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


Journal

JAMA
ISSN: 1538-3598
Titre abrégé: JAMA
Pays: United States
ID NLM: 7501160

Informations de publication

Date de publication:
20 Mar 2024
Historique:
medline: 20 3 2024
pubmed: 20 3 2024
entrez: 20 3 2024
Statut: aheadofprint

Résumé

Finding 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. To evaluate the positivity rate of cutaneous α-synuclein deposition in patients with PD, DLB, MSA, and PAF. This 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. Skin biopsy for detection of phosphorylated α-synuclein. Rates of detection of cutaneous α-synuclein in patients with PD, MSA, DLB, and PAF and controls without synucleinopathy. Of 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. In 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.

Identifiants

pubmed: 38506839
pii: 2816441
doi: 10.1001/jama.2024.0792
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Christopher H Gibbons (CH)

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

Todd Levine (T)

HonorHealth Neurology, Scottsdale, Arizona.
CND Life Sciences, Scottsdale, Arizona.

Charles Adler (C)

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

Bailey Bellaire (B)

CND Life Sciences, Scottsdale, Arizona.

Ningshan Wang (N)

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

Jade Stohl (J)

CND Life Sciences, Scottsdale, Arizona.

Pinky Agarwal (P)

Evergreen Health, Kirkland, Washington.

Georgina M Aldridge (GM)

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

Alexandru Barboi (A)

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

Virgilio G H Evidente (VGH)

Movement Disorder Center of Arizona, Scottsdale.

Douglas Galasko (D)

Department of Neurology, University of California, San Diego.

Michael D Geschwind (MD)

Department of Neurology, University of California, San Franscisco.

Alejandra Gonzalez-Duarte (A)

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

Ramon Gil (R)

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

Mark Gudesblatt (M)

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

Stuart H Isaacson (SH)

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

Horacio Kaufmann (H)

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

Pravin Khemani (P)

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

Rajeev Kumar (R)

Rocky Mountain Movement Disorders Center, Englewood, Colorado.

Guillaume Lamotte (G)

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

Andy J Liu (AJ)

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

Nikolaus R McFarland (NR)

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

Mitchell Miglis (M)

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

Adam Reynolds (A)

Center for Neurosciences, Tuscan, Arizona.

Gregory A Sahagian (GA)

The Neurology Center of Southern California, Carlsbad.

Marie-Helene Saint-Hillaire (MH)

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

Julie B Schwartzbard (JB)

Aventura Associates, Aventura, Florida.

Wolfgang Singer (W)

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

Michael J Soileau (MJ)

Texas Movement Disorder Specialists, Georgetown.

Steven Vernino (S)

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

Oleg Yerstein (O)

Department of Neurology, Lahey Clinic, Burlington, Massachusetts.

Roy Freeman (R)

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

Classifications MeSH