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人类免疫缺陷病毒感染且有认知功能损害的非痴呆患者的壳核肥大

Putamen hypertrophy in nondemented patients with human immunodeficiency virus infection and cognitive compromise.

作者信息

Castelo J Mimi Boer, Courtney Maureen G, Melrose Rebecca J, Stern Chantal E

机构信息

Cognitive Neuroimaging Laboratory, Center for Memory and Brain, Boston University, 2 Cummington St, Room 109, Boston, MA 02215, USA.

出版信息

Arch Neurol. 2007 Sep;64(9):1275-80. doi: 10.1001/archneur.64.9.1275.

DOI:10.1001/archneur.64.9.1275
PMID:17846265
Abstract

BACKGROUND

Documented death and dysfunction of basal ganglia cells in patients seropositive for human immunodeficiency virus (HIV) suggest that the virus may cause structural compromise to these regions.

OBJECTIVES

To examine subcortical volumes in nondemented patients seropositive for HIV (HIV+) by means of a novel automated neuroanatomic morphometric analysis tool, and to investigate relationships among cognitive function, immune health, and subcortical volumes.

DESIGN AND SETTING

Cross-sectional study of subcortical morphometry and cognitive function conducted at the Boston University Center for Memory and Brain and the Massachusetts General Hospital Athinoula A. Martinos Center for Biomedical Imaging.

PATIENTS

Twenty-two nondemented HIV+ patients and 22 age- and education-matched healthy control participants.

MAIN OUTCOME MEASURES

Subcortical segmentation volumes, neuropsychological performance, and immunological variables.

RESULTS

Nondemented HIV+ patients demonstrated relative and isolated putamen hypertrophy compared with control participants. Putamen volume enlargement in HIV+ patients was related to motor slowing and immune status, such that higher CD4 lymphocyte levels were associated with larger putamen volumes. There were no other subcortical volume differences between the groups.

CONCLUSIONS

This study suggests that basal ganglia hypertrophy accompanies HIV-related mild cognitive compromise. These findings may represent a structural imaging parallel to functional imaging studies demonstrating basal ganglia hypermetabolism in HIV+ patients with mild cognitive compromise and early HIV-associated brain disease.

摘要

背景

有记录表明,人类免疫缺陷病毒(HIV)血清反应阳性患者的基底神经节细胞出现死亡和功能障碍,这表明该病毒可能会对这些区域造成结构损伤。

目的

通过一种新型的自动神经解剖形态计量分析工具,检查未患痴呆症的HIV血清反应阳性(HIV+)患者的皮质下体积,并研究认知功能、免疫健康和皮质下体积之间的关系。

设计与地点

在波士顿大学记忆与脑中心以及麻省总医院阿西诺拉·A·马尔蒂诺斯生物医学成像中心进行的关于皮质下形态计量学和认知功能的横断面研究。

患者

22名未患痴呆症的HIV+患者以及22名年龄和教育程度相匹配的健康对照参与者。

主要观察指标

皮质下分割体积、神经心理学表现和免疫学变量。

结果

与对照参与者相比,未患痴呆症的HIV+患者表现出相对孤立的壳核肥大。HIV+患者的壳核体积增大与运动迟缓及免疫状态有关,即较高的CD4淋巴细胞水平与较大的壳核体积相关。两组之间在其他皮质下体积方面没有差异。

结论

本研究表明,基底神经节肥大伴随着与HIV相关的轻度认知损害。这些发现可能代表了一种结构成像,与功能成像研究平行,后者显示了轻度认知损害的HIV+患者和早期HIV相关脑疾病患者的基底神经节代谢亢进。

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