Neuroimaging features of depression-frailty phenotype in older adults: a pilot study

• Published in: International psychogeriatrics 2023-12, Vol.35 (12), p.717-7
• Main Authors: Shuster, Ethan, Miles, Amy E, Heyland, Lindsay K, Calarco, Navona, Jeyachandra, Jerrold, Mansour, Salim, Voineskos, Aristotle N, Steffens, David C, Nikolova, Yuliya S, Diniz, Breno S
• Format: Article
• Language: English
• Subjects: Aged; Analysis of covariance; Brain structure; Comorbidity; Cross-Sectional Studies; Depression - diagnostic imaging; Depressive Disorder, Major; Depressive personality disorders; Diagnostic and Statistical Manual; Diffusion Tensor Imaging; Frail; Frailty; Frailty - diagnostic imaging; Genotype & phenotype; Geriatric psychiatrists; Geriatrics; Health facilities; Humans; Measurement; Medical imaging; Mental depression; Mental disorders; Neuroimaging; Older people; Pilot Projects; Psychosis; Questionnaires; Recurrent; Software; Statistical analysis; Values
• ISSN: 1041-6102; 1741-203X; 1741-203X
• DOI: 10.1017/S1041610223000066

Frailty and late-life depression (LLD) often coexist and share several structural brain changes. We aimed to study the joint effect LLD and frailty have on brain structure. Cross-sectional study. Academic Health Center. Thirty-one participants (14 LLD+Frail and 17 Never-depressed+Robust). LLD was diagnosed by a geriatric psychiatrist according to the Diagnostic and Statistical Manual of Mental Disorders 5th edition for single episode or recurrent major depressive disorder without psychotic features. Frailty was assessed using the FRAIL scale (0-5), classifying subjects as robust (0), prefrail (1-2), and frail (3-5). Participants underwent T1-weighted magnetic resonance imaging in which covariance analysis of subcortical volumes and vertex-wise analysis of cortical thickness values were performed to access changes in grey matter. Participants also underwent diffusion tensor imaging in which tract-based spatial statistics was used with voxel-wise statistical analysis on fractional anisotropy and mean diffusion values to assess changes in white matter (WM). We found a significant difference in mean diffusion values (48,225 voxels; peak voxel: pFWER=0.005, MINI coord. (X,Y,Z) = -26,-11,27) between the LLD-Frail group and comparison group. The corresponding effect size (f=0.808) was large. We showed the LLD+Frailty group is associated with significant microstructural changes within WM tracts compared to Never-depressed+Robust individuals. Our findings indicate the possibility of a heightened neuroinflammatory burden as a potential mechanism underlying the co-occurrence of both conditions and the possibility of a depression-frailty phenotype in older adults.