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. 2022 Aug 22;112(5):1079–1087. doi: 10.1002/cpt.2716

Table 1.

Clinical characteristics of azathioprine‐induced leukopenia (≥ grade 2; WBC ≤ 3,000 cells/μL) patients, general population, and azathioprine tolerant control during 2012–2017

AZA‐induced leukopenia (n = 40) AZA tolerant control (n = 86) General population controls (n = 507) P value
N (%) N (%) N (%)
Age, years, mean ± SD 47.4 ± 18.0 41.2 ± 19.2 56.0 ± 19.2 0.113a
Male, n (%) 17 (42.5) 41 (47.7) 253 (49.9) 0.530c
Initial AZA dose ≥2 mg/kg/day, n (%) 11 (27.5) 21 (24.4) 0.712c
Periods, day 68.2 ± 55.2 314.9 ± 239.7 < 0.001c
Indication, n (%)
Eczema/AD 33 (82.5) 73 (84.9) 0.993c
Urticaria 3 (7.5) 9 (10.5) 0.993c
Bullous pemphigoid 3 (7.5) 2 (5.0) 0.993c
Others 1 (2.5) 2 (5.0) 0.993c
Comorbidity, n (%)
CKD 7 (17.5) 8 (9.3) 0.310c
CVD 11 (27.5) 18 (20.9) 0.648c
DM 4 (10.0) 7 (8.1) 0.810c
Liver disorderb 6 (15.0) 9 (10.4) 0.876c

We excluded AZA users of SLE, sepsis, and patients with leukemia to avoid confounding factors of leukopenia.

AD, atopic dermatitis; AZA, azathioprine; CKD, chronic kidney disease; CVD, cardiovascular disease; DM, diabetes mellitus; SLE, systemic lupus erythematosus; WBC, white blood cell.

a

This P value was calculated by using two‐tailed Student’s t tests.

b

Liver disorders include all kinds of hepatitis, necrosis of liver, hepatic failure, liver replaced by transplant (see Methods section), or patient’s GPT/GOT value was twofold higher than the normal value range (36 U/L) before AZA intake.

c

P values were calculated with AZA‐induced leukopenia comparing to AZA tolerant control by using logistic regression model.