Evidence map›Paper›PMID 40751583›Full record

SynthesisJournal of inherited metabolic disease2025

Effectiveness of Pyridoxal-5'-Phosphate in PNPO Deficiency: A Systematic Review.

Nina N Stolwijk, Laura van Dussen, Niels D Reijnhout, Marion M M G Brands, Bregje Jaeger, Peter T Clayton, Carla E M Hollak, Annet M Bosch

Abstract readSystematic Review
In one paragraph

Synthesis 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 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. 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

8 authors.

Nina N StolwijkMedicines for Society (Medicijn voor de Maatschappij), Platform at Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0002-3498-5747
Laura van DussenDepartment of Endocrinology and Metabolism. Amsterdam UMC, Amsterdam Gastroenterology Endocrinology Metabolism (AGEM) Research Institute, Expertise Center for Inborn Errors of Metabolism, MetabERN, University of Amsterdam, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0002-6539-531X
Niels D ReijnhoutMedicines for Society (Medicijn voor de Maatschappij), Platform at Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.
Marion M M G BrandsDepartment of Pediatrics, Division of Metabolic Diseases, Emma Children's Hospital, Amsterdam Gastroenterology Endocrinology Metabolism (AGEM), Amsterdam UMC Location University of Amsterdam, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0002-2025-5997
Bregje JaegerDepartment of Child Neurology, Emma Children's Hospital, Amsterdam University Medical Centers, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0003-3664-162X
Peter T ClaytonInborn Errors of Metabolism, Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, UK.ORCID https://orcid.org/0000-0001-7592-4302
Carla E M HollakMedicines for Society (Medicijn voor de Maatschappij), Platform at Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0003-0464-1078
Annet M BoschDepartment of Pediatrics, Division of Metabolic Diseases, Emma Children's Hospital, Amsterdam Gastroenterology Endocrinology Metabolism (AGEM), Amsterdam UMC Location University of Amsterdam, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0001-5027-5916

Funding

Postcodeloterij
6 · The paper itself

Abstract

Pyridox(am)ine 5'-phosphate oxidase (PNPO) deficiency is an ultrarare inherited neurometabolic disease, characterized by primarily neonatal-onset B6-responsive epileptic encephalopathies. Treatment often requires sustainable access to high-quality pyridoxal-5'-phosphate (PLP, i.e., active vitamin B6), although some patients (also) respond to pyridoxine (PN). While PN is authorized as a medicinal product, PLP is not, and this forces reliance on lesser-regulated food supplements, which risks dosing inaccuracies. This systematic review evaluates the effectiveness and safety of PLP in PNPO deficiency (PROSPERO, CRD42024542199). A systematic search was conducted in PubMed, Embase, and ClinicalTrials.gov, with risk of bias assessed and observational evidence summarized using a narrative synthesis approach. A total of 30 studies were included reporting on 49 patients treated with PLP. Clinical seizure responsiveness following PLP therapy was observed in the majority of patients (n = 38, 77.6%) and PLP treatment significantly improved survival (p < 0.001) compared with untreated siblings with a similar phenotype. The majority of PLP-responsive patients responded exclusively to PLP, with PN being attempted but ineffective in most of them (n = 30/33, 90.9%) Liver toxicity was the most frequently observed adverse event (n = 10, 20.4%) and although the underlying pathophysiological mechanism remains unclear, it may be associated with high-dose PLP. Therefore, regular liver disease screening is recommended during PLP therapy. This means that PLP remains the only effective therapy for achieving and maintaining seizure control in the majority of PNPO deficient patients, but the therapeutic window for optimal management is narrow. Thus, it is essential to ensure patient access to high-quality and appropriate forms of PLP.

Indexed as

Pyridoxal PhosphatePyridoxaminephosphate OxidaseBrain Diseases, MetabolicHumansHypoxia-Ischemia, BrainPyridoxineSeizuresTreatment OutcomeVitamin B 6Pyridoxal PhosphatePyridoxaminephosphate OxidasePyridoxineVitamin B 6epileptic encephalopathyPNPO deficiencypyridoxal‐5′‐phosphatetreatment accessvitamin B6 disorders

Identifiers

PMID40751583
PMCPMC12317649

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.