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. 2020 Jul 21;15(7):e0236109. doi: 10.1371/journal.pone.0236109

Table 1. Baseline characteristics of the 2484 patients with tuberculosis according to the occurrence of severe adverse events due to pyrazinamide.

Variables Total Serious adverse events due to PZA P value
N = 2478 (‒), N = 2251 (+), N = 227
Age (year) 49.6±18.4 49.0±18.3 55.5±18.5 <0.001
Sex, male (%) 1319 (53.2) 1048 (46.6) 111 (48.9) 0.500
Tuberculosis 0.291
 Pulmonary 2102 (84.8) 1904 (84.6) 198 (87.2)
 Extrapulmonary 376 (15.2) 347 (15.4) 29 (12.8)
Initial diagnosis 0.524
 Sputum AFB 791 (33.7) 722 (33.9) 69 (31.8)
 TB-PCR 1553 (66.3) 1405 (66.1) 148 (68.2)
Comorbidities
 DM 244 (9.8) 214 (9.5) 30 (13.2) 0.074
 Malignancy 133 (5.4) 117 (5.2) 16 (7.0) 0.238
 Renal insufficiency 26 (1.0) 20 (1.0) 4 (1.8) 0.291
Smokinga 0.718
 Never 1069 (56.8) 871 (56.6) 198 (57.7)
 Ex- or current 814 (43.2) 669 (43.4) 145 (42.3)
Alcohol useb 0.553
 Never/social 618 (89.7) 473 (89.2) 145 (91.2)
 Heavy 71 (10.3) 57 (10.8) 14 (8.8)
Long-term steroid use 4 (0.2) 4 (0.2) 0 (0.0) 1.000
Risk factors for hepatotoxicity
HBs Ag (+) 57 (4.2) 51 (4.2) 6 (4.0) 0.912
Anti HCV (+) 12 (0.9) 12 (1.0) 0 (0.0) 0.381
Initial laboratory tests
 AST 22.0±11.8 21.8±11.1 24.2±16.8 0.090
 ALT 19.4±14.6 19.4±14.8 19.6±13.5 0.881
Treatment duration (mo.) 8.0±3.1 7.9±3.1 9.2±3.4 <0.001

AFB, acid-fast blue; TB, tuberculosis; PCR, polymerase chain reaction; DM, diabetes mellitus;

aData were not recorded for 595 (24.0%) patients.

bData were not recorded for 1789 (72.2%) patients.

Data are reported as the mean ± standard deviation and numbers (%).