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Associations of brain morphology with cortical proteins of cognitive resilience.
- Source :
-
Neurobiology of Aging . May2024, Vol. 137, p1-7. 7p. - Publication Year :
- 2024
-
Abstract
- In a recent proteome-wide study, we identified several candidate proteins for drug discovery whose cortical abundance was associated with cognitive resilience to late-life brain pathologies. This study examines the extent to which these proteins are associated with the brain structures of cognitive resilience in decedents from the Religious Orders Study and Memory and Aging Project. Six proteins were associated with brain morphometric characteristics related to higher resilience (i.e., larger anterior and medial temporal lobe volumes), and five were associated with morphometric characteristics related to lower resilience (i.e., enlarged ventricles). Two synaptic proteins, RPH3A and CPLX1, remained inversely associated with the lower resilience signature, after further controlling for 10 neuropathologic indices. These findings suggest preserved brain structure in periventricular regions as a potential mechanism by which RPH3A and CPLX1 are associated with cognitive resilience. Further work is needed to elucidate other mechanisms by which targeting these proteins can circumvent the effects of pathology on individuals at risk for cognitive decline. • We identified two morphometric brain signatures of cognitive resilience • Larger anterior and medial temporal volumes were associated with higher resilience • Larger ventricles were associated with lower resilience • Six previously identified cortical resilience proteins were linked to the volumes • RPH3A and CPLX1 were related to smaller ventricles beyond neuropathological burden. [ABSTRACT FROM AUTHOR]
- Subjects :
- *DRUG discovery
*TEMPORAL lobe
*BRAIN anatomy
*COGNITIVE structures
*BRAIN diseases
Subjects
Details
- Language :
- English
- ISSN :
- 01974580
- Volume :
- 137
- Database :
- Academic Search Index
- Journal :
- Neurobiology of Aging
- Publication Type :
- Academic Journal
- Accession number :
- 176036617
- Full Text :
- https://doi.org/10.1016/j.neurobiolaging.2024.02.005