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Table 2 Characteristics of the TA patients stratified for therapy with PPIs and for the presence of arterial hypertension

From: Chromogranin-A production and fragmentation in patients with Takayasu arteritis

 

Therapy with PPIs

Arterial hypertension

 

No (N = 12)

Yes (N = 30)

p value

No (N = 20)

Yes (N = 22)

p value

Qualitative variables

 Sex (F:M)

11:1

28:2

n.s.

20:0

19:3

n.s.

 Class of arterial involvement:

      

  1

  2A

  2B

  3

  4

  5

1

2

1

0

0

8

3

2

2

1

0

22

n.s.

n.s.

n.s.

n.s.

N.A.

n.s.

2

3

1

1

0

13

2

1

2

0

0

17

n.s.

n.s.

n.s.

n.s.

N.A.

n.s.

 Aneurysms

6

10

n.s.

7

9

n.s.

 Steroids

3

27

<0.001

13

17

n.s.

 Immunosuppressive therapy:

7

23

n.s.

11

19

0.04

 Biologic therapy:

  TNF blockers

  Tocilizumab

4

3

1

15

13

1

n.s.

n.s.

n.s.

10

9

1

9

7

1

n.s.

n.s.

n.s.

 Active disease (NIH criteria)

0

12

0.009

5

6

n.s.

 Anticoagulants

3

4

n.s.

3

4

n.s.

 Arterial hypertension

4

18

n.s.

N.E.

N.E.

 

 Therapy with PPIs

N.E.

N.E.

    

 Cardiac involvement

4

8

n.s.

6

6

n.s.

 Vascular enhancement (N = 30)

1

4

n.s.

3

2

n.s.

 Vascular progression (N = 40)

1

8

n.s.

5

4

n.s.

Scalar variables (median and range)

 Age (years)

51 (31–66)

41 (23–62)

0.060

40 (23–66)

47 (26–65)

n.s.

 Age at TA onset (years)

36 (21–56)

28 (17–56)

n.s.

29 (17–56)

30 (18–56)

n.s.

 Disease duration (years)

12 (4–21)

9 (0–34)

n.s.

9 (2–21)

11 (0–34)

n.s.

 Creatinine (mg/dl)

0.70 (0.44–1.06)

0.70 (0.56–1.60)

n.s.

0.67 (0.49–0.89)

0.75 (0.44–1.61)

0.084

 PDN dose (mg/day)

0 (0–12.5)

5 (0–35)

<0.001

5 (0–25)

5 (0–35)

n.s.

 N vessels

4 (1–6)

4 (1–7)

n.s.

3 (1–-6)

4 (1–7)

n.s.

 ESR (mm/h)

9 (1–23)

18 (2–78)

0.059

13 (2–73)

18 (1–78)

n.s.

 Serum CRP (mg/l)

1.5 (0.1–12)

3.0 (0.3–40)

0.104

2.0 (0.1-40)

2.6 (0.3–36.8)

n.s.

 Plasma PTX3 (ng/ml)

4.1 (1.3–44)

5.9 (2.2–55)

n.s.

5.8 (2.5–43.6)

5.3 (1.3–55.0)

n.s.

 CgAtot (nM)

1.02 (0.45–2.66)

3.40 (0.60–7.85)

<0.001

1.35 (0.5–3-6.31)

3.76 (0.45–7.85)

0.021

 CgA439 (nM)

0 (0-0–19)

0.07 (0–0.78)

n.s.

0.01 (0–0.44)

0.07 (0–0.78)

n.s.

 CgA-FRs (nM)

0.76 (0.22–1.82)

2.18 (0.28–6.68)

<0.001

0.89 (0.39–3.93)

2.45 (0.22–6.68)

0.030

 VS-1 (nM)

0.10 (0.02–0.34)

0.25 (0.06–1.15)

0.001

0.11 (0.02–0.79)

0.32 (0.05–1.15)

0.024

 CgA439/CgAtot

0 % (0–18 %)

2 % (0–24 %)

n.s.

0 % (0–18 %)

2 % (0–24 %)

n.s.

 CgA-FRs/CgAtot

69 % (50–84 %)

66 % (47–94 %)

n.s.

69 % (50–84 %)

66 % (47–94 %)

n.s.

 VS-1/CgAtot

12 % (1–24 %)

10 % (3–27 %)

n.s.

12 % (1–24 %)

10 % (3–27 %)

n.s.

 Rank CgA439+ rank VS-1

27 (5–50)

41 (18–83)

0.002

32 (5–64)

44 (8–83)

0.023

  1. Quantitative and qualitative variables related to TA were evaluated, verifying the impact of the treatment with PPIs and of arterial hypertension. N vessels refers to the number of vessels involved by the disease (see “Methods”)
  2. TA Takayasu arteritis, PPI proton-pump inhibitor, n.s. not significant, N.A. not available, TNF tumour necrosis factor, N.E. not evaluable, PDN prednisone, ESR erythrocyte sedimentation rate, CRP C-reactive protein, PTX3 pentraxin-3, CgA tot total chromogranin-A, CgA 439 full-length CgA (residues 1–439), CgA-FRs fragments of CgA spanning from the N-terminus to the central region but lacking the C-terminal region, VS-1 vasostatin-1