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Table 1 Characteristics of study population at baseline (N = 484)

From: Efficacy and tolerability of lamivudine plus dolutegravir compared with lamivudine plus boosted PIs in HIV-1 positive individuals with virologic suppression: a retrospective study from the clinical practice

Variables

Darunavir/r N = 170

Atazanavir/r N = 141

Dolutegravir N = 183

p

Age*

48 (40–54)

48 (43–53)

51 (43–57)

0.008

Male sex

126 (74.1)

95 (67.4)

127 (69.4)

0.399

Caucasians

157 (92.4)

136 (96.5)

164 (89.6)

0.165

HIV risk factor

0.043

 Heterosexual

74 (43.5)

68 (48.2)

83 (45.4)

 

 MSM

84 (49.4)

49 (34.8)

80 (43.7)

 

 IDUs

11 (6.5)

24 (17.0)

19 (10.4)

 

 Other

1 (0.6)

0

1 (0.5)

 

CDC stage C

48 (28.2)

34 (24.1)

53 (29.0)

0.592

HCV positive serostatus

18 (10.6)

25 (17.7)

26 (14.2)

0.193

Nadir CD4 count (cells/μL)*

219 (64–311)

194 (62–293)

194 (64–284)

0.741

Zenith HIV-RNA (log10 copies/mL)*

4.90 (4.36–5.40)

5.02 (4.48–5.39)

4.93 (4.34–5.40)

0.687

CD4 count at baseline (cells/μL)*

617 (484–793)

616 (509–786)

630 (500–800)

0.671

Years since HIV diagnosis*

9 (5–17)

11 (4–18)

14 (8–20)

< 0.001

Years on antiretroviral therapy*

8 (3–14)

7 (3–13)

12 (5–18)

< 0.001

Previous virological failure

91 (53.5)

78 (55.3)

94 (51.4)

0.775

Previous M184 V resistance mutation

22 (12.9)

17 (12.1)

16 (8.7)

0.419

Years of viral suppression at baseline*

5 (2–8)

4 (2–7)

8 (4–11)

< 0.001

Previous regimen:

< 0.001

 2NRTI + bPI

80 (47.1)

125 (88.7)

14 (7.7)

 2NRTI + NNRTI

20 (11.8)

4 (2.8)

34 (18.6)

 2NRTI + INI

24 (14.1)

1 (0.7)

32 (17.5)

Two-drug regimen

34 (20.0)

8 (5.7)

99 (54.1)

 - Lamivudine plus bPI

32 (18.8)

8 (5.7)

89 (48.6)

 - bPI plus NNRTI, InSTI or MVC

2 (1.2)

0 (0)

6 (3.3)

 - Other regimen

0 (0)

0 (0)

4 (2.2)

Other

12 (7.1)

3 (2.1)

4 (2.2)

TDF in previous regimen

97 (57.1)

119 (84.4)

65 (35.5)

< 0.001

Reasons for switch to dual regimen:

< 0.001

 Simplification

86 (50.6)

100 (70.9)

57 (31.1)

 Dyslipidemia

8 (4.7)

7 (5.0)

60 (32.8)

 GI toxicity

4 (2.4)

2 (1.4)

13 (7.1)

 Liver toxicity

11 (6.5)

0

4 (2.2)

 Renal toxicity

28 (16.5)

12 (8.5)

15 (8.2)

 Bone toxicity

3 (1.8)

3 (2.1)

12 (6.6)

 CNS toxicity

1 (0.6)

0

3 (1.6)

 Other toxicity

14 (8.2)

4 (2.8)

7 (3.8)

 DDI

2 (1.2)

0

6 (3.3)

 Other

13 (7.6)

13 (9.2)

6 (3.3)

 Years on previous regimen*

2 (1–4)

3 (1–5)

2 (1–3)

0.530

Study period:

< 0.001

 2008–2013

37 (21.8)

88 (62.4)

0

 2013–2014

91 (53.5)

33 (23.4)

0

 2014–2015

34 (20.0)

12 (8.5)

77 (42.1)

 2015–2017

8 (4.7)

8 (5.7)

106 (57.9)

  1. Note: bPI boosted protease inhibitor, TDF tenofovir, MVC maraviroc, GI gastrointestinal, CNS central nervous system, DDI drug-drug interaction
  2. *Continuous variables (interquantile range)