Cerebral cortex structure in prodromal Huntington disease
Neuroimaging studies of subjects who are gene-expanded for Huntington Disease, but not yet diagnosed (termed prodromal HD), report that the cortex is “spared,” despite the decrement in striatal and cerebral white-matter volume. Measurement of whole-cortex volume can mask more subtle, but potentially...
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Published in | Neurobiology of disease Vol. 40; no. 3; pp. 544 - 554 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.12.2010
Elsevier |
Subjects | |
Online Access | Get full text |
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Abstract | Neuroimaging studies of subjects who are gene-expanded for Huntington Disease, but not yet diagnosed (termed prodromal HD), report that the cortex is “spared,” despite the decrement in striatal and cerebral white-matter volume. Measurement of whole-cortex volume can mask more subtle, but potentially clinically relevant regional changes in volume, thinning, or surface area. The current study addressed this limitation by evaluating cortical morphology of 523 prodromal HD subjects. Participants included 693 individuals enrolled in the PREDICT-HD protocol. Of these participants, 523 carried the HD gene mutation (prodromal HD group); the remaining 170 were non gene-expanded and served as the comparison group. Based on age and CAG repeat length, gene-expanded subjects were categorized as “Far from onset,” “Midway to onset,” “Near onset,” and “already diagnosed.” MRI scans were processed using FreeSurfer. Cortical volume, thickness, and surface area were not significantly different between the Far from onset group and controls. However, beginning in the Midway to onset group, the cortex showed significant volume decrement, affecting most the posterior and superior cerebral regions. This pattern progressed when evaluating the groups further into the disease process. Areas that remained mostly unaffected included ventral and medial regions of the frontal and temporal cortex. Morphologic changes were mostly in thinning as surface area did not substantially change in most regions. Early in the course of HD, the cortex shows changes that are manifest as cortical thinning and are most robust in the posterior and superior regions of the cerebrum.
►Changes of cerebral cortex are detected in subjects up to a decade prior to onset. ►Structural changes are mostly in thinning rather than in reduction of surface area. ►Affected areas include superior and posterior cerebrum while ventral frontal is spared. |
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AbstractList | Neuroimaging studies of subjects who are gene-expanded for Huntington Disease, but not yet diagnosed (termed prodromal HD), report that the cortex is "spared," despite the decrement in striatal and cerebral white-matter volume. Measurement of whole-cortex volume can mask more subtle, but potentially clinically relevant regional changes in volume, thinning, or surface area. The current study addressed this limitation by evaluating cortical morphology of 523 prodromal HD subjects. Participants included 693 individuals enrolled in the PREDICT-HD protocol. Of these participants, 523 carried the HD gene mutation (prodromal HD group); the remaining 170 were non gene-expanded and served as the comparison group. Based on age and CAG repeat length, gene-expanded subjects were categorized as "Far from onset," "Midway to onset," "Near onset," and "already diagnosed." MRI scans were processed using FreeSurfer. Cortical volume, thickness, and surface area were not significantly different between the Far from onset group and controls. However, beginning in the Midway to onset group, the cortex showed significant volume decrement, affecting most the posterior and superior cerebral regions. This pattern progressed when evaluating the groups further into the disease process. Areas that remained mostly unaffected included ventral and medial regions of the frontal and temporal cortex. Morphologic changes were mostly in thinning as surface area did not substantially change in most regions. Early in the course of HD, the cortex shows changes that are manifest as cortical thinning and are most robust in the posterior and superior regions of the cerebrum. Neuroimaging studies of subjects who are gene-expanded for Huntington Disease, but not yet diagnosed (termed prodromal HD), report that the cortex is “spared,” despite the decrement in striatal and cerebral white-matter volume. Measurement of whole-cortex volume can mask more subtle, but potentially clinically relevant regional changes in volume, thinning, or surface area. The current study addressed this limitation by evaluating cortical morphology of 523 prodromal HD subjects. Participants included 693 individuals enrolled in the PREDICT-HD protocol. Of these participants, 523 carried the HD gene mutation (prodromal HD group); the remaining 170 were non gene-expanded and served as the comparison group. Based on age and CAG repeat length, gene-expanded subjects were categorized as “Far from onset,” “Midway to onset,” “Near onset,” and “already diagnosed.” MRI scans were processed using FreeSurfer. Cortical volume, thickness, and surface area were not significantly different between the Far from onset group and controls. However, beginning in the Midway to onset group, the cortex showed significant volume decrement, affecting most the posterior and superior cerebral regions. This pattern progressed when evaluating the groups further into the disease process. Areas that remained mostly unaffected included ventral and medial regions of the frontal and temporal cortex. Morphologic changes were mostly in thinning as surface area did not substantially change in most regions. Early in the course of HD, the cortex shows changes that are manifest as cortical thinning and are most robust in the posterior and superior regions of the cerebrum. ►Changes of cerebral cortex are detected in subjects up to a decade prior to onset. ►Structural changes are mostly in thinning rather than in reduction of surface area. ►Affected areas include superior and posterior cerebrum while ventral frontal is spared. Neuroimaging studies of subjects who are gene-expanded for Huntington Disease, but not yet diagnosed (termed prodromal HD), report that the cortex is "spared," despite the decrement in striatal and cerebral white-matter volume. Measurement of whole-cortex volume can mask more subtle, but potentially clinically relevant regional changes in volume, thinning, or surface area. The current study addressed this limitation by evaluating cortical morphology of 523 prodromal HD subjects. Participants included 693 individuals enrolled in the PREDICT-HD protocol. Of these participants, 523 carried the HD gene mutation (prodromal HD group); the remaining 170 were non gene-expanded and served as the comparison group. Based on age and CAG repeat length, gene-expanded subjects were categorized as "Far from onset," "Midway to onset," "Near onset," and "already diagnosed." MRI scans were processed using FreeSurfer. Cortical volume, thickness, and surface area were not significantly different between the Far from onset group and controls. However, beginning in the Midway to onset group, the cortex showed significant volume decrement, affecting most the posterior and superior cerebral regions. This pattern progressed when evaluating the groups further into the disease process. Areas that remained mostly unaffected included ventral and medial regions of the frontal and temporal cortex. Morphologic changes were mostly in thinning as surface area did not substantially change in most regions. Early in the course of HD, the cortex shows changes that are manifest as cortical thinning and are most robust in the posterior and superior regions of the cerebrum.Neuroimaging studies of subjects who are gene-expanded for Huntington Disease, but not yet diagnosed (termed prodromal HD), report that the cortex is "spared," despite the decrement in striatal and cerebral white-matter volume. Measurement of whole-cortex volume can mask more subtle, but potentially clinically relevant regional changes in volume, thinning, or surface area. The current study addressed this limitation by evaluating cortical morphology of 523 prodromal HD subjects. Participants included 693 individuals enrolled in the PREDICT-HD protocol. Of these participants, 523 carried the HD gene mutation (prodromal HD group); the remaining 170 were non gene-expanded and served as the comparison group. Based on age and CAG repeat length, gene-expanded subjects were categorized as "Far from onset," "Midway to onset," "Near onset," and "already diagnosed." MRI scans were processed using FreeSurfer. Cortical volume, thickness, and surface area were not significantly different between the Far from onset group and controls. However, beginning in the Midway to onset group, the cortex showed significant volume decrement, affecting most the posterior and superior cerebral regions. This pattern progressed when evaluating the groups further into the disease process. Areas that remained mostly unaffected included ventral and medial regions of the frontal and temporal cortex. Morphologic changes were mostly in thinning as surface area did not substantially change in most regions. Early in the course of HD, the cortex shows changes that are manifest as cortical thinning and are most robust in the posterior and superior regions of the cerebrum. Abstract Neuroimaging studies of subjects who are gene-expanded for Huntington Disease, but not yet diagnosed (termed prodromal HD), report that the cortex is “spared,” despite the decrement in striatal and cerebral white-matter volume. Measurement of whole-cortex volume can mask more subtle, but potentially clinically relevant regional changes in volume, thinning, or surface area. The current study addressed this limitation by evaluating cortical morphology of 523 prodromal HD subjects. Participants included 693 individuals enrolled in the PREDICT-HD protocol. Of these participants, 523 carried the HD gene mutation (prodromal HD group); the remaining 170 were non gene-expanded and served as the comparison group. Based on age and CAG repeat length, gene-expanded subjects were categorized as “Far from onset,” “Midway to onset,” “Near onset,” and “already diagnosed.” MRI scans were processed using FreeSurfer. Cortical volume, thickness, and surface area were not significantly different between the Far from onset group and controls. However, beginning in the Midway to onset group, the cortex showed significant volume decrement, affecting most the posterior and superior cerebral regions. This pattern progressed when evaluating the groups further into the disease process. Areas that remained mostly unaffected included ventral and medial regions of the frontal and temporal cortex. Morphologic changes were mostly in thinning as surface area did not substantially change in most regions. Early in the course of HD, the cortex shows changes that are manifest as cortical thinning and are most robust in the posterior and superior regions of the cerebrum. |
Author | Johnson, Hans J. Ross, Christopher A. Pierson, Ronald K. Mills, James Magnotta, Vincent A. Langbehn, Douglas R. Nopoulos, Peggy C. Aylward, Elizabeth H. Juhl, Andrew R. Paulsen, Jane S. |
AuthorAffiliation | g The Johns Hopkins University, Baltimore, Maryland 21287, Departments of Psychiatry, Neurology, and Neuroscience d University of Iowa Roy and Lucille Carver College of Medicine, Iowa City, Iowa 52242, Department of Radiology b University of Iowa Roy and Lucille Carver College of Medicine, Iowa City, Iowa 52242, Department of Pediatrics e University of Iowa Roy and Lucille Carver College of Medicine, Iowa City, Iowa 52242, Department of Biostatistics c University of Iowa Roy and Lucille Carver College of Medicine, Iowa City, Iowa 52242, Department of Neurology f Seattle Children’s Research Institute, Seattle, Washington 98101, Department of Imaging Science and Neuroscience/Neurodevelopment a University of Iowa Roy and Lucille Carver College of Medicine, Iowa City, Iowa 52242, Department of Psychiatry |
AuthorAffiliation_xml | – name: d University of Iowa Roy and Lucille Carver College of Medicine, Iowa City, Iowa 52242, Department of Radiology – name: b University of Iowa Roy and Lucille Carver College of Medicine, Iowa City, Iowa 52242, Department of Pediatrics – name: a University of Iowa Roy and Lucille Carver College of Medicine, Iowa City, Iowa 52242, Department of Psychiatry – name: e University of Iowa Roy and Lucille Carver College of Medicine, Iowa City, Iowa 52242, Department of Biostatistics – name: g The Johns Hopkins University, Baltimore, Maryland 21287, Departments of Psychiatry, Neurology, and Neuroscience – name: c University of Iowa Roy and Lucille Carver College of Medicine, Iowa City, Iowa 52242, Department of Neurology – name: f Seattle Children’s Research Institute, Seattle, Washington 98101, Department of Imaging Science and Neuroscience/Neurodevelopment |
Author_xml | – sequence: 1 givenname: Peggy C. surname: Nopoulos fullname: Nopoulos, Peggy C. email: peggy-nopoulos@uiowa.edu organization: Department of Psychiatry, University of Iowa Roy and Lucille Carver College of Medicine, Iowa City, IA 52242, USA – sequence: 2 givenname: Elizabeth H. surname: Aylward fullname: Aylward, Elizabeth H. email: elizabeth.aylward@seattlechildrens.org organization: Department of Imaging Science and Neuroscience/Neurodevelopment, Seattle Children's Research Institute, Seattle, WA 98101, USA – sequence: 3 givenname: Christopher A. surname: Ross fullname: Ross, Christopher A. email: caross@jhu.edu organization: Department of Psychiatry, The Johns Hopkins University, Baltimore, MD 21287, USA – sequence: 4 givenname: Hans J. surname: Johnson fullname: Johnson, Hans J. email: hans-johnson@uiowa.edu organization: Department of Psychiatry, University of Iowa Roy and Lucille Carver College of Medicine, Iowa City, IA 52242, USA – sequence: 5 givenname: Vincent A. surname: Magnotta fullname: Magnotta, Vincent A. email: vincent-magnotta@uiowa.edu organization: Department of Psychiatry, University of Iowa Roy and Lucille Carver College of Medicine, Iowa City, IA 52242, USA – sequence: 6 givenname: Andrew R. surname: Juhl fullname: Juhl, Andrew R. email: andrew-juhl@uiowa.edu organization: Department of Psychiatry, University of Iowa Roy and Lucille Carver College of Medicine, Iowa City, IA 52242, USA – sequence: 7 givenname: Ronald K. surname: Pierson fullname: Pierson, Ronald K. email: ronald-pierson@uiowa.edu organization: Department of Psychiatry, University of Iowa Roy and Lucille Carver College of Medicine, Iowa City, IA 52242, USA – sequence: 8 givenname: James surname: Mills fullname: Mills, James email: jamills@healthcare.uiowa.edu organization: Department of Psychiatry, University of Iowa Roy and Lucille Carver College of Medicine, Iowa City, IA 52242, USA – sequence: 9 givenname: Douglas R. surname: Langbehn fullname: Langbehn, Douglas R. email: douglas-langbehn@uiowa.edu organization: Department of Psychiatry, University of Iowa Roy and Lucille Carver College of Medicine, Iowa City, IA 52242, USA – sequence: 10 givenname: Jane S. surname: Paulsen fullname: Paulsen, Jane S. email: jane-paulsen@uiowa.edu organization: Department of Psychiatry, University of Iowa Roy and Lucille Carver College of Medicine, Iowa City, IA 52242, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/20688164$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Contributor | Ross, Christopher A Weaver, Kurt Beglinger, Leigh J Chesire, Amy Suchowersky, Oksana Rae, Daniela Burrows, Maggie Miracle, Dawn Uc, Ergun Magnotta, Vincent A Ecker, Daniel Santos, Rachelle Dar Chua, Phyllis Perlmutter, Joel Schumacher, Jessica Guttman, Mark Craufurd, David Nopoulos, Peg Klimek, Mary Lou Kumar, Rajeev Wood-Siverio, Cathy Quaid, Kimberly Wesson, Melissa Barton, Stacey Welsh, Claire Connor, Carmela Thomsen, Teri Goodman, Anna Doucette, Nicholas Chiu, Edmond Wood, Jessica Johnson, Arik Shpritz, Barnett Kloppel, Stefan Barker, Roger A Vuletich, Elizabeth Baynes, Kathleen McCusker, Elizabeth Price, Kathy Süssmuth, Sigurd Wojcieszek, Joanne DiPietro, Anna Perlman, Susan Landwehrmeyer, Bernhard G Testa, Claudia Geschwind, Michael D Epping, Eric Singer, Adam Howard, Elizabeth Wasserman, Paula Marshall, Frederick Samii, Ali Preston, Joy Rosser, Anne Juhl, Andrew Erickson, Diane Rodnitzky, Robert Wassink, Thomas Suter, Greg Novak, Marianne Tempkin, Terry Komiti, Angela Furtado, Sarah Lipe, Hillary Mallonee, William M Moskowitz, Carol Kimble, My |
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givenname: Maggie surname: Burrows fullname: Burrows, Maggie – sequence: 68 givenname: Marianne surname: Novak fullname: Novak, Marianne – sequence: 69 givenname: Thomasin surname: Andrews fullname: Andrews, Thomasin – sequence: 70 givenname: Elisabeth surname: Rosser fullname: Rosser, Elisabeth – sequence: 71 givenname: Sarah surname: Tabrizi fullname: Tabrizi, Sarah – sequence: 72 givenname: Anne surname: Rosser fullname: Rosser, Anne – sequence: 73 givenname: Kathy surname: Price fullname: Price, Kathy – sequence: 74 givenname: Amy surname: Chesire fullname: Chesire, Amy – sequence: 75 givenname: Frederick surname: Marshall fullname: Marshall, Frederick – sequence: 76 givenname: Mary surname: Wodarski fullname: Wodarski, Mary – sequence: 77 givenname: Oksana surname: Suchowersky fullname: Suchowersky, Oksana – sequence: 78 givenname: Sarah surname: Furtado fullname: Furtado, Sarah – sequence: 79 givenname: Mary Lou surname: Klimek fullname: Klimek, Mary Lou – sequence: 80 givenname: 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Diane surname: Erickson fullname: Erickson, Diane – sequence: 94 givenname: Dawn surname: Miracle fullname: Miracle, Dawn – sequence: 95 givenname: Rajeev surname: Kumar fullname: Kumar, Rajeev – sequence: 96 givenname: Vicki surname: Wheelock fullname: Wheelock, Vicki – sequence: 97 givenname: Terry surname: Tempkin fullname: Tempkin, Terry – sequence: 98 givenname: Nicole surname: Mans fullname: Mans, Nicole – sequence: 99 givenname: Kathleen surname: Baynes fullname: Baynes, Kathleen – sequence: 100 givenname: Joseph surname: Jankovic fullname: Jankovic, Joseph |
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Snippet | Neuroimaging studies of subjects who are gene-expanded for Huntington Disease, but not yet diagnosed (termed prodromal HD), report that the cortex is “spared,”... Abstract Neuroimaging studies of subjects who are gene-expanded for Huntington Disease, but not yet diagnosed (termed prodromal HD), report that the cortex is... Neuroimaging studies of subjects who are gene-expanded for Huntington Disease, but not yet diagnosed (termed prodromal HD), report that the cortex is "spared,"... |
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SubjectTerms | Adult Cerebral cortex Cerebral Cortex - pathology Cortical thickness Early Diagnosis Female Humans Huntington disease Huntington Disease - genetics Huntington Disease - pathology Longitudinal Studies Magnetic Resonance Imaging Male Middle Aged MRI Neurology Surface area |
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Title | Cerebral cortex structure in prodromal Huntington disease |
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