SynthesisMolecular neurodegeneration2025
Diagnostic biomarkers for α-synucleinopathies- state of the art and future developments: a systematic review.
Synthesis in Molecular neurodegeneration, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
3 citing papers in PubMed.
- Alpha-Synuclein in Neurodegeneration: From Shared Biology to Disease-Specific Phenotypes.Cells · 2026Review
- Article
- Sustained attention in dementia with Lewy bodies: a task-based fMRI study.Frontiers in aging neuroscience · 2026Article
Corrections and comments
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Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundAlpha-synucleinopathies are common disorders that are expected to become increasingly prevalent in the future along with the longer life expectancy. However, their diagnosis is problematic as they are mainly based on clinical criteria without the support of disease-specific biomarkers. This leads to frequent misdiagnoses, as underlined by autopsy studies, and an imprecise selection of patients for clinical trials, preventing progress in the development of disease-modifying treatments. In recent years important advances have been made regarding the development of specific biomarkers for the detection of pathological α-synuclein (α-syn), which may improve the diagnosis of patients affected by α-synucleinopathies.
resultsIn this review, we describe in detail the most promising techniques to detect pathological α-syn in patient-derived samples. In particular, we describe the diagnostic accuracy of each individual cerebrospinal fluid (CSF), plasma and skin α-syn biomarker in differentiating α-synucleinopathies from controls, from other neurodegenerative disorders and between different α-synucleinopathies. Furthermore, we underline the main advantages and limitations of these techniques for clinical practice. Finally, we provide our suggestions for further development considering both technical aspects and large-scale standardization. CONCLUSIONS AND RELEVANCE: We conclude that immunofluorescence on biopsied skin tissue and the seed amplification assay on CSF show the best diagnostic accuracy and reliability in the studies that have been performed to date. We discuss the opportunities of these techniques as well as the main current limitations and technical problems that need to be considered before they can be adopted for clinical use.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.