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Longitudinal Structural Brain Changes in Bipolar Disorder: A Multicenter Neuroimaging Study of 1232 Individuals by the ENIGMA Bipolar Disorder Working Group
C. Abé, CRK. Ching, B. Liberg, AV. Lebedev, I. Agartz, TN. Akudjedu, M. Alda, D. Alnæs, S. Alonso-Lana, F. Benedetti, M. Berk, E. Bøen, CDM. Bonnin, F. Breuer, K. Brosch, RM. Brouwer, EJ. Canales-Rodríguez, DM. Cannon, Y. Chye, A. Dahl, O....
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, multicentrická studie, Research Support, N.I.H., Extramural, práce podpořená grantem
Odkazy
PubMed
34809987
DOI
10.1016/j.biopsych.2021.09.008
Knihovny.cz E-zdroje
- MeSH
- bipolární porucha * patologie MeSH
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- magnetická rezonanční tomografie MeSH
- mánie MeSH
- mladý dospělý MeSH
- mozek diagnostické zobrazování patologie MeSH
- multicentrické studie jako téma MeSH
- neurozobrazování MeSH
- ztenčování mozkové kůry MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
BACKGROUND: Bipolar disorder (BD) is associated with cortical and subcortical structural brain abnormalities. It is unclear whether such alterations progressively change over time, and how this is related to the number of mood episodes. To address this question, we analyzed a large and diverse international sample with longitudinal magnetic resonance imaging (MRI) and clinical data to examine structural brain changes over time in BD. METHODS: Longitudinal structural MRI and clinical data from the ENIGMA (Enhancing Neuro Imaging Genetics through Meta Analysis) BD Working Group, including 307 patients with BD and 925 healthy control subjects, were collected from 14 sites worldwide. Male and female participants, aged 40 ± 17 years, underwent MRI at 2 time points. Cortical thickness, surface area, and subcortical volumes were estimated using FreeSurfer. Annualized change rates for each imaging phenotype were compared between patients with BD and healthy control subjects. Within patients, we related brain change rates to the number of mood episodes between time points and tested for effects of demographic and clinical variables. RESULTS: Compared with healthy control subjects, patients with BD showed faster enlargement of ventricular volumes and slower thinning of the fusiform and parahippocampal cortex (0.18
Benito Menni CASM Barcelona Spain
Centro de Investigación Biomédica en Red de Salud Mental Barcelona Spain
Clinic for Radiology University of Münster Münster Germany
Department of Clinical Neuroscience Osher Center Karolinska Institutet Stockholm Sweden
Department of Medical Epidemiology and Biostatistics Karolinska Institutet Stockholm Sweden
Department of Neurology Division of Clinical Neuroscience Oslo University Hospital Oslo Norway
Department of Neurology Oslo University Hospital Oslo Norway
Department of Psychiatric Research Diakonhjemmet Hospital Oslo Norway
Department of Psychiatry and Psychotherapy Philipps University Marburg Marburg Germany
Department of Psychiatry Dalhousie University Halifax Nova Scotia
Department of Psychiatry The University of Melbourne Melbourne Victoria Australia
Department of Psychiatry University of British Columbia Vancouver British Columbia Canada
Department of Psychology University of Oslo Oslo Norway
Department of Public Health and Preventive Medicine Monash University Melbourne Victoria Australia
Djavad Mowafaghian Centre for Brain Health Vancouver British Columbia Canada
FIDMAG Germanes Hospitalàries Research Foundation Barcelona Spain
Hospital general de Granollers Barcelona Spain
Institut d'Investigacions Biomèdiques August Pi i Sunyer Barcelona Spain
Institute for Translational Psychiatry University of Münster Münster Germany
Institute of Clinical Medicine University of Oslo Oslo Norway
Institute of Medical Imaging and Visualisation Bournemouth University Bournemouth United Kingdom
Karolinska University Hospital Department of Neuroradiology Stockholm Sweden
Lee Kong Chian School of Medicine Nanyang Technological University Singapore Singapore
National Institute of Mental Health Klecany Czech Republic
Neuroscience Research Australia Sydney New South Wales Australia
School of Medical Sciences University of New South Wales Sydney New South Wales Australia
School of Psychiatry University of New South Wales Sydney New South Wales Australia
Signal Processing Laboratory École polytechnique fédérale de Lausanne Lausanne Switzerland
Unit of Psychosomatic and CL Psychiatry Oslo University Hospital Oslo Norway
University of Barcelona Barcelona Spain
University of New Mexico Albuquerque New Mexico
University Vita Salute San Raffaele Milano Italy
West Region Institute of Mental Health Singapore Singapore
Yong Loo Lin School of Medicine National University of Singapore Singapore Singapore
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- $a Abé, Christoph $u Department of Clinical Neuroscience, Osher Center, Karolinska Institutet, Stockholm, Sweden. Electronic address: christoph.abe@ki.se
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- $a Longitudinal Structural Brain Changes in Bipolar Disorder: A Multicenter Neuroimaging Study of 1232 Individuals by the ENIGMA Bipolar Disorder Working Group / $c C. Abé, CRK. Ching, B. Liberg, AV. Lebedev, I. Agartz, TN. Akudjedu, M. Alda, D. Alnæs, S. Alonso-Lana, F. Benedetti, M. Berk, E. Bøen, CDM. Bonnin, F. Breuer, K. Brosch, RM. Brouwer, EJ. Canales-Rodríguez, DM. Cannon, Y. Chye, A. Dahl, O. Dandash, U. Dannlowski, K. Dohm, T. Elvsåshagen, L. Fisch, JM. Fullerton, JM. Goikolea, D. Grotegerd, B. Haatveit, T. Hahn, T. Hajek, W. Heindel, M. Ingvar, K. Sim, TTJ. Kircher, RK. Lenroot, UF. Malt, C. McDonald, SR. McWhinney, I. Melle, T. Meller, EMT. Melloni, PB. Mitchell, L. Nabulsi, I. Nenadić, N. Opel, BJ. Overs, F. Panicalli, JK. Pfarr, S. Poletti, E. Pomarol-Clotet, J. Radua, J. Repple, KG. Ringwald, G. Roberts, E. Rodriguez-Cano, R. Salvador, K. Sarink, S. Sarró, S. Schmitt, F. Stein, C. Suo, SI. Thomopoulos, G. Tronchin, E. Vieta, LT. Westlye, AG. White, LN. Yatham, N. Zak, PM. Thompson, OA. Andreassen, M. Landén, ENIGMA Bipolar Disorder Working Group
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- $a BACKGROUND: Bipolar disorder (BD) is associated with cortical and subcortical structural brain abnormalities. It is unclear whether such alterations progressively change over time, and how this is related to the number of mood episodes. To address this question, we analyzed a large and diverse international sample with longitudinal magnetic resonance imaging (MRI) and clinical data to examine structural brain changes over time in BD. METHODS: Longitudinal structural MRI and clinical data from the ENIGMA (Enhancing Neuro Imaging Genetics through Meta Analysis) BD Working Group, including 307 patients with BD and 925 healthy control subjects, were collected from 14 sites worldwide. Male and female participants, aged 40 ± 17 years, underwent MRI at 2 time points. Cortical thickness, surface area, and subcortical volumes were estimated using FreeSurfer. Annualized change rates for each imaging phenotype were compared between patients with BD and healthy control subjects. Within patients, we related brain change rates to the number of mood episodes between time points and tested for effects of demographic and clinical variables. RESULTS: Compared with healthy control subjects, patients with BD showed faster enlargement of ventricular volumes and slower thinning of the fusiform and parahippocampal cortex (0.18 <d < 0.22). More (hypo)manic episodes were associated with faster cortical thinning, primarily in the prefrontal cortex. CONCLUSIONS: In the hitherto largest longitudinal MRI study on BD, we did not detect accelerated cortical thinning but noted faster ventricular enlargements in BD. However, abnormal frontocortical thinning was observed in association with frequent manic episodes. Our study yields insights into disease progression in BD and highlights the importance of mania prevention in BD treatment.
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- 700 1_
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- 700 1_
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