Evidence map›Paper›PMID 41872585›Full record

ArticleEuropean journal of clinical nutrition2026

Alterations in gut microbiota composition in children with methylmalonic acidemia, propionic acidemia, and maple syrup urine disease.

Sabire Gokalp, Ener Cagri Dinleyici, Cansu Muluk, Asli Inci, Emine Aktas, Ilyas Okur, Fatih Ezgu, Leyla Tumer

Abstract read
PubMed Publisher
In one paragraph

Article in European journal of clinical nutrition, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Sabire GokalpDepartment of Pediatric Metabolic Disorders, Gazi University Faculty of Medicine, Ankara, Turkey. sabire32@hotmail.com.ORCID http://orcid.org/0000-0001-5383-5632
Ener Cagri DinleyiciDepartment of Pediatrics, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, Turkey.
Cansu MulukDepartment of Pediatrics, Gazi University Faculty of Medicine, Ankara, Turkey.
Asli InciDepartment of Pediatric Metabolic Disorders, Gazi University Faculty of Medicine, Ankara, Turkey.
Emine AktasDepartment of Pediatric Metabolic Disorders, Gazi University Faculty of Medicine, Ankara, Turkey.
Ilyas OkurDepartment of Pediatric Metabolic Disorders, Gazi University Faculty of Medicine, Ankara, Turkey.
Fatih EzguDepartment of Pediatric Metabolic Disorders, Gazi University Faculty of Medicine, Ankara, Turkey.
Leyla TumerDepartment of Pediatric Metabolic Disorders, Gazi University Faculty of Medicine, Ankara, Turkey.

Funding

Gazi Üniversitesi (Gazi University) TGA-2021-7036
6 · The paper itself

Abstract

aimMethylmalonic acidemia (MMA), propionic acidemia (PA), and maple syrup urine disease (MSUD) are rare monogenic disorders that are described as intoxication-type inborn errors of metabolism (IEMs). They usually present in early life, and long-term management requires strict dietary protein restriction, which may significantly alter gut microbiota composition. Despite growing interest in microbiome research, limited data exist on gut microbiota in these disorders, and no study is available for MMA and MSUD. We aimed to describe the gut microbiota compositions in children with MMA, PA, and MSUD.

methodA total of eight patients (Five MMA, one PA, and two MSUD), and 11age-matched healthy controls were enrolled. All patients were following a medically supervised, protein-restricted diet. Fecal sample was collected from each participant, and gut microbiota composition was evaluated with 16S rRNA sequencing.

resultsPatients with MMA, PA, and MSUD exhibited significantly altered gut microbiota composition compared to healthy controls. Alpha diversity analysis revealed reduced microbial richness in patients, with significantly lower Chao1 and observed OTU indices (p < 0.05). Beta diversity metrics demonstrated distinct clustering between groups, indicating significantly different microbial community structures. Higher relative abundances of opportunistic or dysbiotic taxa have been seen in patient group, while controls were enriched in beneficial taxa like Faecalibacterium prausnitzii, Ruminococcus, and Lactobacillus. LEfSe analysis identified 17 taxa enriched in patients-including members of Proteobacteria, Sphingobacteriia, and Streptococcus anginosus-and 6 taxa enriched in controls, notably Faecalibacterium prausnitzi. DISCUSSION: This is the first descriptive study of the gut microbiota composition of MMA, PA, and MSUD patients. These findings indicate an association between long-term dietary management and altered microbiota composition, although causality cannot be inferred due to the cross-sectional study design. The observed alterations suggest that the gut microbiota may represent a novel therapeutic target in the management of IEMs.

Indexed as

Amino Acid Metabolism, Inborn ErrorsGastrointestinal MicrobiomeMaple Syrup Urine DiseasePropionic AcidemiaCase-Control StudiesChildChild, PreschoolDiet, Protein-RestrictedFecesFemaleHumansInfantMaleRNA, Ribosomal, 16SRNA, Ribosomal, 16S

Identifiers

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.