Evidence map›Paper›PMID 42823914›Full record

ReviewJournal of inherited metabolic disease2026

Consensus Guidelines for Diagnosis and Management of Pyruvate Dehydrogenase Complex Deficiency.

Nandaki Keshavan, Julia Neugebauer, Marcello Bellusci, Enrico Bertini, Garry Brown, Niklas Darin, Suzanne DeBrosse, Lucy Drexler, Stefan Drexler, Gregory M Enns and 14 more

Abstract readConsensus StatementReview
In one paragraph

Review 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. 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

24 authors.

Nandaki KeshavanMetabolic Unit, Great Ormond Street Hospital NHS Foundation Trust, London, UK.ORCID https://orcid.org/0000-0001-6939-4528
Julia NeugebauerDepartment of Paediatric Gastroenterology, Nephrology and Metabolic Medicine, Charité - Universitaetsmedizin Berlin, Berlin, Germany.ORCID https://orcid.org/0000-0002-2576-1012
Marcello BellusciReference Center for Inherited Metabolic Disorders MetabERN, Mitochondrial Disorders Research Group, '12 de Octubre' University Hospital, Madrid, Spain.
Enrico BertiniResearch Unit of Neuromuscular and Neurodegenerative Disease, Translational Pediatrics and Clinical Genetics, Bambino Gesu Children's Hospital, IRCCS, Rome, Italy.ORCID https://orcid.org/0000-0001-9276-4590
Garry BrownOxford Medical Genetics Laboratories, the Churchill Hospital, Oxford, UK.
Niklas DarinDepartment of Pediatrics, Institute of Clinical Sciences, University of Gothenburg, Queen Silvia Children's Hospital, Sahlgrenska University Hospital, Gothenburg, Sweden.
Suzanne DeBrosseCenter for Human Genetics, Department of Genetics and Genome Sciences, University Hospitals Cleveland Medical Center, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
Lucy DrexlerThe Freya Foundation, Bristol, UK.
Stefan DrexlerThe Freya Foundation, Bristol, UK.
Gregory M EnnsDepartment of Pediatrics, Division of Medical Genetics, Stanford University School of Medicine and Lucille Packard Children's Hospital, Palo Alto, California, USA.
Rebecca D GanetzkyDepartment of Pediatrics, Division of Human Genetics, Mitochondrial Medicine Frontier Program, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Kelly GilbertThe Freya Foundation, Bristol, UK.
Austin LarsonSection of Clinical Genetics and Metabolism, Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA.
Rebecca LegiNutrition Services, Stanford University School of Medicine and Lucille Packard Children's Hospital, Palo Alto, USA.
April N LehmanDivision of Genetic and Genomic Medicine, Nationwide Children's Hospital, Columbus, Ohio, USA.
Camile NewbyDepartment of Nutrition and Dietetics, Bristol Royal Hospital for Children, Bristol, UK.
Manuel SchiffReference Center for Mitochondrial Disorders (CARAMMEL) and Reference Center for Inborn Errors of Metabolism, Department of Pediatrics, Necker-Enfants-Malades Hospital, Assistance Publique-Hôpitaux de Paris, University of Paris-Cité, MetabERN, Paris, France.ORCID https://orcid.org/0000-0001-8272-232X
Rachel SkeathDepartment of Dietetics, Great Ormond Street Hospital, London, UK.
Peter W StacpooleDivision of Endocrinology, Diabetes and Metabolism, Departments of Medicine and Biochemistry and Molecular Biology, College of Medicine, University of Florida, Gainesville, Florida, USA.
Sarah ThompsonThe Elizabeth Watt PDCD Research Fund, Centennial, Colorado, USA.
Emma WattThe Elizabeth Watt PDCD Research Fund, Centennial, Colorado, USA.
Saskia B WortmannUniversity Children's Hospital, Expertise Centre for Mitochondrial Diseases (Mitohaus), Paracelsus Private Medical University (PMU), Salzburg, Austria.
Jirair K BedoyanUPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.ORCID https://orcid.org/0000-0002-9580-9747
Shamima RahmanMetabolic Unit, Great Ormond Street Hospital NHS Foundation Trust, London, UK.ORCID https://orcid.org/0000-0003-2088-730X

Funding

Elizabeth Watt PDCD Research FundFreya FoundationSociety for Study of Inborn Errors of Metabolism
6 · The paper itself

Abstract

Primary pyruvate dehydrogenase complex deficiency (PDCD) comprises a group of monogenic disorders caused by pathogenic variants in genes encoding subunits of, or regulatory components affecting, the pyruvate dehydrogenase complex. The clinical phenotype spans a broad continuum, ranging from early onset congenital lactic acidosis to infantile or childhood onset global developmental delay with epilepsy, through to more attenuated adult-onset neurological presentations. Reports from patients and advocacy groups indicate substantial variability in clinical management across both emergency and outpatient settings and between centres internationally. This variability underscores the need for systematic evaluation of the evidence base and the development of harmonised, consensus-driven clinical guidelines to standardise care and improve outcomes. An international consortium of experts from Europe and North America, including metabolic physicians, neurologists, dietitians, geneticists and patient representatives, was convened. The group undertook a structured review of the literature and developed guideline statements addressing disease classification, recognition, diagnostic evaluation, dietary and non-dietary management, surveillance for complications, genetic counselling and transition to adult services. Each recommendation was assigned a GRADE rating reflecting strength and quality of evidence. Consensus was achieved using a Delphi methodology. In total, 199 recommendations reached consensus and constitute the core of these guidelines. These recommendations provide a framework for consistent, high-quality, multidisciplinary care. The process also identified key evidence gaps, highlighting priorities for future research and the ongoing need to develop effective disease-modifying therapies.

Indexed as

Pyruvate Dehydrogenase Complex Deficiency DiseaseConsensusGenetic CounselingHumansPhenotypeclinical guidelineketogenic dietoutcomespyruvate dehydrogenase complex deficiencypyruvate dehydrogenase deficiencytreatments

Identifiers

PMID42823914
PMCPMC13631685

What OpenQuestion holds

Textmetadata
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.