Evidence map›Paper›PMID 35101075›Full record

Observational studyOrphanet journal of rare diseases2022

Aerobic capacity and skeletal muscle characteristics in glycogen storage disease IIIa: an observational study.

Philip J Hennis, Elaine Murphy, Rick I Meijer, Robin H Lachmann, Radha Ramachandran, Claire Bordoli, Gurinder Rayat, David J Tomlinson

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Orphanet journal of rare diseases, 2022. 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
0.9field-weighted citation impact, top 28% 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, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Glycogen storage diseases.Nature reviews. Disease primers · 2023
    Review
  5. 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

8 authors at 5 institutions in 2 countries.

Philip J HennisSport, Health and Performance Enhancement (SHAPE) Research Centre, Nottingham Trent University, Clifton Lane, Clifton, Nottingham, NG11 8NS, UK. philip.hennis@ntu.ac.uk.ORCID 0000-0002-8216-998X
Elaine MurphyCharles Dent Metabolic Unit, The National Hospital for Neurology and Neurosurgery, London, UK.
Rick I MeijerCharles Dent Metabolic Unit, The National Hospital for Neurology and Neurosurgery, London, UK.
Robin H LachmannCharles Dent Metabolic Unit, The National Hospital for Neurology and Neurosurgery, London, UK.
Radha RamachandranDepartment of Adult Inherited Metabolic Disease, St Thomas' Hospital, London, UK.
Claire BordoliSport, Health and Performance Enhancement (SHAPE) Research Centre, Nottingham Trent University, Clifton Lane, Clifton, Nottingham, NG11 8NS, UK.
Gurinder RayatShackleton Department of Anaesthetics, Perioperative Medicine Team, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton, SO16 6YD, UK.
David J TomlinsonMusculoskeletal Science and Sports Medicine Research Centre, Manchester Metropolitan University, Manchester, UK.
National Hospital for Neurology and Neurosurgery · GBNottingham Trent University · GBManchester Metropolitan University · GBSt Thomas' Hospital · GBUniversity Hospital Southampton NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIndividuals with glycogen storage disease IIIa (GSD IIIa) (OMIM #232400) experience muscle weakness and exercise limitation that worsen through adulthood. However, normative data for markers of physical capacity, such as strength and cardiovascular fitness, are limited. Furthermore, the impact of the disease on muscle size and quality is unstudied in weight bearing skeletal muscle, a key predictor of physical function. We aim to produce normative reference values of aerobic capacity and strength in individuals with GSD IIIa, and to investigate the role of muscle size and quality on exercise impairment.

resultsPeak oxygen uptake (V̇O

conclusionsV̇O

Indexed as

Glycogen Storage Disease Type IIIQuality of LifeAdultExerciseHumansMuscle, SkeletalMuscle StrengthAerobic capacityGlycogen storage disease type IIIaMaximum voluntary contractionSkeletal muscle

Identifiers

PMID35101075
PMCPMC8802498
OpenAlexW4210261319

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.