Portegies P, de Gans J, Lange J M, Derix M M, Speelman H, Bakker M, Danner S A, Goudsmit J
Academic Medical Centre, University of Amsterdam, The Netherlands.
BMJ. 1989 Sep 30;299(6703):819-21. doi: 10.1136/bmj.299.6703.819.
To assess the incidence of the AIDS dementia complex and the presence of HIV I p24 antigen in cerebrospinal fluid in relation to zidovudine treatment.
Retrospective study of a consecutive series of patients with AIDS from 1982 to 1988.
An academic centre for AIDS.
196 Patients with AIDS and neurological symptoms examined from 1982 to 1988.
Zidovudine treatment, which was introduced to The Netherlands on 1 May 1987 for patients with severe symptoms of HIV infection (Centers for Disease Control groups IVA, B, C, and D).
Diagnosis of AIDS dementia complex and presence of HIV I p24 antigen in cerebrospinal fluid.
The AIDS dementia complex was diagnosed in 40 of the 196 (20%) patients with AIDS. Thirty eight of 107 patients with AIDS (36%) not taking zidovudine developed the AIDS dementia complex compared with two of the 89 (2%) taking the drug (p less than 0.00001). The incidence of the AIDS dementia complex increased to 53% in the first half of 1987, after the introduction of zidovudine in May 1987, decreasing to 10% in the second half of 1987 and to 3% in 1988. Dementia was diagnosed before definition of the AIDS dementia complex (1986) according to DSM-III criteria and there was good agreement between diagnosis before and after 1986. Sixteen of 61 samples of cerebrospinal fluid (26%) from patients with AIDS (10 with the AIDS dementia complex) not taking zidovudine were positive for HIV I p24 antigen, whereas none of 37 cerebrospinal fluid samples from patients with AIDS (two with the AIDS dementia complex) taking zidovudine were positive.
The incidence of AIDS dementia complex in patients with AIDS declined after the introduction of systematic treatment with zidovudine; the AIDS dementia complex might be prevented by inhibiting viral replication in the central nervous system.
评估艾滋病痴呆综合征的发病率以及脑脊液中HIV I p24抗原的存在情况与齐多夫定治疗的关系。
对1982年至1988年连续一系列艾滋病患者进行回顾性研究。
一个艾滋病学术中心。
196例1982年至1988年期间接受检查的有神经系统症状的艾滋病患者。
齐多夫定治疗,1987年5月1日引入荷兰,用于有严重HIV感染症状的患者(疾病控制中心IVA、B、C和D组)。
艾滋病痴呆综合征的诊断以及脑脊液中HIV I p24抗原的存在情况。
196例艾滋病患者中有40例(20%)被诊断为艾滋病痴呆综合征。107例未服用齐多夫定的艾滋病患者中有38例(36%)出现艾滋病痴呆综合征,而89例服用该药物的患者中有2例(2%)出现该综合征(p<0.00001)。1987年5月引入齐多夫定后,1987年上半年艾滋病痴呆综合征的发病率增至53%,1987年下半年降至10%,1988年降至3%。根据《精神疾病诊断与统计手册》第三版标准,在艾滋病痴呆综合征定义之前(1986年)就诊断出痴呆,1986年前后的诊断结果有很好的一致性。61例未服用齐多夫定的艾滋病患者(10例患有艾滋病痴呆综合征)的脑脊液样本中有16例(26%)HIV I p24抗原呈阳性,而37例服用齐多夫定的艾滋病患者(2例患有艾滋病痴呆综合征)的脑脊液样本中无一例呈阳性。
采用齐多夫定进行系统治疗后,艾滋病患者中艾滋病痴呆综合征的发病率下降;抑制中枢神经系统中的病毒复制可能预防艾滋病痴呆综合征。