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Plasma ACE2 and risk of death or cardiometabolic diseases: a case-cohort analysis
BACKGROUND: Angiotensin-converting enzyme 2 (ACE2) is an endogenous counter-regulator of the renin–angiotensin hormonal cascade. We assessed whether plasma ACE2 concentrations were associated with greater risk of death or cardiovascular disease events. METHODS: We used data from the Prospective Urba...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529405/ https://www.ncbi.nlm.nih.gov/pubmed/33010842 http://dx.doi.org/10.1016/S0140-6736(20)31964-4 |
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author | Narula, Sukrit Yusuf, Salim Chong, Michael Ramasundarahettige, Chinthanie Rangarajan, Sumathy Bangdiwala, Shrikant I van Eikels, Martin Leineweber, Kirsten Wu, Annie Pigeyre, Marie Paré, Guillaume |
author_facet | Narula, Sukrit Yusuf, Salim Chong, Michael Ramasundarahettige, Chinthanie Rangarajan, Sumathy Bangdiwala, Shrikant I van Eikels, Martin Leineweber, Kirsten Wu, Annie Pigeyre, Marie Paré, Guillaume |
author_sort | Narula, Sukrit |
collection | PubMed |
description | BACKGROUND: Angiotensin-converting enzyme 2 (ACE2) is an endogenous counter-regulator of the renin–angiotensin hormonal cascade. We assessed whether plasma ACE2 concentrations were associated with greater risk of death or cardiovascular disease events. METHODS: We used data from the Prospective Urban Rural Epidemiology (PURE) prospective study to conduct a case-cohort analysis within a subset of PURE participants (from 14 countries across five continents: Africa, Asia, Europe, North America, and South America). We measured plasma concentrations of ACE2 and assessed potential determinants of plasma ACE2 levels as well as the association of ACE2 with cardiovascular events. FINDINGS: We included 10 753 PURE participants in our study. Increased concentration of plasma ACE2 was associated with increased risk of total deaths (hazard ratio [HR] 1·35 per 1 SD increase [95% CI 1·29–1·43]) with similar increases in cardiovascular and non-cardiovascular deaths. Plasma ACE2 concentration was also associated with higher risk of incident heart failure (HR 1·27 per 1 SD increase [1·10–1·46]), myocardial infarction (HR 1·23 per 1 SD increase [1·13–1·33]), stroke (HR 1·21 per 1 SD increase [1·10–1·32]) and diabetes (HR 1·44 per 1 SD increase [1·36–1·52]). These findings were independent of age, sex, ancestry, and traditional cardiac risk factors. With the exception of incident heart failure events, the independent relationship of ACE2 with the clinical endpoints, including death, remained robust after adjustment for BNP. The highest-ranked determinants of ACE2 concentrations were sex, geographic ancestry, and body-mass index (BMI). When compared with clinical risk factors (smoking, diabetes, blood pressure, lipids, and BMI), ACE2 was the highest ranked predictor of death, and superseded several risk factors as a predictor of heart failure, stroke, and myocardial infarction. INTERPRETATION: Increased plasma ACE2 concentration was associated with increased risk of major cardiovascular events in a global study. FUNDING: Canadian Institute of Health Research, Heart & Stroke Foundation of Canada, and Bayer. |
format | Online Article Text |
id | pubmed-7529405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75294052020-10-02 Plasma ACE2 and risk of death or cardiometabolic diseases: a case-cohort analysis Narula, Sukrit Yusuf, Salim Chong, Michael Ramasundarahettige, Chinthanie Rangarajan, Sumathy Bangdiwala, Shrikant I van Eikels, Martin Leineweber, Kirsten Wu, Annie Pigeyre, Marie Paré, Guillaume Lancet Articles BACKGROUND: Angiotensin-converting enzyme 2 (ACE2) is an endogenous counter-regulator of the renin–angiotensin hormonal cascade. We assessed whether plasma ACE2 concentrations were associated with greater risk of death or cardiovascular disease events. METHODS: We used data from the Prospective Urban Rural Epidemiology (PURE) prospective study to conduct a case-cohort analysis within a subset of PURE participants (from 14 countries across five continents: Africa, Asia, Europe, North America, and South America). We measured plasma concentrations of ACE2 and assessed potential determinants of plasma ACE2 levels as well as the association of ACE2 with cardiovascular events. FINDINGS: We included 10 753 PURE participants in our study. Increased concentration of plasma ACE2 was associated with increased risk of total deaths (hazard ratio [HR] 1·35 per 1 SD increase [95% CI 1·29–1·43]) with similar increases in cardiovascular and non-cardiovascular deaths. Plasma ACE2 concentration was also associated with higher risk of incident heart failure (HR 1·27 per 1 SD increase [1·10–1·46]), myocardial infarction (HR 1·23 per 1 SD increase [1·13–1·33]), stroke (HR 1·21 per 1 SD increase [1·10–1·32]) and diabetes (HR 1·44 per 1 SD increase [1·36–1·52]). These findings were independent of age, sex, ancestry, and traditional cardiac risk factors. With the exception of incident heart failure events, the independent relationship of ACE2 with the clinical endpoints, including death, remained robust after adjustment for BNP. The highest-ranked determinants of ACE2 concentrations were sex, geographic ancestry, and body-mass index (BMI). When compared with clinical risk factors (smoking, diabetes, blood pressure, lipids, and BMI), ACE2 was the highest ranked predictor of death, and superseded several risk factors as a predictor of heart failure, stroke, and myocardial infarction. INTERPRETATION: Increased plasma ACE2 concentration was associated with increased risk of major cardiovascular events in a global study. FUNDING: Canadian Institute of Health Research, Heart & Stroke Foundation of Canada, and Bayer. Elsevier Ltd. 2020 2020-10-01 /pmc/articles/PMC7529405/ /pubmed/33010842 http://dx.doi.org/10.1016/S0140-6736(20)31964-4 Text en © 2020 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Articles Narula, Sukrit Yusuf, Salim Chong, Michael Ramasundarahettige, Chinthanie Rangarajan, Sumathy Bangdiwala, Shrikant I van Eikels, Martin Leineweber, Kirsten Wu, Annie Pigeyre, Marie Paré, Guillaume Plasma ACE2 and risk of death or cardiometabolic diseases: a case-cohort analysis |
title | Plasma ACE2 and risk of death or cardiometabolic diseases: a case-cohort analysis |
title_full | Plasma ACE2 and risk of death or cardiometabolic diseases: a case-cohort analysis |
title_fullStr | Plasma ACE2 and risk of death or cardiometabolic diseases: a case-cohort analysis |
title_full_unstemmed | Plasma ACE2 and risk of death or cardiometabolic diseases: a case-cohort analysis |
title_short | Plasma ACE2 and risk of death or cardiometabolic diseases: a case-cohort analysis |
title_sort | plasma ace2 and risk of death or cardiometabolic diseases: a case-cohort analysis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529405/ https://www.ncbi.nlm.nih.gov/pubmed/33010842 http://dx.doi.org/10.1016/S0140-6736(20)31964-4 |
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