Evidence map›Paper›PMID 26898293›Full record

ArticleJIMD reports2016

Pilot Experience with an External Quality Assurance Scheme for Acylcarnitines in Plasma/Serum.

P Ruiz Sala, G Ruijter, C Acquaviva, A Chabli, M G M de Sain-van der Velden, J Garcia-Villoria, M R Heiner-Fokkema, E Jeannesson-Thivisol, K Leckstrom, L Franzson and 8 more

Open access · greenAbstract read
In one paragraph

Article in JIMD reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 100% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

18 authors at 12 institutions in 8 countries.

P Ruiz SalaCentro de Diagnóstico de Enfermedades Moleculares, Universidad Autónoma de Madrid, IDIPAZ, CIBER de Enfermedades Raras, 28049, Madrid, Spain.
G RuijterDepartment of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.
C AcquavivaService Maladies Héréditaires du Métabolisme, Centre de Biologie et Pathologie Est, Lyon, France.
A ChabliBiochimie métabolomique et protéomique, Hopital Necker Enfants Malades, Paris, France.
M G M de Sain-van der VeldenDepartment of Medical Genetics, University Medical Centre Utrecht, Utrecht, The Netherlands.
J Garcia-VilloriaDepartment of Biochemistry and Molecular Genetics, Div Inborn Errors Metab, Hospital Clinic, IDIBAPS, CIBERER, Barcelona, Spain.
M R Heiner-FokkemaDepartment of Laboratory Medicine, University Medical Centre Groningen, Groningen, The Netherlands.
E Jeannesson-ThivisolService de Biochimie et Biologie Moléculaire, CHU de Nancy, Vandoeuvre-Nancy, France.
K LeckstromDepartment Clinical Chemistry, Sahlgrenska University Hospital, Gothenburg, Sweden.
L FranzsonDepartment of Genetics and Molecular Medicine, Landspitali, Reykjavik, Iceland.
G LynesNeurometabolic Unit, National Hospital for Neurology and Neurosurgery, London, UK.
J OlesenDepartment of Clinical Genetics, Copenhagen University Hospital, Copenhagen, Denmark.
W OnkenhoutDepartment of Clinical Chemistry and Laboratory Medicine, Leiden University Medical Centre, Leiden, The Netherlands.
P PetrouDepartment of Biochemical Genetics, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.
A DrousiotouDepartment of Biochemical Genetics, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.
A RibesDepartment of Biochemistry and Molecular Genetics, Div Inborn Errors Metab, Hospital Clinic, IDIBAPS, CIBERER, Barcelona, Spain.
C Vianey-SabanService Maladies Héréditaires du Métabolisme, Centre de Biologie et Pathologie Est, Lyon, France.
B MerineroCentro de Diagnóstico de Enfermedades Moleculares, Universidad Autónoma de Madrid, IDIPAZ, CIBER de Enfermedades Raras, 28049, Madrid, Spain. bmerinero@cbm.csic.es.
Centre for Biomedical Network Research on Rare Diseases · ESCyprus Institute of Neurology and Genetics · CYHospital La Paz Institute for Health Research · ESCopenhagen University Hospital · DKErasmus University Rotterdam · NLHôpital Necker-Enfants Malades · FRLeiden University Medical Center · NLNational Hospital for Neurology and Neurosurgery · GBNational University Hospital of Iceland · ISSahlgrenska University Hospital · SEUniversity Medical Center Groningen · NLUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The analysis of acylcarnitines (AC) in plasma/serum is established as a useful test for the biochemical diagnosis and the monitoring of treatment of organic acidurias and fatty acid oxidation defects. External quality assurance (EQA) for qualitative and quantitative AC is offered by ERNDIM and CDC in dried blood spots but not in plasma/serum samples. A pilot interlaboratory comparison between 14 European laboratories was performed over 3 years using serum/plasma samples from patients with an established diagnosis of an organic aciduria or fatty acid oxidation defect. Twenty-three different samples with a short clinical description were circulated. Participants were asked to specify the method used to analyze diagnostic AC, to give quantitative data for diagnostic AC with the corresponding reference values, possible diagnosis, and advice for further investigations.Although the reference and pathological concentrations of AC varied among laboratories, elevated marker AC for propionic acidemia, isovaleric acidemia, medium-chain acyl-CoA dehydrogenase, very long-chain acyl-CoA dehydrogenase, and multiple acyl-CoA dehydrogenase deficiencies were correctly identified by all participants allowing the diagnosis of these diseases. Conversely, the increased concentrations of dicarboxylic AC were not always identified, and therefore the correct diagnosis was not reach by some participants, as exemplified in cases of malonic aciduria and 3-hydroxy-3-methylglutaryl-CoA lyase deficiency. Misinterpretation occurred in those laboratories that used multiple-reaction monitoring acquisition mode, did not derivatize, or did not separate isomers. However, some of these laboratories suggested further analyses to clarify the diagnosis.This pilot experience highlights the importance of an EQA scheme for AC in plasma.

Indexed as

AcylcarnitinesExternal quality assuranceFatty acid oxidation defectsOrganic acidurias

Identifiers

PMID26898293
PMCPMC5110441
OpenAlexW2287865699

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.