Evidence map›Paper›PMID 28114358›Full record

ArticlePloS one2017

Metabolic Syndrome, Neurotoxic 1-Deoxysphingolipids and Nervous Tissue Inflammation in Chronic Idiopathic Axonal Polyneuropathy (CIAP).

Larissa Hube, Maike F Dohrn, Gergely Karsai, Sarah Hirshman, Philip Van Damme, Jörg B Schulz, Joachim Weis, Thorsten Hornemann, Kristl G Claeys

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Demyelination in hereditary sensory neuropathy type-1C.Annals of clinical and translational neurology · 2020
    Article
  9. Article
  10. Macrophage Depletion Ameliorates Peripheral Neuropathy in Aging Mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  11. 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

9 authors at 5 institutions in 3 countries.

Larissa HubeDepartment of Neurology, RWTH Aachen University, Aachen, Germany.
Maike F DohrnDepartment of Neurology, RWTH Aachen University, Aachen, Germany.
Gergely KarsaiCenter for Integrative Human Physiology, University of Zurich, Zurich, Switzerland.
Sarah HirshmanDepartment of Neurology, RWTH Aachen University, Aachen, Germany.
Philip Van DammeDepartment of Neurology, University Hospitals Leuven, Leuven, Belgium.
Jörg B SchulzDepartment of Neurology, RWTH Aachen University, Aachen, Germany.
Joachim WeisInstitute of Neuropathology, RWTH Aachen University, Aachen, Germany.
Thorsten HornemannCenter for Integrative Human Physiology, University of Zurich, Zurich, Switzerland.
Kristl G ClaeysDepartment of Neurology, RWTH Aachen University, Aachen, Germany.
RWTH Aachen University · DEJülich Aachen Research Alliance · DEKU Leuven · BESwiss Integrative Center for Human Health · CHUniversity Hospital of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimChronic idiopathic axonal polyneuropathy (CIAP) is a slowly progressive, predominantly sensory, axonal polyneuropathy, with no aetiology being identified despite extensive investigations. We studied the potential role of the metabolic syndrome, neurotoxic 1-deoxysphingolipids (1-deoxySLs), microangiopathy and inflammation in sural nerve biopsies.

methodsWe included 30 CIAP-patients, 28 with diabetic distal symmetrical polyneuropathy (DSPN) and 31 healthy controls. We assessed standardised scales, tested for the metabolic syndrome, measured 1-deoxySLs in plasma, performed electroneurography and studied 17 sural nerve biopsies (10 CIAP; 7 DSPN).

resultsOne third of the CIAP-patients had a metabolic syndrome, significantly less frequent than DSPN-patients (89%). Although the metabolic syndrome was not significantly more prevalent in CIAP compared to healthy controls, hypercholesterolemia did occur significantly more frequent. 1-deoxySLs were significantly and equally elevated in both patient groups compared to healthy controls. Mean basal lamina thickness of small endoneurial vessels and the number of CD68- or CD8-positive cells in biopsies of CIAP- and DSPN-patients did not differ significantly. However, the number of leucocyte-common-antigen positive cells was significantly increased in CIAP.

conclusionsA non-significant trend towards a higher occurrence of the metabolic syndrome in CIAP-patients compared to healthy controls was found. 1-deoxySLs were significantly increased in plasma of CIAP-patients. Microangiopathy and an inflammatory component were present in CIAP-biopsies.

Indexed as

AgedAxonsCase-Control StudiesChronic DiseaseDiabetic NeuropathiesFemaleHumansMaleMetabolic SyndromeMiddle AgedPolyneuropathiesSphingolipidsSphingolipids

Identifiers

PMID28114358
PMCPMC5256922
OpenAlexW2580480504

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.