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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
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:
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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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