TDP‐43 pathology in pure LATE‐NC differs from when coexisting with Alzheimer's Disease

The histopathologic features of TDP-43 proteinopathy differs in pure LATE-NC vs when coexisting with ADNC, indicating that LATE-NC tends to be modified in the presence of moderate-high levels of ADNC. These data suggest that different mechanisms may underlie TDP-43 aggregation in different amnestic dementias, and that coexisting pathologies can influence each other.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2025-12-01
DOI
https://doi.org/10.1002/alz70855_104302
Primary Topic
Amyotrophic Lateral Sclerosis Research
Type
article
Field-Weighted Citation Impact
0.00
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article

TDP‐43 pathology in pure LATE‐NC differs from when coexisting with Alzheimer's Disease

Klara Gawor, Peter T. Nelson, Dietmar Rudolf Thal, Sandra O. Tomé et al.
Alzheimer s & Dementia
Amyotrophic Lateral Sclerosis Research
article

TDP‐43 pathology in pure LATE‐NC differs from when coexisting with Alzheimer's Disease

Klara Gawor, Peter T. Nelson, Dietmar Rudolf Thal, Sandra O. Tomé, Christine A.F. von Arnim, Rik Vandenberghe
article en

Abstract

The histopathologic features of TDP-43 proteinopathy differs in pure LATE-NC vs when coexisting with ADNC, indicating that LATE-NC tends to be modified in the presence of moderate-high levels of ADNC. These data suggest that different mechanisms may underlie TDP-43 aggregation in different amnestic dementias, and that coexisting pathologies can influence each other.

Alzheimer s & DementiaVol. 21(S1)
University of Kentucky (US), Universitair Ziekenhuis Leuven (BE), Universitätsmedizin Göttingen (DE), VIB-KU Leuven Center for Brain & Disease Research (BE), KU Leuven (BE)
Openalex Percentile: Top 30%
Amyotrophic Lateral Sclerosis Research
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