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. Author manuscript; available in PMC: 2013 Apr 26.
Published in final edited form as: Pharmacogenet Genomics. 2012 Nov;22(11):784–795. doi: 10.1097/FPC.0b013e3283589a76

Table 1.

Clinical characteristics of the study population in the initial discovery sample used for genome-wide association study (n=783) and in the replication cohort (n=307)

N (%) or median (range)
Variables Discovery sample Replication sample
Sex
 Male 329 (42.0) 136 (44.3)
 Female 454 (58.0) 171 (55.7)
Age of onset (years) 57.5 (1.8–98) 54.2 (5.8–88)
Time to onset (days) 24 (0–7045) 39 (0–11463)
Injury type
 Cholestatic 187 (23.9) 90 (29.3)
 Mixed 164 (20.9) 64 (20.8)
 Hepatocellular 256 (32.7) 139 (45.3)
 Unknown/unclassified 176 (22.5) 14 (4.6)
Severity
 Mild 105 (13.4) 50 (16.3)
 Moderate 80 (10.2) 62 (20.2)
 Moderate (hospitalized) 124 (15.8) 48 (15.6)
 Severe 47 (6.0) 32 (10.4)
 Fatal 20 (2.6) 16 (5.2)
 Unknown/unclassified 407 (52.0) 99 (32.2)
Causality score
 ‘Unlikely’ or ‘possible’ 83 (10.6) 35 (11.4)
 ‘Probable’, ‘very likely’, ‘definite’ 622 (79.4) 173 (56.4)
 Unknown/unclassified 78 (10.0) 99 (32.2)
Immunoallergic features
 Eosinophilia 46 (5.9) NA
 Fever 161 (20.6) NA
 Rash 125 (16.0) NA
 Any of above 256 (32.7) NA