Evolocumab for prevention of microvascular dysfunction in patients undergoing percutaneous coronary intervention: the randomised, open-label EVOCATION trial.


Journal

EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology
ISSN: 1969-6213
Titre abrégé: EuroIntervention
Pays: France
ID NLM: 101251040

Informations de publication

Date de publication:
07 Oct 2022
Historique:
pubmed: 16 7 2022
medline: 12 10 2022
entrez: 15 7 2022
Statut: epublish

Résumé

Statins have been shown to prevent microvascular dysfunction that may cause periprocedural myocardial infarction after percutaneous coronary intervention (PCI). Evolocumab has more potent lipid-lowering properties than statins.  Aims: The aims of this study were to investigate whether evolocumab pretreatment on top of statin therapy could prevent periprocedural microvascular dysfunction.  Methods: This study included 100 patients with stable coronary artery disease who were scheduled to undergo PCI and had high low-density lipoprotein cholesterol (LDL-C) under statin therapy. Patients were randomised to receive evolocumab 140 mg every 2 weeks for 2 to 6 weeks before PCI (evolocumab group: N=54) or not (control group: N=46). The primary endpoint was the index of microvascular resistance (IMR) after PCI. Troponin T was measured before and 24 hours after PCI.  Results: Geometric mean LDL-C was 94.1 (95% confidence interval [CI]: 86.8-102.1) mg/dl and 89.4 (95% CI: 83.5-95.7) mg/dl at baseline, and 25.6 (95% CI: 21.9-30.0) mg/dl and 79.8 (95% CI: 73.9-86.3) mg/dl before PCI, in the evolocumab group and in the control group, respectively. PCI was performed 22.1±8.5 days after allocation. Geometric mean IMR was 20.6 (95% CI: 17.2-24.6) in the evolocumab group and 20.6 (95% CI: 17.0-25.0) in the control group (p=0.98). There was no significant difference in the geometric mean of post-PCI troponin T (0.054, 95% CI: 0.041-0.071 ng/ml vs 0.054, 95% CI: 0.038-0.077 ng/ml; p=0.99) and in the incidence of major periprocedural myocardial infarction between the 2 groups (44.4% vs 44.2%; p=1.00).  Conclusions: Evolocumab pretreatment did not prevent periprocedural microvascular dysfunction in patients on modern medical management with statins.

Sections du résumé

BACKGROUND BACKGROUND
Statins have been shown to prevent microvascular dysfunction that may cause periprocedural myocardial infarction after percutaneous coronary intervention (PCI). Evolocumab has more potent lipid-lowering properties than statins.  Aims: The aims of this study were to investigate whether evolocumab pretreatment on top of statin therapy could prevent periprocedural microvascular dysfunction.  Methods: This study included 100 patients with stable coronary artery disease who were scheduled to undergo PCI and had high low-density lipoprotein cholesterol (LDL-C) under statin therapy. Patients were randomised to receive evolocumab 140 mg every 2 weeks for 2 to 6 weeks before PCI (evolocumab group: N=54) or not (control group: N=46). The primary endpoint was the index of microvascular resistance (IMR) after PCI. Troponin T was measured before and 24 hours after PCI.  Results: Geometric mean LDL-C was 94.1 (95% confidence interval [CI]: 86.8-102.1) mg/dl and 89.4 (95% CI: 83.5-95.7) mg/dl at baseline, and 25.6 (95% CI: 21.9-30.0) mg/dl and 79.8 (95% CI: 73.9-86.3) mg/dl before PCI, in the evolocumab group and in the control group, respectively. PCI was performed 22.1±8.5 days after allocation. Geometric mean IMR was 20.6 (95% CI: 17.2-24.6) in the evolocumab group and 20.6 (95% CI: 17.0-25.0) in the control group (p=0.98). There was no significant difference in the geometric mean of post-PCI troponin T (0.054, 95% CI: 0.041-0.071 ng/ml vs 0.054, 95% CI: 0.038-0.077 ng/ml; p=0.99) and in the incidence of major periprocedural myocardial infarction between the 2 groups (44.4% vs 44.2%; p=1.00).  Conclusions: Evolocumab pretreatment did not prevent periprocedural microvascular dysfunction in patients on modern medical management with statins.

Identifiants

pubmed: 35837711
pii: EIJ-D-22-00269
doi: 10.4244/EIJ-D-22-00269
pmc: PMC10241273
pii:
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Cholesterol, LDL 0
Hydroxymethylglutaryl-CoA Reductase Inhibitors 0
Troponin T 0
evolocumab LKC0U3A8NJ

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

e647-e655

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Auteurs

Masaharu Ishihara (M)

Department of Cardiovascular and Renal Medicine, Hyogo College of Medicine, Hyogo, Japan.

Masanori Asakura (M)

Department of Cardiovascular and Renal Medicine, Hyogo College of Medicine, Hyogo, Japan.
Center for Clinical Research and Education, Hyogo College of Medicine, Hyogo, Japan.

Kiyoshi Hibi (K)

Division of Cardiology, Yokohama City University Medical Center, Kanagawa, Japan.

Kozo Okada (K)

Division of Cardiology, Yokohama City University Medical Center, Kanagawa, Japan.

Wataru Shimizu (W)

Department of Cardiovascular Medicine, Nippon Medical School, Tokyo, Japan.

Hitoshi Takano (H)

Department of Cardiovascular Medicine, Nippon Medical School, Tokyo, Japan.

Satoru Suwa (S)

Department of Cardiology, Juntendo University Shizuoka Hospital, Shizuoka, Japan.

Kenshi Fujii (K)

Cardiovascular Center, Sakurabashi-Watanabe Hospital, Osaka, Japan.

Yasuo Okumura (Y)

Division of Cardiology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

Toshiaki Mano (T)

Cardiovascular Center, Kansai Rosai Hospital, Hyogo, Japan.

Kenichi Tsujita (K)

Department of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.

Masataka Igeta (M)

Department of Biostatistics, Hyogo College of Medicine, Hyogo, Japan.

Rika Okamoto (R)

Clinical Study Support Center, Wakayama Medical University Hospital, Wakayama, Japan.

Shinichiro Suna (S)

Department of Cardiovascular and Renal Medicine, Hyogo College of Medicine, Hyogo, Japan.
Center for Clinical Research and Education, Hyogo College of Medicine, Hyogo, Japan.

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