Skin Biopsy Detection of Phosphorylated α-Synuclein in Patients With Synucleinopathies

Author:

Gibbons Christopher H.1,Levine Todd23,Adler Charles4,Bellaire Bailey3,Wang Ningshan1,Stohl Jade3,Agarwal Pinky5,Aldridge Georgina M.6,Barboi Alexandru7,Evidente Virgilio G. H.8,Galasko Douglas9,Geschwind Michael D.10,Gonzalez-Duarte Alejandra11,Gil Ramon12,Gudesblatt Mark13,Isaacson Stuart H.14,Kaufmann Horacio11,Khemani Pravin15,Kumar Rajeev16,Lamotte Guillaume17,Liu Andy J.18,McFarland Nikolaus R.19,Miglis Mitchell20,Reynolds Adam21,Sahagian Gregory A.22,Saint-Hillaire Marie-Helene23,Schwartzbard Julie B.24,Singer Wolfgang25,Soileau Michael J.26,Vernino Steven27,Yerstein Oleg28,Freeman Roy1

Affiliation:

1. Department of Neurology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts

2. HonorHealth Neurology, Scottsdale, Arizona

3. CND Life Sciences, Scottsdale, Arizona

4. Department of Neurology, Mayo Clinic College of Medicine, Scottsdale, Arizona

5. Evergreen Health, Kirkland, Washington

6. Department of Neurology, Carver College of Medicine, University of Iowa, Iowa City

7. Department of Neurology, Northshore University Health System, Glenview, Illinois

8. Movement Disorder Center of Arizona, Scottsdale

9. Department of Neurology, University of California, San Diego

10. Department of Neurology, University of California, San Franscisco

11. Department of Neurology, New York University Grossman School of Medicine, New York

12. Parkinson’s Disease Treatment Center of Southwest Florida, Port Charlotte

13. Department of Neurology, New York University Grossman Long Island School of Medicine, New York

14. Parkinson’s Disease and Movement Disorders Center of Boca Raton, Boca Raton, Florida

15. Department of Neurology, Swedish Medical Center, Seattle, Washington

16. Rocky Mountain Movement Disorders Center, Englewood, Colorado

17. Department of Neurology, University of Utah, Salt Lake City

18. Department of Neurology, Duke University School of Medicine, Durham, North Carolina

19. Department of Neurology, University of Florida Health Center, Gainesville

20. Department of Neurology, Stanford University Medical Center, Palo Alto, California

21. Center for Neurosciences, Tuscan, Arizona

22. The Neurology Center of Southern California, Carlsbad

23. Department of Neurology, Boston Medical Center, Boston, Massachusetts

24. Aventura Associates, Aventura, Florida

25. Department of Neurology, Mayo Clinic Rochester, Rochester, New York

26. Texas Movement Disorder Specialists, Georgetown

27. Department of Neurology, The University of Texas Southwestern Medical Center, Dallas

28. Department of Neurology, Lahey Clinic, Burlington, Massachusetts

Abstract

ImportanceFinding a reliable diagnostic biomarker for the disorders collectively known as synucleinopathies (Parkinson disease [PD], dementia with Lewy bodies [DLB], multiple system atrophy [MSA], and pure autonomic failure [PAF]) is an urgent unmet need. Immunohistochemical detection of cutaneous phosphorylated α-synuclein may be a sensitive and specific clinical test for the diagnosis of synucleinopathies.ObjectiveTo evaluate the positivity rate of cutaneous α-synuclein deposition in patients with PD, DLB, MSA, and PAF.Design, Setting, and ParticipantsThis blinded, 30-site, cross-sectional study of academic and community-based neurology practices conducted from February 2021 through March 2023 included patients aged 40 to 99 years with a clinical diagnosis of PD, DLB, MSA, or PAF based on clinical consensus criteria and confirmed by an expert review panel and control participants aged 40 to 99 years with no history of examination findings or symptoms suggestive of a synucleinopathy or neurodegenerative disease. All participants completed detailed neurologic examinations and disease-specific questionnaires and underwent skin biopsy for detection of phosphorylated α-synuclein. An expert review panel blinded to pathologic data determined the final participant diagnosis.ExposureSkin biopsy for detection of phosphorylated α-synuclein.Main OutcomesRates of detection of cutaneous α-synuclein in patients with PD, MSA, DLB, and PAF and controls without synucleinopathy.ResultsOf 428 enrolled participants, 343 were included in the primary analysis (mean [SD] age, 69.5 [9.1] years; 175 [51.0%] male); 223 met the consensus criteria for a synucleinopathy and 120 met criteria as controls after expert panel review. The proportions of individuals with cutaneous phosphorylated α-synuclein detected by skin biopsy were 92.7% (89 of 96) with PD, 98.2% (54 of 55) with MSA, 96.0% (48 of 50) with DLB, and 100% (22 of 22) with PAF; 3.3% (4 of 120) of controls had cutaneous phosphorylated α-synuclein detected.Conclusions and RelevanceIn this cross-sectional study, a high proportion of individuals meeting clinical consensus criteria for PD, DLB, MSA, and PAF had phosphorylated α-synuclein detected by skin biopsy. Further research is needed in unselected clinical populations to externally validate the findings and fully characterize the potential role of skin biopsy detection of phosphorylated α-synuclein in clinical care.

Publisher

American Medical Association (AMA)

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