Thinning of the cerebral cortex visualized in HIV/AIDS reflects CD4+ T lymphocyte decline

被引:249
作者
Thompson, PM [1 ]
Dutton, RA
Hayashi, KM
Toga, AW
Lopez, OL
Aizenstein, HJ
Becker, JT
机构
[1] Univ Calif Los Angeles, Sch Med, Dept Neurol, Lab Neuro Imaging, Los Angeles, CA 90095 USA
[2] Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Dept Psychiat, Pittsburgh, PA 15213 USA
[4] Univ Pittsburgh, Dept Psychol, Pittsburgh, PA 15213 USA
关键词
brain; MRI; disease; T cell; immunity;
D O I
10.1073/pnas.0502548102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
HIV/AIDS infection is the fourth leading cause of death worldwide, and one in every 100 adults aged 15-49 years is HIV-infected. Forty percent of AIDS patients suffer from neurological symptoms, but the selective profile of damage caused by HIV in the brain is not well understood. Here, we report 3D maps revealing how AIDS affects the human cerebral cortex, identifying the most vulnerable regions and where deficits link with cognitive decline and immune-system suppression. With high-resolution brain MRI scans, we created composite maps of cortical gray-matter thickness in 26 AIDS patients and 14 healthy controls to establish the selective pattern of brain deficits in AIDS. In AIDS, primary sensory, motor, and premotor cortices were 15% thinner. Thinner frontopolar and language cortex correlated with immune system deterioration measured through blood levels of CD4(+) T lymphocytes. Prefrontal and parietal tissue loss correlated with cognitive/motor deficits. T cell depletion and cognitive impairment are, therefore, associated with specific 3D brain-deficit patterns visualized with MRI. These quantitative MRI-based maps reveal that HIV selectively damages the cortex. They provide an approach to gauge the impact of AIDS on the living brain and show that the brain is still vulnerable to infection even when patients are receiving antiretroviral therapy.
引用
收藏
页码:15647 / 15652
页数:6
相关论文
共 30 条
[1]  
[Anonymous], 1992, BRIEF SYMPTOM INVENT
[2]  
[Anonymous], 1992, MMWR-MORBID MORTAL W, V41, P1
[3]   Correlation of in vivo neuroimaging abnormalities with postmortem human immunodeficiency virus encephalitis and dendritic loss [J].
Archibald, SL ;
Masliah, E ;
Fennema-Notestine, C ;
Marcotte, TD ;
Ellis, RJ ;
McCutchan, JA ;
Heaton, RK ;
Grant, I ;
Mallory, M ;
Miller, A ;
Jernigan, TL .
ARCHIVES OF NEUROLOGY, 2004, 61 (03) :369-376
[4]  
Becker JT, 2004, AIDS, V18, pS11, DOI 10.1097/00002030-200401001-00003
[5]   Neurocognitive dysfunction predicts postmortem findings of HIV encephalitis [J].
Cherner, M ;
Masliah, E ;
Ellis, RJ ;
Marcotte, TD ;
Moore, DJ ;
Grant, I ;
Heaton, RK .
NEUROLOGY, 2002, 59 (10) :1563-1567
[6]   THE NEUROPSYCHIATRIC INVENTORY - COMPREHENSIVE ASSESSMENT OF PSYCHOPATHOLOGY IN DEMENTIA [J].
CUMMINGS, JL ;
MEGA, M ;
GRAY, K ;
ROSENBERGTHOMPSON, S ;
CARUSI, DA ;
GORNBEIN, J .
NEUROLOGY, 1994, 44 (12) :2308-2314
[7]   Antiretroviral therapy in HIV infection - Are neurologically active drugs important? [J].
Cysique, LAJ ;
Maruff, P ;
Brew, BJ .
ARCHIVES OF NEUROLOGY, 2004, 61 (11) :1699-1704
[8]   Neurocognitive impairment is an independent risk factor for death in HIV infection [J].
Ellis, RJ ;
Deutsch, R ;
Heaton, RK ;
Marcotte, TD ;
McCutchan, JA ;
Nelson, JA ;
Abramson, I ;
Thal, LJ ;
Atkinson, JH ;
Wallace, MR ;
Grant, I ;
Kelly, M ;
Chandler, JL ;
Spector, SA ;
Jernigan, T ;
Masliah, E ;
Dupont, R .
ARCHIVES OF NEUROLOGY, 1997, 54 (04) :416-424
[9]   A REVIEW OF NEURONAL DAMAGE IN HUMAN-IMMUNODEFICIENCY-VIRUS INFECTION - ITS ASSESSMENT, POSSIBLE MECHANISM AND RELATIONSHIP TO DEMENTIA [J].
EVERALL, I ;
LUTHERT, P ;
LANTOS, P .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1993, 52 (06) :561-566
[10]  
Fahn S, 1987, Recent Dev. Park. Dis, P153