Relationship between cortical iron and tau aggregation in Alzheimer’s disease

Author:

Spotorno Nicola12ORCID,Acosta-Cabronero Julio3ORCID,Stomrud Erik24,Lampinen Björn5,Strandberg Olof T2,van Westen Danielle26ORCID,Hansson Oskar24

Affiliation:

1. Penn Frontotemporal Degeneration Center, Department of Neurology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA

2. Clinical Memory Research Unit, Department of Clinical Sciences, Malmö, Lund University, Lund, Sweden

3. Tenoke Ltd., Cambridge, UK

4. Memory Clinic, Skåne University Hospital, Malmö, Sweden

5. Clinical Sciences Lund, Medical Radiation Physics, Lund University, Lund, Sweden

6. Diagnostic Radiology, Department of Clinical Sciences, Lund University, Lund, Sweden

Abstract

Abstract A growing body of evidence suggests that the dysregulation of neuronal iron may play a critical role in Alzheimer’s disease. Recent MRI studies have established a relationship between iron accumulation and amyloid-β aggregation. The present study provides further insight demonstrating a relationship between iron and tau accumulation using magnetic resonance-based quantitative susceptibility mapping and tau-PET in n = 236 subjects with amyloid-β pathology (from the Swedish BioFINDER-2 study). Both voxel-wise and regional analyses showed a consistent association between differences in bulk magnetic susceptibility, which can be primarily ascribed to an increase in iron content, and tau-PET signal in regions known to be affected in Alzheimer’s disease. Subsequent analyses revealed that quantitative susceptibility specifically mediates the relationship between tau-PET and cortical atrophy measures, thus suggesting a modulatory effect of iron burden on the disease process. We also found evidence suggesting the relationship between quantitative susceptibility and tau-PET is stronger in younger participants (age ≤ 65). Together, these results provide in vivo evidence of an association between iron deposition and both tau aggregation and neurodegeneration, which help advance our understanding of the role of iron dysregulation in the Alzheimer’s disease aetiology.

Funder

European Research Council

Swedish Research Council

Knut and Alice Wallenberg Foundation

Marianne and Marcus Wallenberg Foundation

Swedish Alzheimer’s Foundation

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

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