Evidence map›Paper›PMID 41757235›Full record

Trial reportFrontiers in endocrinology2026

Comparative effectiveness of pemafibrate versus bezafibrate on hepatic and vascular endothelial function in patients with coronary artery disease and metabolic dysfunction-associated steatotic liver disease.

Akihiro Nakamura, Yuta Kagaya, Hiroki Saito, Masanori Kanazawa, Masanobu Miura, Masateru Kondo, Hideaki Endo

Abstract readRandomized Controlled TrialComparative Study
In one paragraph

Trial report in Frontiers in endocrinology, 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

7 authors.

Akihiro NakamuraDepartment of Cardiology, Iwate Prefectural Central Hospital, Morioka, Japan.
Yuta KagayaDepartment of Cardiology, Iwate Prefectural Central Hospital, Morioka, Japan.
Hiroki SaitoDepartment of Cardiology, Iwate Prefectural Central Hospital, Morioka, Japan.
Masanori KanazawaDepartment of Cardiology, Iwate Prefectural Central Hospital, Morioka, Japan.
Masanobu MiuraDepartment of Cardiology, Iwate Prefectural Central Hospital, Morioka, Japan.
Masateru KondoDepartment of Cardiology, Iwate Prefectural Central Hospital, Morioka, Japan.
Hideaki EndoDepartment of Cardiology, Iwate Prefectural Central Hospital, Morioka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Peroxisome proliferator-activated receptor (PPAR) agonists are promising therapeutic agents for metabolic dysfunction-associated steatotic liver disease (MASLD), which increases cardiovascular risk. Methods: We compared the efficacy of pemafibrate, a highly selective PPAR-α agonist, and bezafibrate, a non-selective PPAR-α agonist, in patients with coronary artery disease (CAD) and MASLD. This was a Results: The percentage reduction in ALT levels was significantly greater with pemafibrate treatment than with bezafibrate treatment (-23.1% vs. -9.2%, P = 0.035). FMD significantly increased in both groups, with no difference in the magnitude of the percentage change (P = 0.267). FLI significantly decreased in both groups with no difference in the magnitude of change (P = 0.983), while HSI was not significantly different before and after treatment in either group. Both treatments significantly lowered HOMA-IR; however, the decrease was similar between the groups (P = 0.724). Conclusions: Pemafibrate is more effective than bezafibrate at reducing ALT levels while offering similar beneficial effects on insulin resistance and endothelial function in CAD patients with MASLD.

Indexed as

BenzoxazolesBezafibrateButyratesCoronary Artery DiseaseEndothelium, VascularAgedAlanine TransaminaseCross-Over StudiesFemaleHumansHypolipidemic AgentsInsulin ResistanceLiverMaleMiddle AgedNon-alcoholic Fatty Liver DiseaseAlanine TransaminaseBenzoxazolesBezafibrateButyratesHypolipidemic AgentsPPAR alpha(R)-2-(3-((benzoxazol-2-yl-d4 (3-(4-methoxyphenoxy-d7)propyl)amino)methyl)phenoxy) butanoic acidalanine aminotransferasefatty liver indexflow-mediated vasodilationhomeostasis model assessment of insulin resistanceperoxisome proliferator-activated receptor-α

Identifiers

PMID41757235
PMCPMC12932250

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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.