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Lifetime risk of cardiovascular-renal disease in type 2 diabetes: a population-based study in 473,399 individuals

BACKGROUND: Cardiovascular and renal diseases (CVRD) are major causes of mortality in individuals with type 2 diabetes (T2D). Studies of lifetime risk have neither considered all CVRD together nor the relative contribution of major risk factors to combined disease burden. METHODS: In a population-ba...

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Autores principales: Zhang, Ruiqi, Mamza, Jil Billy, Morris, Tamsin, Godfrey, George, Asselbergs, Folkert W., Denaxas, Spiros, Hemingway, Harry, Banerjee, Amitava
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8822817/
https://www.ncbi.nlm.nih.gov/pubmed/35130878
http://dx.doi.org/10.1186/s12916-022-02234-2
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author Zhang, Ruiqi
Mamza, Jil Billy
Morris, Tamsin
Godfrey, George
Asselbergs, Folkert W.
Denaxas, Spiros
Hemingway, Harry
Banerjee, Amitava
author_facet Zhang, Ruiqi
Mamza, Jil Billy
Morris, Tamsin
Godfrey, George
Asselbergs, Folkert W.
Denaxas, Spiros
Hemingway, Harry
Banerjee, Amitava
author_sort Zhang, Ruiqi
collection PubMed
description BACKGROUND: Cardiovascular and renal diseases (CVRD) are major causes of mortality in individuals with type 2 diabetes (T2D). Studies of lifetime risk have neither considered all CVRD together nor the relative contribution of major risk factors to combined disease burden. METHODS: In a population-based cohort study using national electronic health records, we studied 473,399 individuals with T2D in England 2007–2018. Lifetime risk of individual and combined major adverse renal cardiovascular events, MARCE (including CV death and CVRD: heart failure; chronic kidney disease; myocardial infarction; stroke or peripheral artery disease), were estimated, accounting for baseline CVRD status and competing risk of death. We calculated population attributable risk for individual CVRD components. Ideal cardiovascular health was defined by blood pressure, cholesterol, glucose, smoking, physical activity, diet, and body mass index (i.e. modifiable risk factors). RESULTS: In individuals with T2D, lifetime risk of MARCE was 80% in those free from CVRD and was 97%, 93%, 98%, 89% and 91% in individuals with heart failure, chronic kidney disease, myocardial infarction, stroke and peripheral arterial disease, respectively at baseline. Among CVRD-free individuals, lifetime risk of chronic kidney disease was highest (54%), followed by CV death (41%), heart failure (29%), stroke (20%), myocardial infarction (19%) and peripheral arterial disease (9%). In those with HF only, 75% of MARCE after index T2D can be attributed to HF after adjusting for age, gender, and comorbidities. Compared with those with > 1, < 3 and ≥3 modifiable health risk behaviours, achieving ideal cardiovascular health could reduce MARCE by approximately 41.5%, 23.6% and 17.2%, respectively, in the T2D population. CONCLUSIONS: Four out of five individuals with T2D free from CVRD, and nearly all those with history of CVRD, will develop MARCE over their lifetime. Early preventive measures in T2D patients are clinical, public health and policy priorities. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-022-02234-2.
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spelling pubmed-88228172022-02-08 Lifetime risk of cardiovascular-renal disease in type 2 diabetes: a population-based study in 473,399 individuals Zhang, Ruiqi Mamza, Jil Billy Morris, Tamsin Godfrey, George Asselbergs, Folkert W. Denaxas, Spiros Hemingway, Harry Banerjee, Amitava BMC Med Research Article BACKGROUND: Cardiovascular and renal diseases (CVRD) are major causes of mortality in individuals with type 2 diabetes (T2D). Studies of lifetime risk have neither considered all CVRD together nor the relative contribution of major risk factors to combined disease burden. METHODS: In a population-based cohort study using national electronic health records, we studied 473,399 individuals with T2D in England 2007–2018. Lifetime risk of individual and combined major adverse renal cardiovascular events, MARCE (including CV death and CVRD: heart failure; chronic kidney disease; myocardial infarction; stroke or peripheral artery disease), were estimated, accounting for baseline CVRD status and competing risk of death. We calculated population attributable risk for individual CVRD components. Ideal cardiovascular health was defined by blood pressure, cholesterol, glucose, smoking, physical activity, diet, and body mass index (i.e. modifiable risk factors). RESULTS: In individuals with T2D, lifetime risk of MARCE was 80% in those free from CVRD and was 97%, 93%, 98%, 89% and 91% in individuals with heart failure, chronic kidney disease, myocardial infarction, stroke and peripheral arterial disease, respectively at baseline. Among CVRD-free individuals, lifetime risk of chronic kidney disease was highest (54%), followed by CV death (41%), heart failure (29%), stroke (20%), myocardial infarction (19%) and peripheral arterial disease (9%). In those with HF only, 75% of MARCE after index T2D can be attributed to HF after adjusting for age, gender, and comorbidities. Compared with those with > 1, < 3 and ≥3 modifiable health risk behaviours, achieving ideal cardiovascular health could reduce MARCE by approximately 41.5%, 23.6% and 17.2%, respectively, in the T2D population. CONCLUSIONS: Four out of five individuals with T2D free from CVRD, and nearly all those with history of CVRD, will develop MARCE over their lifetime. Early preventive measures in T2D patients are clinical, public health and policy priorities. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-022-02234-2. BioMed Central 2022-02-07 /pmc/articles/PMC8822817/ /pubmed/35130878 http://dx.doi.org/10.1186/s12916-022-02234-2 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 Article
Zhang, Ruiqi
Mamza, Jil Billy
Morris, Tamsin
Godfrey, George
Asselbergs, Folkert W.
Denaxas, Spiros
Hemingway, Harry
Banerjee, Amitava
Lifetime risk of cardiovascular-renal disease in type 2 diabetes: a population-based study in 473,399 individuals
title Lifetime risk of cardiovascular-renal disease in type 2 diabetes: a population-based study in 473,399 individuals
title_full Lifetime risk of cardiovascular-renal disease in type 2 diabetes: a population-based study in 473,399 individuals
title_fullStr Lifetime risk of cardiovascular-renal disease in type 2 diabetes: a population-based study in 473,399 individuals
title_full_unstemmed Lifetime risk of cardiovascular-renal disease in type 2 diabetes: a population-based study in 473,399 individuals
title_short Lifetime risk of cardiovascular-renal disease in type 2 diabetes: a population-based study in 473,399 individuals
title_sort lifetime risk of cardiovascular-renal disease in type 2 diabetes: a population-based study in 473,399 individuals
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8822817/
https://www.ncbi.nlm.nih.gov/pubmed/35130878
http://dx.doi.org/10.1186/s12916-022-02234-2
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