Literature DB >> 30930344

Clinical Applications of a Novel Selective PPARα Modulator, Pemafibrate, in Dyslipidemia and Metabolic Diseases.

Shizuya Yamashita1,2,3, Daisaku Masuda1, Yuji Matsuzawa4.   

Abstract

Fasting and postprandial hypertriglyceridemia is a risk factor for atherosclerotic cardiovascular diseases (ASCVD). Fibrates have been used to treat dyslipidemia, particularly hypertriglyceridemia, and low HDL-cholesterol (HDL-C). However, conventional fibrates have low selectivity for peroxisome proliferator-activated receptor (PPAR)α. Fibrates' clinical use causes side effects such as worsening liver function and elevating the creatinine level. Large-scale clinical trials of fibrates have shown negative results for prevention of ASCVD. To overcome these issues, the concept of the selective PPARα modulator (SPPARMα), with a superior balance of efficacy and safety, has been proposed. A SPPARMα, pemafibrate (K-877), was synthesized by Kowa Company, Ltd. for better efficacy and safety. Clinical trials conducted in Japan confirmed the superior effects of pemafibrate on triglyceride reduction and HDL-C elevation.Conventional fibrates showed elevated liver function test values and worsened kidney function test values, while pemafibrate demonstrated improved liver function test values and was less likely to increase serum creatinine or decrease the estimated glomerular filtration rate. There were extremely few drug interactions even when it was used concomitantly with various statins. Furthermore, unlike many of the conventional fibrates that are renal excretory-type drugs, pemafibrate is excreted into the bile, so it can be safely used even in patients with impaired renal function and there is no increase in its blood concentration.This novel SPPARMα, pemafibrate, has superior benefit-risk balance compared to conventional fibrates and can be used for patients for whom it was difficult to use existing fibrates, including those who are taking statins and those with renal dysfunction. A large-scale trial PROMINENT using pemafibrate for patients with type 2 diabetes is in progress. In the current review, the latest data on pemafibrate will be summarized.

Entities:  

Keywords:  Dyslipidemia; Pemafibrate; Peroxisome proliferator-activated receptor alpha (PPARα); Selective PPAR alpha modulator (SPPARMα); Triglycerides

Mesh:

Substances:

Year:  2019        PMID: 30930344      PMCID: PMC6514171          DOI: 10.5551/jat.48918

Source DB:  PubMed          Journal:  J Atheroscler Thromb        ISSN: 1340-3478            Impact factor:   4.928


  18 in total

1.  Pemafibrate Dramatically Ameliorated the Values of Liver Function Tests and Fibrosis Marker in Patients with Non-Alcoholic Fatty Liver Disease.

Authors:  Suguru Ikeda; Takaaki Sugihara; Yoshiki Hoshino; Yukako Matsuki; Takakazu Nagahara; Jun-Ichi Okano; Sonoko Kitao; Youhei Fujioka; Kazuhiro Yamamoto; Hajime Isomoto
Journal:  Yonago Acta Med       Date:  2020-08-07       Impact factor: 1.641

Review 2.  New therapeutic approaches for the treatment of hypertriglyceridemia.

Authors:  Ioanna Gouni-Berthold; Jonas Schwarz
Journal:  Herz       Date:  2022-04-22       Impact factor: 1.443

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

Authors:  Atsushi Tanaka; Tsukasa Nakamura; Eiichi Sato; Atsuko Chihara; Koichi Node
Journal:  CEN Case Rep       Date:  2020-01-16

4.  Efficacy and Safety of Pemafibrate, a Novel Selective Peroxisome Proliferator-Activated Receptor α Modulator (SPPARMα): Pooled Analysis of Phase 2 and 3 Studies in Dyslipidemic Patients with or without Statin Combination.

Authors:  Shizuya Yamashita; Hidenori Arai; Koutaro Yokote; Eiichi Araki; Mitsunori Matsushita; Toshiaki Nojima; Hideki Suganami; Shun Ishibashi
Journal:  Int J Mol Sci       Date:  2019-11-06       Impact factor: 5.923

Review 5.  Gene Expression Profiles Induced by a Novel Selective Peroxisome Proliferator-Activated Receptor α Modulator (SPPARMα) Pemafibrate.

Authors:  Yusuke Sasaki; Sana Raza-Iqbal; Toshiya Tanaka; Kentaro Murakami; Motonobu Anai; Tsuyoshi Osawa; Yoshihiro Matsumura; Juro Sakai; Tatsuhiko Kodama
Journal:  Int J Mol Sci       Date:  2019-11-13       Impact factor: 5.923

Review 6.  Impact of peroxisome proliferator-activated receptor-α on diabetic cardiomyopathy.

Authors:  Lin Wang; Yin Cai; Liguo Jian; Chi Wai Cheung; Liangqing Zhang; Zhengyuan Xia
Journal:  Cardiovasc Diabetol       Date:  2021-01-04       Impact factor: 9.951

7.  Efficacy and Safety of Low-Dose Pemafibrate Therapy for Hypertriglyceridemia in Patients with Type 2 Diabetes.

Authors:  Hidenori Bando; Shinji Taneda; Naoki Manda
Journal:  JMA J       Date:  2021-03-26

8.  Genetic Variants and Functional Analyses of the ATG16L1 Gene Promoter in Acute Myocardial Infarction.

Authors:  Falan Han; Shuchao Pang; Zhaoqing Sun; Yinghua Cui; Bo Yan
Journal:  Front Genet       Date:  2021-06-17       Impact factor: 4.599

Review 9.  Hypertriglyceridemia: new approaches in management and treatment.

Authors:  Anna Wolska; Zhi-Hong Yang; Alan T Remaley
Journal:  Curr Opin Lipidol       Date:  2020-12       Impact factor: 4.616

10.  The Alteration of Carnitine Metabolism in Second Trimester in GDM and a Nomogram for Predicting Macrosomia.

Authors:  Man Sun; Baihui Zhao; Sainan He; Ruopeng Weng; Binqiao Wang; Yunping Ding; Xinwen Huang; Qiong Luo
Journal:  J Diabetes Res       Date:  2020-08-11       Impact factor: 4.011

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.