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250名HIV-1血清阳性受试者队列中的临床和生物学进展精算率。拉埃内克HIV研究小组。

Actuarial rate of clinical and biological progression in a cohort of 250 HIV-1-seropositive subjects. Laennec HIV Study Group.

作者信息

Venet A, Tourani J M, Beldjord K, Eme D, Even P, Andrieu J M

出版信息

Clin Exp Immunol. 1990 May;80(2):151-5. doi: 10.1111/j.1365-2249.1990.tb05224.x.

Abstract

This study was undertaken to define the risk of AIDS in a cohort of 250 HIV-seropositive patients identified by their clinical and biological status. All patients were enrolled between October 1985 and March 1988. They were classified according to clinical classes A, asymptomatic (n = 97); B, lymphadenopathic (n = 123); and C, AIDS-related complex, (n = 30). Also as CD4 cell stages 1 (CD4 greater than or equal to 600/microliters; n = 126); 2 (CD4 less than 600 and greater than or equal to 300/microliters; n = 83); and 3 (CD4 less than 300/microliters; n = 41); and serum p24 antigen positive (n = 48) or negative (n = 202). All patients were evaluated every 3-6 months, until AIDS development or April 1989: 29 cases of AIDS occurred during the follow-up period. The risk of AIDS in class C is very high (64% at 2 years) compared with the 3-year risk of classes A (13%) and B (25%). On the other hand the three CD4 stages have significantly different prognosis (stage 1 6%; stage 2 22%; and stage 3 89%; P less than 10(-2]. Antigen p24 negative and positive patients have also different prognosis (18% and 53%; P less than 10(-4]. Interestingly, p24 antigen conserved its prognostic value in stage 2 (positive 37%, negative 16%) while stages 1 are at low risk of AIDS and stages 3 at high risk whatever their p24 antigen status. We have also identified the risk of becoming stage 3 and/or p24 antigen positive in p24 antigen negative patients at stages 1 and 2 (respectively, 18% and 47%). This classification should serve to design randomized trials better with experimental drugs with earlier end-points than AIDS onset.

摘要

本研究旨在确定一组250例根据临床和生物学状况确诊为HIV血清阳性患者的艾滋病风险。所有患者均于1985年10月至1988年3月期间入组。他们根据临床分级进行分类:A类,无症状(n = 97);B类,淋巴结病(n = 123);C类,艾滋病相关综合征(n = 30)。同时还分为CD4细胞阶段1(CD4大于或等于600/微升;n = 126);2(CD4小于600且大于或等于300/微升;n = 83);3(CD4小于300/微升;n = 41);以及血清p24抗原阳性(n = 48)或阴性(n = 202)。所有患者每3 - 6个月评估一次,直至发生艾滋病或1989年4月:随访期间有29例发生艾滋病。与A类(13%)和B类(25%)的3年风险相比,C类的艾滋病风险非常高(2年时为64%)。另一方面,三个CD4阶段的预后有显著差异(阶段1为6%;阶段2为22%;阶段3为89%;P小于10⁻²)。抗原p24阴性和阳性患者的预后也不同(分别为18%和53%;P小于10⁻⁴)。有趣的是,p24抗原在阶段2保留了其预后价值(阳性为37%,阴性为16%),而阶段1无论其p24抗原状态如何,艾滋病风险都较低,阶段3则无论p24抗原状态如何,风险都较高。我们还确定了阶段1和2的p24抗原阴性患者变为阶段3和/或p24抗原阳性的风险(分别为18%和47%)。这种分类应有助于更好地设计随机试验,使用比艾滋病发病更早的终点的实验药物。

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本文引用的文献

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Persistent HIV antigenaemia and decline of HIV core antibodies associated with transition to AIDS.
Br Med J (Clin Res Ed). 1986 Dec 6;293(6560):1459-62. doi: 10.1136/bmj.293.6560.1459.
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Incubation period of AIDS in San Francisco.
Nature. 1989 Mar 16;338(6212):251-3. doi: 10.1038/338251a0.

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