Evidence map›Paper›PMID 19019309›Full record

ReviewNeurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics2008

Therapeutic options in other metabolic myopathies.

Matthias Vorgerd

Abstract readReview
In one paragraph

Review in Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Treatment Opportunities in Patients With Metabolic Myopathies.Current treatment options in neurology · 2017
    Review
  2. Coaxing stem cells for skeletal muscle repair.Advanced drug delivery reviews · 2015
    Review
  3. Article
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

1 author.

Matthias VorgerdDepartment of Neurology, Ruhr-University Bochum, Kliniken Bergmannsheil, Bochum, Germany. matthias.vorgerd@rub.de

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adult patients with metabolic myopathies typically present with exercise-induced pain, cramps, fatigue, and myoglobinuria. The current therapeutic options of glycogen and lipid storage myopathies include dietary treatments, excersise training, and pharmacological supplementations. Herein is a review of evidence from randomized controlled trials in McArdle disease (glycogen storage disease type V, muscle phosphorylase deficiency) and carnitine palmitoyltransferase (CPT) 2 deficiency. A brief overview on current treatment options in rhabdomyolysis is also included because patients with McArdle disease and CPT 2 often experience such potentially life-threatening complications.

Indexed as

AnimalsCarnitine O-PalmitoyltransferaseCreatineExercise TherapyGlycogen Storage DiseaseGlycogen Storage Disease Type VHumansLipid MetabolismMetabolic DiseasesMuscular DiseasesRhabdomyolysisCarnitine O-PalmitoyltransferaseCreatine

Identifiers

PMID19019309
PMCPMC4514707

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.