Evidence map›Paper›PMID 28981487›Full record

ArticlePediatric research2018

Oxygen consumption in platelets as an adjunct diagnostic method for pediatric mitochondrial disease.

Emil Westerlund, Sigurður E Marelsson, Johannes K Ehinger, Fredrik Sjövall, Saori Morota, Eleonor Åsander Frostner, Anders Oldfors, Niklas Darin, Johan Lundgren, Magnus J Hansson and 2 more

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Article in Pediatric research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
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  3. Review
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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

12 authors.

Emil WesterlundMitochondrial Medicine, Department of Clinical Sciences, Lund University, Lund, Sweden.
Sigurður E MarelssonMitochondrial Medicine, Department of Clinical Sciences, Lund University, Lund, Sweden.
Johannes K EhingerMitochondrial Medicine, Department of Clinical Sciences, Lund University, Lund, Sweden.
Fredrik SjövallMitochondrial Medicine, Department of Clinical Sciences, Lund University, Lund, Sweden.
Saori MorotaMitochondrial Medicine, Department of Clinical Sciences, Lund University, Lund, Sweden.
Eleonor Åsander FrostnerMitochondrial Medicine, Department of Clinical Sciences, Lund University, Lund, Sweden.
Anders OldforsDepartment of Pathology, Institute of Biomedicine, University of Gothenburg, Gothenburg, Sweden.
Niklas DarinDepartment of Pediatrics, The Queen Silvia Children's Hospital, University of Gothenburg, Gothenburg, Sweden.
Johan LundgrenDepartment of Pediatrics, Skåne University Hospital, Lund University, Lund, Sweden.
Magnus J HanssonMitochondrial Medicine, Department of Clinical Sciences, Lund University, Lund, Sweden.
Vineta FellmanDepartment of Pediatrics, Skåne University Hospital, Lund University, Lund, Sweden.
Eskil ElmérMitochondrial Medicine, Department of Clinical Sciences, Lund University, Lund, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BackgroundDiagnosing mitochondrial disease (MD) is a challenge. In addition to genetic analyses, clinical practice is to perform invasive procedures such as muscle biopsy for biochemical and histochemical analyses. Blood cell respirometry is rapid and noninvasive. Our aim was to explore its possible role in diagnosing MD.MethodsBlood samples were collected from 113 pediatric patients, for whom MD was a differential diagnosis. A respiratory analysis model based on ratios (independent of mitochondrial specific content) was derived from a group of healthy controls and tested on the patients. The diagnostic accuracy of platelet respirometry was evaluated against routine diagnostic investigation.ResultsMD prevalence in the cohort was 16%. A ratio based on the respiratory response to adenosine diphosphate in the presence of complex I substrates had 96% specificity for disease and a positive likelihood ratio of 5.3. None of the individual ratios had sensitivity above 50%, but a combined model had 72% sensitivity.ConclusionNormal findings of platelet respirometry are not able to rule out MD, but pathological results make the diagnosis more likely and could strengthen the clinical decision to perform further invasive analyses. Our results encourage further study into the role of blood respirometry as an adjunct diagnostic tool for MD.

Indexed as

Oxygen ConsumptionBiopsyBlood PlateletsChildChild, PreschoolFemaleHumansInfantInfant, NewbornLactic AcidMaleMitochondriaMitochondrial DiseasesOxygenPrevalenceSensitivity and SpecificityLactic AcidOxygen

Identifiers

PMID28981487

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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.