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皮质和皮质下神经变性与HIV神经认知障碍有关。

Cortical and subcortical neurodegeneration is associated with HIV neurocognitive impairment.

作者信息

Moore David J, Masliah Eliezer, Rippeth Julie D, Gonzalez Raul, Carey Catherine L, Cherner Mariana, Ellis Ronald J, Achim Cristian L, Marcotte Thomas D, Heaton Robert K, Grant Igor

机构信息

HIV Neurobehavioral Research Center and University of California, San Diego, California 92161, USA.

出版信息

AIDS. 2006 Apr 4;20(6):879-87. doi: 10.1097/01.aids.0000218552.69834.00.

Abstract

OBJECTIVE

To determine the association of markers of regional neurodegeneration (ND) at autopsy to degree of neurocognitive impairment in persons with HIV.

DESIGN

In a prospectively followed cohort of HIV-infected individuals we examined the relationship between antemortem neuropsychological (NP) abilities and postmortem neuropathological data.

METHODS

Twenty-seven HIV-infected individuals with both neuropsychological and neuropathological data were identified. Laser confocal scanning microscopy was used to determine the degree of ND based on: (1) microtubule-associated protein (MAP2; reflecting neuronal cell bodies and dendrites) and (2) synaptophysin (SYN; a measure of presynaptic terminals). A regional combined score, based on the distribution of percentage neuropil occupied by MAP2 and SYN and emphasizing severity of ND, was created for each brain region: midfrontal cortex, hippocampus, and putamen.

RESULTS

The regional combined scores from each brain region studied were better correlated with level of global NP impairment than measures of SYN and MAP2 individually. In a regression, hippocampal and putamen regional combined scores were independent predictors of degree of antemortem NP impairment (F(3,23) = 6.17; P < 0.01; R2 = 0.45). The correlations among regional ND measures demonstrated that ND is unevenly distributed across multiple brain regions.

CONCLUSIONS

As the anatomic distribution and temporal progression of neuropathologic changes appears to differ across individuals, it is important to consider both cortical and subcortical brain regions in studies of neuropathogenesis and treatment of HIV-related brain disease. Furthermore, combining information from several markers of neural injury provided the strongest association with degree of neurocognitive impairment during life.

摘要

目的

确定尸检时区域神经变性(ND)标志物与HIV感染者神经认知障碍程度之间的关联。

设计

在一个前瞻性随访的HIV感染队列中,我们研究了生前神经心理学(NP)能力与死后神经病理学数据之间的关系。

方法

确定了27名同时具有神经心理学和神经病理学数据的HIV感染者。使用激光共聚焦扫描显微镜基于以下因素确定ND程度:(1)微管相关蛋白(MAP2;反映神经元细胞体和树突)和(2)突触素(SYN;突触前终末的一种测量指标)。根据MAP2和SYN所占神经纤维网百分比的分布并强调ND的严重程度,为每个脑区(额中皮质、海马体和壳核)创建一个区域综合评分。

结果

与单独的SYN和MAP2测量指标相比,所研究的每个脑区的区域综合评分与整体NP损伤水平的相关性更好。在一项回归分析中,海马体和壳核区域综合评分是生前NP损伤程度的独立预测指标(F(3,23) = 6.17;P < 0.01;R2 = 0.45)。区域ND测量指标之间的相关性表明,ND在多个脑区的分布不均匀。

结论

由于神经病理变化的解剖分布和时间进程在个体间似乎存在差异,因此在HIV相关脑疾病的神经病理发生机制研究和治疗中,考虑皮质和皮质下脑区都很重要。此外,整合来自多个神经损伤标志物的信息与生命期间神经认知障碍程度的关联最为紧密。

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