Skip to main content
. Author manuscript; available in PMC: 2010 Jul 3.
Published in final edited form as: AIDS. 2009 Jun 1;23(9):1127–1134. doi: 10.1097/QAD.0b013e32832ac34e

Table 3.

Univariate and multivariate logistic modeling of three potential outcomes for emergence of resistance among patients failing antiretroviral therapy based on clinical or immunological criteria in Malawi.

Outcome of interest At least three TAMs
K65R or K70 E tenofovir-associated mutations
Pan-nucleoside resistance Q151M and tenofovir mutations or 69 insertion
Univariate Multivariatea Univariate Multivariatea Univariate Multivariatea
CD4 cell count (cells/μl)
 >100 1.0 1.0 1.0 1.0 1.0 1.0
 100 or less 3.9 (1.2–12.6) 5.57 (1.41–22.02) 5.4 (1.5–19.7) 6.1 (1.47–25.0) 12.2 (1.5–97.0) 9.9 (1.2–84.0)
ZDV use
 No 1.0 1.0 1.0 1.0 1.0 1.0
 Yes 2.3 (0.85–6.05) 3.4 (1.07–10.97) 0.18 (0.04–0.81) 0.18 (0.04–0.94) 0.12 (0.015–0.93) 0.13 (0.02–1.07)

Data are given as odds ratio (95% confidence interval). Outcomes include having at least three TAMs, the development of tenofovir-associated mutations (K65R or K70E) or expected pan-nucleoside resistance mutation (Q151M with K65R or K70E mutations or the 69 insertion). ART, antiretroviral therapy; TAM, thymidine analog mutations; ZDV, zidovudine.

a

Adjusted for HIV-1 RNA (copies/ml), clinical failure, clinic site, and sex. Duration of ART was not considered because of colinearity with the use of zidovudine.

HHS Vulnerability Disclosure