Evidence map›Paper›PMID 33585966›Full record

ArticleArchives of toxicology2021

Assessment of the impact of mitochondrial genotype upon drug-induced mitochondrial dysfunction in platelets derived from healthy volunteers.

Amy L Ball, Katarzyna M Bloch, Lucille Rainbow, Xuan Liu, John Kenny, Jonathan J Lyon, Richard Gregory, Ana Alfirevic, Amy E Chadwick

Open access · hybridAbstract read
In one paragraph

Article in Archives of toxicology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 39% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. 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

9 authors at 2 institutions in 1 country.

Amy L Ball *Department of Pharmacology and Therapeutics, MRC Centre for Drug Safety Science, University of Liverpool, Liverpool, UK.
Katarzyna M Bloch *The Wolfson Centre for Personalised Medicine, Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.
Lucille RainbowCentre for Genomic Research, Institute of Integrative Biology, University of Liverpool, Liverpool, UK.
Xuan LiuCentre for Genomic Research, Institute of Integrative Biology, University of Liverpool, Liverpool, UK.
John KennyCentre for Genomic Research, Institute of Integrative Biology, University of Liverpool, Liverpool, UK.
Jonathan J LyonGSK GlaxoSmithKline, Safety Assessment, Ware, UK.
Richard GregoryCentre for Genomic Research, Institute of Integrative Biology, University of Liverpool, Liverpool, UK.
Ana Alfirevic *The Wolfson Centre for Personalised Medicine, Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.
Amy E ChadwickDepartment of Pharmacology and Therapeutics, MRC Centre for Drug Safety Science, University of Liverpool, Liverpool, UK. Amy.Chadwick@liverpool.ac.uk.ORCID http://orcid.org/0000-0002-7399-8655
University of Liverpool · GBGlaxoSmithKline (United Kingdom) · GB

Funding

Medical Research Council G0700654
6 · The paper itself

Abstract

Mitochondrial DNA (mtDNA) is highly polymorphic and encodes 13 proteins which are critical to the production of ATP via oxidative phosphorylation. As mtDNA is maternally inherited and undergoes negligible recombination, acquired mutations have subdivided the human population into several discrete haplogroups. Mitochondrial haplogroup has been found to significantly alter mitochondrial function and impact susceptibility to adverse drug reactions. Despite these findings, there are currently limited models to assess the effect of mtDNA variation upon susceptibility to adverse drug reactions. Platelets offer a potential personalised model of this variation, as their anucleate nature offers a source of mtDNA without interference from the nuclear genome. This study, therefore, aimed to determine the effect of mtDNA variation upon mitochondrial function and drug-induced mitochondrial dysfunction in a platelet model. The mtDNA haplogroup of 383 healthy volunteers was determined using next-generation mtDNA sequencing (Illumina MiSeq). Subsequently, 30 of these volunteers from mitochondrial haplogroups H, J, T and U were recalled to donate fresh, whole blood from which platelets were isolated. Platelet mitochondrial function was tested at basal state and upon treatment with compounds associated with both mitochondrial dysfunction and adverse drug reactions, flutamide, 2-hydroxyflutamide and tolcapone (10-250 μM) using extracellular flux analysis. This study has demonstrated that freshly-isolated platelets are a practical, primary cell model, which is amenable to the study of drug-induced mitochondrial dysfunction. Specifically, platelets from donors of haplogroup J have been found to have increased susceptibility to the inhibition of complex I-driven respiration by 2-hydroxyflutamide. At a time when individual susceptibility to adverse drug reactions is not fully understood, this study provides evidence that inter-individual variation in mitochondrial genotype could be a factor in determining sensitivity to mitochondrial toxicants associated with costly adverse drug reactions.

Indexed as

AdolescentAdultBlood PlateletsDNA, MitochondrialFemaleFlutamideGenotypeHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedTolcaponeYoung AdultDNA, MitochondrialFlutamidehydroxyflutamideTolcapone2-HydroxyflutamideAdverse drug reactionFlutamideHaplogroupMitochondriamtDNAPlateletsTolcapone

Identifiers

PMID33585966
PMCPMC8032628
OpenAlexW3129530027

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.