Abstract 4352129: Triglyceride Lowering with Pemafibrate to Reduce Fibrinogen - PEMA-TAS study -

M Masanobu Ishii (Kumamoto university, Kumamoto, Japan, Japan) K Koichiro Fujisue (Kumamoto University, Kumamoto, Japan) K Koichi Kaikita K Kenshi Yamanaga (KUMAMOTO UNIVERCITY, Kumamoto, Japan) S Shinsuke Hanatani (Kumamoto University, Kumamoto, Japan) Y yasushi matsuzawa (Kumamoto University, Kumamoto, Japan) M mitsutoshi miura (Fukuoka Tokushukai Medical Center, Fukuoka, Japan) T Takashi Kudo (Fukuoka Tokushukai Medical Center, Fukuoka, Japan) H Hideki Shimomura M Masafumi Takae (Miyazaki Prefectural Nobeoka Hp, Nobeoka, Japan) Y Yuichiro Shirahama (Miyazaki Prefectural Nobeoka Hp, Nobeoka, Japan) N Nobuyasu Yamamoto (Miyazaki Prefectural Nobeoka Hp, Nobeoka, Japan) T teruhiko ito (Kumamoto red cross hospital, Kumamoto, Japan) R ryusuke tsunoda (Kumamoto red cross hospital, Kumamoto, Japan) E Eiji Horio (Saiseikai Kumamoto Hospital, Kumamoto City, Japan) T Tomohiro Sakamoto (Saiseikai Kumamoto Hospital, Kumamoto, Japan) T Taku Rokutanda (Kumamoto Central Hospital, Kumamoto, Japan) K kenji morihisa (Kumamoto Central Hospital, Kumamoto, Japan) K Katsuo Noda (Kumamoto chuo hospital, Kumamoto, Japan) H Hiroki Tanaka (Department of Structural Virology, National Institute of Global Health and Medicine, Japan Institute for Health Security) Y Yunosuke Matsuura E Eiichiro Yamamoto (Kumamoto University Hospital, Kumamoto, Japan) Y Yasuhiro Izumiya (Kumamoto University, Kumamoto, Japan) K Kenichi Tsujita (Department of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University, Japan (K. Tsujita).)

Abstract

Background: Hypertriglyceridemia is associated with an increased risk of adverse cardiovascular outcomes in patients with coronary artery disease (CAD). Although pemafibrate is effective in reducing triglyceride levels, its impact on fibrinogen, a key biomarker linked to thrombotic risk, in those patients remains unclear. This study aimed to evaluate the effect of pemafibrate on fibrinogen levels in CAD patients with hypertriglyceridemia undergoing antiplatelet monotherapy and statin therapy. Methods: This multicenter, randomized, controlled trial enrolled 101 patients with hypertriglyceridemia (fasting triglycerides ≥150 mg/dL) and CAD receiving antiplatelet monotherapy and statin therapy. After exclusion, 98 participants were randomly assigned to receive either pemafibrate 0.1 mg twice daily (intervention group) or standard care without additional lipid-lowering therapy (control group), and 96 patients were finally analyzed. Fibrinogen levels were assessed at baseline and after 3 months of treatment. The primary outcome was the change in fibrinogen levels from baseline to 3 months. Secondary outcomes included the thrombogenicity by Total Thrombus-formation Analysis System (T-TAS). Results: Among 96 patients (median age of 72 years, male; 81%), the median baseline fasting triglyceride level was 175 mg/dL, HDL cholesterol level 45 mg/dL, LDL cholesterol level 72 mg/dL, and fibrinogen level 299 mg/dL. Regarding lipid levels at 3 months, triglyceride level was significantly lower in intervention group than those in control group (99 mg/dL vs. 186 mg/dL, p<0.001), whereas LDL cholesterol level was significantly higher in intervention group than those in control group (81 mg/dL vs. 71 mg/dL, p=0.003). No difference was observed in HDL cholesterol level at 3 months. At 3 months, the intervention group showed a significant reduction in fibrinogen levels compared to the control group (241 mg/dL vs. 300 mg/dL, p < 0.001). However, the intervention group showed a significant increase in AR-AUC and PL-AUC levels compared to the control group (p < 0.001, p=0.004, respectively). Conclusions: Pemafibrate significantly reduced fibrinogen levels in patients with CAD and hypertriglyceridemia, highlighting its primary benefit in lowering thrombotic risk. While increases in AR-AUC and PL-AUC were observed as secondary outcomes, their implications require further investigation to fully understand potential effects on thrombogenicity.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (24)

M

Masanobu Ishii

Kumamoto university, Kumamoto, Japan, Japan

K

Koichiro Fujisue

Kumamoto University, Kumamoto, Japan

K

Koichi Kaikita

K

Kenshi Yamanaga

KUMAMOTO UNIVERCITY, Kumamoto, Japan

S

Shinsuke Hanatani

Kumamoto University, Kumamoto, Japan

Y

yasushi matsuzawa

Kumamoto University, Kumamoto, Japan

M

mitsutoshi miura

Fukuoka Tokushukai Medical Center, Fukuoka, Japan

T

Takashi Kudo

Fukuoka Tokushukai Medical Center, Fukuoka, Japan

H

Hideki Shimomura

M

Masafumi Takae

Miyazaki Prefectural Nobeoka Hp, Nobeoka, Japan

Y

Yuichiro Shirahama

Miyazaki Prefectural Nobeoka Hp, Nobeoka, Japan

N

Nobuyasu Yamamoto

Miyazaki Prefectural Nobeoka Hp, Nobeoka, Japan

T

teruhiko ito

Kumamoto red cross hospital, Kumamoto, Japan

R

ryusuke tsunoda

Kumamoto red cross hospital, Kumamoto, Japan

E

Eiji Horio

Saiseikai Kumamoto Hospital, Kumamoto City, Japan

T

Tomohiro Sakamoto

Saiseikai Kumamoto Hospital, Kumamoto, Japan

T

Taku Rokutanda

Kumamoto Central Hospital, Kumamoto, Japan

K

kenji morihisa

Kumamoto Central Hospital, Kumamoto, Japan

K

Katsuo Noda

Kumamoto chuo hospital, Kumamoto, Japan

H

Hiroki Tanaka

Department of Structural Virology, National Institute of Global Health and Medicine, Japan Institute for Health Security

Y

Yunosuke Matsuura

E

Eiichiro Yamamoto

Kumamoto University Hospital, Kumamoto, Japan

Y

Yasuhiro Izumiya

Kumamoto University, Kumamoto, Japan

K

Kenichi Tsujita

Department of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University, Japan (K. Tsujita).