Evidence map›Paper›PMID 42709008›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2026

Fenofibrate Protects Against Antipsychotic-Induced Hyperglycemia Through Weight Loss and FGF21 Dependent Mechanisms.

Michael Akcan, Stewart Jeromson, Bradley J Baranowski, Annalaura Bellucci, Serena Trang, Katelyn Eisner, Ailish Babicki-Moore, Hadil Alfares, Meagan Arbeau, Kyle Medak and 2 more

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 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

12 authors.

Michael AkcanSchool of Kinesiology, University of British Columbia, Vancouver, British Columbia, Canada.
Stewart JeromsonSchool of Kinesiology, University of British Columbia, Vancouver, British Columbia, Canada.
Bradley J BaranowskiSchool of Kinesiology, University of British Columbia, Vancouver, British Columbia, Canada.
Annalaura BellucciSchool of Kinesiology, University of British Columbia, Vancouver, British Columbia, Canada.
Serena TrangSchool of Kinesiology, University of British Columbia, Vancouver, British Columbia, Canada.
Katelyn EisnerSchool of Kinesiology, University of British Columbia, Vancouver, British Columbia, Canada.
Ailish Babicki-MooreSchool of Kinesiology, University of British Columbia, Vancouver, British Columbia, Canada.
Hadil AlfaresSchool of Kinesiology, University of British Columbia, Vancouver, British Columbia, Canada.
Meagan ArbeauSchool of Kinesiology, University of British Columbia, Vancouver, British Columbia, Canada.
Kyle MedakBC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
Margaret HahnSchizophrenia Division, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
David C WrightSchool of Kinesiology, University of British Columbia, Vancouver, British Columbia, Canada.ORCID https://orcid.org/0000-0003-3867-8901

Funding

Canadian Institutes of Health Research (CIHR) PJT-191735
6 · The paper itself

Abstract

Antipsychotic (AP) medications, such as olanzapine, cause acute weight gain independent of hyperglycemia through a glucagon-dependent mechanism. Previous work has shown that exercise, a ketogenic diet, and fasting can protect against acute AP-induced hyperglycemia and attenuate increases in glucagon. As these interventions all increase circulating concentrations of fibroblast growth factor 21 (FGF21), we hypothesized that increasing endogenous FGF21 through treatment with fenofibrate would protect against AP-induced hyperglycemia. Male C57BL/6J mice were fed a low-fat diet with or without fenofibrate (0.2% w/w) for 1 week prior to an acute olanzapine (OLZ) challenge. Fenofibrate reduced food intake and caused weight loss while protecting against OLZ-induced increases in serum glucagon and blood glucose. Pair feeding mice with the same amount of food as fenofibrate-treated animals conferred a similar degree of protection against OLZ-induced hyperglycemia. Furthermore, an acute oral gavage with fenofibrate, despite increasing circulating FGF21 concentrations to a similar level as fenofibrate feeding, failed to protect against OLZ-induced glucose excursions. The effects of fenofibrate on weight loss and protection against OLZ-induced hyperglycemia were attenuated in FGF21

Indexed as

Antipsychotic AgentsFenofibrateFibroblast Growth FactorsHyperglycemiaHypolipidemic AgentsWeight LossAnimalsBlood GlucoseGlucagonMaleMiceMice, Inbred C57BLOlanzapineAntipsychotic AgentsBlood GlucoseFenofibratefibroblast growth factor 21Fibroblast Growth FactorsGlucagonHypolipidemic AgentsOlanzapineantipsychoticsdyslipidemiaFGF‐21fibrateshyperglycemiametabolismmice

Identifiers

PMID42709008
PMCPMC13552386

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.