Maturation of Hippocampal Subfields in Young Adulthood and Its Relationship With Cognition
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články
Grantová podpora
NU20J-04-00022
Agentura Pro Zdravotnický Výzkum České Republiky
FP7-IEF-2013
Research Executive Agency
6485124
Research Executive Agency
24-12183M
Grantová Agentura České Republiky
857560
Horizon 2020 Framework Programme
CEITEC 2020
The Ministry of Education, Youth and Sports
CZ.02.1.01/0.0/0.0/17 043/0009632
The Ministry of Education, Youth and Sports
LM2018129
The Ministry of Education, Youth and Sports
LM2023069
The Ministry of Education, Youth and Sports
LQ1601
The Ministry of Education, Youth and Sports
LX22NPO5107
The Ministry of Education, Youth and Sports
Marie Curie Intra-European Fellowship for Career Development
European Union-Next Generation EU
PubMed
40747970
PubMed Central
PMC12314922
DOI
10.1002/hbm.70296
Knihovny.cz E-zdroje
- Klíčová slova
- CA1, CA4DG, brain aging, full‐scale IQ, hippocampal subfields, young adulthood,
- MeSH
- dospělí MeSH
- hipokampus * růst a vývoj diagnostické zobrazování anatomie a histologie MeSH
- inteligence fyziologie MeSH
- kognice * fyziologie MeSH
- lidé MeSH
- magnetická rezonanční tomografie MeSH
- mladiství MeSH
- mladý dospělý MeSH
- stárnutí * fyziologie MeSH
- velikost orgánu MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
The hippocampus is a key brain region for memory and cognitive functions, which consists of distinct subregions with different developmental trajectories throughout adolescence. However, trajectories of hippocampal subfield change in young adulthood remain uncharacterized, as is their potential relationship with cortical brain aging and cognitive ability during this time. We conducted two magnetic resonance imaging (MRI) follow-ups of a prenatal birth cohort in young adulthood and studied the effects of chronological age and cortical brain age on the volume of hippocampal subfields in the early 20s (n = 109; 51% men) and late 20s (n = 251; 53% men) and how these age-related volumetric changes might relate to full-scale IQ (FSIQ). We showed that CA1 and CA4DG subfields continue to grow in the third decade of life and that this growth can be observed both at the level of chronological age as well as estimated cortical brain age at both MRI timepoints. Moreover, in men, a larger size of these age-related subfields was associated with higher FSIQ, and the deviations between cortical brain age and chronological age mediated the relationships between right CA1 and FSIQ, as well as right CA4DG and FSIQ. These findings reveal that coordinated patterns of advanced cortical brain aging and hippocampal maturation may confer a cognitive advantage in young adulthood.
Centre for Addiction and Mental Health University of Toronto Toronto Canada
Cerebral Imaging Centre Douglas Mental Health University Institute Montreal Canada
Department of Psychiatry McGill University Montreal Canada
RECETOX Faculty of Science Masaryk University Brno Czech Republic
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