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Kochan, N. A.

Publications and source records attributed to Kochan, N. A..

2 recordsLinked to original sources

Associations between volumes of grey matter regions and white matter hyperintensities with cognitive empathy in oldest-old adults

OBJECTIVESTo study the differential associations of regional volumes of grey matter (GM) and white matter hyperintensities (WMH) with behavioural and informant-reported measures of cognitive empathy (CE), especially in brain regions understood to have functional connectivity involvement with CE abilities. METHODSCommunity-dwelling participants from the Sydney Memory and Ageing Study (Sydney MAS) underwent whole brain MRI. Regional cortical GM volumes were derived using FreeSurfer v7.1 for, and WMH volumes were derived using UBO Detector. On follow-up four years later, CE was indexed via the Reading the Mind in the Eyes Test (RMET; a behavioural task) and Interpersonal Reactivity Index - Perspective Taking subscale (IRI-PT; an informant-reported measure). RESULTSIn 129 participants (mean age 87.01 years), Structural equation modelling (SEM) showed associations between insula GM volumes and RMET scores (p=0.001), and between supramarginal gyrus (SMG) GM volumes and IRI-PT scores (p=0.016). Associations remained significant after inclusion of covariates accounting for age, global cognition, affective symptoms, and social networks. DISCUSSIONCE abilities assessed with RMET (a behavioural task) were positively associated with insula GM volumes. CE abilities on the IRI-PT (an informant-reported measure) were positively associated with SMG GM volumes. No associations between WMH volumes and CE measures were found. These findings may inform clinical workflows that use structural MRI investigations looking at social cognitive disturbances in older adults and provide further evidence of the divergent nature of behavioural and self-report measures of CE.

neuroscience↗

Dissociable Cellular and Genetic Mechanisms of Cortical Thinning at Different Life Stages

Mechanisms underpinning age-related variations in cortical thickness in the human brain remain poorly understood. We investigated whether inter-regional age-related variations in cortical thinning (in a multicohort neuroimaging dataset from the ENIGMA Lifespan Working Group totalling 14,248 individuals, aged 4-89 years) depended on cell-specific marker gene expression levels. We found differences amidst early-life (<20 years), mid-life (20-60 years), and late-life (>60 years) in the patterns of association between inter-regional profiles of cortical thickness and expression profiles of marker genes for CA1 and S1 pyramidal cells, astrocytes, and microglia. Gene ontology and enrichment analyses indicated that each of the three life-stages was associated with different biological processes and cellular components: synaptic modeling in early life, neurotransmission in mid-life, and neurodegeneration in late-life. These findings provide mechanistic insights into age-related cortical thinning during typical development and aging.

neuroscience↗