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 in | Psychiatry research. Neuroimaging Vol. 260; pp. 1 - 5 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Netherlands
Elsevier B.V
28.02.2017
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Online Access | Get full text |
ISSN | 0925-4927 1872-7506 1872-7506 |
DOI | 10.1016/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. |
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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 |
AuthorAffiliation_xml | – name: f McLean Imaging Center, McLean Hospital, Department of Psychiatry, Harvard Medical School, 115 Mill St., Belmont, MA USA, 02478 – name: d Departments of Psychiatry, Neurology and Radiology, Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA, USA – name: b Department of Psychiatry, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA – name: a Psychiatry Neuroimaging Laboratory, Department of Psychiatry, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – name: e Department of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – name: c Biological Psychiatry Laboratory, McLean Hospital, Belmont, Massachusetts, USA, and Department of Psychiatry, Harvard Medical School, Boston, Massachusetts, USA |
Author_xml | – sequence: 1 givenname: Johanna surname: Seitz fullname: Seitz, Johanna organization: Psychiatry Neuroimaging Laboratory, Department of Psychiatry, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – sequence: 2 givenname: Amanda E. surname: Lyall fullname: Lyall, Amanda E. organization: Psychiatry Neuroimaging Laboratory, Department of Psychiatry, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – sequence: 3 givenname: Gen surname: Kanayama fullname: Kanayama, Gen organization: Biological Psychiatry Laboratory, McLean Hospital, Belmont, Massachusetts, USA, and Department of Psychiatry, Harvard Medical School, Boston, MA, USA – sequence: 4 givenname: Nikos surname: Makris fullname: Makris, Nikos organization: Psychiatry Neuroimaging Laboratory, Department of Psychiatry, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – sequence: 5 givenname: James I. surname: Hudson fullname: Hudson, James I. organization: Biological Psychiatry Laboratory, McLean Hospital, Belmont, Massachusetts, USA, and Department of Psychiatry, Harvard Medical School, Boston, MA, USA – sequence: 6 givenname: Marek surname: Kubicki fullname: Kubicki, Marek organization: Psychiatry Neuroimaging Laboratory, Department of Psychiatry, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – sequence: 7 givenname: Harrison G. surname: Pope fullname: Pope, Harrison G. organization: Biological Psychiatry Laboratory, McLean Hospital, Belmont, Massachusetts, USA, and Department of Psychiatry, Harvard Medical School, Boston, MA, USA – sequence: 8 givenname: Marc J. surname: Kaufman fullname: Kaufman, Marc J. email: kaufman@mclean.harvard.edu organization: Department of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27988413$$D View this record in MEDLINE/PubMed |
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Keywords | Inferior-fronto-occipital fasciculus (IFOF) Tract-based spatial statistics (TBSS) Diffusion tensor imaging (DTI) Anabolic-androgenic steroids (AAS) |
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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 |
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