Evidence map›Paper›PMID 42863838›Full record

ArticleJournal of inherited metabolic disease2026

Tailored Amino Acid Treatment for Pediatric Patients With Mitochondrial Aminoacyl-tRNA Synthetase Deficiencies.

I J J Muffels, G Kok, Z Tang, L S Medeiros, F O Poswar, W P Vermeij, R Rodenburg, K Smit, S K Sukumaran, S B Wortmann and 12 more

Abstract read
In one paragraph

Article in Journal of inherited metabolic disease, 2026. 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
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. 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

22 authors.

I J J MuffelsDepartment of Metabolic Diseases, Division Pediatrics, Wilhelmina Children's Hospital University Medical Centre Utrecht, Utrecht University, Utrecht, the Netherlands.ORCID https://orcid.org/0000-0002-4335-5034
G KokDepartment of Metabolic Diseases, Division Pediatrics, Wilhelmina Children's Hospital University Medical Centre Utrecht, Utrecht University, Utrecht, the Netherlands.
Z TangPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
L S MedeirosPostgraduate Program in Genetics and Molecular Biology, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.ORCID https://orcid.org/0000-0002-0276-7817
F O PoswarPostgraduate Program in Genetics and Molecular Biology, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.ORCID https://orcid.org/0000-0002-0804-2876
W P VermeijPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID https://orcid.org/0000-0002-9690-1385
R RodenburgRadboud Center for Mitochondrial Medicine, Department of Human Genetics, Radboud UMC, Nijmegen, the Netherlands.ORCID https://orcid.org/0000-0001-5227-3527
K SmitPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID https://orcid.org/0000-0002-6702-4045
S K SukumaranDepartment of Cardiology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India.ORCID https://orcid.org/0000-0003-1712-802X
S B WortmannUniversity Children's Hospital, Paracelsus Private Medical University, Salzburg, Austria.ORCID https://orcid.org/0000-0002-1968-8103
L AverdunkDepartment of General Pediatrics, Neonatology and Pediatric Cardiology, Medical Faculty, University Hospital Düsseldorf, Heinrich-Heine-University, Düsseldorf, Germany.ORCID https://orcid.org/0000-0003-0719-1607
J MunchDepartment of General Pediatrics, Neonatology and Pediatric Cardiology, Medical Faculty, University Hospital Düsseldorf, Heinrich-Heine-University, Düsseldorf, Germany.
J Pak-Lam HoDepartment of Pediatrics, The Hong Kong Children's Hospital, Hong Kong, China.ORCID https://orcid.org/0009-0006-8265-720X
A M K KwokDepartment of Pediatrics, The Hong Kong Children's Hospital, Hong Kong, China.ORCID https://orcid.org/0000-0002-3995-6718
E E S NieuwenhuisPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID https://orcid.org/0000-0001-8094-1211
P M van HasseltDepartment of Metabolic Diseases, Division Pediatrics, Wilhelmina Children's Hospital University Medical Centre Utrecht, Utrecht University, Utrecht, the Netherlands.ORCID https://orcid.org/0000-0001-9821-8398
I V D SchwartzPostgraduate Program in Genetics and Molecular Biology, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.ORCID https://orcid.org/0000-0002-7933-6687
C M A LuboutDepartment of Metabolic Diseases, Beatrix Children's Hospital, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.ORCID https://orcid.org/0000-0002-8058-440X
A M BoschDepartment of Pediatrics, Division of Metabolic Diseases, Amsterdam Gastroenterology Endocrinology and Metabolism, Emma Children's Hospital, Amsterdam UMC-AMC, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0001-5027-5916
K KoopDepartment of Metabolic Diseases, Division Pediatrics, Wilhelmina Children's Hospital University Medical Centre Utrecht, Utrecht University, Utrecht, the Netherlands.ORCID https://orcid.org/0000-0003-4027-9723
E M M Hoytema van KonijnenburgDepartment of Metabolic Diseases, Division Pediatrics, Wilhelmina Children's Hospital University Medical Centre Utrecht, Utrecht University, Utrecht, the Netherlands.ORCID https://orcid.org/0000-0002-3086-8447
S A FuchsDepartment of Metabolic Diseases, Division Pediatrics, Wilhelmina Children's Hospital University Medical Centre Utrecht, Utrecht University, Utrecht, the Netherlands.ORCID https://orcid.org/0000-0001-9147-2406

Funding

Tjallingh Roorda
6 · The paper itself

Abstract

Aminoacyl-tRNA synthetases (ARSs) facilitate the loading of transfer RNAs with their cognate amino acids in the cytosol (ARS1), mitochondria (ARS2), or both (dual ARS). ARS deficiencies are clinically heterogeneous and can cause severe, occasionally fatal disease. Supplementation with cognate amino acids to prevent local amino acid depletion has shown promise in ARS1 deficiencies, but its potential in ARS2 deficiencies remains largely unexplored. We investigated the effects of cognate amino acid depletion on mitochondrial function in fibroblasts from seven patients with ARS2 deficiencies using Seahorse respirometry and imaging flow cytometry. During amino acid depletion, patient fibroblasts showed decreased mitochondrial membrane potential and reduced basal and maximal respiratory capacity. We additionally evaluated oral cognate amino acid supplementation in nine patients with SARS2, EARS2, LARS2, WARS2, FARS2, or VARS2 deficiencies. Supplementation was well tolerated, with no adverse effects observed. Several patients showed clinical improvements during treatment, including improved development, increased growth, and/or improved cardiac function. In two patients, treatment discontinuation coincided with severe neurological regression. Together, these findings demonstrate that assessing mitochondrial function during cognate amino acid depletion provides a novel functional assay for ARS2 deficiencies that may aid variant interpretation and supports a biological rationale for cognate amino acid supplementation. Clinical supplementation was well tolerated and showed preliminary beneficial effects. These findings support further investigation of cognate amino acid supplementation as a potential supportive treatment strategy for patients with ARS2 deficiencies.

Indexed as

Amino AcidsAmino Acyl-tRNA SynthetasesMitochondriaMitochondrial DiseasesChildChild, PreschoolDietary SupplementsFemaleFibroblastsHumansInfantMaleMembrane Potential, MitochondrialAmino AcidsAmino Acyl-tRNA Synthetasesamino acid supplementationaminoacyl‐tRNA synthetase deficiencygenetic diseasemetabolic disordermitochondrial diseaseseahorse

Identifiers

PMID42863838
PMCPMC13657799

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.