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Abstract #3868

Brain asymmetries from midlife to old adulthood and hemispheric brain age

Max Korbmacher1,2,3, Dennis van der Meer2,4, Dani Beck2,5,6, Eli Nina Eikefjord1,3, Ann-Marie de Lange2,7,8, Arvid Lundervold1,3,9,10, Ole A. Andreassen2,11, Lars T. Westlye2,6,11, and Ivan I. Maximov1,2
1Department of Health and Functioning, Western Norway University of Applied Sciences, Bergen, Norway, 2NORMENT Centre for Psychosis Research, Division of Mental Health and Addiction, University of Oslo and Oslo University Hospital, Oslo, Norway, 3Mohn Medical Imaging and Visualization Centre (MMIV), Bergen, Norway, 4Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, Netherlands, 5Department of Psychiatric Research, Diakonhjemmet Hospital, Oslo, Norway, 6Department of Psychology, University of Oslo, Oslo, Norway, 7LREN, Centre for Research in Neurosciences - Department of Clinical Neurosciences, CHUV and University of Lausanne, Lausanne, Switzerland, 8Department of Psychiatry, Oxford University, Oxford, United Kingdom, 9Department of Radiology, Haukeland University Hospital, Bergen, Norway, 10Department of Biomedicine, University of Bergen, Bergen, Norway, 11KG Jebsen Centre for Neurodevelopmental Disorders, University of Oslo, Oslo, Norway

Synopsis

Keywords: Aging, Aging, Asymmetry

Motivation: The human brain demonstrates structural and functional asymmetries which have implications for ageing and the development of mental and neurological diseases. Age-relationships
of these asymmetries are largely unknown.

Goal(s): We aimed to map brain asymmetries from midlife to older ages and develop hemispheric
brain age (HBA) models, which consider apparent hemispheric differences.

Approach: We used structural and diffusion magnetic resonance imaging metrics (N=48,040, UK Biobank) to evaluate the age-relationship of brain asymmetry.

Results: Most metrics indicated asymmetry, which appears lower at higher age in white matter and
higher in grey matter. HBA reflects other brain ages and unique information of each hemisphere.

Impact: We present for the first time comprehensive analyses of brain asymmetries throughout midlife and older ages and establish a new conceptualisation of BrainAge. This ”hemispheric” BrainAge can serve as a marker of asymmetry by comparing left to right hemisphere-derived BrainAges.

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Keywords