A hemochromatosis allele that protects against Alzheimer's disease injury: A role for H-ferritin

Recent epidemiological evidence showed that mutations to the HFE-63 allele of this hemochromatosis-associated iron-assimilation protein improve chances of avoiding Alzheimer's disease (AD). This is unexpected since increased brain ferroptosis in gray-matter increases the risk for vascular dementia and AD. However, diffusion tensor imaging from a key Alzheimer's Disease Neuroimaging Initiative biomarker study showed that the hemochromatosis H63D allele protected white matter tracts and improved cognitive performance in individuals when <i>APOE4</i> accelerates AD. H63D-carrying individuals exhibit elevated serum ferritin levels. We suggest coordinate increased levels of H-ferritin in iron-rich oligodendrocytes in H63D carriers generates sufficient neuroprotection to enhance myelin sheath integrity in white matter axons.

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Publication Details

Journal
Journal of Alzheimer s Disease
Published
2025-12-22
DOI
https://doi.org/10.1177/13872877251404974
Primary Topic
Iron Metabolism and Disorders
Type
article
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article

A hemochromatosis allele that protects against Alzheimer's disease injury: A role for H-ferritin

Catherine M. Cahill, C. K. John Wang, Jack T. Rogers, K. Arai et al.
Journal of Alzheimer s Disease
Iron Metabolism and Disorders
article

A hemochromatosis allele that protects against Alzheimer's disease injury: A role for H-ferritin

Catherine M. Cahill, C. K. John Wang, Jack T. Rogers, K. Arai, Amy Tsurumi
article en

Abstract

Recent epidemiological evidence showed that mutations to the HFE-63 allele of this hemochromatosis-associated iron-assimilation protein improve chances of avoiding Alzheimer's disease (AD). This is unexpected since increased brain ferroptosis in gray-matter increases the risk for vascular dementia and AD. However, diffusion tensor imaging from a key Alzheimer's Disease Neuroimaging Initiative biomarker study showed that the hemochromatosis H63D allele protected white matter tracts and improved cognitive performance in individuals when <i>APOE4</i> accelerates AD. H63D-carrying individuals exhibit elevated serum ferritin levels. We suggest coordinate increased levels of H-ferritin in iron-rich oligodendrocytes in H63D carriers generates sufficient neuroprotection to enhance myelin sheath integrity in white matter axons.

Journal of Alzheimer s DiseaseVol. 109(3)
Massachusetts General Hospital (US)
Good health and well-being
Openalex Percentile: Top 25%
Iron Metabolism and Disorders
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