White matter abnormalities in long-term anabolic-androgenic steroid users: A pilot study

Recent studies of long-term anabolic-androgenic steroid (AAS) users reported amygdala structural and functional connectivity abnormalities. We assessed white matter microstructure in the inferior-fronto-occipital fasciculus (IFOF), a major associative bundle of the amygdala network. Diffusion weight...

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Published inPsychiatry research. Neuroimaging Vol. 260; pp. 1 - 5
Main Authors Seitz, Johanna, Lyall, Amanda E., Kanayama, Gen, Makris, Nikos, Hudson, James I., Kubicki, Marek, Pope, Harrison G., Kaufman, Marc J.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 28.02.2017
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Online AccessGet full text
ISSN0925-4927
1872-7506
1872-7506
DOI10.1016/j.pscychresns.2016.12.003

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Abstract Recent studies of long-term anabolic-androgenic steroid (AAS) users reported amygdala structural and functional connectivity abnormalities. We assessed white matter microstructure in the inferior-fronto-occipital fasciculus (IFOF), a major associative bundle of the amygdala network. Diffusion weighted images acquired from 9 male long-term AAS users and 8 matched controls aged 36–51 years old were processed using a standardized pipeline (Tract-Based Spatial Statistics). Group differences were examined using linear regression with adjustment for age and current testosterone level. Compared to nonusers, AAS users exhibited significantly higher fractional anisotropy (FA) in the IFOF. Users showed markedly greater FA than nonusers on the left IFOF but only a modest, nonsignificant difference on the right IFOF. Moreover, FA was positively associated with lifetime cumulative AAS dose. Our results suggest that long-term AAS use alters IFOF white matter organization and integrity, which in turn might affect amygdala-related processes such as reward system function. Accordingly, further studies are needed to replicate findings in larger subject groups to determine the functional significance of the FA abnormality. •Anabolic-androgenic steroids (AAS) cause psychiatric and cognitive abnormalities.•We performed the first Diffusion Tensor Imaging study of long-term AAS users.•Fractional anisotropy (FA) was higher in AAS users in an amygdala network tract.•Among AAS users, FA in this tract was positively associated with lifetime AAS dose.•The FA abnormality is consistent with prior human and animal studies of AAS effects.
AbstractList Abstract Recent studies of long-term anabolic-androgenic steroid (AAS) users reported amygdala structural and functional connectivity abnormalities. We assessed white matter microstructure in the inferior-fronto-occipital fasciculus (IFOF), a major associative bundle of the amygdala network. Diffusion weighted images acquired from 9 male long-term AAS users and 8 matched controls aged 36–51 years old were processed using a standardized pipeline (Tract-Based Spatial Statistics). Group differences were examined using linear regression with adjustment for age and current testosterone level. Compared to nonusers, AAS users exhibited significantly higher fractional anisotropy (FA) in the IFOF. Users showed markedly greater FA than nonusers on the left IFOF but only a modest, nonsignificant difference on the right IFOF. Moreover, FA was positively associated with lifetime cumulative AAS dose. Our results suggest that long-term AAS use alters IFOF white matter organization and integrity, which in turn might affect amygdala-related processes such as reward system function. Accordingly, further studies are needed to replicate findings in larger subject groups to determine the functional significance of the FA abnormality.
Recent studies of long-term anabolic-androgenic steroid (AAS) users reported amygdala structural and functional connectivity abnormalities. We assessed white matter microstructure in the inferior-fronto-occipital fasciculus (IFOF), a major associative bundle of the amygdala network. Diffusion weighted images acquired from 9 male long-term AAS users and 8 matched controls aged 36-51 years old were processed using a standardized pipeline (Tract-Based Spatial Statistics). Group differences were examined using linear regression with adjustment for age and current testosterone level. Compared to nonusers, AAS users exhibited significantly higher fractional anisotropy (FA) in the IFOF. Users showed markedly greater FA than nonusers on the left IFOF but only a modest, nonsignificant difference on the right IFOF. Moreover, FA was positively associated with lifetime cumulative AAS dose. Our results suggest that long-term AAS use alters IFOF white matter organization and integrity, which in turn might affect amygdala-related processes such as reward system function. Accordingly, further studies are needed to replicate findings in larger subject groups to determine the functional significance of the FA abnormality.
Recent studies of long-term anabolic-androgenic steroid (AAS) users reported amygdala structural and functional connectivity abnormalities. We assessed white matter microstructure in the inferior-fronto-occipital fasciculus (IFOF), a major associative bundle of the amygdala network. Diffusion weighted images acquired from 9 male long-term AAS users and 8 matched controls aged 36-51 years old were processed using a standardized pipeline (Tract-Based Spatial Statistics). Group differences were examined using linear regression with adjustment for age and current testosterone level. Compared to nonusers, AAS users exhibited significantly higher fractional anisotropy (FA) in the IFOF. Users showed markedly greater FA than nonusers on the left IFOF but only a modest, nonsignificant difference on the right IFOF. Moreover, FA was positively associated with lifetime cumulative AAS dose. Our results suggest that long-term AAS use alters IFOF white matter organization and integrity, which in turn might affect amygdala-related processes such as reward system function. Accordingly, further studies are needed to replicate findings in larger subject groups to determine the functional significance of the FA abnormality.Recent studies of long-term anabolic-androgenic steroid (AAS) users reported amygdala structural and functional connectivity abnormalities. We assessed white matter microstructure in the inferior-fronto-occipital fasciculus (IFOF), a major associative bundle of the amygdala network. Diffusion weighted images acquired from 9 male long-term AAS users and 8 matched controls aged 36-51 years old were processed using a standardized pipeline (Tract-Based Spatial Statistics). Group differences were examined using linear regression with adjustment for age and current testosterone level. Compared to nonusers, AAS users exhibited significantly higher fractional anisotropy (FA) in the IFOF. Users showed markedly greater FA than nonusers on the left IFOF but only a modest, nonsignificant difference on the right IFOF. Moreover, FA was positively associated with lifetime cumulative AAS dose. Our results suggest that long-term AAS use alters IFOF white matter organization and integrity, which in turn might affect amygdala-related processes such as reward system function. Accordingly, further studies are needed to replicate findings in larger subject groups to determine the functional significance of the FA abnormality.
Recent studies of long-term anabolic-androgenic steroid (AAS) users reported amygdala structural and functional connectivity abnormalities. We assessed white matter microstructure in the inferior-fronto-occipital fasciculus (IFOF), a major associative bundle of the amygdala network. Diffusion weighted images acquired from 9 male long-term AAS users and 8 matched controls aged 36–51 years old were processed using a standardized pipeline (Tract-Based Spatial Statistics). Group differences were examined using linear regression with adjustment for age and current testosterone level. Compared to nonusers, AAS users exhibited significantly higher fractional anisotropy (FA) in the IFOF. Users showed markedly greater FA than nonusers on the left IFOF but only a modest, nonsignificant difference on the right IFOF. Moreover, FA was positively associated with lifetime cumulative AAS dose. Our results suggest that long-term AAS use alters IFOF white matter organization and integrity, which in turn might affect amygdala-related processes such as reward system function. Accordingly, further studies are needed to replicate findings in larger subject groups to determine the functional significance of the FA abnormality. •Anabolic-androgenic steroids (AAS) cause psychiatric and cognitive abnormalities.•We performed the first Diffusion Tensor Imaging study of long-term AAS users.•Fractional anisotropy (FA) was higher in AAS users in an amygdala network tract.•Among AAS users, FA in this tract was positively associated with lifetime AAS dose.•The FA abnormality is consistent with prior human and animal studies of AAS effects.
Author Pope, Harrison G.
Kaufman, Marc J.
Kanayama, Gen
Lyall, Amanda E.
Seitz, Johanna
Makris, Nikos
Hudson, James I.
Kubicki, Marek
AuthorAffiliation d Departments of Psychiatry, Neurology and Radiology, Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA, USA
b Department of Psychiatry, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA
e Department of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA
f McLean Imaging Center, McLean Hospital, Department of Psychiatry, Harvard Medical School, 115 Mill St., Belmont, MA USA, 02478
a Psychiatry Neuroimaging Laboratory, Department of Psychiatry, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA
c Biological Psychiatry Laboratory, McLean Hospital, Belmont, Massachusetts, USA, and Department of Psychiatry, Harvard Medical School, Boston, Massachusetts, USA
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Keywords Inferior-fronto-occipital fasciculus (IFOF)
Tract-based spatial statistics (TBSS)
Diffusion tensor imaging (DTI)
Anabolic-androgenic steroids (AAS)
Language English
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Snippet Recent studies of long-term anabolic-androgenic steroid (AAS) users reported amygdala structural and functional connectivity abnormalities. We assessed white...
Abstract Recent studies of long-term anabolic-androgenic steroid (AAS) users reported amygdala structural and functional connectivity abnormalities. We...
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SubjectTerms Adult
Anabolic-androgenic steroids (AAS)
Androgens - administration & dosage
Anisotropy
Brain - diagnostic imaging
Brain - drug effects
Brain - physiopathology
Diffusion Magnetic Resonance Imaging
Diffusion Tensor Imaging
Diffusion tensor imaging (DTI)
Humans
Inferior-fronto-occipital fasciculus (IFOF)
Male
Middle Aged
Pilot Projects
Psychiatry
Radiology
Testosterone Congeners - administration & dosage
Tract-based spatial statistics (TBSS)
White Matter - diagnostic imaging
White Matter - drug effects
White Matter - physiopathology
Title White matter abnormalities in long-term anabolic-androgenic steroid users: A pilot study
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0925492716301986
https://www.clinicalkey.es/playcontent/1-s2.0-S0925492716301986
https://dx.doi.org/10.1016/j.pscychresns.2016.12.003
https://www.ncbi.nlm.nih.gov/pubmed/27988413
https://www.proquest.com/docview/1851296022
https://pubmed.ncbi.nlm.nih.gov/PMC5272808
Volume 260
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