Evidence map›Paper›PMID 34791566›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2022

Sudomotor dysfunction in patients with gluten neuropathy.

Panagiotis Zis, Faiza Shafique, Ptolemaios G Sarrigiannis, Artemios Artemiadis, Dasappaiah G Rao, David S Sanders, Marios Hadjivassiliou

Open access · hybridAbstract read
In one paragraph

Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 43% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Panagiotis ZisMedical School, University of Cyprus, Nicosia, Cyprus. takiszis@gmail.com.ORCID http://orcid.org/0000-0001-8567-3092
Faiza ShafiqueSheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
Ptolemaios G SarrigiannisDepartment of Clinical Neurophysiology, Royal Devon and Exeter NHS Foundation Trust, Exeter, UK.
Artemios ArtemiadisMedical School, University of Cyprus, Nicosia, Cyprus.
Dasappaiah G RaoSheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
David S SandersMedical School, University of Sheffield, Sheffield, UK.
Marios HadjivassiliouMedical School, University of Sheffield, Sheffield, UK.
Sheffield Teaching Hospitals NHS Foundation Trust · GBUniversity of Cyprus · CYRoyal Devon & Exeter NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimGluten neuropathy (GN) is a common neurological manifestation of gluten sensitivity (GS), characterized by serological evidence of GS, while other risk factors for developing neuropathy are absent. The degree of small fiber dysfunction in GN has not been studied in depth to date. Small fiber involvement may lead to pain, thermal perception abnormalities, and sweat gland dysfunction. Sudomotor innervation refers to the cholinergic innervation of the sympathetic nervous system through small fibers in the sweat glands. The aim of our study was to assess the sudomotor function of GN patients.

methodsPatients with GN were recruited. Clinical and neurophysiological data were obtained. HLA-DQ genotyping was performed. The skin electrochemical conductance (ESC) was measured with SUDOSCAN

resultsThirty-two patients (25 males, mean age 69.5±10.2 years) were recruited. Thirteen patients (40.6%) had abnormal sudomotor function of the hands. Sixteen patients (50%) had abnormal sudomotor function of the feet. Twenty-one patients (65.6%) had abnormal sudomotor function of either the hands or feet. Sudomotor dysfunction did not correlate with the type of neuropathy (length-dependent neuropathy or sensory ganglionopathy), gluten-free diet adherence, severity of neuropathy, and duration of disease or HLA-DQ genotype. No differences in the ESC were found between patients with painful and patients with painless GN.

conclusionSudomotor dysfunction affects two-thirds of patients with GN. The lack of correlation between pain and sudomotor dysfunction suggests different patterns of small fiber involvement in patients with GN.

Indexed as

GlutensPeripheral Nervous System DiseasesAgedFemaleGalvanic Skin ResponseHandHLA-DQ AntigensHumansMaleMiddle AgedPainGlutensHLA-DQ AntigensAutonomicGluten neuropathySmall fiberSudomotorSUDOSCAN

Identifiers

PMID34791566
PMCPMC9018627
OpenAlexW3213410241

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.