Brain network reorganisation and spatial lesion distribution in systemic lupus erythematosus

Author:

Valdés Hernández Maria del C12,Smith Keith34,Bastin Mark E1,Nicole Amft E.5,Ralston Stuart H6,Wardlaw Joanna M12,Wiseman Stewart J12ORCID

Affiliation:

1. Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK

2. UK Dementia Research Institute, University of Edinburgh, Edinburgh, UK

3. Usher Institute for Population Health Science and Informatics, University of Edinburgh, Edinburgh, UK

4. Health Data Research UK, London, UK

5. University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK

6. Centre for Genomic and Experimental Medicine, University of Edinburgh, Edinburgh, UK

Abstract

Objective This work investigates network organisation of brain structural connectivity in systemic lupus erythematosus (SLE) relative to healthy controls and its putative association with lesion distribution and disease indicators. Methods White matter hyperintensity (WMH) segmentation and connectomics were performed in 47 patients with SLE and 47 healthy age-matched controls from structural and diffusion MRI data. Network nodes were divided into hierarchical tiers based on numbers of connections. Results were compared between patients and controls to assess for differences in brain network organisation. Voxel-based analyses of the spatial distribution of WMH in relation to network measures and SLE disease indicators were conducted. Results Despite inter-individual differences in brain network organization observed across the study sample, the connectome networks of SLE patients had larger proportion of connections in the peripheral nodes. SLE patients had statistically larger numbers of links in their networks with generally larger fractional anisotropy weights (i.e. a measure of white matter integrity) and less tendency to aggregate than those of healthy controls. The voxels exhibiting connectomic differences were coincident with WMH clusters, particularly the left hemisphere’s intersection between the anterior limb of the internal and external capsules. Moreover, these voxels also associated more strongly with disease indicators. Conclusion Our results indicate network differences reflective of compensatory reorganization of the neural circuits, reflecting adaptive or extended neuroplasticity in SLE.

Funder

European Union Horizon 2020

Stroke Association

NIH

Lupus UK

Mrs Gladys Row Fogo Charitable Trust

Publisher

SAGE Publications

Subject

Rheumatology

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