Geographical variation in disease progression in HIV-1 seroconverted injecting drug users in europe?

• Published in: International journal of epidemiology Vol. 28; no. 3; pp. 541 - 549
• Main Authors: PRINS, M, BRETTLE, R. P, ROBERTSON, J. R, HERNANDEZ AGUADO, I, BROERS, B, CARRE, N, GOLDBERG, D. J, ZANGERLE, R, COUTINHO, R. A, VAN DEN HOEK, A
• Format: Journal Article
• Language: English
• Published: Oxford Oxford University Press 01-06-1999; Oxford Publishing Limited (England)
• Subjects: Adult; Biological and medical sciences; CD4 Lymphocyte Count; Confounding Factors (Epidemiology); Disease Progression; Europe - epidemiology; Female; HIV Infections - epidemiology; HIV Infections - immunology; HIV Infections - transmission; HIV Seropositivity - immunology; HIV-1 - immunology; Human viral diseases; Humans; Infectious diseases; Male; Medical sciences; Proportional Hazards Models; Substance Abuse, Intravenous - immunology; Viral diseases; Viral diseases of the lymphoid tissue and the blood. Aids; Europe; Human; Immunopathology; Drug addiction; Prevalence; Mortality; AIDS; Immune deficiency; Epidemiology; Infection; Viral disease; Evolution; Public health; Geographical variation
• DOI: 10.1093/ije/28.3.541
• EISSN: 1464-3685
• ISSN: 0300-5771

Human immunodeficiency virus (HIV) disease progression might vary by geographical region due to differences in the spectrum of HIV-related illnesses and (access to) health care. Therefore, the effect of geographical region, next to the effect of other potential cofactors, on disease progression in 664 injecting drug users (IDU) with documented HIV seroconversion from eight cohorts in Europe was studied.
Kaplan-Meier methods and Cox proportional hazards analysis were performed to assess the effect of geographical region, other sociodemographics, drug use and repeated HIV exposure on progression from HIV seroconversion to immunosuppression, AIDS and death with AIDS. We considered the confounding effect of study-design related factors (e.g. setting of follow-up), and accounted for pre-AIDS death from natural causes by imputing when each endpoint would have occurred, had they not died without AIDS.
Estimates of progression to AIDS and death with AIDS were substantially faster after taking pre-AIDS mortality into account. Median incubation time from seroconversion to the first CD4 count < 200 cells/microliter was 7.7 years (95% CI: 7.1-8.3) and to AIDS 10.4 years (95% CI: 9.8-infinity). The 10-year survival was 70.3% (95% CI: 62.8-76.6). The relative hazards (RH) of AIDS for IDU from central and southern Europe compared with IDU from northern Europe was 1.9 (95% CI: 1.2-3.0) and 1.2 (95% CI: 0.6-2.3), respectively, before, and 1.5 (95% CI: 0.7-3.2) and 1.1 (95% CI: 0.6-2.3) after taking differences in study-design related factors into account. Accounting for these factors, the RH of death with AIDS was 0.9 (95% CI: 0.3-2.5) for central and 1.2 (95% CI: 0.4-3.4) for southern Europe compared with northern Europe. For the first CD4 count < 200 cells/microliter these figures were 0.8 (95% CI: 0.5-1.4) and 0.8 (95% CI: 0.5-1.4). Age at seroconversion was the strongest predictor of disease progression. No statistically significant differences in disease progression were found by gender, foreign nationality, drug use and potential repeated HIV exposure.
We found no evidence for regional variability in HIV disease progression among European IDU. Future studies evaluating geographical differences should consider the confounding effect of study-design related factors and differential non-AIDS mortality. As age is an important determinant of disease progression, it should be considered in recommending treatment.