Evidence map›Paper›PMID 40713718›Full record

ArticleCell communication and signaling : CCS2025

Intestinal inflammation and microbiota modulation impact cochlear function: emerging insights in gut-ear axis.

Anna Pisani, Valentina Petito, Fabiola Paciello, Valeria Emoli, Letizia Masi, Veronica Mohamed Hizam, Pierluigi Puca, Raffaele Montuoro, Federica Del Chierico, Lorenza Putignani and 10 more

Abstract read
In one paragraph

Article in Cell communication and signaling : CCS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. The Gut-Ear Axis: From Dysbiosis to Auditory and Vestibular Disorders.International journal of molecular sciences · 2026
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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

20 authors.

Anna Pisani *Dipartimento di Neuroscienze, Unità di Audiologia, Università degli Studi di Napoli Federico II, Naples, 80131, Italy.
Valentina Petito *CeMAD Translational Research Laboratories Digestive Disease Center, Department of Medical and Surgical sciences, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, 00168, Italy.
Fabiola PacielloDipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, Rome, 00168, Italy. fabiola.paciello@unicatt.it.
Valeria EmoliCeMAD Translational Research Laboratories Digestive Disease Center, Department of Medical and Surgical sciences, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, 00168, Italy.
Letizia MasiCeMAD Translational Research Laboratories Digestive Disease Center, Department of Medical and Surgical sciences, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, 00168, Italy.
Veronica Mohamed HizamDipartimento Testa-collo e organi di senso, Università Cattolica del Sacro Cuore, Rome, 00168, Italy.
Pierluigi PucaCeMAD Translational Research Laboratories Digestive Disease Center, Department of Medical and Surgical sciences, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, 00168, Italy.
Raffaele MontuoroDipartimento Testa-collo e organi di senso, Università Cattolica del Sacro Cuore, Rome, 00168, Italy.
Federica Del ChiericoUnità di Microbiomica e Microbioma Umano, Ospedale Pediatrico Bambino Gesù IRCCS, Rome, 00165, Italy.
Lorenza PutignaniImmunologia, Reumatologia e Malattie Infettive, Unità di microbioma umano, IRCCS, Ospedale Pediatrico Bambino Gesù, Rome, Italy.
Claudio GrassiDipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, Rome, 00168, Italy.
Jacopo GalliFondazione Policlinico Universitario A. Gemelli IRCCS, Rome, 00168, Italy.
Maurizio TaglialatelaDipartimento di Neuroscienze, Unità di Audiologia, Università degli Studi di Napoli Federico II, Naples, 80131, Italy.
Maria Emiliana CaristoCen.Ri.S., Università Cattolica del Sacro Cuore, Rome, 00168, Italy.
Gianluca IaniroCeMAD Translational Research Laboratories Digestive Disease Center, Department of Medical and Surgical sciences, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, 00168, Italy.
Loris Riccardo LopetusoCeMAD Translational Research Laboratories Digestive Disease Center, Department of Medical and Surgical sciences, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, 00168, Italy.
Giovanni CammarotaDigestive Disease Center "CeMAD", Internal Medicine and Gastroenterology, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, 00168, Italy.
Antonio GasbarriniCeMAD Translational Research Laboratories Digestive Disease Center, Department of Medical and Surgical sciences, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, 00168, Italy.
Anna Rita Fetoni *Dipartimento di Neuroscienze, Unità di Audiologia, Università degli Studi di Napoli Federico II, Naples, 80131, Italy. annarita.fetoni@unina.it.
Franco Scaldaferri *CeMAD Translational Research Laboratories Digestive Disease Center, Department of Medical and Surgical sciences, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, 00168, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough several evidence demonstrates a "gut-microbiota-brain axis", suggesting a bidirectional communication between gut microbiota and the central nervous system, less is known about a possible link between the gut and the peripheral nervous system, including the inner ear.

methodsHere, we investigated the impact of intestinal inflammation and the modulation of gut microbiota through fecal microbiota transplantation on hearing sensitivity. Female C57BL/6 mice were assigned to four groups: control (Ctrl), DSS-induced colitis (DSS), FMT from patients with active ulcerative colitis (FMT aUC), and FMT from patients with ulcerative colitis in remission (FMT rUC). Auditory function was evaluated by auditory brainstem responses (ABR). Morphological and molecular analyses on cochlear tissues were performed using immunofluorescence, histological staining, and Western blot to assess inflammation, oxidative stress, and blood-labyrinth barrier integrity. Donor microbiota composition was characterized by 16S rRNA sequencing, and systemic inflammation was evaluated by measuring serum lipopolysaccharide (LPS) levels.

resultsWe found that intestinal dysbiosis is associated with functional, morphological, and molecular alterations in the cochlea, such as increased oxidative stress, inflammation, and altered blood-labyrinth barrier permeability. This leads to macrophage infiltration and immune response activation through the MyD88/NF-κB pathway. Notably, these effects were exacerbated by FMT from subjects with aUC, while FMT from patients with rUC provided a protective effect on cochlear functions.

conclusionsOverall, our findings suggest that gut inflammation, microbiota alteration, or its therapeutic modulation can impact inner ear pathology: worsening gut inflammatory status negatively affects hearing sensitivity, while the restoration of gut microbiota positively impacts auditory function.

Indexed as

CochleaGastrointestinal MicrobiomeInflammationIntestinesAnimalsColitis, UlcerativeDysbiosisFecal Microbiota TransplantationFemaleHumansMiceMice, Inbred C57BLMyeloid Differentiation Factor 88Myeloid Differentiation Factor 88CochleaGut dysbiosisGut microbiotaInflammation

Identifiers

PMID40713718
PMCPMC12297715

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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.