Evidence map›Paper›PMID 31471628›Full record

ArticleJournal of molecular medicine (Berlin, Germany)2019

Clinical relevance of circadian melatonin release in relapsing-remitting multiple sclerosis.

Simone Kern, Michael Geiger, Madlen Paucke, Alina Kästner, Katja Akgün, Tjalf Ziemssen

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of molecular medicine (Berlin, Germany), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.9field-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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Time to activin on pathogenic T cells.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  10. The role of melatonin in Multiple Sclerosis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2020
    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

6 authors at 1 institution in 1 country.

Simone KernZentrum für Klinische Neurowissenschaften, Klinik und Poliklinik für Neurologie, CGC Universitätsklinikum Dresden, Fetscherstr. 74, 01307, Dresden, Germany. Simone.Kern@uniklinikum-dresden.de.ORCID 0000-0001-7173-1482
Michael GeigerZentrum für Klinische Neurowissenschaften, Klinik und Poliklinik für Neurologie, CGC Universitätsklinikum Dresden, Fetscherstr. 74, 01307, Dresden, Germany.
Madlen PauckeZentrum für Klinische Neurowissenschaften, Klinik und Poliklinik für Neurologie, CGC Universitätsklinikum Dresden, Fetscherstr. 74, 01307, Dresden, Germany.
Alina KästnerZentrum für Klinische Neurowissenschaften, Klinik und Poliklinik für Neurologie, CGC Universitätsklinikum Dresden, Fetscherstr. 74, 01307, Dresden, Germany.
Katja AkgünZentrum für Klinische Neurowissenschaften, Klinik und Poliklinik für Neurologie, CGC Universitätsklinikum Dresden, Fetscherstr. 74, 01307, Dresden, Germany.
Tjalf ZiemssenZentrum für Klinische Neurowissenschaften, Klinik und Poliklinik für Neurologie, CGC Universitätsklinikum Dresden, Fetscherstr. 74, 01307, Dresden, Germany.
Klinik und Poliklinik für Neurologie · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A growing body of evidence indicates the role of melatonin (MT) in the pathogenesis of multiple sclerosis (MS): It modulates immune function, alleviates oxidative stress and it is linked to seasonality of MS relapse. This report addresses the potential clinical relevance of circadian MT rhythms in relapsing-remitting MS (RRMS) patients. The study sample comprised of fifty-five RRMS patients and fifty age- and sex-matched healthy control (HC) subjects. Circadian salivary MT was measured non-invasively at 12 time points over day in participants' home environment. 6-Hydroxy-melatoninsulfate (MT sulfate) concentration in night-time urine was assessed as an estimate for nocturnal MT. Ratings for neurological disability, health-related quality of life (HrQoL), fatigue, depressive symptoms and sleep patterns were additionally obtained. There was no evidence for an overall disturbed MT rhythm in RRMS patients. However, lower MT levels within the first hour after awakening were associated with longer disease duration. MT levels only correlated moderately with neurological disability. Sleep disruptions were more common in patients than in controls and were associated with lower nocturnal MT sulfate levels. MT also correlated moderately with fatigue and HrQoL. We did not find evidence for a generally disturbed circadian MT rhythm in RRMS patients but longer disease duration was associated with significantly lower MT levels. Moreover, MT correlated with a series of clinical features. The exact nature of this relationship remains unclear and future studies are needed in order to determine whether MT could serve as a potential therapeutic target in MS. KEY MESSAGES: Melatonin acts as a free radical scavenger and modulates immune function. In multiple sclerosis, low melatonin levels were associated with acute exacerbations. Melatonin levels are not generally disturbed in multiple sclerosis patients. But lower levels are associated with disease duration and clinical aspects. Salivary melatonin after awakening might serve as a good measure of melatonin.

Indexed as

AdultCircadian RhythmFemaleFree Radical ScavengersHumansMaleMelatoninMiddle AgedMultiple SclerosisQuality of LifeSalivary GlandsFree Radical ScavengersMelatoninCircadian rhythmsFatigueMelatoninMultiple sclerosisNeurological disability

Identifiers

PMID31471628
OpenAlexW2971310893

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.