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Lipoprotein(a) levels in a global population with established atherosclerotic cardiovascular disease.
Nissen, Steven E; Wolski, Kathy; Cho, Leslie; Nicholls, Stephen J; Kastelein, John; Leitersdorf, Eran; Landmesser, Ulf; Blaha, Michael; Lincoff, A Michael; Morishita, Ryuichi; Tsimikas, Sotirios; Liu, Junhao; Manning, Brian; Kozlovski, Plamen; Lesogor, Anastasia; Thuren, Tom; Shibasaki, Taro; Matei, Florin; Silveira, Fábio Serra; Meunch, Andreas; Bada, Aysha; Vijan, Vinod; Bruun, Niels Eske; Nordestgaard, Borge G.
Afiliação
  • Nissen SE; Cleveland Clinic Cardiovascular Coordinating Center, Cleveland, Ohio, USA nissens@ccf.org.
  • Wolski K; Cleveland Clinic Cardiovascular Coordinating Center, Cleveland, Ohio, USA.
  • Cho L; Cleveland Clinic Cardiovascular Coordinating Center, Cleveland, Ohio, USA.
  • Nicholls SJ; Victorian Heart Institute, Monash University, Clayton, Victoria, Australia.
  • Kastelein J; Academic Medical Center, Amsterdam, The Netherlands.
  • Leitersdorf E; Department of Medicine, Hadassah Medical Center, Jerusalem, Israel.
  • Landmesser U; Israel and Faculty of Medicine, the Hebrew University, Jerusalem, Israel.
  • Blaha M; Department of Cardiology, Charité University Medicine Berlin, German Center for Cardiovascular Research (DZHK), Partner Site Berlin, Berlin Institute of Health, Berlin, Germany.
  • Lincoff AM; Johns Hopkins, Ciccarone Center for the Prevention of Cardiovascular Disease, Baltimore, Maryland, USA.
  • Morishita R; Cleveland Clinic Cardiovascular Coordinating Center, Cleveland, Ohio, USA.
  • Tsimikas S; Center of Medical Innovation and Translational Research School of Medicine, Osaka University, Suita, Osaka, Japan.
  • Liu J; Division of Cardiovascular Medicine, University of California San Diego, La Jolla, California, USA.
  • Manning B; Novartis Pharmaceuticals, East Hanover, New Jersey, USA.
  • Kozlovski P; Novartis Pharmaceuticals, East Hanover, New Jersey, USA.
  • Lesogor A; Novartis Pharma AG, Basel, Switzerland.
  • Thuren T; Novartis Pharma AG, Basel, Switzerland.
  • Shibasaki T; Novartis Pharmaceuticals, East Hanover, New Jersey, USA.
  • Matei F; Saitama Sekishinkai Hospital, Sayama-city, Saitama, Japan.
  • Silveira FS; Clinica Matcord, Buzau, Romania.
  • Meunch A; Research Center Clínica do Coração, Aracaju-SE, Brazil.
  • Bada A; SEC Clinical Research, Andalusia, Alabama, USA.
  • Vijan V; Chris Hani Baragwanath Hospital, Soweto, South Africa.
  • Bruun NE; Vijan Cardiac & Critical Care Centre, Maharashtra, India.
  • Nordestgaard BG; Zealand University Hospital, Roskilde, Denmark.
Open Heart ; 9(2)2022 10.
Article em En | MEDLINE | ID: mdl-36252994
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Isquemia Encefálica / Acidente Vascular Cerebral / Aterosclerose Tipo de estudo: Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Open Heart Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Isquemia Encefálica / Acidente Vascular Cerebral / Aterosclerose Tipo de estudo: Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Open Heart Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos