Association of virus load, CD4 cell count, and treatment with clinical progression in human immunodeficiency virus-infected patients with very low CD4 cell counts

被引:51
作者
Miller, V
Phillips, AN
Clotet, B
Mocroft, A
Ledergerber, B
Kirk, O
Ormaasen, V
Gargalianos-Kakolyris, P
Vella, S
Lundgren, JD
机构
[1] Univ Frankfurt Klinikum, Zentrum Inneren Med, D-6000 Frankfurt, Germany
[2] UCL Royal Free & Univ Coll Med Sch, Royal Free Ctr HIV Med, London, England
[3] UCL Royal Free & Univ Coll Med Sch, Dept Primary Care & Populat Sci, London, England
[4] Hosp Badalona Germans Trias & Pujol, Fdn Caixa, Barcelona, Spain
[5] Univ Zurich Hosp, Div Infect Dis, Zurich, Switzerland
[6] Univ Copenhagen, Hvidovre Hosp, DK-1168 Copenhagen, Denmark
[7] Ulleval Hosp, Dept Infect Dis, Oslo, Norway
[8] Gen Hosp Athens, Dept Med 1, Special Infect Unit, Athens, Greece
[9] Inst Super Sanita, Virol Lab, Rome, Italy
关键词
D O I
10.1086/341466
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
This study prospectively assessed the impact of treatment modality, virus load, and CD4 cell count of <50 cells/mm(3) on human immunodeficiency virus disease progression. The incidence rate of new AIDS disease or death was 54.8 (95% confidence interval, 48.7-59.9) per 100 person-years of follow-up. Independent predictors related to progression were latest CD4 cell count (relative risk [RR], 0.84/10 mm(3) higher; P < .0001), latest hemoglobin level (RR, P 0.79/ g/L higher; P < .0001), Pneumocystis carinii pneumonia prophylaxis (RR, 0.49; P <.0001), latest body mass index (RR, 0.93/kg/m(2) higher; P = .002), latest virus load (RR, 1.11/ log(10) higher; P = .03), and intensity of treatment (RR, 1.82, P = .004; RR 2.27, P < .0001;RR 2.46, P = .0001; RR 2.33 P < .0006; 5.10, P < .0001, respectively, for 4, 3, 2, 1, or no drugs vs. >= 5 drugs). Although reverse causality cannot be excluded, more intense antiviral treatment appears to decrease the risk of progression in immunocompromised patients.
引用
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页码:189 / 197
页数:9
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