Evidence map›Paper›PMID 38572327›Full record

ArticleJGH open : an open access journal of gastroenterology and hepatology2024

Impact of pemafibrate in patients with metabolic dysfunction-associated steatotic liver disease complicated by dyslipidemia: A single-arm prospective study.

Hiroki Ono, Masanori Atsukawa, Akihito Tsubota, Taeang Arai, Kenta Suzuki, Tetsuyuki Higashi, Michika Kitamura, Kaori Shioda-Koyano, Tadamichi Kawano, Yuji Yoshida and 7 more

Open access · goldAbstract read
In one paragraph

Article in JGH open : an open access journal of gastroenterology and hepatology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.1field-weighted citation impact, top 8% of its field
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

9 citing papers in PubMed, 8 citations in OpenAlex.

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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

17 authors at 3 institutions in 1 country.

Hiroki OnoDivision of Gastroenterology and Hepatology Nippon Medical School Tokyo Japan.
Masanori AtsukawaDivision of Gastroenterology and Hepatology Nippon Medical School Tokyo Japan.ORCID https://orcid.org/0000-0003-3374-7111
Akihito TsubotaProject Research Units (PRU) Research Center for Medical Science The Jikei University School of Medicine Tokyo Japan.
Taeang AraiDivision of Gastroenterology and Hepatology Nippon Medical School Tokyo Japan.
Kenta SuzukiDivision of Gastroenterology and Hepatology Nippon Medical School Tokyo Japan.
Tetsuyuki HigashiDivision of Gastroenterology and Hepatology Nippon Medical School Tokyo Japan.
Michika KitamuraDivision of Gastroenterology and Hepatology Nippon Medical School Tokyo Japan.
Kaori Shioda-KoyanoDivision of Gastroenterology and Hepatology Nippon Medical School Tokyo Japan.
Tadamichi KawanoDivision of Gastroenterology and Hepatology Nippon Medical School Tokyo Japan.
Yuji YoshidaDivision of Gastroenterology Nippon Medical School Chiba Hokusoh Hospital Chiba Japan.
Tomomi OkuboDivision of Gastroenterology Nippon Medical School Chiba Hokusoh Hospital Chiba Japan.
Korenobu HayamaDivision of Gastroenterology Nippon Medical School Chiba Hokusoh Hospital Chiba Japan.
Norio ItokawaDivision of Gastroenterology and Hepatology Nippon Medical School Tokyo Japan.
Chisa KondoDivision of Gastroenterology and Hepatology Nippon Medical School Tokyo Japan.
Mototsugu NagaoDivision of Endocrinology, Diabetes and Metabolism Nippon Medical School Tokyo Japan.
Masato IwabuDivision of Endocrinology, Diabetes and Metabolism Nippon Medical School Tokyo Japan.
Katsuhiko IwakiriDivision of Gastroenterology and Hepatology Nippon Medical School Tokyo Japan.ORCID https://orcid.org/0000-0002-5558-6104
Nippon Medical School · JPChiba Hokusou Hospital · JPJikei University School of Medicine · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aim: This study aimed to clarify the efficacy and safety of 48-week pemafibrate treatment in patients with metabolic dysfunction-associated steatotic liver disease (MASLD) complicated by dyslipidemia. Methods: A total of 110 patients diagnosed with MASLD complicated by dyslipidemia received pemafibrate at a dose of 0.1 mg twice daily for 48 weeks. Results: The participants were 54 males and 37 females, with a median age of 63 (52-71) years. Besides improvement in lipid profile, significant reductions from baseline to 48 weeks of treatment were found in liver-related enzymes, such as aspartate aminotransferase, alanine aminotransferase (ALT), gamma-glutamyl transpeptidase, and alkaline phosphatase ( Conclusion: This study demonstrated that 48-week pemafibrate administration improved liver-related enzymes and surrogate marker of liver fibrosis in patients with MASLD. The improvement of insulin resistance by pemafibrate may contribute to the favorable effect on MASLD complicated by dyslipidemia.

Indexed as

homeostasis model assessment‐insulin resistanceliver fibrosismetabolic dysfunction‐associated steatotic liver diseasenon‐alcoholic fatty liver diseasepemafibrate

Identifiers

PMID38572327
PMCPMC10986296
OpenAlexW4393410386

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.