Objectives
Certain prescribed opioids have immunosuppressive properties, yet their impact on clinically relevant outcomes, including antiretroviral therapy (ART) response among HIV-infected patients, remains understudied.
Methods
Using the Veterans Aging Cohort Study data, we conducted a longitudinal analysis of 4,358 HIV-infected patients initiating ART between 2002 and 2010 and then followed them for 24 months. The primary independent variable was prescribed opioid duration, categorized using pharmacy data as none prescribed, short-term (<90 days), and long-term (≥90 days). Outcomes included CD4 cell count over time. Analyses adjusted for demographics, comorbid conditions, ART type and year of initiation, and overall disease severity (ascertained with the VACS index). Sensitivity analyses examined whether effects varied according to baseline CD4 cell count, achievement of viral load suppression, and opioid properties (i.e., dose and known immunosuppressive properties).
Results
Compared to those with none, patients with short-term prescribed opioids had a similar increase in CD4 cell count (rise per year: 74 vs. 68 cells/mm3, p=0.11), as did those with long-term prescribed opioids (rise per year: 74 vs. 75 cells/mm3, p=0.98). In sensitivity analysis, compared to those with none, short-term prescribed opioid effects were statistically significant among those with baseline CD4 cell count ≥500 cells/mm3 (rise per year: 52 vs. 20 cells/mm3, p=0.04); findings were otherwise unchanged.
Conclusions
Despite immunosuppressive properties intrinsic to opioids, prescribed opioids appeared to have no effect on CD4 cell counts over 24 months among HIV-infected patients initiating antiretroviral therapy.