Effect of pemafibrate, a novel selective peroxisome proliferator-activated receptor-alpha modulator (SPPARMα), on urinary protein excretion in IgA nephropathy with hypertriglyceridemia

  • Atsushi TanakaEmail author
  • Tsukasa Nakamura
  • Eiichi Sato
  • Atsuko Chihara
  • Koichi Node
Case Report


Lipid abnormalities, including hypertriglyceridemia, are one of the most common comorbidities in patients with chronic kidney disease (CKD) and are independently associated with disease progression. However, it remains uncertain whether treatment for hypertriglyceridemia has favorable effects on the clinical course of IgA nephropathy (IgAN). Pemafibrate is a novel selective peroxisome proliferator-activated receptor-alpha modulator and may be distinct from conventional fibrates in terms of its pharmacological activity and hepatic and renal safety. A recent clinical study demonstrated that pemafibrate was safe and effective for correcting pro-atherogenic lipid abnormalities in CKD patients with a wide range of renal insufficiency. However, the effect of pemafibrate on renal function in patients with IgAN and hypertriglyceridemia has not been verified. This paper is the first to show that 12 months of pemafibrate (0.1 mg daily) administration in three drug-naïve and mild IgAN patients with variable renal dysfunction and histopathology proven IgAN decreased serum triglyceride level and excretion of urinary protein and liver-type fatty acid-binding protein with no change in estimated glomerular filtration rate (eGFR). These findings suggest that pemafibrate is safe and effective for correcting hypertriglyceridemia and decreasing urinary protein excretion without changing eGFR and blood pressure levels in mild IgAN patients with hypertriglyceridemia.


Pemafibrate Selective peroxisome proliferator-activated receptor-alpha modulator (SPPARMα) IgA nephropathy Urinary protein excretion 



The authors wish to thank Aya Yamada for her excellent secretarial assistance.


This case report was not supported by any funding bodies.

Compliance with ethical standards

Conflict of interest

AT has received a research grant from GlaxoSmithKline. KN has received honoraria from Ono, Takeda, Daiichi Sankyo, Astellas, MSD, Boehringer Ingelheim, and Mitsubishi Tanabe; research grants from Asahi Kasei, Astellas, Boehringer Ingelheim, Mitsubishi Tanabe, Teijin, and Terumo; scholarship from Bayer, Takeda, Astellas, Daiichi Sankyo, Teijin, and Bristol-Myers Squibb. The remaining authors declare no conflict of interest.

Ethical approval

This article does not contain any studies with human participants performed by any of the authors.

Informed consent

Informed consent was obtained from the participant included in the article.


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Copyright information

© Japanese Society of Nephrology 2020

Authors and Affiliations

  1. 1.Department of Cardiovascular MedicineSaga UniversitySagaJapan
  2. 2.Division of Nephrology, Department of Internal MedicineShinmatsudo Central General HospitalMatsudoJapan

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