Evidence map›Paper›PMID 37468577›Full record

ArticleEuropean journal of human genetics : EJHG2023

A biallelic variant in COX18 cause isolated Complex IV deficiency associated with neonatal encephalo-cardio-myopathy and axonal sensory neuropathy.

Dario Ronchi, Manuela Garbellini, Francesca Magri, Francesca Menni, Megi Meneri, Maria Francesca Bedeschi, Robertino Dilena, Valeria Cecchetti, Irene Picciolli, Francesca Furlan and 16 more

Open access · greenAbstract readCase Reports
In one paragraph

Article in European journal of human genetics : EJHG, 2023. 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
1.7field-weighted citation impact, top 16% 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, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. 2023 in the European Journal of Human Genetics.European journal of human genetics : EJHG · 2024
    Article
  7. Ambivalence and regret in genome sequencing.European journal of human genetics : EJHG · 2023
    Article
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors at 3 institutions in 1 country.

Dario RonchiDino Ferrari Center, Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy.ORCID 0000-0002-6093-9816
Manuela GarbelliniFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurology Unit, Milan, Italy.
Francesca MagriFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurology Unit, Milan, Italy.
Francesca MenniFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Regional Clinical Center for expanded newborn screening, Milan, Italy.
Megi MeneriDino Ferrari Center, Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy.
Maria Francesca BedeschiFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Medical Genetics Unit, Milan, Italy.
Robertino DilenaFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, UO Neurofisiopatologia, Milan, Italy.
Valeria CecchettiFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neonatal Intensive Care Unit, Milan, Italy.
Irene PicciolliFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neonatal Intensive Care Unit, Milan, Italy.
Francesca FurlanFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Regional Clinical Center for expanded newborn screening, Milan, Italy.
Valentina PolimeniFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neonatal Intensive Care Unit, Milan, Italy.
Sabrina SalaniFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurology Unit, Milan, Italy.
Laura PezzoliASST Papa Giovanni XXIII, Laboratorio di Genetica Medica, Bergamo, Italy.
Francesco FortunatoDino Ferrari Center, Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy.
Matteo BelliniASST Papa Giovanni XXIII, Laboratorio di Genetica Medica, Bergamo, Italy.
Daniela PigaFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurology Unit, Milan, Italy.
Michela RipoloneFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neuromuscular and Rare Disease Unit, Milan, Italy.ORCID 0000-0001-9293-6823
Simona ZanottiFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neuromuscular and Rare Disease Unit, Milan, Italy.
Laura NapoliFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neuromuscular and Rare Disease Unit, Milan, Italy.
Patrizia CiscatoFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neuromuscular and Rare Disease Unit, Milan, Italy.
Monica SciaccoFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neuromuscular and Rare Disease Unit, Milan, Italy.
Giovanna MangiliASST Papa Giovanni XXIII, Neonatology and NICU, Bergamo, Italy.
Fabio MoscaFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neonatal Intensive Care Unit, Milan, Italy.
Stefania CortiDino Ferrari Center, Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy.
Maria IasconeASST Papa Giovanni XXIII, Laboratorio di Genetica Medica, Bergamo, Italy.ORCID 0000-0002-4707-212X
Giacomo Pietro ComiDino Ferrari Center, Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy. giacomo.comi@unimi.it.ORCID 0000-0002-1383-5248
Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITUniversity of Milan · ITOspedale Papa Giovanni XXIII · IT

Funding

Ministero della Salute (Ministry of Health, Italy) Ricerca Corrente
6 · The paper itself

Abstract

Pathogenic variants impacting upon assembly of mitochondrial respiratory chain Complex IV (Cytochrome c Oxidase or COX) predominantly result in early onset mitochondrial disorders often leading to CNS, skeletal and cardiac muscle manifestations. The aim of this study is to describe a molecular defect in the COX assembly factor gene COX18 as the likely cause of a neonatal form of mitochondrial encephalo-cardio-myopathy and axonal sensory neuropathy. The proband is a 19-months old female displaying hypertrophic cardiomyopathy at birth and myopathy with axonal sensory neuropathy and failure to thrive developing in the first months of life. Serum lactate was consistently increased. Whole exome sequencing allowed the prioritization of the unreported homozygous substitution NM_001297732.2:c.667 G > C p.(Asp223His) in COX18. Patient's muscle biopsy revealed severe and diffuse COX deficiency and striking mitochondrial abnormalities. Biochemical and enzymatic studies in patient's myoblasts and in HEK293 cells after COX18 silencing showed a severe impairment of both COX activity and assembly. The biochemical defect was partially rescued by delivery of wild-type COX18 cDNA into patient's myoblasts. Our study identifies a novel defect of COX assembly and expands the number of nuclear genes involved in a mitochondrial disorder due to isolated COX deficiency.

Indexed as

Cytochrome-c Oxidase DeficiencyMuscular DiseasesElectron Transport Complex IVFemaleHEK293 CellsHumansInfantMembrane ProteinsMitochondrial ProteinsMutationCOX18 protein, humanElectron Transport Complex IVMembrane ProteinsMitochondrial Proteins

Identifiers

PMID37468577
PMCPMC10689781
OpenAlexW4384819059

What OpenQuestion holds

Textmetadata
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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.