Evidence map›Paper›PMID 36583842›Full record

ArticleHepatology international2023

Pemafibrate improves liver dysfunction and non-invasive surrogates for liver fibrosis in patients with non-alcoholic fatty liver disease with hypertriglyceridemia: a multicenter study.

Asahiro Morishita, Kyoko Oura, Kei Takuma, Mai Nakahara, Tomoko Tadokoro, Koji Fujita, Joji Tani, Tingting Shi, Takashi Himoto, Miwa Tatsuta and 7 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Hepatology international, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 30 citations in OpenAlex.

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  7. 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
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  11. Targeting Metabolism: Innovative Therapies for MASLD Unveiled.International journal of molecular sciences · 2025
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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 5 institutions in 1 country.

Asahiro MorishitaDepartment of Gastroenterology and Neurology, Kagawa University, Kita-gun, Kagawa, 761-0793, Japan. morishita.asahiro@kagawa-u.ac.jp.ORCID http://orcid.org/0000-0002-0760-3045
Kyoko OuraDepartment of Gastroenterology and Neurology, Kagawa University, Kita-gun, Kagawa, 761-0793, Japan.
Kei TakumaDepartment of Gastroenterology and Neurology, Kagawa University, Kita-gun, Kagawa, 761-0793, Japan.
Mai NakaharaDepartment of Gastroenterology and Neurology, Kagawa University, Kita-gun, Kagawa, 761-0793, Japan.
Tomoko TadokoroDepartment of Gastroenterology and Neurology, Kagawa University, Kita-gun, Kagawa, 761-0793, Japan.
Koji FujitaDepartment of Gastroenterology and Neurology, Kagawa University, Kita-gun, Kagawa, 761-0793, Japan.
Joji TaniDepartment of Gastroenterology and Neurology, Kagawa University, Kita-gun, Kagawa, 761-0793, Japan.
Tingting ShiDepartment of Gastroenterology and Neurology, Kagawa University, Kita-gun, Kagawa, 761-0793, Japan.
Takashi HimotoDepartment of Medical Technology, Kagawa Prefectural University of Health Sciences, Takamatsu, Japan.
Miwa TatsutaDepartment of Gastroenterology, KKR Takamatsu Hospital, Takamatsu, Japan.
Akio MoriyaDepartment of Gastroenterology, Mitoyo General Hospital, Kanonji, Japan.
Tomonori SenooDepartment of Hepatology, Kagawa Prefectural Central Hospital, Takamatsu, Japan.
Akemi TsutsuiDepartment of Hepatology, Kagawa Prefectural Central Hospital, Takamatsu, Japan.
Takuya NaganoDepartment of Hepatology, Kagawa Prefectural Central Hospital, Takamatsu, Japan.
Koichi TakaguchiDepartment of Hepatology, Kagawa Prefectural Central Hospital, Takamatsu, Japan.
Masafumi OnoDepartment of Gastroenterology and Neurology, Kagawa University, Kita-gun, Kagawa, 761-0793, Japan.
Tsutomu MasakiDepartment of Gastroenterology and Neurology, Kagawa University, Kita-gun, Kagawa, 761-0793, Japan.
Kagawa University · JPKagawa Prefectural Central Hospital · JPKagawa Prefectural College of Health Sciences · JPMito Saiseikai General Hospital · JPNational Hospital Organization Takamatsu Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis retrospective, multicenter study evaluated the effect of pemafibrate treatment on liver function and fibrosis by liver function tests (LFTs) and various fibrotic biomarkers including FibroScan in non-alcoholic fatty liver disease (NAFLD) with hypertriglyceridemia.

methodsA total of 138 NAFLD patients treated with pemafibrate at three hospitals between September 2018 and April 2021 were included. To evaluate the effect of pemafibrate treatment, FibroScan-aspartate aminotransferase (FAST) score, a novel index of steatohepatitis that can be calculated based on the aspartate aminotransferase (AST) value, controlled attenuation parameter (CAP), and liver stiffness measurement (LSM) was used.

resultsSerum TG levels were significantly decreased 4 weeks after pemafibrate treatment (p = 0.003). The levels of AST (p = 0.038), alanine aminotransferase (ALT) (p = 0.003), and gamma-glutamyl transferase (GGT) (p = 0.047) also significantly diminished 12 weeks after pemafibrate administration compared to before administration (p < 0.05). However, serum HDL-cholesterol (p = 0.193), LDL-cholesterol (p = 0.967), and eGFR (p = 0.909) levels were not significantly altered 12 weeks after pemafibrate administration. In addition, the fibrosis biomarkers' Type IV collagen (p = 0.753) and FIB-4 index (p = 0.333) did not significantly differ, while Autotaxin (p = 0.006) and the AST-to-platelet ratio index (APRI) (p = 0.003) significantly decreased 48 weeks after pemafibrate administration. No significant reductions in LSM (p = 0.959) and CAP (p = 0.266) were detected using FibroScan 48 weeks after pemafibrate administration. FAST score was significantly improved (p = 0.0475).

conclusionPemafibrate improved LFTs, including fibrotic biomarkers and FAST score, due to the hepatic anti-inflammatory effect, suggesting that pemafibrate may prevent disease progression in NAFLD patients with hypertriglyceridemia.

Indexed as

HypertriglyceridemiaNon-alcoholic Fatty Liver DiseaseAspartate AminotransferasesBenzoxazolesBiomarkersButyratesCholesterolFibrosisHumansLiver CirrhosisRetrospective StudiesAspartate AminotransferasesBenzoxazolesBiomarkersButyratesCholesterol(R)-2-(3-((benzoxazol-2-yl-d4 (3-(4-methoxyphenoxy-d7)propyl)amino)methyl)phenoxy) butanoic acidFAST scoreFibrotic biomarkersHypertriglyceridemiaNAFLDPemafibrate

Identifiers

PMID36583842
PMCPMC10224826
OpenAlexW4313304103

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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.