4.2 Article

fMRI brain activation during a delay discounting task in HIV-positive adults with and without cocaine dependence

期刊

PSYCHIATRY RESEARCH-NEUROIMAGING
卷 192, 期 3, 页码 167-175

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.pscychresns.2010.12.011

关键词

Cocaine dependence; HIV/AIDS; Functional magnetic resonance imaging; Delay discounting; Decision making

资金

  1. amfAR, The Foundation for AIDS Research [106884-42-RFBR]
  2. National Institute on Drug Abuse [T32-DA01536, K25-DA016612, K05-DA00343]
  3. Harvard University Center for AIDS Research [P30-AI60354]

向作者/读者索取更多资源

Cocaine use is associated with poorer HIV clinical outcomes and may contribute to neurobiological impairments associated with impulsive decision making. This study examined the effect of cocaine dependence on brain activation during a delay discounting task involving choices between smaller immediate rewards and larger delayed ones. Participants were 39 HIV-positive adults on antiretroviral therapy who had current cocaine dependence (active, n = 15), past cocaine dependence (recovered, n = 13), or no lifetime substance dependence (naive, n = 11). Based on responses on a traditional delay discounting task, three types of choices were individualized for presentation during functional magnetic resonance imaging: hard (similarly valued), easy (disparately valued), and no (single option). Active participants had significantly smaller increases in activation than naive participants during hard versus easy choices bilaterally in the precentral gyrus and anterior cingulate cortex and in the right frontal pole (including dorsolateral, ventrolateral, and orbitofrontal cortex). During hard and easy choices relative to no choices, active participants had smaller increases in activation compared to naive participants in frontoparietal cortical regions. These deficits in the executive network during delay discounting choices may contribute to impulsive decision making among HIV-positive cocaine users, with implications for risk behaviors associated with disease transmission and progression. (C) 2010 Elsevier Ireland Ltd. All rights reserved.

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