Early and short-term use of proprotein convertase anti-subtilisin-kexin type 9 inhibitors on coronary plaque stability in acute coronary syndrome

被引:3
作者
Uehara, Hiroki [1 ,2 ]
Kajiya, Takashi [3 ]
Abe, Masami [4 ]
Nakata, Marohito [5 ]
Hosogi, Shingo [6 ]
Ueda, Shinichiro [2 ]
机构
[1] Urasoe Gen Hosp, Dept Cardiol, 1-56-1-Maeda, Urasoe, Okinawa 9012102, Japan
[2] Univ Ryukyus, Dept Clin Res Educ & Management, Grad Sch Med, 207 Uebaru Nishihara Town, Nishihara, Okinawa 9030215, Japan
[3] Tenyoukai Cent Hosp, Dept Cardiol, Kagoshima, Japan
[4] Yuai Med Ctr Hosp, Dept Cardiol, Tomigusuku, Okinawa, Japan
[5] Naha City Hosp, Dept Cardiol, Naha, Okinawa, Japan
[6] Chikamori Hosp, Dept Cardiol, Kochi, Japan
来源
EUROPEAN HEART JOURNAL OPEN | 2024年 / 4卷 / 04期
关键词
PCSK9; inhibitor; Acute coronary syndrome; LDL-cholesterol; Statin; Optical coherence tomography; WORKING GROUP; PROTEIN;
D O I
10.1093/ehjopen/oeae055
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Proprotein convertase anti-subtilisin-kexin type 9 inhibitors (PCSK9Is) improve plaque volume and composition and reduce major adverse coronary events in chronic coronary artery disease. We evaluated the effects of the short-term use of PCSK9Is on coronary plaque stability in patients with acute coronary syndrome (ACS) using optical coherence tomography (OCT). Methods and results This is a multicentre, open-label randomized controlled trial. The enrolled 80 subjects met the inclusion criteria. Of these, 52 patients (age 60 +/- 11 years, 38 men, 14 women) with ST-elevated ACS had undergone successful primary percutaneous coronary intervention with LDL-cholesterol (LDL-C) levels > 70 mg/dL while receiving high-intensity statins. Participants were randomly assigned to the PCSK9I group (evolocumab 420 mg for 3 months, n = 29) or the standard of care (SoC) group (n = 23). Optical coherence tomography was performed at baseline (BL) and 3 and 9 months after randomization to assess lipid-rich plaques in non-culprit lesions. The change in the minimum fibrous cap thickness (MFCT) from BL to 9 months was the primary endpoint. The percentage change in LDL-C levels from BL to 3 months was significantly greater in the PCSK9I group (-67.8 +/- 21.5% in the PCSK9I group vs. -16.3 +/- 21.8% in the SoC group; P < 0.0001), and the difference between the two groups disappeared from BL to 9 months (-20.0 +/- 37.8% in the PCSK9I group vs. -6.7 +/- 34.2% in the SoC group; P = 0.20). The changes in MFCT from BL to 9 months were significantly greater in the PCSK9I group, even after PCSK9I discontinuation {100 mu m [interquartile range (IQR): 45-180 mu m] vs. 50 mu m [IQR: 0-110 mu m]; P = 0.032}. Conclusion Combination treatment with PCSK9Is and statins resulted in more marked plaque stabilization after ACS than SoC alone, and this effect persisted for 6 months after PCSK9I discontinuation.
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页数:9
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