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. 2011 May 5;6(5):e19562. doi: 10.1371/journal.pone.0019562

Table 1. Clinical information of the study participants.

Participant Gender Age at infection Risk exposurea HCV genotype HCV RNA range (log10 IU/ml)b Early specimen Late specimen
Years infected KnodellFibrosis stage AST (U/L)c ALT (U/L)c AFP (ng/ml)c Years infected KnodellFibrosis stage AST (U/L)c ALT (U/L)c AFP (ng/ml)c
1 M 16 IDU 1a 4.7–7.3 26 4 176 258 8.9 38 4 47 72 5.2
2 F 44 IDU 1a 5.8–6.7 3 1 50 62 1.5 14 1 38 43 3.7
3 F 30 Others 1a 4.7–6.2 15 1 57 71 9.0 25 3 32 30 14.0
4 F 29 Others 1a 5.7–6.3 7 0 52 49 2.0 13 0–1 43 38 3.2
5 M 25 IDU 1a 6.0–7.3 29 N/A 25 32 2.9 35 N/A 24 33 3.7
6 M 25 IDU 1a 6.1–7.0 13 1 55 126 3.8 20 N/A 30 67 5.7
7 F 27 IDU 1a 6.4–7.2 2 N/A N/A N/A N/A 23 3 66 81 3.4
8 F 15 BT, IDU 1b 5.6–6.3 32 1 68 32 3.0 37 1 44 35 3.6
9 F 32 Others 1a 5.7–6.8 10 1 38 74 1.7 15 1 41 63 1.7
a

IDU, intravenous drug use; BT, blood transfusion; others include tattooing, body piercing, sharing personal care items, blood-to-blood contact during sexual activity, intranasal cocaine use, and unknown.

b

HCV RNA range (log10 IU/ml) was estimated as the range of all documented RNA titers of the archived specimens until the late time point for each participant.

c

AST, ALT and AFP levels were estimated as the mean of all documented enzymatic levels of the year of the early or late time points for each participant.