Evidence map›Paper›PMID 36001607›Full record

ArticlePloS one2022

A Metabologenomic approach reveals alterations in the gut microbiota of a mouse model of Alzheimer's disease.

Francesco Favero, Elettra Barberis, Mara Gagliardi, Stefano Espinoza, Liliana Contu, Stefano Gustincich, Francesca Boccafoschi, Chiara Borsotti, Dmitry Lim, Vito Rubino and 6 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 20% of its field
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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
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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

16 authors at 3 institutions in 1 country.

Francesco FaveroDepartment of Translational Medicine (DIMET) & Center for Translational Research on Autoimmune and Allergic Disease (CAAD), University of Piemonte Orientale, Novara, Italy.
Elettra BarberisDepartment of Translational Medicine (DIMET) & Center for Translational Research on Autoimmune and Allergic Disease (CAAD), University of Piemonte Orientale, Novara, Italy.
Mara GagliardiDepartment of Health Science (DSS) & Center for Translational Research on Autoimmune and Allergic Disease (CAAD), University of Piemonte Orientale, Novara, Italy.
Stefano EspinozaDepartment of Health Science (DSS), University of Piemonte Orientale, Novara, Italy.
Liliana ContuCentral RNA Laboratory, Istituto Italiano di Tecnologia, Erzelli, Genova, Italy.
Stefano GustincichCentral RNA Laboratory, Istituto Italiano di Tecnologia, Erzelli, Genova, Italy.
Francesca BoccafoschiDepartment of Health Science (DSS) & Center for Translational Research on Autoimmune and Allergic Disease (CAAD), University of Piemonte Orientale, Novara, Italy.
Chiara BorsottiDepartment of Health Science (DSS), University of Piemonte Orientale, Novara, Italy.
Dmitry LimDepartment of Pharmaceutical Sciences (DSF), University of Piemonte Orientale, Novara, Italy.
Vito RubinoDepartment of 'Studi per l'Economia e l'Impresa' (DISEI), University of Piemonte Orientale, Novara, Italy.
Flavio MignoneDepartment of Science and Technological Innovation, University of Piemonte Orientale, Alessandria, Italy.
Edoardo PasolliDepartment of Agriculture, University of Naples Federico II, Naples, Italy.
Marcello ManfrediDepartment of Translational Medicine (DIMET) & Center for Translational Research on Autoimmune and Allergic Disease (CAAD), University of Piemonte Orientale, Novara, Italy.
Silvia ZucchelliDepartment of Health Science (DSS) & Center for Translational Research on Autoimmune and Allergic Disease (CAAD), University of Piemonte Orientale, Novara, Italy.
Davide CoràDepartment of Translational Medicine (DIMET) & Center for Translational Research on Autoimmune and Allergic Disease (CAAD), University of Piemonte Orientale, Novara, Italy.
Marco CorazzariDepartment of Health Science (DSS), Center for Translational Research on Autoimmune and Allergic Disease (CAAD) & Interdisciplinary Research Center of Autoimmune Diseases (IRCAD), University of Piemonte Orientale, Novara, Italy.ORCID 0000-0002-6246-5968
Università degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITItalian Institute of Technology · ITUniversity of Naples Federico II · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The key role played by host-microbiota interactions on human health, disease onset and progression, and on host response to treatments has increasingly emerged in the latest decades. Indeed, dysbiosis has been associated to several human diseases such as obesity, diabetes, cancer and also neurodegenerative disease, such as Parkinson, Huntington and Alzheimer's disease (AD), although whether causative, consequence or merely an epiphenomenon is still under investigation. In the present study, we performed a metabologenomic analysis of stool samples from a mouse model of AD, the 3xTgAD. We found a significant change in the microbiota of AD mice compared to WT, with a longitudinal divergence of the F/B ratio, a parameter suggesting a gut dysbiosis. Moreover, AD mice showed a significant decrease of some amino acids, while data integration revealed a dysregulated production of desaminotyrosine (DAT) and dihydro-3-coumaric acid. Collectively, our data show a dysregulated gut microbiota associated to the onset and progression of AD, also indicating that a dysbiosis can occur prior to significant clinical signs, evidenced by early SCFA alterations, compatible with gut inflammation.

Indexed as

Alzheimer DiseaseGastrointestinal MicrobiomeNeurodegenerative DiseasesAnimalsDisease Models, AnimalDysbiosisHumansMice

Identifiers

PMID36001607
PMCPMC9401139
OpenAlexW3202511111

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.