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. 2015 Jul 7;21(25):7795–7804. doi: 10.3748/wjg.v21.i25.7795

Table 4.

Stratified multivariate analysis

Adjusted variables Adjusted OR (95%CI)
All cohort (n = 351) Female (n = 185) Male (n = 166)
Age at Thiopurine prescription > 40 (sex-by-age interaction, P = 0.04) 2.4 (1.4-4.2) 2.8 (1.4-5.6) 0.9 (0.4-2.1)
Female vs male (referent) 1.2 (0.7-2.0) NA NA
Smoking history (current/past) 1.5 (0.9-2.5) 1.5 (0.8-3.1) 1.6 (0.8-3.6)
Pre-thiopurine intestinal resection vs no resection (referent) 0.86 (0.43-1.71) 0.7 (0.3-1.8) 1.0 (0.4-2.8)
L1 vs L2 (referent) 1.4 (0.6-3.2) 1.2 (0.4-3.6) 3.1 (0.9-10.4)
L3 vs L2 (referent) 1.5 (0.7-3.0) 1.1 (0.4-2.7) 2.1 (0.7-6.3)
B2 vs B1 (referent) 1 (0.5-2.2) 1.0 (0.3-2.8) 0.7 (0.2-2.4)
B3 vs B1 (referent) 1.1 (0.5-2.5) 1.0 (0.3-2.8) 0.8 (0.3-2.5)
Pre-thiopurine perianal disease vs no perianal disease (referent) 0.7 (0.4-1.3) 1.1 (0.5-2.7) 0.7 (0.3-1.8)
5-ASA at time of thiopurine vs past or never (referent) 0.8 (0.4-1.5) 0.7 (0.3-1.8) 1.0 (0.4-2.4)
Corticosteroid at diagnosis vs no exposure at diagnosis (referent) 0.9 (0.5-1.6) 0.7 (0.3-1.5) 0.9 (0.4-2.2)
L4 vs L2 (referent) 1.8 (0.7-4.3) 3.4 (0.9-12.2) 0.9 (0.3-3.1)

Predictors of thiopurine discontinuation in all cohort and as determined by this stratified multivariate analysis by sex. Demographic data suggests a higher incidence of adverse events in female patients over the age of 40 years. An age-by-gender interaction is seen as described in this multivariate analysis of thiopurine-exposed patients in female subjects over the age of 40 years. ASA: Aminosalicylic acid; NA: Not available.