Evidence mapPaperPMID 38730247Full record

ArticleNature communications2024

The pan-PPAR agonist lanifibranor improves cardiometabolic health in patients with metabolic dysfunction-associated steatohepatitis.

Michael P Cooreman, Javed Butler, Robert P Giugliano, Faiez Zannad, Lucile Dzen, Philippe Huot-Marchand, Martine Baudin, Daniel R Beard, Jean-Louis Junien, Pierre Broqua and 2 more

Registry-linked trialAbstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03008070 (A Randomized, Double-blind, Placebo-controlled, Multicenter, Dose-range, Proof-of-concept, 24-week Treatment Study of IVA337 in Adult Subjects With Nonalcoholic Steatohepatitis), which is not on this map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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.

NCT03008070 phase2completednot on this map

A Randomized, Double-blind, Placebo-controlled, Multicenter, Dose-range, Proof-of-concept, 24-week Treatment Study of IVA337 in Adult Subjects With Nonalcoholic Steatohepatitis (NASH)

TypeinterventionalSponsorInventiva PharmaRan2017 to 2020Enrolled247ConditionsNon-Alcoholic Steatohepatitis (NASH)ArmsIVA337, Placebo
3 · Its place in the literature

Who cites it

35 citing papers in PubMed.

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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

12 authors.

Michael P CooremanResearch and Development, Inventiva, New York, NY, USA. Michael.Cooreman@inventivapharma.com.ORCID http://orcid.org/0009-0007-3230-7591
Javed ButlerBaylor Scott and White Research Institute, Dallas, TX, USA.ORCID http://orcid.org/0000-0001-7683-4720
Robert P GiuglianoBrigham and Women's Hospital, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Faiez ZannadCentre d'Investigations Cliniques Plurithématique 1433, Université de Lorraine, Nancy, France.ORCID http://orcid.org/0000-0001-7456-1570
Lucile DzenResearch and Development, Inventiva, New York, NY, USA.
Philippe Huot-MarchandResearch and Development, Inventiva, New York, NY, USA.
Martine BaudinResearch and Development, Inventiva, New York, NY, USA.
Daniel R BeardTranslational Medicine Academy, Basel, Switzerland.
Jean-Louis JunienResearch and Development, Inventiva, New York, NY, USA.
Pierre BroquaResearch and Development, Inventiva, New York, NY, USA.
Manal F AbdelmalekDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
Sven M FrancqueDepartment of Gastroenterology and Hepatology, Antwerp University Hospital and University of Antwerp, Antwerp, Belgium.ORCID http://orcid.org/0000-0002-7527-4714

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lanifibranor, a pan-PPAR agonist, improves liver histology in patients with metabolic dysfunction-associated steatohepatitis (MASH), who have poor cardiometabolic health (CMH) and cardiovascular events as major mortality cause. NATIVE trial secondary and exploratory outcomes (ClinicalTrials.gov NCT03008070) were analyzed for the effect of lanifibranor on IR, lipid and glucose metabolism, systemic inflammation, blood pressure (BP), hepatic steatosis (imaging and histological grading) for all patients of the original analysis. With lanifibranor, triglycerides, HDL-C, apolipoproteins, insulin, HOMA-IR, HbA1c, fasting glucose (FG), hs-CRP, ferritin, diastolic BP and steatosis improved significantly, independent of diabetes status: most patients with prediabetes returned to normal FG levels. Significant adiponectin increases correlated with hepatic and CMH marker improvement; patients had an average weight gain of 2.5 kg, with 49% gaining ≥2.5% weight. Therapeutic benefits were similar regardless of weight change. Here, we show that effects of lanifibranor on liver histology in MASH are accompanied with CMH improvement, indicative of potential cardiovascular clinical benefits.

Indexed as

ChalconesAdiponectinAdultAgedBlood GlucoseBlood PressureCardiovascular DiseasesFatty LiverFemaleHumansInsulin ResistanceLipid MetabolismLiverMaleMiddle AgedPeroxisome Proliferator-Activated ReceptorsAdiponectinBlood GlucoseChalconesPeroxisome Proliferator-Activated ReceptorsPropionatesTriglycerides

Identifiers

PMID38730247
PMCPMC11087475

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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 Socratic graph.