Evidence map›Paper›PMID 39293976›Full record

ArticleInternal medicine (Tokyo, Japan)2025

Pemafibrate Reduced Liver Stiffness in Patients with Metabolic Dysfunction-associated Steatotic Liver Disease Complicated with Hyperlipidemia and Liver Fibrosis with a Fibrosis-4 Index Above 1.3.

Tatsuki Ichikawa, Mio Yamashima, Shinobu Yamamichi, Makiko Koike, Yusuke Nakano, Hiroyuki Yajima, Osamu Miyazaki, Tomonari Ikeda, Takuma Okamura, Naohiro Komatsu and 3 more

Abstract read
In one paragraph

Article in Internal medicine (Tokyo, Japan), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Effect of Pemafibrate on Metabolic Dysfunction-Associated Steatotic Liver Disease: A Nationwide Multicenter Study.JGH open : an open access journal of gastroenterology and hepatology · 2025
    Article
  4. Review
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

13 authors.

Tatsuki IchikawaDepartment of Gastroenterology, Nagasaki Harbor Medical Center, Japan.
Mio YamashimaDepartment of Gastroenterology, Nagasaki Harbor Medical Center, Japan.
Shinobu YamamichiDepartment of Gastroenterology, Nagasaki Harbor Medical Center, Japan.
Makiko KoikeInnovation and Translational Research Center, Nagasaki Harbor Medical Center, Japan.
Yusuke NakanoInnovation and Translational Research Center, Nagasaki Harbor Medical Center, Japan.
Hiroyuki YajimaDepartment of Gastroenterology, Nagasaki Harbor Medical Center, Japan.
Osamu MiyazakiDepartment of Gastroenterology, Nagasaki Harbor Medical Center, Japan.
Tomonari IkedaDepartment of Gastroenterology, Nagasaki Harbor Medical Center, Japan.
Takuma OkamuraDepartment of Gastroenterology, Nagasaki Harbor Medical Center, Japan.
Naohiro KomatsuDepartment of Gastroenterology, Nagasaki Harbor Medical Center, Japan.
Sayuri SugioDepartment of Gastroenterology, Nagasaki Harbor Medical Center, Japan.
Miruki YoshinoDepartment of Gastroenterology, Nagasaki Harbor Medical Center, Japan.
Hisamitsu MiyaakiDepartment of Gastroenterology and Hepatology, Graduate School of Biomedical Sciences, Nagasaki University, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective To evaluate the effect of pemafibrate (PEM) on metabolic dysfunction-associated steatotic liver disease (MASLD). Methods We retrospectively evaluated 43 patients with hyperlipidemia and MASLD to determine changes in clinical factors between the start of PEM treatment and 0.5 years later. Using FibroScan, 39 of 43 patients were evaluated for liver stiffness (LS; kPa) and controlled attenuation parameter (CAP; dB/m). None of the patients had decompensated cirrhosis. Results Thirty patients were women, the median age was 66 years old, the median fibrosis-4 (FIB-4) score was 2.52, the median LS was 8.05 kPa, and the median CAP was 280.5 dB/m at the start of PEM treatment. AST, ALT, ALP, γGTP, and triglyceride levels decreased 0.5 years after starting PEM treatment, but FIB-4, LS, and CAP values did not decrease. However, LS decreased in patients with a FIB-4 index ≥1.3 at the start of PEM treatment, whereas it did not change in patients with a FIB-4 index <1.3. Similarly, LS decreased in patients with a value ≥8 kPa at the start of treatment and did not change in those with <8 kPa. The decreased LS group had higher baseline ALT and LS levels and lower ALT levels during 0.5 years of follow-up than the increased LS group. Conclusion At the initiation of PEM treatment, the LS decreased in patients with MASLD complicated by hyperlipidemia and moderate LS (FIB-4>1.3 or LS >8 kPa). Although there is currently no approved treatment for MASLD, PEM may be a viable treatment option for MASLD with mild LS.

Indexed as

Antifibrotic AgentsBenzoxazolesButyratesFatty LiverHyperlipidemiasLiverLiver CirrhosisAgedElasticity Imaging TechniquesFemaleHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeAntifibrotic AgentsBenzoxazolesButyrates(R)-2-(3-((benzoxazol-2-yl-d4 (3-(4-methoxyphenoxy-d7)propyl)amino)methyl)phenoxy) butanoic acidliver stiffnessMASLDpemafibrate

Identifiers

PMID39293976
PMCPMC12120207

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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.