Kaposi's sarcoma and human herpesvirus 8 infection do not protect HIV-1 infected homosexual men from AIDS dementia complex

被引:4
|
作者
Renwick, N
Weverling, GJ
Halaby, T
Portegies, P
Bakker, M
Schulz, TF
Goudsmit, J
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Human Retrovirol, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Clin Epidemiol & Biostat, NL-1105 AZ Amsterdam, Netherlands
[3] Univ Limburg, Acad Hosp Maastricht, Dept Med Microbiol, Maastricht, Netherlands
[4] Univ Amsterdam, Acad Med Ctr, Dept Neurol, NL-1105 AZ Amsterdam, Netherlands
[5] Hannover Med Sch, Dept Virol, Hannover, Germany
关键词
AIDS dementia complex; epidemiology; HHV8; KSHV; Kaposi's sarcoma; risk;
D O I
10.1097/00002030-200111090-00012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To examine the association between Kaposi's sarcoma (KS), human herpes virus 8 (HHV8) and AIDS dementia complex (ADC). Design: A total of 599 HIV-1 infected homosexual men participated in a prospective cohort study (Amsterdam, 1984-1996). Methods: The risk for ADC in patients with prior KS or HHV8 infection was estimated using the Cox proportional hazards method with adjustments for antiretroviral medication and low CD4 cell counts. Results: Of the 599 participants, 290 (48.4%) had HHV8 antibodies, 99 (16.5%) had KS and 30 (5.0%) had ADC. ADC was diagnosed in 5.2% of participants with KS and 5.0% of those without KS, and in 4.8% of HHV8 seropositive compared to 5.2% seronegative individuals and thus was not associated with KS or HHV8 infection. Using a time-dependent Cox proportional hazards analysis with the date of KS as risk factor, the risk for ADC was 2.7 (95% confidence interval (CI), 0.92-7.96; P=0.07) and when only definite ADC was considered it was 3.5 (95% CI, 1.00-12.26; P=0.05). After adjusting for decreases in CD4 cell count and use of medication, the hazards ratio for participants with KS to develop ADC was 2.0 (95% CI, 0.66-5.77; P=0.23) and 2.6 (95% Cl, 0.73-9.12; P=0.14), respectively. HHV8 seropositivity, adjusted for the same variables, showed a risk for ADC of 0.85 (95% Cl, 0.41-1.77; P=0.66) and for definite ADC 0.69 (95% Cl, 0.27-1.73; P=0.42). The expected neuroprotective effects of antiretroviral medication were observed. Conclusions: KS or HHV8 does not significantly influence the risk for developing ADC in a group with a uniform risk for developing KS therefore we recommend caution in searching for a KS-associated or HHV8-derived therapy for ADC. (C) 2001 Lippincott Williams & Wilkins.
引用
收藏
页码:2165 / 2169
页数:5
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