# Biochemical and Plasma Lipid Responses to Pemafibrate in Patients With Primary Biliary Cholangitis and Dyslipidemia: A Four-Year Analysis

**Authors:** Hiroyuki Kobayashi, Ayumi Sugiura, Mizuki Koyama-Otagiri, Takayuki Nimura, Yukifumi Kurasawa, Haruaki Shirakawa, Satoru Joshita

PMC · DOI: 10.7759/cureus.83176 · Cureus · 2025-04-29

## TL;DR

This study shows that pemafibrate, when used with UDCA, improves liver enzymes and is safe for PBC patients with dyslipidemia who don't respond well to standard treatment.

## Contribution

The study provides four-year evidence that pemafibrate improves liver function and lipid profiles in PBC patients refractory to UDCA or bezafibrate.

## Key findings

- Pemafibrate with UDCA significantly reduced alkaline phosphatase levels over four years.
- ALP normalization increased from 36% to 86% during the treatment period.
- Gamma-glutamyl transferase and alanine aminotransferase levels also improved significantly.

## Abstract

Background and aims

Primary biliary cholangitis (PBC) is a chronic autoimmune liver disease treated with ursodeoxycholic acid (UDCA), though some patients respond inadequately. This study evaluated the mid-term effects of pemafibrate on liver function and lipid profiles in PBC patients with dyslipidemia who were refractory to UDCA alone or with bezafibrate.

Methods

A retrospective review was conducted on 25 PBC patients (17 female; median age: 71) who began treatment with pemafibrate and UDCA at Shinshu University Hospital or NHI Yodakubo Hospital in 2021. Patients were either given pemafibrate as an add-on to UDCA (n = 10) or switched from UDCA + bezafibrate (n = 15). Biochemical markers were monitored over four years.

Results

Median alkaline phosphatase (ALP) declined from 138 U/L to 85, 78, 82, and 77 U/L at years 1-4, respectively. ALP normalization increased from 36% to 86% over the same period (P < 0.001). Gamma-glutamyl transferase dropped from 53 to 36 U/L at one year and remained stable. Alanine aminotransferase improved similarly (26-19 U/L, P = 0.007). No significant changes were seen in aspartate aminotransferase, bilirubin, creatinine, or estimated glomerular filtration rate (eGFR). No serious adverse effects were reported.

Conclusions

Pemafibrate with UDCA led to sustained liver enzyme improvement and was well-tolerated in dyslipidemic PBC patients refractory to standard therapy. Prospective studies are warranted to evaluate its long-term benefits, including in patients without dyslipidemia.

## Linked entities

- **Chemicals:** pemafibrate (PubChem CID 11526038), ursodeoxycholic acid (PubChem CID 31401), bezafibrate (PubChem CID 39042)
- **Diseases:** Primary biliary cholangitis (MONDO:0005388), dyslipidemia (MONDO:0002525)

## Full-text entities

- **Genes:** ALPP (alkaline phosphatase, placental) [NCBI Gene 250] {aka ALP, PALP, PLAP, PLAP-1}, GGT1 (gamma-glutamyltransferase 1) [NCBI Gene 2678] {aka CD224, D22S672, D22S732, GGT, GGT 1, GGTD}
- **Diseases:** PBC (MESH:D008105), Dyslipidemia (MESH:D050171), autoimmune liver disease (MESH:D008107)
- **Chemicals:** bezafibrate (MESH:D001629), UDCA (MESH:D014580), Lipid (MESH:D008055), creatinine (MESH:D003404), Pemafibrate (MESH:C540740), bilirubin (MESH:D001663)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12121969/full.md

## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12121969/full.md

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Source: https://tomesphere.com/paper/PMC12121969