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Table 1 Demographic and clinical characteristics at start of anti-hepatitis C virus (HCV) treatment of chronically HIV/HCV co-infected patients, 1998-2011

From: Effect of abacavir on sustained virologic response to HCV treatment in HIV/HCV co-infected patients, Cohere in Eurocoord

 

Sustained virologic response

 

Total

No

Yes

p-value

Number of patients (%)

1309

819 (63)a

490 (37)a

 

Age baseline, years

42 (38–46)

42 (38–46)

42 (37–46)

0.04

Baseline BMI

   

<0.0001

  < 25

329 (25b)

234 (71)

95 (29)

 

  > =25

123 (9)

96 (78)

27 (22)

 

 Unknown

857 (66)

489 (57)

368 (43)

 

Gender

   

0.57

 Male

960 (73)

605 (63)

355 (37)

 

 Female

349 (39)

214 (61)

135 (39)

 

HIV transmission route:

   

0.05

 Men who have sex with men

175 (13)

91 (52)

84 (48)

 

 Male, injection drug use (IDU)

595 (45)

393 (66)

202 (34)

 

 Female IDU

209 (16)

127 (61)

82 (39)

 

 Male heterosexual

84 (6)

55 (65)

29 (35)

 

 Female heterosexual

96 (7)

62 (65)

34 (35)

 

 Male other/unknown

106 (8)

66 (62)

40 (38)

 

 Female other/unknown

44 (3)

25 (57)

19 (43)

 

Region of origin:

   

0.06

 Western

1101 (84)

700 (64)

401 (36)

 

 Other

116 (9)

72 (62)

44 (38)

 

 Unknown

92 (7)

47 (51)

45 (49)

 

CD4 at baseline (cells/μl)

    

 0–349

264 (20)

163 (62)

101 (38)

0.02

 350–499

306 (23)

194 (63)

112 (37)

 

  > =500

491 (38)

288 (59)

203 (41)

 

 Missing

248 (19)

174 (70)

74 (30)

 

Nadir CD4 (cells/ μl)

   

<0.001

  < 200

689 (53)

434 (63)

255 (37)

 

  > =200

583 (45)

381 (65)

202 (35)

 

 Missing

37 (3)

4 (11)

33 (89)

 

HIV RNA levels at baseline (copies/ml)

   

0.99

  < =400

1082 (83)

677 (63)

405 (37)

 

  > 400

227 (17)

142 (63)

85 (37)

 

Hepatitis B virus co-infection

   

0.64

 No

1214 (93)

762 (63)

452 (37)

 

 Yes

53 (4)

30 (57)

23 (43)

 

 Unknown

42 (3)

27 (64)

14 (33)

 

HCV RNA load at baseline

   

<0.0001

  < 600,000

222 (17)

99 (45)

123 (55)

 

  ≥ 600,000

724 (55)

485 (67)

239 (33)

 

 Missing

363 (28)

235 (65)

128 (35)

 

HCV genotypes

   

<0.0001

 1

82 (6)

53 (65)

29 (35)

 

 1a

307 (23)

234 (76)

83 (27)

 

 1b

147 (11)

108 (73)

39 (27)

 

 2&3

315 (24)

154 (49)

161 (51)

 

 4

143 (11)

103 (72)

40 (28)

 

 Other/unknown

315 (24)

177 (56)

138 (44)

 

APRIc score:

   

<0.0001

  < 0.5

409 (31)

206 (50)

203 (50)

 

 0.5–1.5

426 (32)

312 (73)

114 (27)

 

  > =1.5

195 (15)

155 (79)

40 (21)

 

 Unknown

279 (21)

146 (52)

133 (48)

 

Decline in haemoglobin (g/dl)

   

0.0017

 No decline

179 (14)

126 (70)

53 (30)

 

  < =2.5

227 (17)

157 (69)

70 (31)

 

  > 2.5

230 (18)

127 (55)

103 (45)

 

 Missing

637 (49)

409 (64)

264 (41)

 

Duration of HCV treatment in weeks

   

<0.0001

  < =24

496 (38)

390 (79)

106 (21)

 

 24-48

437 (33)

242 (55)

195 (45)

 

  > 48

376 (29)

187 (50)

189 (50)

 

Calendar year of start HCV treatment

   

<0.0001

  < =2003

266 (20)

201 (76)

65(24)

 

 2003–2006

421 (32)

258 (61)

163 (39)

 

  > =2006

622 (48)

360 (58)

262 (42)

 

cART regimen

   

0.003

 PI

158 (12)

104 (66)

54 (34)

 

 Boosted PI

444 (34)

296 (67)

148 (33)

 

 NNRTI

284 (22)

154 (54)

130 (46)

 

 PI + NNRTI

50 (6)

35 (70)

15 (30)

 

 No PI and/or NNRTI

131 (10)

90 (69)

41 (31)

 

 no cART

242 (18)

140 (58)

102 (42)

 

Backbone

   

<0.0001

 Start after HCV treatment

242 (18)

140 (58)

102 (42)

 

 ABC + 3TC

189 (14)

117 (62)

72 (38)

 

 AZT + 3TC

140 (11)

99 (62)

41 (29)

 

 FTC + TDF

262 (20)

147 (56)

115 (44)

 

 TDF + 3TC

130 (10)

68 (52)

62 (48)

 

 TDF + ABC

44 (3)

27 (61)

17 (39)

 

 d4T + 3TC

90 (7)

68 (76)

22 (24)

 

 other

212 (16)

153 (72)

59 (28)

 
  1. apercentage in these colums are representing the percentage of the total number of patients in a specific category/row
  2. bPercentage from total number of patients included in this study (n = 1309)
  3. cAPRI, aspartate amino transferase-to-platelet ratio; PI, protease inhibitor; NNRTI, non-nucleoside reverse transcriptase; NRTI, nucleoside analog reverse-transcriptaseinhibitor; ABC, abacavir, 3TC, lamivudine; AZT, zidovudine; FTC, emtricitabine; TDF, tenofovir; d4T, stavudine