Evidence map›Paper›PMID 39291161›Full record

ArticleBrain communications2024

New phenotyping questionnaire for diagnosing sarcoidosis-associated small fiber neuropathy.

Lisette R M Raasing, Oscar J M Vogels, Mirjam Datema, Carmen A Ambarus, Martijn R Tannemaat, Jan C Grutters, Marcel Veltkamp

Abstract read
In one paragraph

Article in Brain communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Lisette R M RaasingILD Center of Excellence, Department of Pulmonology, St Antonius Hospital, 3435 CM Nieuwegein, The Netherlands.ORCID https://orcid.org/0000-0003-0474-7550
Oscar J M VogelsILD Center of Excellence, Department of Neurology, St Antonius Hospital, 3435 CM Nieuwegein, The Netherlands.
Mirjam DatemaILD Center of Excellence, Department of Clinical Neurophysiology, St Antonius Hospital, 3435 CM Nieuwegein, The Netherlands.
Carmen A AmbarusILD Center of Excellence, Department of Pathology, St Antonius Hospital, 3435 CM Nieuwegein, The Netherlands.
Martijn R TannemaatDepartment of Clinical Neurophysiology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.ORCID https://orcid.org/0000-0003-2929-0390
Jan C GruttersILD Center of Excellence, Department of Pulmonology, St Antonius Hospital, 3435 CM Nieuwegein, The Netherlands.
Marcel VeltkampILD Center of Excellence, Department of Pulmonology, St Antonius Hospital, 3435 CM Nieuwegein, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Small fiber neuropathy is a common complication in patients with sarcoidosis and its prevalence is estimated at 40-86%. The underlying mechanism influences the presentation of small fiber neuropathy. For example, patients with metabolic diseases are often associated with a classic length-dependent small fiber neuropathy pattern, while patients with inflammatory diseases are more often present with a non-length-dependent small fiber neuropathy. Detailed phenotyping may be useful to improve diagnostic efficiency, as a clue to underlying mechanisms and as a precondition for personalized medicine. This study examined four phenotypes distinguishing between length-dependent and non-length-dependent presentation with a new subdivision for continuous and intermittent presentation. Forty-eight sarcoid patients with symptoms and at least two clinical signs of small fiber neuropathy and normal nerve conduction studies were classified as having probable small fiber neuropathy. A new small fiber neuropathy phenotyping questionnaire has been developed that allows patients to mark the anatomical locations of pain at three different levels: the skin, muscles, and joints. The location of symptoms was used to define length dependence, and two colors were used to distinguish continuous (red) from intermittent (blue) symptoms. In addition, skin biopsy, corneal confocal microscopy, Sudoscan and water immersion skin wrinkling were used to investigate a correlation between the four phenotypes, sensory function, nerve fiber density, and autonomic nerve function. Overall, 35% of patients with probable small fiber neuropathy showed length-dependent symptoms and 44% showed non-length-dependent symptoms while 21% suffered from non-neuropathic musculoskeletal pain. The distinction between intermittent and continuous symptoms showed significantly less continuous than intermittent non-length-dependent symptoms (odds ratio = 0.3,

Indexed as

nerve fiber densitypainsensory testingSFNSLthermal threshold testing

Identifiers

PMID39291161
PMCPMC11406462

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