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Recreational use of GHB is associated with alterations of resting state functional connectivity of the central executive and default mode networks

Gamma‐hydroxybutyrate acid (GHB) is a recreational drug with a high addictive potential. Severe side effects such as GHB‐induced coma are common and linked to increased emergency room attendances. Task‐based functional‐imaging studies have revealed an association between the regular use of GHB and m...

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Autores principales: Raposo Pereira, Filipa, Zhutovsky, Paul, Mcmaster, Minni T.B., Polderman, Nikki, de Vries, Yvon D.A.T., van den Brink, Wim, van Wingen, Guido A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6590661/
https://www.ncbi.nlm.nih.gov/pubmed/30720906
http://dx.doi.org/10.1002/hbm.24532
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author Raposo Pereira, Filipa
Zhutovsky, Paul
Mcmaster, Minni T.B.
Polderman, Nikki
de Vries, Yvon D.A.T.
van den Brink, Wim
van Wingen, Guido A.
author_facet Raposo Pereira, Filipa
Zhutovsky, Paul
Mcmaster, Minni T.B.
Polderman, Nikki
de Vries, Yvon D.A.T.
van den Brink, Wim
van Wingen, Guido A.
author_sort Raposo Pereira, Filipa
collection PubMed
description Gamma‐hydroxybutyrate acid (GHB) is a recreational drug with a high addictive potential. Severe side effects such as GHB‐induced coma are common and linked to increased emergency room attendances. Task‐based functional‐imaging studies have revealed an association between the regular use of GHB and multiple GHB‐induced comas, and altered neurocognitive function. However the effects of multiple GHB‐induced comas and regular GHB‐use on intrinsic brain connectivity during rest remain unknown. The study population consisted of 23 GHB‐users with ≥4 GHB‐induced comas (GHB‐Coma), 22 GHB‐users who never experienced a GHB‐induced coma (GHB‐NoComa) and 24 polydrug users who never used GHB (No‐GHB). Resting‐state scans were collected to assess resting‐state functional‐connectivity within and between the default mode network (DMN), the bilateral central executive network (CEN) and the salience network (SN). The GHB‐NoComa group showed decreased rsFC of the right CEN with a region in the anterior cingulate cortex (p (FWE) = 0.048) and decreased rsFC between the right CEN and the DMN (p (FWE) = 0.048) when compared with the No‐GHB group. These results suggest that regular GHB‐use is associated with decreased rsFC within the right CEN and between the right CEN and the DMN. The presence of multiple GHB‐induced comas is not associated with (additional) alterations in rsFC.
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spelling pubmed-65906612019-07-08 Recreational use of GHB is associated with alterations of resting state functional connectivity of the central executive and default mode networks Raposo Pereira, Filipa Zhutovsky, Paul Mcmaster, Minni T.B. Polderman, Nikki de Vries, Yvon D.A.T. van den Brink, Wim van Wingen, Guido A. Hum Brain Mapp Research Articles Gamma‐hydroxybutyrate acid (GHB) is a recreational drug with a high addictive potential. Severe side effects such as GHB‐induced coma are common and linked to increased emergency room attendances. Task‐based functional‐imaging studies have revealed an association between the regular use of GHB and multiple GHB‐induced comas, and altered neurocognitive function. However the effects of multiple GHB‐induced comas and regular GHB‐use on intrinsic brain connectivity during rest remain unknown. The study population consisted of 23 GHB‐users with ≥4 GHB‐induced comas (GHB‐Coma), 22 GHB‐users who never experienced a GHB‐induced coma (GHB‐NoComa) and 24 polydrug users who never used GHB (No‐GHB). Resting‐state scans were collected to assess resting‐state functional‐connectivity within and between the default mode network (DMN), the bilateral central executive network (CEN) and the salience network (SN). The GHB‐NoComa group showed decreased rsFC of the right CEN with a region in the anterior cingulate cortex (p (FWE) = 0.048) and decreased rsFC between the right CEN and the DMN (p (FWE) = 0.048) when compared with the No‐GHB group. These results suggest that regular GHB‐use is associated with decreased rsFC within the right CEN and between the right CEN and the DMN. The presence of multiple GHB‐induced comas is not associated with (additional) alterations in rsFC. John Wiley & Sons, Inc. 2019-02-05 /pmc/articles/PMC6590661/ /pubmed/30720906 http://dx.doi.org/10.1002/hbm.24532 Text en © 2019 The Authors. Human Brain Mapping published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Raposo Pereira, Filipa
Zhutovsky, Paul
Mcmaster, Minni T.B.
Polderman, Nikki
de Vries, Yvon D.A.T.
van den Brink, Wim
van Wingen, Guido A.
Recreational use of GHB is associated with alterations of resting state functional connectivity of the central executive and default mode networks
title Recreational use of GHB is associated with alterations of resting state functional connectivity of the central executive and default mode networks
title_full Recreational use of GHB is associated with alterations of resting state functional connectivity of the central executive and default mode networks
title_fullStr Recreational use of GHB is associated with alterations of resting state functional connectivity of the central executive and default mode networks
title_full_unstemmed Recreational use of GHB is associated with alterations of resting state functional connectivity of the central executive and default mode networks
title_short Recreational use of GHB is associated with alterations of resting state functional connectivity of the central executive and default mode networks
title_sort recreational use of ghb is associated with alterations of resting state functional connectivity of the central executive and default mode networks
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6590661/
https://www.ncbi.nlm.nih.gov/pubmed/30720906
http://dx.doi.org/10.1002/hbm.24532
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