Evidence map›Paper›PMID 41951373›Full record

ArticleJournal of atherosclerosis and thrombosis2026

Switching from Conventional Fibrates to Pemafibrate Improves Lipid Profiles, Liver Enzymes, Renal Function, and Fibrosis Markers in Dyslipidemic Patients with MASLD: A Multicenter Real-World Study.

Takao Sato, Toshihiro Miyamoto, Ryoma Fukuoka, Kazumasa Sugimoto, Yoko Tanimoto, Takashi Nakayama, Kojiro Tanimoto, Koichiro Sugimura, Yoshihide Fujimoto, Takahiko Kiyooka and 1 more

Abstract readMulticenter Study
In one paragraph

Article in Journal of atherosclerosis and thrombosis, 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

11 authors.

Takao SatoDepartment of Cardiology, IUHW Narita hospital.
Toshihiro MiyamotoDepartment of Cardiology, IUHW Narita hospital.
Ryoma FukuokaDepartment of Cardiology, IUHW Narita hospital.
Kazumasa SugimotoDepartment of Cardiology, IUHW Narita hospital.
Yoko TanimotoDepartment of Cardiology, IUHW Narita hospital.
Takashi NakayamaDepartment of Cardiology, IUHW Narita hospital.
Kojiro TanimotoDepartment of Cardiology, IUHW Narita hospital.
Koichiro SugimuraDepartment of Cardiology, IUHW Narita hospital.
Yoshihide FujimotoDepartment of Cardiology, IUHW Narita hospital.
Takahiko KiyookaDepartment of Cardiology, IUHW Atami hospital.
Akio KawamuraDepartment of Cardiology, IUHW Narita hospital.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsMetabolic dysfunction-associated steatotic liver disease (MASLD) is highly prevalent worldwide. Conventional fibrates effectively lower triglycerides but may elevate liver enzymes and creatinine, limiting long-term use. Pemafibrate, a selective PPARα modulator (SPPARMα), offers potent triglyceride reduction with favorable hepatic and renal safety. This study evaluated the effects of switching from conventional fibrates to pemafibrate on lipid profiles, liver enzyme, fibrosis indices(Fibrosis-4 index) with particular emphasis on renal safety in clinical practice.

methodsWe retrospectively analyzed 144 patients with dyslipidemia, including those with MASLD or chronic kidney disease, who were switched from bezafibrate 200mg (N = 24) or 400mg (N = 30), or fenofibrate 80mg (N = 51) or 160mg (N = 39), to pemafibrate (0.2mg/day). Laboratory parameters were assessed at baseline and 6 months post-switch.

resultsTriglycerides decreased significantly, particularly in the bezafibrate 200 mg and fenofibrate 80 mg groups, while other lipid profiles remained stable. Serum alanine aminotransferase decreased significantly with bezafibrate 200mg (29±27 to 17±13U/L, p<0.05) and fenofibrate 80mg (26±18 to 20±10 U/L, p<0.05), whereas treatment with bezafibrate (400mg) and fenofibrate (160mg) showed a trend toward reduction. The glutamyl transferase showed a similar trend. The Fibrosis-4 index showed reductions across all groups, reaching statistical significance in bezafibrate200mg (1.51±0.63→1.36±0.47, p = 0.02) and fenofibrate 80mg (1.17±0.37→1.07±0.33, p = 0.001). Renal function remained stable across all groups, with no clinically significant deterioration in estimated glomerular filtration rate, supporting the renal safety of pemafibrate.

conclusionSwitching from conventional fibrates to pemafibrate improved triglyceride levels, liver enzymes, and fibrosis indices in patients with MASLD, while maintaining a favorable renal safety profile.

Indexed as

BenzoxazolesBiomarkersButyratesDyslipidemiasFatty LiverFibric AcidsAgedBezafibrateFemaleFenofibrateFollow-Up StudiesHumansHypolipidemic AgentsKidney Function TestsLipidsLiverBenzoxazolesBezafibrateBiomarkersButyratesFenofibrateFibric AcidsHypolipidemic AgentsLipids(R)-2-(3-((benzoxazol-2-yl-d4 (3-(4-methoxyphenoxy-d7)propyl)amino)methyl)phenoxy) butanoic acidTriglyceridesA selective PPARα modulatorFIB-4 indexFibrateRenal function

Identifiers

PMID41951373
PMCPMC13345723

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.