HIV-1 RNA levels and the development of clinical disease

被引:70
作者
Phillips, AN
Eron, JJ
Bartlett, JA
Rubin, M
Johnson, J
Price, S
Self, P
Hill, AM
Akil, B
Beall, G
Bellos, N
Berry, P
Brummit, C
Cameron, B
Cohen, C
Donabedian, H
Mayar, K
McKinley, G
Sepulveda, G
Thompson, M
Tsoukas, C
Walmsley, S
Horton, J
Kerkering, T
Matthew, E
Pearce, D
Peterson, D
Pottage, J
Sampson, J
Smith, W
Yangco, B
Cowan, J
Kaczka, C
Zameck, R
Dawson, D
Pobiner, B
Gilbert, C
ScottLennox, J
DeMasi, R
Jarrett, P
Yuen, G
Esinhart, J
Quinn, J
Fallon, MA
Benoit, S
机构
[1] GLAXO WELLCOME,ANTIVIRAL CLIN RES,RES TRIANGLE PK,NC 27709
[2] UNIV LONDON,ROYAL FREE HOSP,SCH MED,HIV RES UNIT,DEPT PRIMARY CARE & POPULAT SCI,LONDON NW3 2PF,ENGLAND
[3] UNIV N CAROLINA,SCH MED,DEPT MED,DIV INFECT DIS,CHAPEL HILL,NC
[4] DUKE UNIV,MED CTR,DURHAM,NC
[5] GLAXO WELLCOME UK,DEPT MED STAT,GREENFORD,MIDDX,ENGLAND
关键词
viral load; HIV RNA; AIDS; CD4 lymphocyte count;
D O I
10.1097/00002030-199607000-00009
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 assess the prognostic value of HIV RNA levels for predicting clinical disease independently of the CD4 lymphocyte count in patients on antiretroviral therapy. Design: Cohort of HIV-infected patients from two trials of lamivudine therapy. Patients: For 620 patients randomized in the North American NUCA3001 and NUCA3002 trials of lamivudine, HIV RNA levels were measured (median, seven measures per patient) and CD4 counts were assessed at a central laboratory (median, 13 counts per patient). Patients were in the 1993 Centers for Disease Control and Prevention (CDC) stages A (n = 439), B (n = 135) or C (n = 46) at baseline. Outcome measures: For patients who were in CDC stage A at baseline we considered the ability of HIV RNA levels and CD4 counts to predict the development of CDC stage B or C disease. A Cox proportional hazards model was used. In a second analysis, patients who were AIDS-free at baseline were considered, and the endpoint was AIDS (CDC stage C). Results: Patients' initial CD4 counts ranged (5-95% centiles) from 104 to 529x10(6)/l (median, 274x10(6)/l) and HIV RNA levels from 1 900 to 339 680 copies/ml (median, 44 240 copies/ml). For the first analysis, with CDC stage B or C disease as endpoint, both the most recent HIV RNA level and CD4 count predicted the development of clinical disease [relative hazard (RH) for HIV RNA, 1.96 per 10-fold difference in HIV RNA; 95% confidence interval (CI), 1.41-2.73; P=0.0001; and RH for CD4 count, 1.82 per twofold difference in CD4 count; 95% CI, 1.27-2.56; P=0.0009]. When both HIV RNA and CD4 count were included in a multiple regression model, both markers provided information additional to that given by the other (RH for HIV RNA, 1.75; 95% CI, 1.23-2.50; P=0.002; and RH for CD4 count, 1.40; 95% CI, 0.95-2.07; P=0.09). In the second analysis, with AIDS as endpoint, both HIV RNA level (P=0.02) and CD4 count (P=0.004) were independently associated with clinical progression. These results were essentially unchanged after adjustment for treatment arm (zidovudine/lamivudine versus control arms). Conclusion: The HIV RNA level shows ability to predict the development of clinical disease and may thus be of importance in addition to the CD4 count in patient monitoring.
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收藏
页码:859 / 865
页数:7
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