Evidence map›Paper›PMID 28389989›Full record

ArticleClinical rheumatology2018

Single vagus nerve stimulation reduces early postprandial C-peptide levels but not other hormones or postprandial metabolism.

M W Tang, F S van Nierop, F A Koopman, H M Eggink, D M Gerlag, M W Chan, R Zitnik, F M Vaz, J A Romijn, P P Tak and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Clinical rheumatology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. 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

11 authors at 4 institutions in 4 countries.

M W TangDepartment of Clinical Immunology & Rheumatology, Amsterdam Rheumatology and Immunology Centre, Academic Medical Centre, University of Amsterdam, Room F4-105, PO Box 22700, 1100 DE, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0001-9726-9943
F S van NieropDepartment of Endocrinology and Metabolism, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands.
F A KoopmanDepartment of Clinical Immunology & Rheumatology, Amsterdam Rheumatology and Immunology Centre, Academic Medical Centre, University of Amsterdam, Room F4-105, PO Box 22700, 1100 DE, Amsterdam, The Netherlands.
H M EgginkDepartment of Endocrinology and Metabolism, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands.
D M GerlagDepartment of Clinical Immunology & Rheumatology, Amsterdam Rheumatology and Immunology Centre, Academic Medical Centre, University of Amsterdam, Room F4-105, PO Box 22700, 1100 DE, Amsterdam, The Netherlands.
M W ChanDepartment of Clinical Immunology & Rheumatology, Amsterdam Rheumatology and Immunology Centre, Academic Medical Centre, University of Amsterdam, Room F4-105, PO Box 22700, 1100 DE, Amsterdam, The Netherlands.
R ZitnikSetPoint Medical Corporation, Valencia, CA, USA.
F M VazLaboratory of Genetic Metabolic Disease, Department of clinical chemistry, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands.
J A RomijnDepartment of Internal Medicine, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands.
P P TakDepartment of Clinical Immunology & Rheumatology, Amsterdam Rheumatology and Immunology Centre, Academic Medical Centre, University of Amsterdam, Room F4-105, PO Box 22700, 1100 DE, Amsterdam, The Netherlands. p.p.tak@amc.uva.nl.
M R SoetersDepartment of Endocrinology and Metabolism, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands.
University of Amsterdam · NLAlta Bates Summit Medical Center · USGlaxoSmithKline (United Kingdom) · GBUniversity College Ghent · BE

Funding

IMI EU funded project BeTheCure 001423
6 · The paper itself

Abstract

A recent study in rheumatoid arthritis (RA) patients using electrical vagus nerve stimulation (VNS) to activate the inflammatory reflex has shown promising effects on disease activity. Innervation by the autonomic nerve system might be involved in the regulation of many endocrine and metabolic processes and could therefore theoretically lead to unwanted side effects. Possible effects of VNS on secretion of hormones are currently unknown. Therefore, we evaluated the effects of a single VNS on plasma levels of pituitary hormones and parameters of postprandial metabolism. Six female patients with RA were studied twice in balanced assignment (crossover design) to either VNS or no stimulation. The patients selected for this substudy had been on VNS therapy daily for at least 3 months and at maximum of 24 months. We compared 10-, 20-, and 30-min poststimulus levels to baseline levels, and a 4-h mixed meal test was performed 30 min after VNS. We also determined energy expenditure (EE) by indirect calorimetry before and after VNS. VNS did not affect pituitary hormones (growth hormone, thyroid stimulating hormone, adrenocorticotropic hormone, prolactin, follicle-stimulating hormone, and luteinizing hormone), postprandial metabolism, or EE. Of note, VNS reduced early postprandial insulin secretion, but not AUC of postprandial plasma insulin levels. Cortisol and catecholamine levels in serum did not change significantly. Short stimulation of vagal activity by VNS reduces early postprandial insulin secretion, but not other hormone levels and postprandial response. This suggests VNS as a safe treatment for RA patients.

Indexed as

Vagus Nerve StimulationAdrenocorticotropic HormoneAdultArthritis, RheumatoidCalorimetry, IndirectC-PeptideCross-Over StudiesEnergy MetabolismFemaleFollicle Stimulating HormoneHuman Growth HormoneHumansLuteinizing HormoneMiddle AgedPostprandial PeriodProlactinAdrenocorticotropic HormoneC-PeptideFollicle Stimulating HormoneHuman Growth HormoneLuteinizing HormoneProlactinThyrotropinBrainClinical trials and methodsEndocrineGastrointestinalHormonesMetabolic diseaseMetabolomicsRheumatoid arthritisStudy design

Identifiers

PMID28389989
PMCPMC5775981
OpenAlexW2605167837

What OpenQuestion holds

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Registered trials

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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.