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Admission glucose as a prognostic marker for all-cause mortality and cardiovascular disease
BACKGROUND: Diabetes and prediabetes are known risk factors for cardiovascular disease and associated with increased mortality risk. Whether patients with a random elevated blood glucose level but no history of diabetes are at a higher mortality and cardiovascular risk is not entirely known. METHODS...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9701417/ https://www.ncbi.nlm.nih.gov/pubmed/36435766 http://dx.doi.org/10.1186/s12933-022-01699-y |
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author | Djupsjö, Catarina Kuhl, Jeanette Andersson, Tomas Lundbäck, Magnus Holzmann, Martin J. Nyström, Thomas |
author_facet | Djupsjö, Catarina Kuhl, Jeanette Andersson, Tomas Lundbäck, Magnus Holzmann, Martin J. Nyström, Thomas |
author_sort | Djupsjö, Catarina |
collection | PubMed |
description | BACKGROUND: Diabetes and prediabetes are known risk factors for cardiovascular disease and associated with increased mortality risk. Whether patients with a random elevated blood glucose level but no history of diabetes are at a higher mortality and cardiovascular risk is not entirely known. METHODS: A retrospective cohort study where patients (18–80 years) with no history of diabetes between 2006 and 2016 attending the emergency department (ED) in Sweden were included. Based on the first (index) blood glucose level patients were categorized into four groups: hypoglycemia (< 3.9 mmol/L), normal glucose tolerance (NGT) (3.9–7.8 mmol/L), dysglycemia (7.8–11.1 mmol/L), and hyperglycemia (> 11.1 mmol/L). Data was collected from four nationwide registers (National Patient Register, National Cause of Death Register, Prescribed Drug Register and Statistics Sweden). Cox regression was used to calculate adjusted hazard ratios (HR) with 95% confidence intervals (CI) for all-cause mortality and cardiovascular outcomes using NGT as reference. RESULTS: 618,694 patients were included during a mean follow-up time of 3.9 years. According to the index blood glucose level: 1871 (0.3%) had hypoglycemia, 525,636 (85%) had NGT, 77,442 (13%) had dysglycemia, and 13,745 (2%) patients had hyperglycemia, respectively. During follow-up 44,532 (7.2%) deaths occurred. After multiple adjustments, mortality risk was highest in patients with hypoglycemia HR 2.58 (2.26–2.96) followed by patients with hyperglycemia HR 1.69 (1.63–1.76) and dysglycemia HR 1.16 (1.13–1.19). Risk for cardiovascular events: i.e., myocardial infarction, stroke and heart failure, were highest among patients with hyperglycemia HR 2.28 (2.13–2.44), HR 1.62 (1.51–1.74) and HR 1.60 (1.46–1.75), respectively. CONCLUSION: Patients with disturbed blood glucose level at ED admission have a higher mortality risk than patients with NGT. Patients with hyperglycemia have almost a two folded increased long-term mortality risk and more than a doubled risk for cardiovascular events compared to patients with NGT. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12933-022-01699-y. |
format | Online Article Text |
id | pubmed-9701417 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97014172022-11-28 Admission glucose as a prognostic marker for all-cause mortality and cardiovascular disease Djupsjö, Catarina Kuhl, Jeanette Andersson, Tomas Lundbäck, Magnus Holzmann, Martin J. Nyström, Thomas Cardiovasc Diabetol Research BACKGROUND: Diabetes and prediabetes are known risk factors for cardiovascular disease and associated with increased mortality risk. Whether patients with a random elevated blood glucose level but no history of diabetes are at a higher mortality and cardiovascular risk is not entirely known. METHODS: A retrospective cohort study where patients (18–80 years) with no history of diabetes between 2006 and 2016 attending the emergency department (ED) in Sweden were included. Based on the first (index) blood glucose level patients were categorized into four groups: hypoglycemia (< 3.9 mmol/L), normal glucose tolerance (NGT) (3.9–7.8 mmol/L), dysglycemia (7.8–11.1 mmol/L), and hyperglycemia (> 11.1 mmol/L). Data was collected from four nationwide registers (National Patient Register, National Cause of Death Register, Prescribed Drug Register and Statistics Sweden). Cox regression was used to calculate adjusted hazard ratios (HR) with 95% confidence intervals (CI) for all-cause mortality and cardiovascular outcomes using NGT as reference. RESULTS: 618,694 patients were included during a mean follow-up time of 3.9 years. According to the index blood glucose level: 1871 (0.3%) had hypoglycemia, 525,636 (85%) had NGT, 77,442 (13%) had dysglycemia, and 13,745 (2%) patients had hyperglycemia, respectively. During follow-up 44,532 (7.2%) deaths occurred. After multiple adjustments, mortality risk was highest in patients with hypoglycemia HR 2.58 (2.26–2.96) followed by patients with hyperglycemia HR 1.69 (1.63–1.76) and dysglycemia HR 1.16 (1.13–1.19). Risk for cardiovascular events: i.e., myocardial infarction, stroke and heart failure, were highest among patients with hyperglycemia HR 2.28 (2.13–2.44), HR 1.62 (1.51–1.74) and HR 1.60 (1.46–1.75), respectively. CONCLUSION: Patients with disturbed blood glucose level at ED admission have a higher mortality risk than patients with NGT. Patients with hyperglycemia have almost a two folded increased long-term mortality risk and more than a doubled risk for cardiovascular events compared to patients with NGT. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12933-022-01699-y. BioMed Central 2022-11-26 /pmc/articles/PMC9701417/ /pubmed/36435766 http://dx.doi.org/10.1186/s12933-022-01699-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Djupsjö, Catarina Kuhl, Jeanette Andersson, Tomas Lundbäck, Magnus Holzmann, Martin J. Nyström, Thomas Admission glucose as a prognostic marker for all-cause mortality and cardiovascular disease |
title | Admission glucose as a prognostic marker for all-cause mortality and cardiovascular disease |
title_full | Admission glucose as a prognostic marker for all-cause mortality and cardiovascular disease |
title_fullStr | Admission glucose as a prognostic marker for all-cause mortality and cardiovascular disease |
title_full_unstemmed | Admission glucose as a prognostic marker for all-cause mortality and cardiovascular disease |
title_short | Admission glucose as a prognostic marker for all-cause mortality and cardiovascular disease |
title_sort | admission glucose as a prognostic marker for all-cause mortality and cardiovascular disease |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9701417/ https://www.ncbi.nlm.nih.gov/pubmed/36435766 http://dx.doi.org/10.1186/s12933-022-01699-y |
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