Karolinska Institute
Department of Neurobiology, Care Sciences and Society
I am a postdoctoral researcher at Karolinska Institutet, Sweden. My research revolves around neural and cognitive networks in healthy ageing and neurodegenerative disorders. I am interested in distinct alterations of brain network topology that reflect specific psychopathology traits but also neural changes that reveal transdiagnostic brain network features, e.g. cognitive impairments as encountered in both schizophrenia as well as age-related dementias. To this end, I employ graphtheoretical analyses on neuroimaging cognitive data to characterize the the network impacts of cognitive impairments and investigate possible targets for treatments.

Presenter of 1 Presentation

NEURAL CONNECTIVITY CHANGES IN DEMENTIA WITH LEWY BODIES – A SYSTEMATIC REVIEW

Session Type
SYMPOSIUM
Date
Sat, 19.03.2022
Session Time
09:10 AM - 11:10 AM
Room
ONSITE: 133-134
Lecture Time
10:10 AM - 10:25 AM

Abstract

Aims

Studies on dementia with Lewy bodies (DLB) have mainly focussed on the deterioration of distinct cortical and subcortical regions related to the deposition of Lewy bodies. In view of the proposed trans-synaptic spread of the alpha-synuclein-pathology, investigating the disease in this segregated fashion only, would be detrimental to our understanding of its progression. Over the past two decades, an increasing number of studies have examined the effects of the disease on structural and functional brain connectivity. Here, we aim to summarize the current state of research on connectivity changes in DLB compared to healthy age-matched controls and other dementias.

Methods

In August 2021, we conducted a search of relevant peer-reviewed literature across several electrophysiological and imaging modalities on PubMed, following PRISMA guidelines.

Results

Out of 337 identified articles, 38 articles were selected and systematically reviewed. Positron emission tomography (PET), magnetic resonance imaging (MRI), and electroencephalography (EEG) assessments of patients revealed widespread abnormalities within and across brain networks in DLB. Most changes occurred within the default mode network and its connections to other cortical regions. Further, advanced mathematical analysis methods demonstrated disease-related changes in local and global network efficiency measures. A subset of studies revealed correlations between connectivity measures and cognitive impairments.

Conclusions

This review shows that the exploration of structural and functional connectivity changes in DLB allows reconstructing the spread of the disease along neural tracts. This knowledge may help to understand clinical presentations and to identify targets for future disease-modifying treatments in DLB.

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