Evidence map›Paper›PMID 42712877›Full record

ArticleInternational journal of microbiology2026

Microbiota-Metabolome Alterations Suggest Pro-Inflammatory Phenotype in Congenital Central Hypoventilation Syndrome.

Leandro Di Gloria, Marta Peruzzi, Marzia Vasarri, Marta Menicatti, Gianluca Bartolucci, Monica Annunziata, Arianna Bedeschi, Matteo Ramazzotti, Donatella Degl'Innocenti, Niccolò Nassi

Abstract read
In one paragraph

Article in International journal of microbiology, 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

10 authors.

Leandro Di GloriaDepartment of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy, unifi.it.ORCID https://orcid.org/0000-0002-8630-8166
Marta PeruzziSleep Disorder Breathing and SIDS Center, Meyer Children's Hospital IRCCS, Florence, Italy.ORCID https://orcid.org/0009-0007-7583-6936
Marzia VasarriDepartment of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy, unifi.it.ORCID https://orcid.org/0000-0002-4241-3992
Marta MenicattiDepartment of Neurosciences, Psychology, Drug Research and Child Health Section of Pharmaceutical and Nutraceutical Sciences, University of Florence, Florence, Italy, unifi.it.ORCID https://orcid.org/0000-0001-8302-7644
Gianluca BartolucciDepartment of Neurosciences, Psychology, Drug Research and Child Health Section of Pharmaceutical and Nutraceutical Sciences, University of Florence, Florence, Italy, unifi.it.ORCID https://orcid.org/0000-0002-5631-8769
Monica AnnunziataSleep Disorder Breathing and SIDS Center, Meyer Children's Hospital IRCCS, Florence, Italy.
Arianna BedeschiGastroenterology Unit, Meyer Children's Hospital IRCCS, Florence, Italy.ORCID https://orcid.org/0009-0000-8735-0131
Matteo RamazzottiDepartment of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy, unifi.it.ORCID https://orcid.org/0000-0002-6862-9409
Donatella Degl'InnocentiDepartment of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy, unifi.it.ORCID https://orcid.org/0000-0002-3342-5537
Niccolò NassiSleep Disorder Breathing and SIDS Center, Meyer Children's Hospital IRCCS, Florence, Italy.ORCID https://orcid.org/0000-0003-0827-5319

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital central hypoventilation syndrome (CCHS) is a genetic disorder caused by mutations in the PHOX2B gene, characterized by impaired autonomic control of breathing and systemic consequences that may affect gut homeostasis. This study provides the first integrated multi-omics analysis in a CCHS group and matched controls, combining fecal DNA-based gut taxonomic profiling with targeted quantification of fatty acids and aromatic carboxylic acids. While overall microbial diversity and community structure remained largely preserved, significant alterations were observed in specific taxa within the CCHS group. Notably, the control group exhibited an enrichment of short-chain fatty acid (SCFA)-producing genera, which are associated with eubiotic gut ecosystems, whereas the CCHS group showed higher abundance of taxa commonly linked to inflammatory contexts. Consistently, fecal levels of beneficial SCFAs-particularly valeric acid, and to a lesser extent butyric acid-were reduced in CCHS group. These findings point to a dysbiotic gut microbiota in patients with CCHS, likely supporting putative inflammatory processes that would further worsen overall health status if confirmed. Furthermore, this work provides exploratory functional signatures for future studies aimed at understanding systemic consequences, guiding mechanistic investigations, and informing strategies to improve supportive care and long-term health outcomes in this rare patient population.

Indexed as

CCHSdysbiosisinflammationmetabolic profilingmicrobiota

Identifiers

PMID42712877
PMCPMC13550528

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.