CSF α-Synuclein Seed Amplification Assays and Skin Immunofluorescence

The development of biomarkers capable of reliably detecting pathologic forms of α-synuclein (aSyn) in vivo marks a significant step forward in the field of neurodegeneration. Over the recent years, CSF aSyn seed amplification assays (aSyn-SAA) and skin biopsy phospho-aSyn immunofluorescence (skin aSyn-IF) testing were developed that detect pathologic aSyn seeds and phosphorylated aSyn aggregates, respectively, in patients with synucleinopathies, which include Parkinson disease, dementia with Lewy bodies, and also multiple system atrophy. High rates of positivity have also been documented in research participants at a risk of developing future aSyn-related disease (e.g., hyposmia and REM sleep behavior disorder), as well as other contexts. These assays have numerous potential applications in research settings and clinical care. Here, we review the currently published evidence supporting CSF aSyn-SAA and skin aSyn-IF testing and discuss their potential research applications in clinical trials. As CSF aSyn-SAA and skin aSyn-IF testing is now commercially available to clinicians in nonresearch settings, we also explore their current utility and limitations as diagnostic tools and call for the development of a formal clinical use guidelines. We also highlight where critical knowledge gaps remain and explore emerging developments related to these assays.

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Publication Details

Journal
Neurology
Published
2026-01-13
DOI
https://doi.org/10.1212/wnl.0000000000214648
Primary Topic
Parkinson's Disease Mechanisms and Treatments
Type
article
Field-Weighted Citation Impact
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article

CSF α-Synuclein Seed Amplification Assays and Skin Immunofluorescence

George T. Kannarkat, Thomas Francis Tropea, Juan Diego Martínez-Lemus, Danielle Thordarson et al.
Neurology
Parkinson's Disease Mechanisms and Treatments
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CSF α-Synuclein Seed Amplification Assays and Skin Immunofluorescence

George T. Kannarkat, Thomas Francis Tropea, Juan Diego Martínez-Lemus, Danielle Thordarson, David G. Coughlin, Cayla Vila, Alexander Pantelyat, Jamie L. Adams, Liana Rosenthal, Anthony E. Lang, Charles H. Adler, Andrew D. Siderowf, for the Parkinson Study Group Biomarkers Working Group, William Barbosa, Joohi Jimenez-Shahed, Steven A. Gunzler, Douglas Galasko, Tanya Simuni, Jeanne Feuerstein, Peter A. LeWitt, Mya C. Schiess, Michael Schwarzschild
article en

Abstract

The development of biomarkers capable of reliably detecting pathologic forms of α-synuclein (aSyn) in vivo marks a significant step forward in the field of neurodegeneration. Over the recent years, CSF aSyn seed amplification assays (aSyn-SAA) and skin biopsy phospho-aSyn immunofluorescence (skin aSyn-IF) testing were developed that detect pathologic aSyn seeds and phosphorylated aSyn aggregates, respectively, in patients with synucleinopathies, which include Parkinson disease, dementia with Lewy bodies, and also multiple system atrophy. High rates of positivity have also been documented in research participants at a risk of developing future aSyn-related disease (e.g., hyposmia and REM sleep behavior disorder), as well as other contexts. These assays have numerous potential applications in research settings and clinical care. Here, we review the currently published evidence supporting CSF aSyn-SAA and skin aSyn-IF testing and discuss their potential research applications in clinical trials. As CSF aSyn-SAA and skin aSyn-IF testing is now commercially available to clinicians in nonresearch settings, we also explore their current utility and limitations as diagnostic tools and call for the development of a formal clinical use guidelines. We also highlight where critical knowledge gaps remain and explore emerging developments related to these assays.

NeurologyVol. 106(3)
Northwestern University (US), University Health Network (CA), Johns Hopkins University (US), University of California, Los Angeles (US), Wayne State University (US), University Hospitals of Cleveland (US), University of California San Diego (US), Massachusetts General Hospital (US), Institute for Neurodegenerative Disorders (US), Mayo Clinic Hospital (US), University of Colorado Anschutz Medical Campus (US), University of Rochester (US), University of Pennsylvania (US), The University of Texas Health Science Center at Houston (US), University of Colorado Denver (US), Icahn School of Medicine at Mount Sinai (US)
Partnerships for the goals
Openalex Percentile: Top 89%
Parkinson's Disease Mechanisms and Treatments
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