The potential of TDP-43 PET ligands for a biological diagnosis of TDP-43 proteinopathies

Candidate PET ligands targeting pathological TDP-43 aggregates are characterized by Vokali and colleagues in a series of human tissue, cell/animal model, and non-human primate experiments. Their preclinical data suggests favorable specificity and pharmacokinetic profiles of their two candidate tracers, which could translate into a disease-specific biomarker in TDP-43 proteinopathies.

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Publication Details

Journal
Nature Communications
Published
2025-10-24
DOI
https://doi.org/10.1038/s41467-025-64541-5
Citations
2
Primary Topic
Amyotrophic Lateral Sclerosis Research
Type
article
Field-Weighted Citation Impact
2.78
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article

The potential of TDP-43 PET ligands for a biological diagnosis of TDP-43 proteinopathies

David J. Irwin
2 citations
Nature Communications
Amyotrophic Lateral Sclerosis Research
2.78
article

The potential of TDP-43 PET ligands for a biological diagnosis of TDP-43 proteinopathies

David J. Irwin
article en
2 citations

Abstract

Candidate PET ligands targeting pathological TDP-43 aggregates are characterized by Vokali and colleagues in a series of human tissue, cell/animal model, and non-human primate experiments. Their preclinical data suggests favorable specificity and pharmacokinetic profiles of their two candidate tracers, which could translate into a disease-specific biomarker in TDP-43 proteinopathies.

Nature CommunicationsVol. 16(1)
Penn Center for AIDS Research (US), University of Pennsylvania (US)
Openalex Percentile: Top 8%
Amyotrophic Lateral Sclerosis Research
2.78
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