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. 2022 Mar 16;13:840935. doi: 10.3389/fimmu.2022.840935

Table 1.

Baseline characteristics.

Cohort 1 Cohort 2
PSC-UC (n=17) UC (n=17) Healthycontrols (n=12) p-value PSC-UC (n=10) UC (n=10) Healthy controls (n=10) p-value
Male [n (%)] 17 (100) 17 (100) 12 (100) 10 (100) 10 (100) 10 (100)
Age [median (IQR)] 41 (30-55) 34 (31-54) 39 (29-50) 0.911 40 (35-58) 58 (49-62) 30 (28-53) 0.022
Age at diagnosis PSC [median (IQR)] 33 (24-46) 33 (25-37)
Duration PSC in years [median (IQR)] 5 (2-12) 7 (6-15)
Age at diagnosis UC [median (IQR)] 27 (20-37) 29 (19-40) 0.865 35 (22-39) 30 (19-46) 0.796
Duration UC in years [median (IQR)] 16 (7-21) 11 (5-15) 0.218 9 (5-19) 22 (14-34) 0.019
Medication use [n (%)]
 UDCA 17 (100) 0 (0) 0.000 8 (80) 0 (0) 0.001
 Anti-TNF-α 0 (0) 0 (0) 0 (0) 0 (0)
 Mesalazine 17 (100) 17 (100) 9 (90) 9 (90) 1.000
 Thiopurines 8 (47) 9 (53) 1.000 0 (0) 1 (10) 1.000
Montreal classification [n (%)] 0.144 0.164
 Pancolitis 15 (88) 10 (59) 7 (70) 6 (60)
 Left sided 2 (12) 5 (29) 1 (10) 4 (40)
 Proctitis 0 (0) 1 (6) 2 (20) 0 (0)

For continuous variables the Kruskal Wallis test was used for comparing 3 groups, whereas the Mann Whitney-U test was used for comparing 2 groups. For dichotomous variables, Fisher’s Exact test was used. P-value < 0.05 was considered statistically significant. PSC, primary sclerosing cholangitis; UC, ulcerative colitis; IQR, interquartile range; UDCA, Ursodeoxycholic acid.