Clinically‐relevant proteomic and metabolomic signatures with effective neuroprotective treatment of the Tg4344AD rat model of Alzheimer's disease

We have identified common and unique molecular signatures of AD at the proteomic and metabolomic levels that are held in common across the TgF344 AD rat model and the human AD brain. We additionally determined which of the aberrant expression patterns held in common across rat and human AD brain are normalized by a neuroprotective treatment that prevents the onset of disease in these rats. This points us towards new insight into mechanisms underlying effective prevention of AD.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2025-12-01
DOI
https://doi.org/10.1002/alz70856_103515
Primary Topic
Metabolomics and Mass Spectrometry Studies
Type
article
Field-Weighted Citation Impact
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Clinically‐relevant proteomic and metabolomic signatures with effective neuroprotective treatment of the Tg4344AD rat model of Alzheimer's disease

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Clinically‐relevant proteomic and metabolomic signatures with effective neuroprotective treatment of the Tg4344AD rat model of Alzheimer's disease

Kathryn Franke, Jaymie R. Voorhees, Kalyani Chaubey, Edwin Vázquez‐Rosa, Andrew A. Pieper, Lijun Dou, Coral Cintrón‐Pérez, Feixiong Cheng
article en

Abstract

We have identified common and unique molecular signatures of AD at the proteomic and metabolomic levels that are held in common across the TgF344 AD rat model and the human AD brain. We additionally determined which of the aberrant expression patterns held in common across rat and human AD brain are normalized by a neuroprotective treatment that prevents the onset of disease in these rats. This points us towards new insight into mechanisms underlying effective prevention of AD.

Alzheimer s & DementiaVol. 21(S2)
Cleveland Clinic (US), Washington University in St. Louis (US), University Hospitals Cleveland Medical Center (US), Louis Stokes Cleveland VA Medical Center (US), Case Western Reserve University (US)
Openalex Percentile: Top 36%
Metabolomics and Mass Spectrometry Studies
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