Evidence map›Paper›PMID 29107524›Full record

ArticleMolecular metabolism2017

A polyphenol-rich cranberry extract reverses insulin resistance and hepatic steatosis independently of body weight loss.

Fernando F Anhê, Renato T Nachbar, Thibault V Varin, Vanessa Vilela, Stéphanie Dudonné, Geneviève Pilon, Maryse Fournier, Marc-André Lecours, Yves Desjardins, Denis Roy and 2 more

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
9.3field-weighted citation impact, top 1% 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

77 citing papers in PubMed, 179 citations in OpenAlex.

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  9. Proanthocyanidin-Rich Cranberry Extract Lowers Glycemia in Established Obesity by Delaying Glucose Absorption.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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  11. Frontiers in microbiology · 2026
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  13. Calafate (Antioxidants (Basel, Switzerland) · 2025
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17 more citing papers are in PubMed but not listed here.

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

12 authors at 3 institutions in 2 countries.

Fernando F AnhêDepartment of Medicine, Faculty of Medicine, Cardiology Axis of the Québec Heart and Lung Institute, Canada; Institute of Nutrition and Functional Foods, Laval University, Québec, Canada. Electronic address: fernando.forato@criucpq.ulaval.ca.
Renato T NachbarDepartment of Medicine, Faculty of Medicine, Cardiology Axis of the Québec Heart and Lung Institute, Canada. Electronic address: renatotnt.uem@gmail.com.
Thibault V VarinInstitute of Nutrition and Functional Foods, Laval University, Québec, Canada. Electronic address: Thibaut.Varin.1@ulaval.ca.
Vanessa VilelaDepartment of Medicine, Faculty of Medicine, Cardiology Axis of the Québec Heart and Lung Institute, Canada. Electronic address: vilelarvanessa@hotmail.com.
Stéphanie DudonnéInstitute of Nutrition and Functional Foods, Laval University, Québec, Canada. Electronic address: Stephanie.Dudonne.1@ulaval.ca.
Geneviève PilonDepartment of Medicine, Faculty of Medicine, Cardiology Axis of the Québec Heart and Lung Institute, Canada; Institute of Nutrition and Functional Foods, Laval University, Québec, Canada. Electronic address: Genevieve.Pilon@criucpq.ulaval.ca.
Maryse FournierResearch Centre, Sainte-Justine Hospital, Montréal, Québec, Canada. Electronic address: fourniermaryse1@gmail.com.
Marc-André LecoursResearch Centre, Sainte-Justine Hospital, Montréal, Québec, Canada. Electronic address: malecours@hotmail.com.
Yves DesjardinsInstitute of Nutrition and Functional Foods, Laval University, Québec, Canada. Electronic address: Yves.Desjardins@fsaa.ulaval.ca.
Denis RoyInstitute of Nutrition and Functional Foods, Laval University, Québec, Canada. Electronic address: Denis.Roy@fsaa.ulaval.ca.
Emile LevyResearch Centre, Sainte-Justine Hospital, Montréal, Québec, Canada. Electronic address: emile.levy@recherche-ste-justine.qc.ca.
André MaretteDepartment of Medicine, Faculty of Medicine, Cardiology Axis of the Québec Heart and Lung Institute, Canada; Institute of Nutrition and Functional Foods, Laval University, Québec, Canada. Electronic address: Andre.Marette@criucpq.ulaval.ca.
Montreal Heart Institute · CAUniversité Laval · CACentre Hospitalier Universitaire Sainte-Justine · CA

Funding

CIHR FDN 143247
6 · The paper itself

Abstract

objectivePrevious studies have reported that polyphenol-rich extracts from various sources can prevent obesity and associated gastro-hepatic and metabolic disorders in diet-induced obese (DIO) mice. However, whether such extracts can reverse obesity-linked metabolic alterations remains unknown. In the present study, we aimed to investigate the potential of a polyphenol-rich extract from cranberry (CE) to reverse obesity and associated metabolic disorders in DIO-mice.

methodsMice were pre-fed either a Chow or a High Fat-High Sucrose (HFHS) diet for 13 weeks to induce obesity and then treated either with CE (200 mg/kg, Chow + CE, HFHS + CE) or vehicle (Chow, HFHS) for 8 additional weeks.

resultsCE did not reverse weight gain or fat mass accretion in Chow- or HFHS-fed mice. However, HFHS + CE fully reversed hepatic steatosis and this was linked to upregulation of genes involved in lipid catabolism (e.g., PPARα) and downregulation of several pro-inflammatory genes (eg, COX2, TNFα) in the liver. These findings were associated with improved glucose tolerance and normalization of insulin sensitivity in HFHS + CE mice. The gut microbiota of HFHS + CE mice was characterized by lower Firmicutes to Bacteroidetes ratio and a drastic expansion of Akkermansia muciniphila and, to a lesser extent, of Barnesiella spp, as compared to HFHS controls.

conclusionsTaken together, our findings demonstrate that CE, without impacting body weight or adiposity, can fully reverse HFHS diet-induced insulin resistance and hepatic steatosis while triggering A. muciniphila blooming in the gut microbiota, thus underscoring the gut-liver axis as a primary target of cranberry polyphenols.

Indexed as

Insulin ResistanceAnimalsFatty LiverGastrointestinal MicrobiomeMaleMiceMice, Inbred C57BLPlant ExtractsPolyphenolsVaccinium macrocarponWeight GainPlant ExtractsPolyphenolsAkkermansiaBarnesiellaFlavonoidsObesityVaccinium macrocarpon

Identifiers

PMID29107524
PMCPMC5699918
OpenAlexW2765599500

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.