Evidence map›Paper›PMID 31801616›Full record

Observational studyJournal of translational medicine2019

Microbiota, type 2 diabetes and non-alcoholic fatty liver disease: protocol of an observational study.

Benedetta M Motta, Christoph Grander, Martin Gögele, Luisa Foco, Vladimir Vukovic, Roberto Melotti, Christian Fuchsberger, Alessandro De Grandi, Chiara Cantaloni, Anne Picard and 5 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Journal of translational medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

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  7. Cells · 2020
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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

15 authors at 3 institutions in 3 countries.

Benedetta M MottaInstitute for Biomedicine (affiliated to the University of Lübeck), Eurac Research, 39100, Bolzano, Italy. benedetta.motta@eurac.edu.ORCID 0000-0002-6681-2170
Christoph GranderDepartment of Internal Medicine I, Gastroenterology, Hepatology, Endocrinology & Metabolism, Medical University Innsbruck, Innsbruck, Austria.
Martin GögeleInstitute for Biomedicine (affiliated to the University of Lübeck), Eurac Research, 39100, Bolzano, Italy.
Luisa FocoInstitute for Biomedicine (affiliated to the University of Lübeck), Eurac Research, 39100, Bolzano, Italy.
Vladimir VukovicInstitute for Biomedicine (affiliated to the University of Lübeck), Eurac Research, 39100, Bolzano, Italy.
Roberto MelottiInstitute for Biomedicine (affiliated to the University of Lübeck), Eurac Research, 39100, Bolzano, Italy.
Christian FuchsbergerInstitute for Biomedicine (affiliated to the University of Lübeck), Eurac Research, 39100, Bolzano, Italy.
Alessandro De GrandiInstitute for Biomedicine (affiliated to the University of Lübeck), Eurac Research, 39100, Bolzano, Italy.
Chiara CantaloniInstitute for Biomedicine (affiliated to the University of Lübeck), Eurac Research, 39100, Bolzano, Italy.
Anne PicardInstitute for Biomedicine (affiliated to the University of Lübeck), Eurac Research, 39100, Bolzano, Italy.
Deborah MascalzoniInstitute for Biomedicine (affiliated to the University of Lübeck), Eurac Research, 39100, Bolzano, Italy.
Alessandra RossiniInstitute for Biomedicine (affiliated to the University of Lübeck), Eurac Research, 39100, Bolzano, Italy.
Cristian PattaroInstitute for Biomedicine (affiliated to the University of Lübeck), Eurac Research, 39100, Bolzano, Italy.
Herbert TilgDepartment of Internal Medicine I, Gastroenterology, Hepatology, Endocrinology & Metabolism, Medical University Innsbruck, Innsbruck, Austria. herbert.tilg@i-med.ac.at.
Peter P PramstallerInstitute for Biomedicine (affiliated to the University of Lübeck), Eurac Research, 39100, Bolzano, Italy.
Eurac Research · ITInnsbruck Medical University · ATUppsala University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNon-alcoholic fatty liver disease (NAFLD) is characterized by triglyceride accumulation in the hepatocytes in the absence of alcohol overconsumption, commonly associated with insulin resistance and obesity. Both NAFLD and type 2 diabetes (T2D) are characterized by an altered microbiota composition, however the role of the microbiota in NAFLD and T2D is not well understood. To assess the relationship between alteration in the microbiota and NAFLD while dissecting the role of T2D, we established a nested study on T2D and non-T2D individuals within the Cooperative Health Research In South Tyrol (CHRIS) study, called the CHRIS-NAFLD study. Here, we present the study protocol along with baseline and follow-up characteristics of study participants.

methodsAmong the first 4979 CHRIS study participants, 227 individuals with T2D were identified and recalled, along with 227 age- and sex-matched non-T2D individuals. Participants underwent ultrasound and transient elastography examination to evaluate the presence of hepatic steatosis and liver stiffness. Additionally, sampling of saliva and faeces, biochemical measurements and clinical interviews were carried out.

resultsWe recruited 173 T2D and 183 non-T2D participants (78% overall response rate). Hepatic steatosis was more common in T2D (63.7%) than non-T2D (36.3%) participants. T2D participants also had higher levels of liver stiffness (median 4.8 kPa, interquartile range (IQR) 3.7, 5.9) than non-T2D participants (median 3.9 kPa, IQR 3.3, 5.1). The non-invasive scoring systems like the NAFLD fibrosis score (NFS) suggests an increased liver fibrosis in T2D (mean - 0.55, standard deviation, SD, 1.30) than non-T2D participants (mean - 1.30, SD, 1.17). DISCUSSION: Given the comprehensive biochemical and clinical characterization of study participants, once the bioinformatics classification of the microbiota will be completed, the CHRIS-NAFLD study will become a useful resource to further our understanding of the relationship between microbiota, T2D and NAFLD.

Indexed as

MicrobiotaAgedBacteriaDiabetes Mellitus, Type 2FemaleHumansMaleMetabolic SyndromeNon-alcoholic Fatty Liver DiseaseCooperative Health Research In South TyrolMicrobiotaNAFLDType 2 diabetes

Identifiers

PMID31801616
PMCPMC6891972
OpenAlexW2994308056

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.