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Longitudinal analysis of a dominantly inherited Alzheimer disease mutation carrier protected from dementia. | LitMetric

Article Synopsis

  • The study examines a unique case of an individual with the presenilin 2 p.Asn141Ile mutation, linked to Alzheimer's disease, who has not shown symptoms past the usual onset age.
  • Through genetic, neuroimaging, and biomarker analyses, researchers identified factors such as localized tau pathology and genetic variants that could explain this person's resilience against cognitive decline.
  • The findings suggest that environmental influences, alongside a rich profile of heat shock proteins, might play a role in protecting against Alzheimer's, emphasizing the need for more research on potential therapeutic strategies focused on tau deposition.

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Article Abstract

We conducted an in-depth longitudinal study on an individual carrying the presenilin 2 p.Asn141Ile mutation, traditionally associated with dominantly inherited Alzheimer's disease (AD), who has remarkably remained asymptomatic past the expected age of clinical onset. This study combines genetic, neuroimaging and biomarker analyses to explore the underpinnings of this resilience. Unlike typical progression in dominantly inherited AD, tau pathology in this case was confined to the occipital region without evidence of spread, potentially explaining the preservation of cognitive functions. Genetic analysis revealed several variants that, although not previously associated with protection against AD, suggest new avenues for understanding disease resistance. Notably, environmental factors such as significant heat exposure and a unique proteomic profile rich in heat shock proteins might indicate adaptive mechanisms contributing to the observed phenotype. This case underscores the complexity of Alzheimer's pathology and suggests that blocking tau deposition could be a promising target for therapeutic intervention. The study highlights the need for further research to identify and validate the mechanisms that could inhibit or localize tau pathology as a strategy to mitigate or delay the onset of Alzheimer's dementia.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12024232PMC
http://dx.doi.org/10.1038/s41591-025-03494-0DOI Listing

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