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The relationship between Lp(a) and CVD outcomes: a systematic review

Robust associations between lipoprotein(a) [Lp(a)] and CVD outcomes among general populations have been published in previous studies. However, associations in high risk primary prevention and secondary prevention populations are less well defined. In order to investigate this further, a systematic...

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Autores principales: Forbes, Carol A., Quek, Ruben G. W., Deshpande, Sohan, Worthy, Gill, Wolff, Robert, Stirk, Lisa, Kleijnen, Jos, Gandra, Shravanthi R., Djedjos, Stephen, Wong, Nathan D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4869344/
https://www.ncbi.nlm.nih.gov/pubmed/27184891
http://dx.doi.org/10.1186/s12944-016-0258-8
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author Forbes, Carol A.
Quek, Ruben G. W.
Deshpande, Sohan
Worthy, Gill
Wolff, Robert
Stirk, Lisa
Kleijnen, Jos
Gandra, Shravanthi R.
Djedjos, Stephen
Wong, Nathan D.
author_facet Forbes, Carol A.
Quek, Ruben G. W.
Deshpande, Sohan
Worthy, Gill
Wolff, Robert
Stirk, Lisa
Kleijnen, Jos
Gandra, Shravanthi R.
Djedjos, Stephen
Wong, Nathan D.
author_sort Forbes, Carol A.
collection PubMed
description Robust associations between lipoprotein(a) [Lp(a)] and CVD outcomes among general populations have been published in previous studies. However, associations in high risk primary prevention and secondary prevention populations are less well defined. In order to investigate this further, a systematic review was performed including prospective studies, which assessed the relationship between Lp(a) and CVD outcomes using multivariable analyses. Additional information was gathered on Lp(a) assays, multivariable modelling and population characteristics. Literature searches from inception up to December 2015 retrieved 2850 records. From these 60 studies were included. Across 39 primary prevention studies in the general population (hazard ratios ranged from 1.16 to 2.97) and seven high risk primary prevention studies (hazard ratios ranged from 1.01 to 3.7), there was evidence of a statistically significant relationship between increased Lp(a) and an increased risk of future CVD. Results in 14 studies of secondary prevention populations were also suggestive of a modest statistically significant relationship (hazard ratios ranged from 0.75 to 3.7). Therefore current evidence would suggest that increased Lp(a) levels are associated with modest increases in the risk of future CVD events in both general and higher risk populations. However, further studies are required to confirm these findings. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12944-016-0258-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-48693442016-05-18 The relationship between Lp(a) and CVD outcomes: a systematic review Forbes, Carol A. Quek, Ruben G. W. Deshpande, Sohan Worthy, Gill Wolff, Robert Stirk, Lisa Kleijnen, Jos Gandra, Shravanthi R. Djedjos, Stephen Wong, Nathan D. Lipids Health Dis Review Robust associations between lipoprotein(a) [Lp(a)] and CVD outcomes among general populations have been published in previous studies. However, associations in high risk primary prevention and secondary prevention populations are less well defined. In order to investigate this further, a systematic review was performed including prospective studies, which assessed the relationship between Lp(a) and CVD outcomes using multivariable analyses. Additional information was gathered on Lp(a) assays, multivariable modelling and population characteristics. Literature searches from inception up to December 2015 retrieved 2850 records. From these 60 studies were included. Across 39 primary prevention studies in the general population (hazard ratios ranged from 1.16 to 2.97) and seven high risk primary prevention studies (hazard ratios ranged from 1.01 to 3.7), there was evidence of a statistically significant relationship between increased Lp(a) and an increased risk of future CVD. Results in 14 studies of secondary prevention populations were also suggestive of a modest statistically significant relationship (hazard ratios ranged from 0.75 to 3.7). Therefore current evidence would suggest that increased Lp(a) levels are associated with modest increases in the risk of future CVD events in both general and higher risk populations. However, further studies are required to confirm these findings. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12944-016-0258-8) contains supplementary material, which is available to authorized users. BioMed Central 2016-05-17 /pmc/articles/PMC4869344/ /pubmed/27184891 http://dx.doi.org/10.1186/s12944-016-0258-8 Text en © Forbes et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Forbes, Carol A.
Quek, Ruben G. W.
Deshpande, Sohan
Worthy, Gill
Wolff, Robert
Stirk, Lisa
Kleijnen, Jos
Gandra, Shravanthi R.
Djedjos, Stephen
Wong, Nathan D.
The relationship between Lp(a) and CVD outcomes: a systematic review
title The relationship between Lp(a) and CVD outcomes: a systematic review
title_full The relationship between Lp(a) and CVD outcomes: a systematic review
title_fullStr The relationship between Lp(a) and CVD outcomes: a systematic review
title_full_unstemmed The relationship between Lp(a) and CVD outcomes: a systematic review
title_short The relationship between Lp(a) and CVD outcomes: a systematic review
title_sort relationship between lp(a) and cvd outcomes: a systematic review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4869344/
https://www.ncbi.nlm.nih.gov/pubmed/27184891
http://dx.doi.org/10.1186/s12944-016-0258-8
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