Evidence map›Paper›PMID 39529390›Full record

ArticleJournal of inherited metabolic disease2025

Current global vitamin and cofactor prescribing practices for primary mitochondrial diseases: Results of a European reference network survey.

Julia Neugebauer, Karit Reinson, Marcello Bellusci, Julien H Park, Omar Hikmat, Enrico Bertini, Manuel Schiff, MetabERN PM‐MD Consortium authors, Shamima Rahman

Abstract read
In one paragraph

Article in Journal of inherited metabolic disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Therapies for Mitochondrial Disease: Past, Present, and Future.Journal of inherited metabolic disease · 2025
    Review
  5. 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.

Julia NeugebauerDepartment of Paediatric Gastroenterology, Nephrology and Metabolic Medicine, Charité - Universitaetsmedizin Berlin, Berlin, Germany.ORCID 0000-0002-2576-1012
Karit ReinsonDepartment of Clinical Genetics, Genetics and Personalized Medicine Clinic, Tartu University Hospital, Tartu, Estonia.
Marcello BellusciReference Center for Inherited Metabolic Disorders MetabERN, Mitochondrial Disorders Research Group (imas12) '12 de Octubre' University Hospital, Madrid, Spain.
Julien H ParkDepartment of General Paediatrics, University Hospital Muenster, Muenster, Germany.
Omar HikmatDepartment of Paediatrics and Adolescent Medicine, Haukeland University Hospital, Norway.
Enrico BertiniResearch Unit of Neuromuscular and Neurodegenerative Disease, Translational Pediatrics and Clinical Genetics, Bambino Gesu' Children's Hospital, IRCCS, Rome, Italy.
Manuel SchiffUniversité Paris Cité, Institut Imagine, Genetics of Mitochondrial Disorders, INSERM UMR, Paris, France.
MetabERN PM‐MD Consortium authors
Shamima RahmanMitochondrial Research Group, Genetics and Genomic Medicine Department, UCL Great Ormond Street Institute of Child Health, London, UK.ORCID 0000-0003-2088-730X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary mitochondrial diseases (PMD) account for a group of approximately 400 different genetic disorders with diverse clinical presentations and pathomechanisms. Although each individual disorder is rare, collectively they represent one of the largest groups in the field of inherited metabolic disorders. The complexity of PMD results in a continued lack of therapeutic options, necessitating a predominantly symptomatic treatment approach for affected patients. While a subset of diseases responds exceptionally well to treatment with specific vitamins or cofactors, for most PMD systematic reviews were not able to show significant benefit. This is in discrepancy to their continued frequent use among specialists. To gain further insight into the current clinical practice of vitamin and cofactor supplementation among clinicians treating children and adults affected by PMD, we conducted a worldwide cross-sectional questionnaire study exploring the choice of substances and the specific diseases where they are applied. To our knowledge, this is the first global study exploring this topic and featuring a high response rate from paediatricians. The vast majority (95%, 106/112) of responding specialists recommended the use of vitamins and cofactors, either in an agnostic approach irrespective of the specific PMD or directed to the treatment of specific diseases or phenotypes. Our study highlights significant regional and specialty-specific differences in supplementation practices. We provide some preliminary insights into specialist-based opinions regarding the use of vitamins and cofactors in PMD and highlight the need for more rigorous clinical and preclinical investigations and/or clear consensus statements.

Indexed as

Mitochondrial DiseasesPractice Patterns, Physicians'VitaminsAdultChildCoenzymesCross-Sectional StudiesDietary SupplementsEuropeHumansSurveys and QuestionnairesCoenzymesVitaminscofactorscross sectional studyinherited metabolic diseaseprimary mitochondrial diseasesurveytreatmentvitamins

Identifiers

PMID39529390
PMCPMC11670042

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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.