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Lipoprotein(a) levels in a global population with established atherosclerotic cardiovascular disease
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, re...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9577925/ https://www.ncbi.nlm.nih.gov/pubmed/36252994 http://dx.doi.org/10.1136/openhrt-2022-002060 |
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author | 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 |
author_facet | 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 |
author_sort | Nissen, Steven E |
collection | PubMed |
description | 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. TRIAL REGISTRATION NUMBER: |
format | Online Article Text |
id | pubmed-9577925 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-95779252022-10-19 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 Open Heart Coronary Artery Disease 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. TRIAL REGISTRATION NUMBER: BMJ Publishing Group 2022-10-17 /pmc/articles/PMC9577925/ /pubmed/36252994 http://dx.doi.org/10.1136/openhrt-2022-002060 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Coronary Artery 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 Lipoprotein(a) levels in a global population with established atherosclerotic cardiovascular disease |
title | Lipoprotein(a) levels in a global population with established atherosclerotic cardiovascular disease |
title_full | Lipoprotein(a) levels in a global population with established atherosclerotic cardiovascular disease |
title_fullStr | Lipoprotein(a) levels in a global population with established atherosclerotic cardiovascular disease |
title_full_unstemmed | Lipoprotein(a) levels in a global population with established atherosclerotic cardiovascular disease |
title_short | Lipoprotein(a) levels in a global population with established atherosclerotic cardiovascular disease |
title_sort | lipoprotein(a) levels in a global population with established atherosclerotic cardiovascular disease |
topic | Coronary Artery Disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9577925/ https://www.ncbi.nlm.nih.gov/pubmed/36252994 http://dx.doi.org/10.1136/openhrt-2022-002060 |
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