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Association between lipid levels and all-cause and cause-specific mortality in critically ill patients

Extremely low lipid levels are considered a sign of debilitation and illness. The association between lipid levels and the risk of mortality in critically ill patients has not been well investigated. This study was designed to evaluate the association between lipid levels and all-cause and cause-spe...

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Autores principales: Li, Shan, Zhang, Wei, Liu, Hongbin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10060260/
https://www.ncbi.nlm.nih.gov/pubmed/36991035
http://dx.doi.org/10.1038/s41598-023-32209-z
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author Li, Shan
Zhang, Wei
Liu, Hongbin
author_facet Li, Shan
Zhang, Wei
Liu, Hongbin
author_sort Li, Shan
collection PubMed
description Extremely low lipid levels are considered a sign of debilitation and illness. The association between lipid levels and the risk of mortality in critically ill patients has not been well investigated. This study was designed to evaluate the association between lipid levels and all-cause and cause-specific mortality in critically ill patients using a large collaborative research database known as the eICU database. In total, 27,316 individuals with low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), total cholesterol (TC) and triglyceride (TG) measurements were analyzed. A J-shaped association was observed between LDL-C, HDL-C, and TC levels and all-cause and noncardiovascular mortality, with low concentrations associated with higher risk. LDL-C, HDL-C and TC levels in the first quintile were associated with higher all-cause and noncardiovascular mortality but not with cardiovascular mortality compared to the reference quintile. There was a marked synergistic effect between low LDL-C combined with low HDL-C on the risk of mortality. Individuals with LDL-C ≤ 96 mg/dL and HDL-C ≤ 27 mg/dL had an increased risk of all-cause mortality (OR 1.52, 95% CI: 1.26–1.82), cardiovascular mortality (OR 1.07, 95% CI: 1.37–1.76) and noncardiovascular mortality (OR 1.82, 95% CI: 1.37–2.43). The results of this observational cohort showed that low LDL-C, HDL-C and TC levels were independently associated with higher all-cause and noncardiovascular mortality in critically ill patients.
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spelling pubmed-100602602023-03-31 Association between lipid levels and all-cause and cause-specific mortality in critically ill patients Li, Shan Zhang, Wei Liu, Hongbin Sci Rep Article Extremely low lipid levels are considered a sign of debilitation and illness. The association between lipid levels and the risk of mortality in critically ill patients has not been well investigated. This study was designed to evaluate the association between lipid levels and all-cause and cause-specific mortality in critically ill patients using a large collaborative research database known as the eICU database. In total, 27,316 individuals with low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), total cholesterol (TC) and triglyceride (TG) measurements were analyzed. A J-shaped association was observed between LDL-C, HDL-C, and TC levels and all-cause and noncardiovascular mortality, with low concentrations associated with higher risk. LDL-C, HDL-C and TC levels in the first quintile were associated with higher all-cause and noncardiovascular mortality but not with cardiovascular mortality compared to the reference quintile. There was a marked synergistic effect between low LDL-C combined with low HDL-C on the risk of mortality. Individuals with LDL-C ≤ 96 mg/dL and HDL-C ≤ 27 mg/dL had an increased risk of all-cause mortality (OR 1.52, 95% CI: 1.26–1.82), cardiovascular mortality (OR 1.07, 95% CI: 1.37–1.76) and noncardiovascular mortality (OR 1.82, 95% CI: 1.37–2.43). The results of this observational cohort showed that low LDL-C, HDL-C and TC levels were independently associated with higher all-cause and noncardiovascular mortality in critically ill patients. Nature Publishing Group UK 2023-03-29 /pmc/articles/PMC10060260/ /pubmed/36991035 http://dx.doi.org/10.1038/s41598-023-32209-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Li, Shan
Zhang, Wei
Liu, Hongbin
Association between lipid levels and all-cause and cause-specific mortality in critically ill patients
title Association between lipid levels and all-cause and cause-specific mortality in critically ill patients
title_full Association between lipid levels and all-cause and cause-specific mortality in critically ill patients
title_fullStr Association between lipid levels and all-cause and cause-specific mortality in critically ill patients
title_full_unstemmed Association between lipid levels and all-cause and cause-specific mortality in critically ill patients
title_short Association between lipid levels and all-cause and cause-specific mortality in critically ill patients
title_sort association between lipid levels and all-cause and cause-specific mortality in critically ill patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10060260/
https://www.ncbi.nlm.nih.gov/pubmed/36991035
http://dx.doi.org/10.1038/s41598-023-32209-z
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