Cortico-limbic volume abnormalities in late life depression are distinct from β amyloid and white matter pathologies

Autor: Mackin, R. Scott, Rhodes, Emma, Kassel, Michelle, Kryza-Lacombe, Maria, Burns, Emily, Bickford, David, Morin, Ruth, Tosun, Duygu, Landau, Susan, Butters, Meryl A., Aisen, Paul, Raman, Rema, Saykin, Andrew J., Toga, Arthur, Koeppe, Robert, Jack, Clifford, Weiner, Michael W., Nelson, Craig, Insel, Philip S.
Zdroj: Molecular Psychiatry; 20240101, Issue: Preprints p1-10, 10p
Abstrakt: This study was conducted to clarify patterns of cortico-limbic volume abnormalities in late life depression (LLD) relative to non-depressed (ND) adults matched for amyloid β (Aβ) deposition and to evaluate the relationship of volume abnormalities with cognitive performance. Participants included 116 LLD and 226 ND. Classification accuracy of LLD status was estimated using area under the receiver operator characteristic curve. Twenty-one percent of LLD and ND participants were Aβ positive and the groups did not differ on white matter hyperintensity volume (WMH (logscale); β = 0.12, p= 0.28). Compared to ND, the LLD group exhibited significantly lower bilateral volume in the lateral orbitofrontal cortex, hippocampus, accumbens area, superior temporal lobe, temporal pole, and amygdala after multiple comparison correction (p< 0.009 for all). Cortico-limbic volumes significantly improved classification of LLD beyond demographic characteristics, Aβ status, and WMH (AUCVol= 0.71, AUCWMH, Aβ= 0.62, AUC difference, 0.09 [0.03 to 0.15]). LLD exhibited poorer performance on measures of global cognition, set shifting, and verbal learning and memory relative to ND. Cognitive function was positively associated with cortico-limbic volumes and these relationships did not differ by group. Secondary analyses with an ND sample additionally matched for Mild Cognitive Impairment (MCI) diagnosis showed a similar but attenuated pattern of volume abnormalities. Overall, our results support LLD as being associated with cortico-limbic volume abnormalities that are distinct from Aβ and white matter pathologies and that these volume abnormalities are important factors associated with cognitive dysfunction in LLD.
Databáze: Supplemental Index
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