Evidence map›Paper›PMID 33942428›Full record

ArticleHuman mutation2021

Bi-allelic KARS1 pathogenic variants affecting functions of cytosolic and mitochondrial isoforms are associated with a progressive and multisystem disease.

Gerarda Cappuccio, Camilla Ceccatelli Berti, Enrico Baruffini, Jennifer Sullivan, Vandana Shashi, Tamison Jewett, Tara Stamper, Silvia Maitz, Francesco Canonico, Anya Revah-Politi and 18 more

Open access · hybridAbstract readCase Reports
In one paragraph

Article in Human mutation, 2021. 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
0.8field-weighted citation impact, top 29% 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, 16 citations in OpenAlex.

  1. Article
  2. Hyperkinetic Movement Disorder inNeurology international · 2025
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. 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

28 authors at 14 institutions in 5 countries.

Gerarda CappuccioDepartment of Translational Medicine, Federico II University, Naples, Italy.ORCID 0000-0003-3934-2342
Camilla Ceccatelli BertiDepartment of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.ORCID 0000-0002-6527-4462
Enrico BaruffiniDepartment of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.ORCID 0000-0002-8280-7849
Jennifer SullivanDivision of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, North Carolina, USA.
Vandana ShashiDivision of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, North Carolina, USA.ORCID 0000-0002-5011-7501
Tamison JewettDepartment of Pediatrics, Section on Medical Genetics, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
Tara StamperDepartment of Pediatrics, Section on Medical Genetics, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
Silvia MaitzClinical Pediatric Genetics Unit, Pediatrics Clinics, MBBM Foundation, Hospital San Gerardo, Monza, Italy.
Francesco CanonicoDepartment of Neuroradiology, San Gerardo Hospital, ASST di Monza, Università degli Studi di Milano Bicocca, Monza, Italy.
Anya Revah-PolitiDepartment of Pathology and Cell Biology, Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, New York, USA.
Gabriel S KupchikDivision of Medical Genetics, Maimonides Children's Hospital of Brooklyn at Maimonides Medical Center, Downstate Medical Center, State University of New York, New York, New York, USA.
Kwame Anyane-YeboaDepartment of Pediatrics, Institute for Genomic Medicine Columbia University Medical Center, New York, New York, USA.
Vimla AggarwalDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York, USA.
Andreas BennecheDepartment of Medical Genetics, Haukeland University Hospital, Bergen, Norway.
Eirik BratlandDepartment of Medical Genetics, Haukeland University Hospital, Bergen, Norway.
Siren BerlandDepartment of Medical Genetics, Haukeland University Hospital, Bergen, Norway.
Felice D'ArcoDepartment of Paediatric Neuroradiology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Cesar A AlvesDivision of Neuroradiology, Department of Radiology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Adeline VanderverDivision of Neurology, Children's Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Daniela LongoDepartment of Diagnostic Imaging, Pediatric Hospital Bambino Gesù, Rome, Italy.
Enrico BertiniDepartment of Neuroscience, Unit of Neuromuscular and Neurodegenerative Diseases, IRCCS Bambino Gesù Children's Hospital, Rome, Italy.ORCID 0000-0001-9276-4590
Annalaura TorellaTelethon Institute of Genetics and Medicine, Pozzuoli, Naples, Italy.
Vincenzo NigroTelethon Institute of Genetics and Medicine, Pozzuoli, Naples, Italy.
Telethon Undiagnosed Diseases Program
Alessandra D'AmicoDepartment of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
Marjo S van der KnaapDepartment of Child Neurology, Amsterdam Leukodystrophy Center, Emma Children's Hospital, Amsterdam University Medical Centers and Amsterdam Neuroscience, Amsterdam, The Netherlands.ORCID 0000-0001-8912-0954
Paola GoffriniDepartment of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.
Nicola Brunetti-PierriDepartment of Translational Medicine, Federico II University, Naples, Italy.ORCID 0000-0002-6895-8819
University of Parma · ITColumbia University Irving Medical Center · USFederico II University Hospital · ITHaukeland University Hospital · NOBambino Gesù Children's Hospital · ITChildren's Hospital of Philadelphia · USDuke Medical Center · USUniversity of Campania "Luigi Vanvitelli" · ITWake Forest University · USAzienda Ospedaliera San Gerardo · ITEmma Kinderziekenhuis · NLGreat Ormond Street Hospital for Children NHS Foundation Trust · GBMaimonides Medical Center · USUniversity of Milano-Bicocca · IT

Funding

Clinical and Translational Science AwardUL1TR001873 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI REILLY, MUREDACH P · 2016 to 2025
$99.0M
NCATS NIH HHS UL1 TR001873Wellcome Trust
6 · The paper itself

Abstract

KARS1 encodes a lysyl-transfer RNA synthetase (LysRS) that links lysine to its cognate transfer RNA. Two different KARS1 isoforms exert functional effects in cytosol and mitochondria. Bi-allelic pathogenic variants in KARS1 have been associated to sensorineural hearing and visual loss, neuropathy, seizures, and leukodystrophy. We report the clinical, biochemical, and neuroradiological features of nine individuals with KARS1-related disorder carrying 12 different variants with nine of them being novel. The consequences of these variants on the cytosol and/or mitochondrial LysRS were functionally validated in yeast mutants. Most cases presented with severe neurological features including congenital and progressive microcephaly, seizures, developmental delay/intellectual disability, and cerebral atrophy. Oculo-motor dysfunction and immuno-hematological problems were present in six and three cases, respectively. A yeast growth defect of variable severity was detected for most variants on both cytosolic and mitochondrial isoforms. The detrimental effects of two variants on yeast growth were partially rescued by lysine supplementation. Congenital progressive microcephaly, oculo-motor dysfunction, and immuno-hematological problems are emerging phenotypes in KARS1-related disorder. The data in yeast emphasize the role of both mitochondrial and cytosolic isoforms in the pathogenesis of KARS1-related disorder and supports the therapeutic potential of lysine supplementation at least in a subset of patients.

Indexed as

Abnormalities, MultipleAdolescentAllelesBrain Diseases, Metabolic, InbornChildChild, PreschoolCohort StudiesCytosolDisease ProgressionFemaleHomozygoteHumansInfantIsoenzymesLysine-tRNA LigaseMaleIsoenzymesLysine-tRNA LigaseKARSKARS1LysRSlysyl-transfer RNA synthetasemitochondrial disease

Identifiers

PMID33942428
PMCPMC8251883
OpenAlexW3157689224

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.