Suppr超能文献

神经认知障碍是HIV感染患者死亡的独立危险因素。圣地亚哥HIV神经行为研究中心团队。

Neurocognitive impairment is an independent risk factor for death in HIV infection. San Diego HIV Neurobehavioral Research Center Group.

作者信息

Ellis R J, Deutsch R, Heaton R K, Marcotte T D, McCutchan J A, Nelson J A, Abramson I, Thal L J, Atkinson J H, Wallace M R, Grant I

机构信息

Department of Neurosciences, University of California, Department of Medicine, San Diego, USA.

出版信息

Arch Neurol. 1997 Apr;54(4):416-24. doi: 10.1001/archneur.1997.00550160054016.

Abstract

OBJECTIVE

To determine if mortality is increased in individuals with human immunodeficiency virus type 1 (HIV-1)-associated neurocognitive disorders less severe than frank dementia.

DESIGN

A prospective cohort study; median duration of follow-up was 2.4 years. Kaplan-Meier analysis and Cox proportional hazards models were used to compare survival times according to neurocognitive classification.

SETTING

University-based research unit.

PARTICIPANTS

A volunteer sample of 414 individuals seropositive for HIV-1. Subjects were classified at their baseline evaluation as neuropsychologically (NP) normal or abnormal (impaired in > or = 2 NP test domains). A subgroup of NP abnormal subjects met operational criteria for HIV-associated minor cognitive motor disorder; the remaining subjects were designated NP impaired. Subjects with frank dementia were excluded.

MAIN OUTCOME MEASURE

Mortality.

RESULTS

At the baseline evaluation, 256 (62%) of 414 subjects were designated normal; 109 (26%). NP impaired; and 49 (12%), minor cognitive motor disorder. One hundred six participants (26%) died during follow-up. Compared with the NP normal group, the unadjusted relative risk (RR) of death for all NP abnormal subjects (minor cognitive motor disorder and NP impaired) was significantly increased (RR, 1.7; 95% confidence interval [CI], 1.2-2.6; P < .005). After adjusting for concurrently measured predictors of survival (CD4 lymphocyte counts, Centers for Disease Control and Prevention HIV disease classification, hemoglobin concentration, and serum beta 2-microglobulin) in proportional hazards models, mortality for all NP abnormal subjects remained elevated (RR, 1.8; 95% CI, 1.2-2.8; P < .01). The elevation in mortality risk for subjects with minor cognitive motor disorder was statistically significant (RR, 2.2; 95% CI, 1.2-3.8; P < .01); for NP impaired subjects it was marginally significant (RR, 1.6; 95% CI, 1.0-2.8; P = .06).

CONCLUSIONS

The HIV-infected individuals with NP impairment had a higher risk of dying than those without impairment. This was particularly true for those meeting syndromic diagnostic criteria.

摘要

目的

确定1型人类免疫缺陷病毒(HIV-1)相关神经认知障碍程度低于明显痴呆的个体死亡率是否增加。

设计

一项前瞻性队列研究;随访中位时间为2.4年。采用Kaplan-Meier分析和Cox比例风险模型,根据神经认知分类比较生存时间。

地点

大学研究单位。

参与者

414名HIV-1血清学阳性个体的志愿者样本。受试者在基线评估时被分类为神经心理学(NP)正常或异常(在≥2个NP测试领域受损)。NP异常受试者的一个亚组符合HIV相关轻度认知运动障碍的操作标准;其余受试者被指定为NP受损。排除明显痴呆的受试者。

主要观察指标

死亡率。

结果

在基线评估时,414名受试者中有256名(62%)被指定为正常;109名(26%)NP受损;49名(12%)为轻度认知运动障碍。106名参与者(26%)在随访期间死亡。与NP正常组相比,所有NP异常受试者(轻度认知运动障碍和NP受损)未经调整的死亡相对风险(RR)显著增加(RR,1.7;95%置信区间[CI],1.2 - 2.6;P <.005)。在比例风险模型中对同时测量的生存预测因素(CD4淋巴细胞计数、疾病控制和预防中心HIV疾病分类、血红蛋白浓度和血清β2微球蛋白)进行调整后,所有NP异常受试者的死亡率仍然升高(RR,1.8;95%CI,1.2 - 2.8;P <.01)。轻度认知运动障碍受试者的死亡风险升高具有统计学意义(RR,2.2;95%CI,1.2 - 3.8;P <.01);NP受损受试者的死亡风险升高边缘显著(RR,1.6;95%CI,1.0 - 2.8;P =.06)。

结论

HIV感染且有NP损害的个体比无损害的个体死亡风险更高。对于符合综合征诊断标准的个体尤其如此。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验