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Lipoprotein(a) levels in a global population with established atherosclerotic cardiovascular disease

  • Steven E. Nissen*
  • , Kathy Wolski
  • , Leslie Cho
  • , Stephen J. Nicholls
  • , John Kastelein
  • , Eran Leitersdorf
  • , Ulf Landmesser
  • , Michael Blaha
  • , A. Michael Lincoff
  • , Ryuichi Morishita
  • , Sotirios Tsimikas
  • , Junhao Liu
  • , Brian Manning
  • , Plamen Kozlovski
  • , Anastasia Lesogor
  • , Tom Thuren
  • , Taro Shibasaki
  • , Florin Matei
  • , F. bio Serra Silveira
  • , Andreas Meunch
  • Aysha Bada, Vinod Vijan, Niels Eske Bruun, Borge G. Nordestgaard
*Corresponding author for this work
  • Cleveland Clinic Foundation
  • Monash University
  • Hadassah University Medical Centre
  • Hebrew University of Jerusalem
  • Berlin Institute of Health, Comprehensive Allergy Center, Department of Dermatology and Allergy, Berlin
  • Johns Hopkins University
  • The University of Osaka
  • University of California at San Diego
  • Novartis
  • Saitama Sekishinkai Hospital
  • Clinica Matcord
  • Centro de Pesquisa Clínica do Coração
  • SEC Clinical Research
  • Chris Hani Baragwanath Hospital
  • Vijan Cardiac & Critical Care Centre
  • Department of Surgery, Zealand University Hospital, Denmark
  • University of Copenhagen

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Objective Lipoprotein(a) (Lp(a)) is an important genetically determined risk factor for atherosclerotic vascular disease (ASCVD). With the development of Lp(a)-lowering therapies, this study sought to characterise patterns of Lp(a) levels in a global ASCVD population and identify racial, ethnic, regional and gender differences. Methods A multicentre cross-sectional epidemiological study to estimate the prevalence of elevated Lp(a) in patients with a history of myocardial infarction, ischaemic stroke or peripheral artery disease conducted at 949 sites in 48 countries in North America, Europe, Asia, South America, South Africa and Australia between April 2019 and July 2021. Low-density lipoprotein cholesterol (LDL-C) and Lp(a) levels were measured either as mass (mg/dL) or molar concentration (nmol/L). Results Of 48 135 enrolled patients, 13.9% had prior measurements of Lp(a). Mean age was 62.6 (SD 10.1) years and 25.9% were female. Median Lp(a) was 18.0 mg/dL (IQR 7.9-57.1) or 42.0 nmol/L (IQR 15.0-155.4). Median LDL-C was 77 mg/dL (IQR 58.4-101.0). Lp(a) in women was higher, 22.8 (IQR 9.0-73.0) mg/dL, than in men, 17.0 (IQR 7.1-52.2) mg/dL, p<0.001. Black patients had Lp(a) levels approximately threefold higher than white, Hispanic or Asian patients. Younger patients also had higher levels. 27.9% of patients had Lp(a) levels >50 mg/dL, 20.7% had levels >70 mg/dL, 12.9% were >90 mg/dL and 26.0% of patients exceeded 150 nmol/L. Conclusions Globally, Lp(a) is measured in a small minority of patients with ASCVD and is highest in black, younger and female patients. More than 25% of patients had levels exceeding the established threshold for increased cardiovascular risk, approximately 50 mg/dL or 125 nmol/L.
Original languageEnglish
Article number002060
JournalOpen heart
Volume9
Issue number2
DOIs
Publication statusPublished - 17 Oct 2022

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • atherosclerosis
  • global burden of disease
  • hyperlipidemias

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