Abstract 4360395: Stroke and Myocardial Infarction Rates in Patients at High Risk for a First Major Atherosclerotic Cardiovascular Event: The VESALIUS-REAL Global Burden Study

Q Queenie Chan A Adrienne Chan (Aston University, Birmingham, United Kingdom) C Celine Chui (The University of Hong Kong, Hong Kong, Hong Kong) E Emil Hagstrom (Uppsala Clinical Research Centre, Uppsala, Sweden) E Edward Lai (National Cheng Kung University, Tainan, Taiwan) S Shih-Chieh Shao (Keelung Chang Gung Memorial Hospital, Keelung, Taiwan) A Andreas Ochs (Amgen Ltd, London, United Kingdom) G Gabriel Paiva da Silva Lima (Amgen, Thousand Oaks, CA) M Mahendra Sibartie (Amgen Ltd, London, United Kingdom) T Thomas Cars (Sence Research AV, Uppsala, Sweden) N Naomi Reimes (PHARMO Institute, Utrecht, Netherlands) M Matthew Budoff (The Lundquist Institute, Torrance, California, United States) J Jaimini Cegla (Imperial College London, London) J Jan Cornel (Radboud University Medical Center, Nijmegen, Netherlands) H Huei-kai Huang (Buddhist Tzu Chi General Hospital, Hualien City, Taiwan) U Ulrich Laufs K Kenichi Tsujita (Department of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University, Japan (K. Tsujita).) K Kai Hang Yiu I Ian Wong (Aston University, Birmingham, United Kingdom)

Abstract

Background: VESALIUS-CV (Effect of EVolocumab in PatiEntS at High CArdiovascuLar RIsk WithoUt Prior Myocardial Infarction or Stroke – CardioVascular; NCT03872401) is an ongoing clinical trial investigating the benefits of intensified lipid-lowering therapy (LLT) in patients at high risk for a first atherosclerotic cardiovascular disease (ASCVD) event. We conducted an observational study to examine a similar population in the real world (VESALIUS-REAL) across different healthcare settings. Aim: To examine the rate of ASCVD events across eight countries in a high-risk population similar to that of VESALIUS-CV. Methods: Using eligibility criteria aligned with VESALIUS-CV, selected patients were aged ≥50 years, had evaluated low-density lipoprotein cholesterol (LDL-C) ≥2.3 mmol/L (≥90 mg/dL), and had coronary artery disease, cerebrovascular disease, peripheral artery disease, or high-risk diabetes in addition to another high cardiovascular risk factor, without history of myocardial infarction (MI) or stroke. Index was defined as the earliest date patients met all eligibility criteria. Patients with an index date between 2017 and 2022 were identified in medical and pharmacy claims (DeSC [Japan], German Disease Analyzer [Germany], HealthVerity [US]) or in electronic medical records (Hospital Authority [Hong Kong], PHARMO Data Network [The Netherlands], National and Regional Patient Registries [Sweden], Chang Gung Research Database [Taiwan], Clinical Practice Research Datalink Aurum [UK]). Incidence of first MI and first stroke was age and sex standardized to the 2020 global population and reported per 1,000 person-years (pys). Results: Of 1,076,773 patients at high risk for an ASCVD event, the proportion not receiving LLT at index ranged from 38% in Hong Kong to 72% in Germany and Taiwan. The age-sex standardized incidence rates of MI ranged from 2.6 (95% confidence interval [CI], 2.5–2.8) in Japan to 13.6 (95% CI, 12.6–14.7) in Hong Kong. For stroke, incidence rates ranged from 5.6 (95% CI, 5.3–5.8) in the US to 27.7 (95% CI, 26.4–29.2) in Taiwan ( Figure ). Conclusions: Despite being at high risk for a first ASCVD event, most patients in VESALIUS-REAL were not receiving LLT. Variation between countries may reflect differences in treatment. Differences in data sources and collection practices may impact incidence rates. These results highlight a missed opportunity to optimize lipid management in this high-risk population to prevent the burden of ASCVD events.

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 (19)

Q

Queenie Chan

A

Adrienne Chan

Aston University, Birmingham, United Kingdom

C

Celine Chui

The University of Hong Kong, Hong Kong, Hong Kong

E

Emil Hagstrom

Uppsala Clinical Research Centre, Uppsala, Sweden

E

Edward Lai

National Cheng Kung University, Tainan, Taiwan

S

Shih-Chieh Shao

Keelung Chang Gung Memorial Hospital, Keelung, Taiwan

A

Andreas Ochs

Amgen Ltd, London, United Kingdom

G

Gabriel Paiva da Silva Lima

Amgen, Thousand Oaks, CA

M

Mahendra Sibartie

Amgen Ltd, London, United Kingdom

T

Thomas Cars

Sence Research AV, Uppsala, Sweden

N

Naomi Reimes

PHARMO Institute, Utrecht, Netherlands

M

Matthew Budoff

The Lundquist Institute, Torrance, California, United States

J

Jaimini Cegla

Imperial College London, London

J

Jan Cornel

Radboud University Medical Center, Nijmegen, Netherlands

H

Huei-kai Huang

Buddhist Tzu Chi General Hospital, Hualien City, Taiwan

U

Ulrich Laufs

K

Kenichi Tsujita

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

K

Kai Hang Yiu

I

Ian Wong

Aston University, Birmingham, United Kingdom