Biopsy-Proven Small-Fiber Neuropathy in Primary Sjögren's Syndrome: Neuropathic Pain Characteristics, Autoantibody Findings, and Histopathologic Features.


Journal

Arthritis care & research
ISSN: 2151-4658
Titre abrégé: Arthritis Care Res (Hoboken)
Pays: United States
ID NLM: 101518086

Informations de publication

Date de publication:
07 2019
Historique:
received: 02 01 2018
accepted: 11 09 2018
pubmed: 18 9 2018
medline: 25 2 2020
entrez: 18 9 2018
Statut: ppublish

Résumé

Painful small-fiber neuropathies (SFNs) in primary Sjögren's syndrome (SS) may present as pure or mixed with concurrent large-fiber involvement. SFN can be diagnosed by punch skin biopsy results that identify decreased intra-epidermal nerve-fiber density (IENFD) of unmyelinated nerves. We compared 23 consecutively evaluated patients with SS with pure and mixed SFN versus 98 patients without SFN. We distinguished between markers of dorsal root ganglia (DRG) degeneration (decreased IENFD in the proximal thigh versus the distal leg) versus axonal degeneration (decreased IENFD in the distal leg versus the proximal thigh). There were no differences in pain intensity, pain quality, and treatment characteristics in the comparison of 13 patients with pure SFN versus 10 patients with mixed SFN. Ten patients with SFN (approximately 45%) had neuropathic pain preceding sicca symptoms. Opioid analgesics were prescribed to approximately 45% of patients with SFN. When compared to 98 patients without SFN, the 23 patients with SFN had an increased frequency of male sex (30% versus 9%; P < 0.01), a decreased frequency of anti-Ro 52 (P = 0.01) and anti-Ro 60 antibodies (P = 0.01), rheumatoid factor positivity (P < 0.01), and polyclonal gammopathy (P < 0.01). Eleven patients had stocking-and-glove pain, and 12 patients had nonstocking-and-glove pain. Skin biopsy results disclosed patterns of axonal (16 patients) and DRG injury (7 patients). SS SFN had an increased frequency among male patients, a decreased frequency of multiple antibodies, frequent treatment with opioid analgesics, and the presence of nonstocking-and-glove pain. Distinguishing between DRG versus axonal injury is significant, especially given that mechanisms targeting the DRG may result in irreversible neuronal cell death. Altogether, these findings highlight clinical, autoantibody, and pathologic features that can help to define mechanisms and treatment strategies.

Identifiants

pubmed: 30221483
doi: 10.1002/acr.23762
pmc: PMC7556316
mid: NIHMS1627500
doi:

Substances chimiques

Autoantibodies 0
Biomarkers 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

936-948

Subventions

Organisme : NIDCR NIH HHS
ID : R01 DE012354
Pays : United States
Organisme : Jerome L. Greene Foundation
Pays : International
Organisme : NIDCR NIH HHS
ID : R37 DE012354
Pays : United States
Organisme : NIAMS NIH HHS
ID : P30 AR070254
Pays : United States
Organisme : NIH HHS
ID : DE-12354-15A1
Pays : United States
Organisme : NIAMS NIH HHS
ID : K23 AR064279
Pays : United States
Organisme : NIAMS NIH HHS
ID : P30 AR053503
Pays : United States

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2018, American College of Rheumatology.

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Auteurs

Julius Birnbaum (J)

Johns Hopkins University School of Medicine, Baltimore, Maryland.

Aliya Lalji (A)

Johns Hopkins University School of Medicine, Baltimore, Maryland.

Aveen Saed (A)

Johns Hopkins University School of Medicine, Baltimore, Maryland.

Alan N Baer (AN)

Johns Hopkins University School of Medicine, Baltimore, Maryland.

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Classifications MeSH