In 6 months, the probability of remaining in state 1 is about 0.20. The chances of being in the other states as HPV status changes and/or VL decreases are: 0.08 for HPV positive

and VL > 400 copies/mL (state 2); 0.60 for HPV negative and VL < 400 copies/mL (state 3) and 0.12 for HPV positive and VL < 400 copies/mL (state 4). The probabilities stabilize in about 2.5 years to around 0.11, 0.08, 0.58 and 0.23 for the four states, respectively. They suggest that, whereas the probabilities of being HPV positive and HPV negative are similar when VL > 400 copies/mL (at around 0.10), the probability of being HPV positive is about 0.4 times the probability of being HPV negative when VL ≤ 400 copies/mL. There were 145 subjects included in this analysis, because two of the subjects did BTK inhibitor price not provide CD4 cell counts. Of the 140 subjects with both HPV and CD4 results at baseline, 107 subjects (76%) started with a CD4 count <350 cells/μL, and HPV was detected in 86 subjects (61%). Data availability trends over time were similar to those for the VL model above. In the CD4 model (Fig. 1b), similar conclusions were drawn for the two HPV sets (set 2 results are shown). Comparison between γ21 and γ43 suggested that a woman with a current CD4 count >350 cells/μL was more likely to clear HPV than a woman with a CD4 count ≤ 350 cells/μL

(hazard ratio γ43/γ21 = 2.65; P = 0.018). The statistical tests on other comparisons were not significant. There was no evidence that HPV detection rates differed between Ganetespib order subjects with CD4 counts ≤350 and >350 cells/μL (γ12/γ34 = 1.03; P = 0.94), and HPV status did not seem to affect CD4 state transition rates (γ13/γ24 = 0.920; P = 0.78; γ31/γ42 = 0.408; P = 0.18). Figure 2b presents the model-based probability curves over 5 years for a HAART-initiating woman,

starting as HPV negative and with a CD4 count ≤350 cells/μL (state 1). The probabilities stabilize in about 3.5 years to around 0.12 in state 1, 0.11 in state 2 (HPV positive and CD4 count ≤350 cells/μL), 0.56 in state 3 (HPV negative and CD4 count >350 cells/μL) and 0.21 in state 4 (HPV positive and CD4 count >350 cells/μL). The probability of being HPV positive is about 0.4 times the probability Dichloromethane dehalogenase of being HPV negative when the CD4 count is >350 cells/μL. Studies have shown varying effects of HAART on HPV infection and HPV-related cervical dysplasia. Several studies have shown a higher HPV prevalence in women with a lower CD4 cell count and higher likelihood of clearance of HPV with improved CD4 cell count [9, 13, 14]. Research on the association between HIV VL and HPV detection has been limited. One study showed that HIV VL and CD4 cell count in combination appeared to be associated with HPV detection, with varying effects of HIV RNA level on HPV prevalence and incident detection depending on the CD4 cell count stratum [4].