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February 19, 2013; 80 (8) Article

Skin sympathetic fiber α-synuclein deposits

A potential biomarker for pure autonomic failure

Vincenzo Donadio, Alex Incensi, Pietro Cortelli, Maria Pia Giannoccaro, Masen Abdel Jaber, Agostino Baruzzi, Rocco Liguori
First published February 6, 2013, DOI: https://doi.org/10.1212/WNL.0b013e3182825127
Vincenzo Donadio
From IRCCS Istituto delle Scienze Neurologiche di Bologna e Dipartimento di Scienze Neurologiche, Università di Bologna, Bologna, Italy.
MD, PhD
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Alex Incensi
From IRCCS Istituto delle Scienze Neurologiche di Bologna e Dipartimento di Scienze Neurologiche, Università di Bologna, Bologna, Italy.
BSc
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Pietro Cortelli
From IRCCS Istituto delle Scienze Neurologiche di Bologna e Dipartimento di Scienze Neurologiche, Università di Bologna, Bologna, Italy.
MD
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Maria Pia Giannoccaro
From IRCCS Istituto delle Scienze Neurologiche di Bologna e Dipartimento di Scienze Neurologiche, Università di Bologna, Bologna, Italy.
MD
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Masen Abdel Jaber
From IRCCS Istituto delle Scienze Neurologiche di Bologna e Dipartimento di Scienze Neurologiche, Università di Bologna, Bologna, Italy.
MD
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Agostino Baruzzi
From IRCCS Istituto delle Scienze Neurologiche di Bologna e Dipartimento di Scienze Neurologiche, Università di Bologna, Bologna, Italy.
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Rocco Liguori
From IRCCS Istituto delle Scienze Neurologiche di Bologna e Dipartimento di Scienze Neurologiche, Università di Bologna, Bologna, Italy.
MD
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Citation
Skin sympathetic fiber α-synuclein deposits
A potential biomarker for pure autonomic failure
Vincenzo Donadio, Alex Incensi, Pietro Cortelli, Maria Pia Giannoccaro, Masen Abdel Jaber, Agostino Baruzzi, Rocco Liguori
Neurology Feb 2013, 80 (8) 725-732; DOI: 10.1212/WNL.0b013e3182825127

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This article has a correction. Please see:

  • Skin sympathetic fiber α-synuclein deposits: A potential biomarker for pure autonomic failure - January 07, 2014
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Abstract

Objective: This study aimed to test whether peripheral α-synuclein staining might be useful for pure autonomic failure (PAF) diagnosis, helping to differentiate degenerative from acquired peripheral autonomic neuropathy.

Methods: We studied 21 patients with chronic peripheral autonomic neuropathy showing sympathetic and parasympathetic involvement as confirmed by cardiovascular reflexes and microneurography from the peroneal nerve. Twelve patients showed a specific cause of neuropathy (acquired autonomic neuropathy) whereas 9 had no specific acquired causes fulfilling the diagnostic criteria for PAF. Fifteen matched healthy subjects served as controls. Subjects underwent skin biopsy from thigh and leg to study skin innervation and phosphorylated α-synuclein deposits in the peripheral axons.

Results: Somatic and autonomic skin innervations were significantly decreased in patients with peripheral autonomic neuropathy compared to controls. No differences were found between acquired autonomic neuropathy and PAF. The deposits of α-synuclein were not found in controls but served to distinguish acquired from degenerative autonomic peripheral neuropathy: all patients with PAF showed α-synuclein deposits, which were absent in patients with acquired autonomic neuropathy. Colocalization study disclosed α-synuclein neuritic inclusions in the postganglionic sympathetic adrenergic and cholinergic nerve fibers.

Conclusions: Our study demonstrated that a search for neuritic inclusions of phosphorylated α-synuclein in the skin sympathetic nerve fibers could provide a sensitive in vivo biomarker for degenerative peripheral autonomic neuropathy and may shed more light on the pathogenesis of PAF.

GLOSSARY

AChR=
acetylcholine receptor;
DβH=
dopamine-β-hydroxylase;
LB=
Lewy body;
MAP=
muscle arrector pilorum;
PAF=
pure autonomic failure;
PAN=
peripheral autonomic neuropathy;
PGP 9.5=
protein gene product 9.5;
PGP-ir=
protein gene product immunoreactive;
SG=
sweat gland;
VIP=
vasoactive intestinal peptide

Footnotes

  • Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Received July 27, 2012.
  • Accepted October 15, 2012.
  • © 2013 American Academy of Neurology
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