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The prognostic value of serum amyloid A for long‐term mortality among patients with subclinical carotid atherosclerosis
BACKGROUND AND PURPOSE: Despite extensive research in the last decade, the role of serum amyloid A (SAA) in atherogenesis remains highly controversial. The aim of this study was therefore to assess whether SAA is associated with long‐term mortality in patients with subclinical carotid artery disease...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593658/ https://www.ncbi.nlm.nih.gov/pubmed/30810222 http://dx.doi.org/10.1111/eci.13095 |
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author | Mayer, Florian J. Binder, Christoph J. Krychtiuk, Konstantin A. Schillinger, Martin Minar, Erich Hoke, Matthias |
author_facet | Mayer, Florian J. Binder, Christoph J. Krychtiuk, Konstantin A. Schillinger, Martin Minar, Erich Hoke, Matthias |
author_sort | Mayer, Florian J. |
collection | PubMed |
description | BACKGROUND AND PURPOSE: Despite extensive research in the last decade, the role of serum amyloid A (SAA) in atherogenesis remains highly controversial. The aim of this study was therefore to assess whether SAA is associated with long‐term mortality in patients with subclinical carotid artery disease. METHODS: One thousand sixty‐five patients with neurological asymptomatic carotid atherosclerosis as evaluated by duplex sonography were prospectively followed for cause‐specific mortality. RESULTS: During a median of 11.8 years, a total of 549 deaths, including 362 cardiovascular deaths, were recorded. Patients who died within the follow‐up period had significantly higher baseline SAA serum levels compared to those who survived (12.9 vs 9.5 mg/dL; P < 0.001). In univariable Cox regression analysis, the risk of all‐cause and cardiovascular mortality significantly increased in patients with elevated serum levels of SAA (crude hazard ratio for cardiovascular mortality per increase of 1 SD of SAA levels was 1.14, 95% CI 1.08‐1.22], P < 0.0001). However, SAA lost its significance after adjusting for high‐sensitivity C‐reactive protein (hsCRP), suggesting that SAA might not be directly associated with atherogenesis, but rather be a mere reflection of the individual patient's inflammatory status. CONCLUSIONS: Serum amyloid A is not independently associated with (cardiovascular) mortality in patients with subclinical carotid atherosclerosis. |
format | Online Article Text |
id | pubmed-6593658 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65936582019-07-10 The prognostic value of serum amyloid A for long‐term mortality among patients with subclinical carotid atherosclerosis Mayer, Florian J. Binder, Christoph J. Krychtiuk, Konstantin A. Schillinger, Martin Minar, Erich Hoke, Matthias Eur J Clin Invest Original Articles BACKGROUND AND PURPOSE: Despite extensive research in the last decade, the role of serum amyloid A (SAA) in atherogenesis remains highly controversial. The aim of this study was therefore to assess whether SAA is associated with long‐term mortality in patients with subclinical carotid artery disease. METHODS: One thousand sixty‐five patients with neurological asymptomatic carotid atherosclerosis as evaluated by duplex sonography were prospectively followed for cause‐specific mortality. RESULTS: During a median of 11.8 years, a total of 549 deaths, including 362 cardiovascular deaths, were recorded. Patients who died within the follow‐up period had significantly higher baseline SAA serum levels compared to those who survived (12.9 vs 9.5 mg/dL; P < 0.001). In univariable Cox regression analysis, the risk of all‐cause and cardiovascular mortality significantly increased in patients with elevated serum levels of SAA (crude hazard ratio for cardiovascular mortality per increase of 1 SD of SAA levels was 1.14, 95% CI 1.08‐1.22], P < 0.0001). However, SAA lost its significance after adjusting for high‐sensitivity C‐reactive protein (hsCRP), suggesting that SAA might not be directly associated with atherogenesis, but rather be a mere reflection of the individual patient's inflammatory status. CONCLUSIONS: Serum amyloid A is not independently associated with (cardiovascular) mortality in patients with subclinical carotid atherosclerosis. John Wiley and Sons Inc. 2019-03-12 2019-06 /pmc/articles/PMC6593658/ /pubmed/30810222 http://dx.doi.org/10.1111/eci.13095 Text en © 2019 The Authors. European Journal of Clinical Investigation published by John Wiley & Sons Ltd on behalf of Stichting European Society for Clinical Investigation Journal Foundation. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Mayer, Florian J. Binder, Christoph J. Krychtiuk, Konstantin A. Schillinger, Martin Minar, Erich Hoke, Matthias The prognostic value of serum amyloid A for long‐term mortality among patients with subclinical carotid atherosclerosis |
title | The prognostic value of serum amyloid A for long‐term mortality among patients with subclinical carotid atherosclerosis |
title_full | The prognostic value of serum amyloid A for long‐term mortality among patients with subclinical carotid atherosclerosis |
title_fullStr | The prognostic value of serum amyloid A for long‐term mortality among patients with subclinical carotid atherosclerosis |
title_full_unstemmed | The prognostic value of serum amyloid A for long‐term mortality among patients with subclinical carotid atherosclerosis |
title_short | The prognostic value of serum amyloid A for long‐term mortality among patients with subclinical carotid atherosclerosis |
title_sort | prognostic value of serum amyloid a for long‐term mortality among patients with subclinical carotid atherosclerosis |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593658/ https://www.ncbi.nlm.nih.gov/pubmed/30810222 http://dx.doi.org/10.1111/eci.13095 |
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