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. Author manuscript; available in PMC: 2016 Jan 1.
Published in final edited form as: JAMA Intern Med. 2015 Jan 1;175(1):88–99. doi: 10.1001/jamainternmed.2014.4010

Table 2.

Rate of Achieving CD4+ T-Cell Count Normalization

Model Rate Ratio
(95% CI)a
P Value
Univariate
 Sex, female vs male 1.18 (0.73–1.89) .51
 Ethnicity
  African American vs European American 0.92 (0.73–1.15) .44
  Other vs European American 0.80 (0.56–1.14) .22
 Age at ART initiation, each increase of 1 y 1.00 (0.99–1.02) .86
 Time from EDS to ART initiation, ≤12 vs>12 mo 1.53 (1.22–1.91) <.001
 Time from entry to ART initiation, ≤12 vs >12 mo 1.51 (1.21–1.89) <.001
 Study entry CD4+, ≥500 vs <500 cells/μL 2.45 (1.98–3.05) <.001
 Pre-ART CD4+, each increase of 10 cells 1.06 (1.05–1.06) <.001
 Pre-ART CD4+, ≥500 vs <500 cells/μL 5.91 (4.77–7.32) <.001
 Pre-ART viral load, each increase of 1 log10 copies/mL 1.05 (0.90–1.21) .57
 Calendar year of ART initiation, each increase of 1 y 1.06 (1.04–1.09) <.001
 Antiretroviral regimenb
  PI-based vs NNRTI-based 1.39 (1.06–1.82) .02
  Other vs NNRTI-based 0.61 (0.47–0.80) <.001
  Other vs PI-based 0.44 (0.34–0.57) <.001
 Duration of VL-suppressive ART, each increase of 1 yc 0.88 (0.84–0.92) <.001
 Time from ART initiation to VL suppression, each increase of 1 mo 0.98 (0.97–0.98) <.001
Multivariated
 Model1: time from EDS to ART initiation, ≤12 vs>12 mo 1.32 (1.04–1.67) .02
 Model 2: time from study entry to ART initiation, ≤12 vs >12 mo 1.77 (1.38–2.26) <.001
 Model 3: study entry CD4+, ≥500 vs <500 cells/μL 2.00 (1.51–2.64) <.001
 Model 4: pre-ART CD4+, ≥500 vs <500 cells/μL 4.08 (3.14–5.30) <.001

Abbreviations: ART, antiretroviral therapy; EDS, estimated date of seroconversion; NNRTI, nonnucleoside reverse transcriptase inhibitor; PI, protease inhibitor; VL, viral load.

a

The Cox proportional hazards model was used to estimate the rate ratio for achievement of the first CD4+ count of 900 cells/μL or more after ART initiation.

b

PI-based was defined as PI therapy without any NNRTI, NNRTI-based was defined as NNRTI therapy without any PI, and the other treatment options were a combination of PI and NNRTI therapy or neither of these drug classes.

c

Duration of VL-suppressive ART was indexed from the date of starting ART.

d

The covariates adjusted for in models 1 and 2 were study entry CD4+ counts 500 cells/μL or more or less than 500 cells/μL, pre-ART CD4+ count 500 cells/μL or more or less than 500 cells/μL, calendar year of ART initiation, ART regimen, length of follow-up (years), and duration of VL-suppressive ART. The covariates adjusted for in model 3 were pre-ART CD4+ counts 500 cells/μL or more or less than 500 cells/μL, and time from study entry to ART initiation within 12 months or more than 12 months, calendar year of ART initiation, ART regimen, length of follow-up (years), and duration of VL-suppressive ART. Similar results were found when the model was adjusted for time from EDS to ART initiation within 12 months or more than 12 months instead of time from entry to ART. The covariates adjusted for in model 4 were study entry CD4+ counts 500 cells/μL or more or less than 500 cells/μL; time from study entry to ART initiation within 12 months or more than 12 months, calendar year of ART initiation, ART regimen, length of follow-up (years), and duration of VL-suppressive ART. Similar results were found when the model was adjusted for time from EDS to ART initiation within 12 months or more than 12 months instead of time from entry to ART.