Subcortical volumes across the lifespan: Data from 18,605 healthy individuals aged 3–90years
Age has a major effect on brain volume. However, the normative studies available are constrained by small sample sizes, restricted age coverage and significant methodological variability. These limitations introduce inconsistencies and may obscure or distort the lifespan trajectories of brain morpho...
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Published in | Human brain mapping Vol. 43; no. 1; pp. 452 - 469 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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San Antonio
John Wiley & Sons, Inc
01.01.2022
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Abstract | Age has a major effect on brain volume. However, the normative studies available are constrained by small sample sizes, restricted age coverage and significant methodological variability. These limitations introduce inconsistencies and may obscure or distort the lifespan trajectories of brain morphometry. In response, we capitalized on the resources of the Enhancing Neuroimaging Genetics through Meta‐Analysis (ENIGMA) Consortium to examine age‐related trajectories inferred from cross‐sectional measures of the ventricles, the basal ganglia (caudate, putamen, pallidum, and nucleus accumbens), the thalamus, hippocampus and amygdala using magnetic resonance imaging data obtained from 18,605 individuals aged 3–90 years. All subcortical structure volumes were at their maximum value early in life. The volume of the basal ganglia showed a monotonic negative association with age thereafter; there was no significant association between age and the volumes of the thalamus, amygdala and the hippocampus (with some degree of decline in thalamus) until the sixth decade of life after which they also showed a steep negative association with age. The lateral ventricles showed continuous enlargement throughout the lifespan. Age was positively associated with inter‐individual variability in the hippocampus and amygdala and the lateral ventricles. These results were robust to potential confounders and could be used to examine the functional significance of deviations from typical age‐related morphometric patterns. |
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AbstractList | Age has a major effect on brain volume. However, the normative studies available are constrained by small sample sizes, restricted age coverage and significant methodological variability. These limitations introduce inconsistencies and may obscure or distort the lifespan trajectories of brain morphometry. In response, we capitalized on the resources of the Enhancing Neuroimaging Genetics through Meta‐Analysis (ENIGMA) Consortium to examine age‐related trajectories inferred from cross‐sectional measures of the ventricles, the basal ganglia (caudate, putamen, pallidum, and nucleus accumbens), the thalamus, hippocampus and amygdala using magnetic resonance imaging data obtained from 18,605 individuals aged 3–90 years. All subcortical structure volumes were at their maximum value early in life. The volume of the basal ganglia showed a monotonic negative association with age thereafter; there was no significant association between age and the volumes of the thalamus, amygdala and the hippocampus (with some degree of decline in thalamus) until the sixth decade of life after which they also showed a steep negative association with age. The lateral ventricles showed continuous enlargement throughout the lifespan. Age was positively associated with inter‐individual variability in the hippocampus and amygdala and the lateral ventricles. These results were robust to potential confounders and could be used to examine the functional significance of deviations from typical age‐related morphometric patterns. |
Author | Jernigan, Terry L Lebedeva, Irina Stein, Dan J Klaus‐Peter Lesch Swagerman, Suzanne C Machielsen, Marise W J Lochner, Christine Nic J A van der Wee Ehrlich, Stefan Portella, Maria J Harrison, Ben J Sim, Kang Glahn, David C Radua, Joaquim Clark, Vincent P Dennis van't Ent Worker, Amanda Papachristou, Efstathios Asherson, Philip Nordvik, Jan E Chubar, Victoria Sommer, Iris Rosa, Pedro G P Walter, Henrik Borgwardt, Stefan Bonvino, Aurora Hickie, Ian B Naaijen, Jilly Lee, Won Hee Tamnes, Christian K Nakao, Tomohiro Ignacio Martínez‐Zalacaín Andreassen, Ole A Huyser, Chaim Doan, Nhat Trung McDonald, Colm Anton Albajes‐Eizagirre Gur, Rachel E Saykin, Andrew J Kahn, Rene Uhlmann, Anne Andersson, Micael Castellanos, Francisco X Edith Pomarol‐Clotet Schumann, Gunter Akudjedu, Theophilus N Klein, Marieke Alpert, Kathryn I West, John D Wittfeld, Katharina Medland, Sarah E Hilleke E Hulshoff Pol Wen, Wei Bargallo, Nuria Andreas Meyer‐Lindenberg Ramona Baur‐Streubel Anthony, James den Braber, Anouk Jönsson, Erik G Frangou, Sophia Kalnin, Andrew Zanetti, Marc |
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SubjectTerms | Age Alzheimer's disease Amygdala Attention deficit hyperactivity disorder Basal ganglia Brain Brain research Cognition & reasoning Ganglia Genetics Globus pallidus Hippocampus HIV Human immunodeficiency virus Life span Magnetic resonance imaging Medical imaging Memory Morphometry Neuroimaging Nucleus accumbens Obsessive compulsive disorder Putamen Thalamus Ventricle (lateral) Working groups |
Title | Subcortical volumes across the lifespan: Data from 18,605 healthy individuals aged 3–90years |
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