HIV Infection Is Associated with Impaired Striatal Function during Inhibition with Normal Cortical Functioning on Functional MRI

被引:20
作者
du Plessis, Stefan [1 ]
Vink, Matthijs [2 ]
Joska, John A. [3 ]
Koutsilieri, Eleni [4 ]
Bagadia, Asif [5 ]
Stein, Dan J. [3 ,6 ]
Emsley, Robin [1 ]
机构
[1] Univ Stellenbosch, Dept Psychiat, Fac Heath Sci, 2nd Floor Clin Bldg,Fransie van Zijl Ave, ZA-7505 Cape Town, South Africa
[2] Brain Ctr Rudolf Magnus, Cg Utrecht, Netherlands
[3] Univ Cape Town, Dept Psychiat, Groote Schuur Hosp, ZA-7925 Cape Town, South Africa
[4] Univ Wurzburg, Inst Virol & Immunbiol, Wurzburg, Germany
[5] Univ Stellenbosch, Dept Radiol, Fac Heath Sci, ZA-7505 Cape Town, South Africa
[6] Univ Stellenbosch, MRC, Fac Heath Sci, Unit Anxiety & Stress Disorders, ZA-7505 Cape Town, South Africa
基金
英国医学研究理事会;
关键词
Brain; Inhibition; Dementia; fMRI; Putamen; HIV; HUMAN-IMMUNODEFICIENCY-VIRUS; TIME-TASK PERFORMANCE; CEREBRAL-BLOOD-FLOW; ANTIRETROVIRAL THERAPY; PROACTIVE-INHIBITION; BRAIN ACTIVATION; SUBSTANCE-ABUSE; WORKING-MEMORY; BASAL GANGLIA; FMRI;
D O I
10.1017/S1355617715000971
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The aim of the present study was to investigate the effect of HIV infection on cortical and subcortical regions of the frontal-striatal system involved in the inhibition of voluntary movement. Functional MRI (fMRI) studies suggest that human immunodeficiency virus (HIV) infection is associated with frontostriatal dysfunction. While frontostriatal systems play a key role in behavioral inhibition, there are to our knowledge no fMRI studies investigating the potential impact of HIV on systems involved during the inhibition of voluntary movement. A total of 17 combined antiretroviral therapy (cART) naive HIV+ participants as well as 18 age, gender, ethnic, education matched healthy controls performed a modified version of the stop-signal paradigm. This paradigm assessed behavior as well as functional brain activity associated with motor execution, reactive inhibition (outright stopping) and proactive inhibition (anticipatory response slowing before stopping). HIV+ participants showed significantly slower responses during motor execution compared to healthy controls, whereas they had normal proactive response slowing. Putamen hypoactivation was evident in the HIV+ participants based on successful stopping, indicating subcortical dysfunction during reactive inhibition. HIV+ participants showed normal cortical functioning during proactive inhibition. Our data provide evidence that HIV infection is associated with subcortical dysfunction during reactive inhibition, accompanied by relatively normal higher cortical functioning during proactive inhibition. This suggests that HIV infection may primarily involve basic striatal-mediated control processes in cART naive participants.
引用
收藏
页码:722 / 731
页数:10
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