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Table 1 Demographics and clinical characteristics of the subjects

From: Altered expressions of CXCR4 and CD26 on T-helper lymphocytes in hereditary hemorrhagic telangiectasia

 

HHT (n = 36)

Controls (n = 18)

 

Age (mean, SD)

60.2 (10.4)

59.7 (10.2)

p = 0.868

Sex (males, %)

26 (72%)

13 (72%)

p = 1

History of severe infection (n, %)

18 (50%)

0 (0%)

 

Mutation (n, %):

 ENG

18 (50%)

  

 ACVRL1

16 (44%)

  

 SMAD4

0 (0%)

  

 Not identified

2 (6%)

  

Visible telangiectases (median, min–max)

70 (0–242)

  

Epistaxis frequency1 (n, %)

 Daily

13 (36%)

  

 Weekly

13 (36%)

  

 Monthly or more rarely

10 (28%)

  

Arteriovenous malformations (n, %2)

 Lung3

12 (34%)

  

 Digestive tract

19 (73%)

  

 Liver

15 (44%)

  

 Brain

6 (25%)

  

Treatment (n, %)

 IV iron or blood transfusion (at least 5)

20 (56%)

  

 Tranexamic acid

6 (17%)

  

 Bevacizumab

4 (11%)

  
  1. n: Number of patients
  2. 1During the last month before blood sampling
  3. 2% of patients with a screening performed for the specified organ
  4. 3Only those large enough to be considered for treatment (usually diameter of the feeding artery > 3 mm)