Long-Term Cocaine Self-administration Produces Structural Brain Changes That Correlate With Altered Cognition
An enduring question from cross-sectional clinical studies is whether the structural and functional differences often observed between cocaine users and healthy control subjects result from a history of drug use or instead reflect preexisting differences. To assess causality from drug exposure, true...
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Published in | Biological psychiatry (1969) Vol. 89; no. 4; pp. 376 - 385 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
15.02.2021
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Subjects | |
Online Access | Get full text |
ISSN | 0006-3223 1873-2402 1873-2402 |
DOI | 10.1016/j.biopsych.2020.08.008 |
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Abstract | An enduring question from cross-sectional clinical studies is whether the structural and functional differences often observed between cocaine users and healthy control subjects result from a history of drug use or instead reflect preexisting differences. To assess causality from drug exposure, true predrug baseline imaging and neurocognitive assessments are needed.
We addressed this fundamental question of causality using longitudinal anatomical magnetic resonance imaging and neurocognitive assessments in rhesus macaques. Cognitive tasks employed were stimulus reversal learning as a measure of cognitive flexibility/inhibitory control and delayed match to sample as a measure of visual working memory. Time points examined were before and following 12 months of chronic cocaine (n = 8) or water (n = 6) self-administration. A magnetic resonance imaging–only time point was also obtained following 2 years of forced abstinence.
We identified localized patterns of gray matter density (GMD) changes that were largely concordant with cross-sectional clinical studies. These included decreases in orbitofrontal cortex, insula, amygdala, and temporal cortex. There was also a prominent increase in GMD in the caudate putamen. GMD decreases were significantly correlated with cognitive impairments across individuals only in select cortical regions. Following abstinence, changes in GMD in some regions, including the orbitofrontal cortex, insula, and amygdala, were persistent and thus may play an important role in risk of relapse following extended abstinence.
Cocaine use is causal in producing regional changes in GMD, and those changes appear to drive cognitive impairments. |
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AbstractList | An enduring question from cross-sectional clinical studies is whether the structural and functional differences often observed between cocaine users and healthy control subjects result from a history of drug use or instead reflect preexisting differences. To assess causality from drug exposure, true predrug baseline imaging and neurocognitive assessments are needed.
We addressed this fundamental question of causality using longitudinal anatomical magnetic resonance imaging and neurocognitive assessments in rhesus macaques. Cognitive tasks employed were stimulus reversal learning as a measure of cognitive flexibility/inhibitory control and delayed match to sample as a measure of visual working memory. Time points examined were before and following 12 months of chronic cocaine (n = 8) or water (n = 6) self-administration. A magnetic resonance imaging–only time point was also obtained following 2 years of forced abstinence.
We identified localized patterns of gray matter density (GMD) changes that were largely concordant with cross-sectional clinical studies. These included decreases in orbitofrontal cortex, insula, amygdala, and temporal cortex. There was also a prominent increase in GMD in the caudate putamen. GMD decreases were significantly correlated with cognitive impairments across individuals only in select cortical regions. Following abstinence, changes in GMD in some regions, including the orbitofrontal cortex, insula, and amygdala, were persistent and thus may play an important role in risk of relapse following extended abstinence.
Cocaine use is causal in producing regional changes in GMD, and those changes appear to drive cognitive impairments. AbstractBackgroundAn enduring question from cross-sectional clinical studies is whether the structural and functional differences often observed between cocaine users and healthy control subjects result from a history of drug use or instead reflect preexisting differences. To assess causality from drug exposure, true predrug baseline imaging and neurocognitive assessments are needed. MethodsWe addressed this fundamental question of causality using longitudinal anatomical magnetic resonance imaging and neurocognitive assessments in rhesus macaques. Cognitive tasks employed were stimulus reversal learning as a measure of cognitive flexibility/inhibitory control and delayed match to sample as a measure of visual working memory. Time points examined were before and following 12 months of chronic cocaine ( n = 8) or water ( n = 6) self-administration. A magnetic resonance imaging–only time point was also obtained following 2 years of forced abstinence. ResultsWe identified localized patterns of gray matter density (GMD) changes that were largely concordant with cross-sectional clinical studies. These included decreases in orbitofrontal cortex, insula, amygdala, and temporal cortex. There was also a prominent increase in GMD in the caudate putamen. GMD decreases were significantly correlated with cognitive impairments across individuals only in select cortical regions. Following abstinence, changes in GMD in some regions, including the orbitofrontal cortex, insula, and amygdala, were persistent and thus may play an important role in risk of relapse following extended abstinence. ConclusionsCocaine use is causal in producing regional changes in GMD, and those changes appear to drive cognitive impairments. An enduring question from cross-sectional clinical studies is whether the structural and functional differences often observed between cocaine users and healthy control subjects result from a history of drug use or instead reflect preexisting differences. To assess causality from drug exposure, true predrug baseline imaging and neurocognitive assessments are needed.BACKGROUNDAn enduring question from cross-sectional clinical studies is whether the structural and functional differences often observed between cocaine users and healthy control subjects result from a history of drug use or instead reflect preexisting differences. To assess causality from drug exposure, true predrug baseline imaging and neurocognitive assessments are needed.We addressed this fundamental question of causality using longitudinal anatomical magnetic resonance imaging and neurocognitive assessments in rhesus macaques. Cognitive tasks employed were stimulus reversal learning as a measure of cognitive flexibility/inhibitory control and delayed match to sample as a measure of visual working memory. Time points examined were before and following 12 months of chronic cocaine (n = 8) or water (n = 6) self-administration. A magnetic resonance imaging-only time point was also obtained following 2 years of forced abstinence.METHODSWe addressed this fundamental question of causality using longitudinal anatomical magnetic resonance imaging and neurocognitive assessments in rhesus macaques. Cognitive tasks employed were stimulus reversal learning as a measure of cognitive flexibility/inhibitory control and delayed match to sample as a measure of visual working memory. Time points examined were before and following 12 months of chronic cocaine (n = 8) or water (n = 6) self-administration. A magnetic resonance imaging-only time point was also obtained following 2 years of forced abstinence.We identified localized patterns of gray matter density (GMD) changes that were largely concordant with cross-sectional clinical studies. These included decreases in orbitofrontal cortex, insula, amygdala, and temporal cortex. There was also a prominent increase in GMD in the caudate putamen. GMD decreases were significantly correlated with cognitive impairments across individuals only in select cortical regions. Following abstinence, changes in GMD in some regions, including the orbitofrontal cortex, insula, and amygdala, were persistent and thus may play an important role in risk of relapse following extended abstinence.RESULTSWe identified localized patterns of gray matter density (GMD) changes that were largely concordant with cross-sectional clinical studies. These included decreases in orbitofrontal cortex, insula, amygdala, and temporal cortex. There was also a prominent increase in GMD in the caudate putamen. GMD decreases were significantly correlated with cognitive impairments across individuals only in select cortical regions. Following abstinence, changes in GMD in some regions, including the orbitofrontal cortex, insula, and amygdala, were persistent and thus may play an important role in risk of relapse following extended abstinence.Cocaine use is causal in producing regional changes in GMD, and those changes appear to drive cognitive impairments.CONCLUSIONSCocaine use is causal in producing regional changes in GMD, and those changes appear to drive cognitive impairments. |
Author | Jedema, Hank P. Bonner, Alexandra R. Stein, Elliot A. Yang, Yihong Aizenstein, Howard J. Bradberry, Charles W. Song, Xiaowei |
AuthorAffiliation | 3 VA Pittsburgh Healthcare System, Pittsburgh PA, USA 1 Dept of Psychiatry, University of Pittsburgh, Pittsburgh PA, USA 2 Intramural Research Program, National Institute on Drug Abuse, Baltimore MD, USA 4 Current address, Cleveland Clinic Children’s Hospital |
AuthorAffiliation_xml | – name: 3 VA Pittsburgh Healthcare System, Pittsburgh PA, USA – name: 1 Dept of Psychiatry, University of Pittsburgh, Pittsburgh PA, USA – name: 4 Current address, Cleveland Clinic Children’s Hospital – name: 2 Intramural Research Program, National Institute on Drug Abuse, Baltimore MD, USA |
Author_xml | – sequence: 1 givenname: Hank P. orcidid: 0000-0002-7869-2110 surname: Jedema fullname: Jedema, Hank P. organization: Department of Psychiatry, University of Pittsburgh, Pittsburgh, Pennsylvania – sequence: 2 givenname: Xiaowei surname: Song fullname: Song, Xiaowei organization: Intramural Research Program, National Institute on Drug Abuse, Baltimore, Maryland – sequence: 3 givenname: Howard J. surname: Aizenstein fullname: Aizenstein, Howard J. organization: Department of Psychiatry, University of Pittsburgh, Pittsburgh, Pennsylvania – sequence: 4 givenname: Alexandra R. surname: Bonner fullname: Bonner, Alexandra R. organization: Department of Psychiatry, University of Pittsburgh, Pittsburgh, Pennsylvania – sequence: 5 givenname: Elliot A. surname: Stein fullname: Stein, Elliot A. organization: Intramural Research Program, National Institute on Drug Abuse, Baltimore, Maryland – sequence: 6 givenname: Yihong surname: Yang fullname: Yang, Yihong organization: Intramural Research Program, National Institute on Drug Abuse, Baltimore, Maryland – sequence: 7 givenname: Charles W. surname: Bradberry fullname: Bradberry, Charles W. email: charles.bradberry@nih.gov organization: Department of Psychiatry, University of Pittsburgh, Pittsburgh, Pennsylvania |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33012519$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Addiction Animals Brain - diagnostic imaging Cocaine Cocaine - adverse effects Cocaine-Related Disorders - diagnostic imaging Cognition Cross-Sectional Studies Impairment Macaca mulatta Macaque Magnetic Resonance Imaging Psychiatric/Mental Health Structural imaging |
Title | Long-Term Cocaine Self-administration Produces Structural Brain Changes That Correlate With Altered Cognition |
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