Evidence map›Paper›PMID 35191616›Full record

ArticleAnnals of clinical and translational neurology2022

Validity and reliability of the German multidimensional fatigue inventory in spinal muscular atrophy.

Camilla Binz, Alma Osmanovic, Nele H Thomas, Benjamin Stolte, Maren Freigang, Isabell Cordts, Ramona Griep, Zeljko Uzelac, Claudia D Wurster, Christoph Kamm and 11 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Annals of clinical and translational neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Pathophysiology and Management of Fatigue in Neuromuscular Diseases.International journal of molecular sciences · 2023
    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

21 authors at 8 institutions in 1 country.

Camilla Binz *Department of Neurology, Hannover Medical School, Hanover, Germany.ORCID 0000-0003-3035-4638
Alma Osmanovic *Department of Neurology, Hannover Medical School, Hanover, Germany.ORCID 0000-0002-6012-8423
Nele H ThomasDepartment of Biometry, Hannover Medical School, Hanover, Germany.
Benjamin StolteDepartment of Neurology, University Hospital Essen, Essen, Germany.
Maren FreigangDepartment of Neurology, Technische Universität Dresden, Dresden, Germany.ORCID 0000-0002-0941-6075
Isabell CordtsDepartment of Neurology, Klinikum rechts der Isar der Technischen Universität München, Munich, Germany.
Ramona GriepDepartment of Neurology, Center for ALS, SMA and other Motor Neuron Disorders, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Zeljko UzelacDepartment of Neurology, Ulm University, Ulm, Germany.
Claudia D WursterDepartment of Neurology, Ulm University, Ulm, Germany.
Christoph KammTranslational Neurodegeneration Section "Albrecht-Kossel", Department of Neurology, University Medical Center Rostock, University of Rostock, Rostock, Germany.
Hannah A SieglerDepartment of Neurology, Hannover Medical School, Hanover, Germany.
Gary WieselmannDepartment of Neurology, Hannover Medical School, Hanover, Germany.
Andreas HermannTranslational Neurodegeneration Section "Albrecht-Kossel", Department of Neurology, University Medical Center Rostock, University of Rostock, Rostock, Germany.ORCID 0000-0002-7364-7791
Paul LingorDepartment of Neurology, Klinikum rechts der Isar der Technischen Universität München, Munich, Germany.ORCID 0000-0001-9362-7096
Marcus DeschauerDepartment of Neurology, Klinikum rechts der Isar der Technischen Universität München, Munich, Germany.
Albert C LudolphDepartment of Neurology, Ulm University, Ulm, Germany.
Thomas MeyerDepartment of Neurology, Center for ALS, SMA and other Motor Neuron Disorders, Charité - Universitätsmedizin Berlin, Berlin, Germany.
René GüntherDepartment of Neurology, Technische Universität Dresden, Dresden, Germany.
Tim HagenackerDepartment of Neurology, University Hospital Essen, Essen, Germany.ORCID 0000-0002-3631-3450
Susanne Petri *Department of Neurology, Hannover Medical School, Hanover, Germany.
Olivia Schreiber-Katz *Department of Neurology, Hannover Medical School, Hanover, Germany.ORCID 0000-0001-5621-4487
Medizinische Hochschule Hannover · DETUM Klinikum · DEUniversität Ulm · DEAmbulatory Rehabilitation Center Berlin Adlershof · DEEssen University Hospital · DEGerman Center for Neurodegenerative Diseases · DETechnische Universität Dresden · DEUniversity of Rostock · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveFatigue is a common and burdensome symptom of spinal muscular atrophy. Given its complex interactions, different dimensions of fatigue need to be investigated. The Multidimensional Fatigue Inventory is a widely used instrument that captures five distinct dimensions. The aim of this study was to investigate the validity and reliability of the German Multidimensional Fatigue Inventory in spinal muscular atrophy and to evaluate the presence of clinically relevant fatigue.

methodsOne hundred and forty adult spinal muscular atrophy patients completed the Multidimensional Fatigue Inventory in a nationwide, multicenter, cross-sectional study. Structural validity was explored using principal component analysis. Cronbach's α was calculated to evaluate internal consistency. Convergent validity was assessed by correlation with a Visual Analog Scale for fatigue and the EuroQol-Five Dimension-Five Level Scale as a measure of quality of life.

resultsThe original five-component model of the questionnaire constituted an acceptable fit. Internal consistency and convergent validity of general, physical, mental fatigue, and reduced activity were good. We observed a floor effect for mental fatigue. While physical fatigue exceeded the cutoff for clinically relevant fatigue, all dimensions but reduced motivation correlated negatively with quality of life. Age, depression, and ≥4 copies of the survival motor neuron 2 gene were associated with higher general/physical fatigue; unemployed participants reported higher scores for reduced activity/motivation.

interpretationThe Multidimensional Fatigue Inventory is a valid and reliable instrument to assess different dimensions of fatigue in spinal muscular atrophy. Fatigue is a relevant problem in spinal muscular atrophy and its assessment should be incorporated into standard care.

Indexed as

Muscular Atrophy, SpinalQuality of LifeAdultCross-Sectional StudiesHumansMental FatiguePsychometricsReproducibility of Results

Identifiers

PMID35191616
PMCPMC8935281
OpenAlexW4213350957

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.