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. 2018 Sep 21;8:336. doi: 10.3389/fcimb.2018.00336

Table 1.

Characteristics of patients included in the three cohorts.

Cohort 1, (O'Brien et al., 2014) Cohort 2, (unpublished) Cohort 3, (Fumery et al., 2017)
All participants n = 65 n = 62 n = 211
Disease status CD
UC
No-IBD controls
52%
12%
35%
27%
24%
48%
100%
0%
0%
Gender Males 60% 53% 45%
Age (year) Median (interquartile range) 45.1 (23–95)a 23.6 (9.5–62)b 33.8 (25–70)b
Smoking habits Never smokers
Past smokers
Active smokers
NA 58%
21%
21%
38%
28%
34%
Genotyping NOD2 wt
NOD2 mutated*
68%
32%
89%
11%
56%
44%
ATG16L1 (AA)
ATG16L1 (AG + GG)
18%
82%
29%
70%
21%
79%
IRGM (CC)
IRGM (CT + TT)
85%
15%
74%
26%
62%
38%
CD patients only n = 34 n = 17 n = 211
Age at diagnosis A1 (< 17 years)
A2 (17–40 years)
A3 (>40 years)
16%
59%
25%
55%
45%
0%
10%
80%
10%
Disease Location L1 (ileum)
L2 (colon)
L3 (ileocolon)
L4 (upper gastrointestinal)
59%
13%
25%
3%
20%
50%
30%
0%
60%
1%
38%
2%
Disease Behavior B1 (inflamatory)
B2 (stricturing)
B3 (penetrating)
6%
72%
22%
80%
0%
20%
16%
48%
36%

CD, Crohn's Disease; UC, Ulcerative Colitis; IBD, Inflammatory Bowel Disease;

a

at diagnosis;

b

at enrolment;

*

one or more of the R702W, G908R, or L1007fs-insC mutations.

Cohort 1 and 3: post-surgical resected tissues, cohort 2: endoscopic mucosal biopsies.

Montreal Classification is reported for CD patients (Satsangi et al., 2006).