Skip to main content
. 2015 Jun 14;21(22):6952–6964. doi: 10.3748/wjg.v21.i22.6952

Table 6.

Antiphospholipid antibodies, thrombophilia markers and clinical characteristics of total Crohn’s disease according to presence and type of thrombosis n (%)

Factor Follow-up of CD Total Cohort from diagnosis (n = 265)
No thrombosis Arterial thrombosis Venous thrombosis No pregnancy loss Pregnancy loss
(n = 251) (n = 3) (n = 11) (n = 146) (n = 10)
Male/female 104/147 1/2 7/4 146/0 10/0
Age at presentation (yr)1 25.0 (19.0-33.0) 40.0 (28.0-42.0) 29.5 (23.3-39.3) 26.0 (20.0-35.0) 25.5 (21.0-35.0)
Frequent relapse 48 (20.2) 0 (0.0) 4 (36.4) 33 (24.1) 2 (20.0)
Previous thrombosis 1 (0.4)3 0 (0.0) 4 (36.4)3 2 (1.4) 0 (0.0)
Smoking habits yes 48 (19.1) 0 (0.0) 3 (27.3) 22 (15.1) 2 (20.0)
Follow up time from diagnosis, mo1 102.2 (63.3-172.8)2 149.9 (130.8-219.8) 186.3 (142.0-244.2)2 109.0 (61.8-184.6) 136.5 (95.4-180.6)
Positive markers (%)
Anti-β2-GPI IgG and/or IgM 4.8 0 9.1 4.9 10
Anti-β2-GPI IgA 2.8 0 0 4.9 0
ACA IgG and/or IgM 12.1 0 27.3 13.9 10
ACA IgA 19.0 66.7 0 20.1 10
Anti-PS/PT IgG and/or IgM 14.6 50.0 36.4 18.3 40
Anti-PS/PT IgA 8.9 50.0 9.1 7.7 10
At least 1 APLA pos 48.0 66.7 54.5 52.8 60
At least 2 APLA pos 16.1 33.3 9.1 18.1 10
At least 3 APLA pos 3.2 0 9.1 4.9 0
Thrombophilia markers3 (%)
LA 7.5 0 0 5.1 0
PS deficiency (inherited and/or acquired) 8.1 0 25.0 12.7 0
ATIII deficiency (inherited and/or acquired) 0 0 0 0 0
PC deficiency (inherited and/or acquired) 3.0 0 0 4.8 0
FV Leiden 5.94 0 42.94 7.8 0
FII20210A 5.9 0 16.7 7.8 0
1

Median (IQR);

2

Using Kruskal-Wallis test (P ≤ 0.01);

3

Using χ2-test with Yates correction (P ≤ 0.05);

4

Serologic and genetic markers of thrombophilia were available in 105 patients. pts: Patients; APLA: Antiphospholipid antibodies; β2-GPI: Beta2-glycoprotein-I; ACA: Anti-cardiolipin antibody; PS/PT: Phosphatidylserine/prothrombin complex.