EVolution in ALS diagnosis: molecular markers in extracellular vesicles
Philippe Codron1, Stéphanie Millecamps2, Philippe Corcia3
1Centre de Référence sur la SLA d'Angers, Centre Hospitalier Universitaire d'Angers, Angers, France; Laboratoire de Neurobiologie et Neuropathologie, Centre Hospitalier Universitaire d'Angers, Angers, France; University of Angers, Inserm, CNRS, MITOVASC, SFR ICAT, Angers, France.
Researchers identified a new biomarker for amyotrophic lateral sclerosis (ALS). Blood extracellular vesicles (EVs) containing transactive response DNA-binding protein 43 (TDP-43) can help diagnose ALS and track disease progression.
Area of Science:
- Neuroscience
- Biochemistry
- Biomarker Discovery
Background:
- Identifying reliable biomarkers for amyotrophic lateral sclerosis (ALS) is crucial for disease management.
- Current diagnostic and monitoring methods for ALS require improvement.
Purpose of the Study:
- To evaluate the potential of blood extracellular vesicles (EVs) as biomarkers for ALS.
- To assess the correlation between transactive response DNA-binding protein 43 (TDP-43) levels in EVs and ALS patient status and severity.
Main Methods:
- Analysis of extracellular vesicles (EVs) isolated from blood samples.
- Quantification of transactive response DNA-binding protein 43 (TDP-43) levels within EVs.
- Comparison of TDP-43 levels in EVs between ALS patients and healthy controls.
Main Results:
- Elevated levels of transactive response DNA-binding protein 43 (TDP-43) were found in blood extracellular vesicles (EVs) of ALS patients.
- TDP-43 levels in EVs accurately distinguished ALS patients from controls.
- TDP-43 levels in EVs correlated with ALS disease severity.
Conclusions:
- Blood extracellular vesicles (EVs) expressing high levels of TDP-43 represent a promising biomarker for amyotrophic lateral sclerosis (ALS).
- This biomarker shows potential for early diagnosis and monitoring of ALS progression.
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