)

100% (13)

52% (12)

0% (0)

BNP (pg/mL)

 Mean (SD)

261 (313)

411 (494)

 Median (range)

140 (42–1054)

148 (12–1630)

Date of sample

 At time of RHC, % (n)

100% (13)

91% (21)

36% (4)

  1. aMissing values
  2. BNP, brain natriuretic peptide; lcSSc-PAH, limited cutaneous systemic sclerosis pulmonary arterial hypertension; ILD, interstitial lung disease; mPAP, mean pulmonary artery pressure; mPCWP, mean pulmonary capillary wedge pressure; PVR, pulmonary vascular resistance; RHC, right heart catheterization