To investigate the causal pathways by which age and the CCR5-Δ32, CCR2-64I, and SDF-1 3′A alleles influence progression to AIDS.Design:
Analysis of follow-up data from 2 cohort studies among homosexual men (n = 400), having >10 years of follow-up.Methods:
The effects of the 4 cofactors on the CD4 and HIV-1 RNA trajectories after seroconversion were modeled in a random-effects model. A proportional hazards model was used to investigate their effect on the risk of AIDS after correction for CD4 cell count and RNA level. This approach allows investigation as to whether they influence AIDS progression by affecting CD4 count and RNA level or by other pathways.Results:
Persons of younger age or having the CCR2-64I or SDF-1 3′A mutation have significantly higher CD4 levels. Persons with the CCR5-Δ32 deletion or CCR2-64I mutation have significantly lower RNA levels. After correction for both CD4 count and RNA level, only the SDF-1 3′A mutation significantly increases the AIDS risk.Conclusions:
Age and the CCR5-Δ32 deletion and CCR2-64I mutation influence AIDS progression by affecting CD4 and HIV-1 RNA. The SDF-1 3′A allele increases the AIDS risk, but this effect is countered by its effect on CD4 and HIV-1 RNA level.