The additive effect of late-life depression and olfactory dysfunction on the risk of dementia was mediated by hypersynchronization of the hippocampus/fusiform gyrus
Fusiform gyrus
Lingual gyrus
Temporal cortex
Orbitofrontal cortex
DOI:
10.1038/s41398-021-01291-0
Publication Date:
2021-03-17T10:04:05Z
AUTHORS (15)
ABSTRACT
Abstract Early detection of patients with late-life depression (LLD) a high risk developing dementia contributes to early intervention. Odor identification (OI) dysfunction serves as marker for predicting dementia, but whether OI increases the in LLD remains unclear. The present study aimed explore interactive effect and on its underlying neuroimaging changes. One hundred fifty-seven 101 normal controls were recruited, data their OI, cognition, activity daily living (ADL), resting-state functional magnetic resonance imaging collected. Two × two factorial analyses used analyze effects neuropsychological abnormalities. Mediation abnormalities detected by mediated associations between cognition/ADL. results suggested that exhibited additive reduced ADL, global cognition memory scores, well variables including (i) increased fractional amplitude low-frequency fluctuation (fALFF) right orbitofrontal cortex precentral cortex, (ii) regional homogeneity (ReHo) left hippocampus/fusiform gyrus, etc. In addition, these fALFF ReHo values associated scores (ADL, memory, language). Moreover, gyrus completely relationship partially cognition. Overall, hypersynchronization may increase patients.
SUPPLEMENTAL MATERIAL
Coming soon ....
REFERENCES (50)
CITATIONS (16)
EXTERNAL LINKS
PlumX Metrics
RECOMMENDATIONS
FAIR ASSESSMENT
Coming soon ....
JUPYTER LAB
Coming soon ....