Charting human subcortical maturation across the adult lifespan with in vivo 7 T MRI
The human subcortex comprises hundreds of unique structures. Subcortical functioning is crucial for behavior, and disrupted function is observed in common neurodegenerative diseases. Despite their importance, human subcortical structures continue to be difficult to study in vivo. Here we provide a d...
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Published in | NeuroImage (Orlando, Fla.) Vol. 249; p. 118872 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Inc
01.04.2022
Elsevier Limited Elsevier |
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Abstract | The human subcortex comprises hundreds of unique structures. Subcortical functioning is crucial for behavior, and disrupted function is observed in common neurodegenerative diseases. Despite their importance, human subcortical structures continue to be difficult to study in vivo. Here we provide a detailed account of 17 prominent subcortical structures and ventricles, describing their approximate iron and myelin contents, morphometry, and their age-related changes across the normal adult lifespan. The results provide compelling insights into the heterogeneity and intricate age-related alterations of these structures. They also show that the locations of many structures shift across the lifespan, which is of direct relevance for the use of standard magnetic resonance imaging atlases. The results further our understanding of subcortical morphometry and neuroimaging properties, and of normal aging processes which ultimately can improve our understanding of neurodegeneration. |
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AbstractList | The human subcortex comprises hundreds of unique structures. Subcortical functioning is crucial for behavior, and disrupted function is observed in common neurodegenerative diseases. Despite their importance, human subcortical structures continue to be difficult to study in vivo. Here we provide a detailed account of 17 prominent subcortical structures and ventricles, describing their approximate iron and myelin contents, morphometry, and their age-related changes across the normal adult lifespan. The results provide compelling insights into the heterogeneity and intricate age-related alterations of these structures. They also show that the locations of many structures shift across the lifespan, which is of direct relevance for the use of standard magnetic resonance imaging atlases. The results further our understanding of subcortical morphometry and neuroimaging properties, and of normal aging processes which ultimately can improve our understanding of neurodegeneration. |
ArticleNumber | 118872 |
Author | Bazin, Pierre-Louis Isherwood, Scott J.S. Miletić, Steven Alkemade, Anneke Keuken, Max C. Forstmann, Birte U. |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/34999202$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1016_j_neuroimage_2022_119680 crossref_primary_10_1016_j_neuroimage_2022_119660 crossref_primary_10_1371_journal_pone_0301520 crossref_primary_10_1016_j_biopsych_2023_01_006 crossref_primary_10_1002_advs_202303381 crossref_primary_10_3389_fnhum_2022_838228 crossref_primary_10_1002_hbm_26147 crossref_primary_10_1080_15294145_2023_2197002 |
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Keywords | Aging Iron Subcortex Morphometry Myelin |
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SubjectTerms | Adolescent Adult Age Aged Aged, 80 and over Aging Alzheimer's disease Atrophy Brain - anatomy & histology Brain - diagnostic imaging Brain - growth & development Brain - metabolism Female Humans Iron Life span Magnetic Resonance Imaging Male Methods Middle Aged Morphometry Myelin Neurodegeneration Neurodegenerative diseases Neuroimaging Parkinson's disease Subcortex Young Adult |
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Title | Charting human subcortical maturation across the adult lifespan with in vivo 7 T MRI |
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