4.0 Article

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

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ARCHIVES OF NEUROLOGY
卷 64, 期 9, 页码 1275-1280

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AMER MEDICAL ASSOC
DOI: 10.1001/archneur.64.9.1275

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资金

  1. NCRR NIH HHS [RR14075] Funding Source: Medline
  2. NIMH NIH HHS [P50 MH071702] Funding Source: Medline
  3. NINDS NIH HHS [R01 NS040239, F31 NS054570, F31 NS052126, R01 NS40239] Funding Source: Medline

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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 non-demented 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.

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