Evidence map›Paper›PMID 18210050›Full record

ArticleDer Nervenarzt2008

[Fumaric acid and its esters in the treatment of multiple sclerosis: studies and effects].

M Stangel, D Moharregh-Khiabani, R A Linker, R Gold

Abstract readEnglish Abstract
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In one paragraph

Article in Der Nervenarzt, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

M StangelKlink für Neurologie, Medizinische Hochschule Hannover, Carl-Neuberg-Strasse 1, Hannover, Germany. stangel.martin@mh-hannover.de
D Moharregh-Khiabani
R A Linker
R Gold

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The currently licensed medications for relapsing-remitting multiple sclerosis (RRMS) are only partially effective and require a parenteral route of administration. Thus there is a need for new, preferably orally available therapeutics. Such a substance could be fumaric acid and its esters (FAE). These compounds are already in use for treatment of psoriasis and are known to have an immunomodulatory effect. In addition there is a potential for neuroprotective effects as suggested by in vitro studies and experiments in the animal model of experimental autoimmune encephalomyelitis. A phase II clinical study in RRMS patients with the modified fumaric acid ester BG-12 showed as "proof of principle" in a frequent MRI design that FAE significantly reduce the number of gadolinium-enhancing lesions after 24 weeks of treatment. Further phase III studies have been started to explore the long-term efficacy of this substance. The results of these studies will show if FAE can be another treatment option, maybe for combination therapy, in patients with MS.

Indexed as

AnimalsClinical Trials, Phase II as TopicClinical Trials, Phase III as TopicDimethyl FumarateEstersFumaratesHumansImmunosuppressive AgentsMiceMice, Inbred C57BLMultiple Sclerosis, Relapsing-RemittingNeuroprotective AgentsTreatment OutcomeDimethyl FumarateEstersFumaratesImmunosuppressive AgentsNeuroprotective Agents

Identifiers

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.