Evidence map›Paper›PMID 25348629›Full record

ArticleBrain : a journal of neurology2014

The relationship of nerve fibre pathology to sensory function in entrapment neuropathy.

Annina B Schmid, Jeremy D P Bland, Manzoor A Bhat, David L H Bennett

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Brain : a journal of neurology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02672059 (Pain In Neuropathy Study), which is not on this map. Cited by 59 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 7 pooled it
3.3field-weighted citation impact, top 7% 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.

NCT02672059 unknown statusnot on this map

Pain In Neuropathy Study

TypeobservationalSponsorKing's College LondonRan2011Enrolled700ConditionsDiabetic Neuropathy, Neuropathic Pain, Chronic Pain, Carpal Tunnel SyndromeArmsObservation
3 · Its place in the literature

Who cites it

59 citing papers in PubMed, 7 syntheses or guidelines pooled it, 138 citations in OpenAlex.

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  4. Atraumatic proximal radial nerve entrapment. Illustrative cases and systematic review of literature.European journal of orthopaedic surgery & traumatology : orthopedie traumatologie · 2022
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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

4 authors at 4 institutions in 3 countries.

Annina B SchmidNuffield Department of Clinical Neurosciences, University of Oxford, OX3 9DU, Headington, UK School of Health and Rehabilitation Sciences, The University of Queensland, St Lucia, QLD 4072, Australia.
Jeremy D P BlandDepartment of Clinical Neurophysiology, Kent and Canterbury Hospital, CT1 3NG, Canterbury Kent, UK.
Manzoor A BhatDepartment of Physiology, Centre for Biomedical Neuroscience, School of Medicine, University of Texas Health Science Centre, San Antonio, TX, USA.
David L H BennettNuffield Department of Clinical Neurosciences, University of Oxford, OX3 9DU, Headington, UK annina.schmid@neuro-research.ch david.bennett@ndcn.ox.ac.uk.
Kent and Canterbury Hospital · GBThe University of Texas Health Science Center at San Antonio · USUniversity of Oxford · GBUniversity of Queensland · AU

Funding

Molecular Organization &Function of Paranodal JunctionsR01GM063074 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BHAT, MANZOOR A. · 2001 to 2023
$5.8M
NIGMS NIH HHS GM063074NIGMS NIH HHS R01 GM063074Wellcome Trust 095698Wellcome Trust 095698z/11/zWellcome Trust 102645
6 · The paper itself

Abstract

Surprisingly little is known about the impact of entrapment neuropathy on target innervation and the relationship of nerve fibre pathology to sensory symptoms and signs. Carpal tunnel syndrome is the most common entrapment neuropathy; the aim of this study was to investigate its effect on the morphology of small unmyelinated as well as myelinated sensory axons and relate such changes to somatosensory function and clinical symptoms. Thirty patients with a clinical and electrophysiological diagnosis of carpal tunnel syndrome [17 females, mean age (standard deviation) 56.4 (15.3)] and 26 age and gender matched healthy volunteers [18 females, mean age (standard deviation) 51.0 (17.3)] participated in the study. Small and large fibre function was examined with quantitative sensory testing in the median nerve territory of the hand. Vibration and mechanical detection thresholds were significantly elevated in patients with carpal tunnel syndrome (P<0.007) confirming large fibre dysfunction and patients also presented with increased thermal detection thresholds (P<0.0001) indicative of C and Aδ-fibre dysfunction. Mechanical and thermal pain thresholds were comparable between groups (P>0.13). A skin biopsy was taken from a median nerve innervated area of the proximal phalanx of the index finger. Immunohistochemical staining for protein gene product 9.5 and myelin basic protein was used to evaluate morphological features of unmyelinated and myelinated axons. Evaluation of intraepidermal nerve fibre density showed a striking loss in patients (P<0.0001) confirming a significant compromise of small fibres. The extent of Meissner corpuscles and dermal nerve bundles were comparable between groups (P>0.07). However, patients displayed a significant increase in the percentage of elongated nodes (P<0.0001), with altered architecture of voltage-gated sodium channel distribution. Whereas neither neurophysiology nor quantitative sensory testing correlated with patients' symptoms or function deficits, the presence of elongated nodes was inversely correlated with a number of functional and symptom related scores (P<0.023). Our findings suggest that carpal tunnel syndrome does not exclusively affect large fibres but is associated with loss of function in modalities mediated by both unmyelinated and myelinated sensory axons. We also document for the first time that entrapment neuropathies lead to a clear reduction in intraepidermal nerve fibre density, which was independent of electrodiagnostic test severity. The presence of elongated nodes in the target tissue further suggests that entrapment neuropathies affect nodal structure/myelin well beyond the focal compression site. Interestingly, nodal lengthening may be an adaptive phenomenon as it inversely correlates with symptom severity.

Indexed as

AdultAgedAged, 80 and overArthrogryposisBiopsyCarpal Tunnel SyndromeFemaleHereditary Sensory and Motor NeuropathyHumansMaleMedian NerveMiddle AgedNerve FibersNeural ConductionPainSkincarpal tunnel syndromeentrapment neuropathynodes of Ranvierquantitative sensory testingskin biopsysmall fibres

Identifiers

PMID25348629
PMCPMC4240296
OpenAlexW2119258910

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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.