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- Publisher Website: 10.1016/j.jacc.2023.07.012
- Scopus: eid_2-s2.0-85170550222
- PMID: 37730288
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Article: Impaired Renal Function and Major Cardiovascular Events in Young Adults
Title | Impaired Renal Function and Major Cardiovascular Events in Young Adults |
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Authors | |
Keywords | cardiovascular disease chronic epidemiology hypertension kidney failure prevention |
Issue Date | 2023 |
Citation | Journal of the American College of Cardiology, 2023, v. 82, n. 13, p. 1316-1327 How to Cite? |
Abstract | Background: Cardiovascular (CV) disease in young adults (aged 18-39 years) is on the rise. Whether subclinical reductions in kidney function (ie, estimated glomerular filtration rate [eGFR] above the current threshold for chronic kidney disease but below age-expected values) are associated with elevated CV risk is unknown. Objectives: The goal of this study was to examine age-specific associations of subclinical eGFR reductions in young adults with major adverse cardiovascular events (MACEs) and MACE plus heart failure (MACE+). Methods: A retrospective cohort study of 8.7 million individuals (3.6 million aged 18-39 years) was constructed using linked provincial health care data sets from Ontario, Canada (January 2008-March 2021). Cox models were used to examine the association of categorized eGFR (50-120 mL/min/1.73 m2) with MACE (first of CV mortality, acute coronary syndrome, and ischemic stroke) and MACE+, stratified according to age (18-39, 40-49, and 50-65 years). Results: In the study cohort (mean age 41.3 years; mean eGFR 104.2 mL/min/1.73 m2; median follow-up 9.2 years), a stepwise increase in the relative risk of MACE and MACE+ was observed as early as eGFR <80 mL/min/1.73 m2 in young adults (eg, for MACE, at eGFR 70-79 mL/min/1.73 m2, ages 18-30 years: 2.37 events per 1,000 person years [HR: 1.31; 95% CI: 1.27-1.40]; ages 40-49 years: 6.26 events per 1,000 person years [HR: 1.09; 95% CI: 1.06-1.12]; ages 50-65 years: 14.9 events per 1,000 person years [HR: 1.07; 95% CI: 1.05-1.08]). Results persisted for each MACE component and in additional analyses (stratifying according to past CV disease, accounting for albuminuria at index, and using repeated eGFR measures). Conclusions: In young adults, eGFR below age-expected values were associated with an elevated risk for MACE and MACE+, warranting age-appropriate risk stratification, proactive monitoring, and timely intervention. |
Persistent Identifier | http://hdl.handle.net/10722/347068 |
ISSN | 2023 Impact Factor: 21.7 2023 SCImago Journal Rankings: 8.762 |
DC Field | Value | Language |
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dc.contributor.author | Hussain, Junayd | - |
dc.contributor.author | Imsirovic, Haris | - |
dc.contributor.author | Canney, Mark | - |
dc.contributor.author | Clark, Edward G. | - |
dc.contributor.author | Elliott, Meghan J. | - |
dc.contributor.author | Ravani, Pietro | - |
dc.contributor.author | Tanuseputro, Peter | - |
dc.contributor.author | Akbari, Ayub | - |
dc.contributor.author | Hundemer, Gregory L. | - |
dc.contributor.author | Ramsay, Tim | - |
dc.contributor.author | Tangri, Navdeep | - |
dc.contributor.author | Knoll, Greg A. | - |
dc.contributor.author | Sood, Manish M. | - |
dc.date.accessioned | 2024-09-17T04:15:09Z | - |
dc.date.available | 2024-09-17T04:15:09Z | - |
dc.date.issued | 2023 | - |
dc.identifier.citation | Journal of the American College of Cardiology, 2023, v. 82, n. 13, p. 1316-1327 | - |
dc.identifier.issn | 0735-1097 | - |
dc.identifier.uri | http://hdl.handle.net/10722/347068 | - |
dc.description.abstract | Background: Cardiovascular (CV) disease in young adults (aged 18-39 years) is on the rise. Whether subclinical reductions in kidney function (ie, estimated glomerular filtration rate [eGFR] above the current threshold for chronic kidney disease but below age-expected values) are associated with elevated CV risk is unknown. Objectives: The goal of this study was to examine age-specific associations of subclinical eGFR reductions in young adults with major adverse cardiovascular events (MACEs) and MACE plus heart failure (MACE+). Methods: A retrospective cohort study of 8.7 million individuals (3.6 million aged 18-39 years) was constructed using linked provincial health care data sets from Ontario, Canada (January 2008-March 2021). Cox models were used to examine the association of categorized eGFR (50-120 mL/min/1.73 m2) with MACE (first of CV mortality, acute coronary syndrome, and ischemic stroke) and MACE+, stratified according to age (18-39, 40-49, and 50-65 years). Results: In the study cohort (mean age 41.3 years; mean eGFR 104.2 mL/min/1.73 m2; median follow-up 9.2 years), a stepwise increase in the relative risk of MACE and MACE+ was observed as early as eGFR <80 mL/min/1.73 m2 in young adults (eg, for MACE, at eGFR 70-79 mL/min/1.73 m2, ages 18-30 years: 2.37 events per 1,000 person years [HR: 1.31; 95% CI: 1.27-1.40]; ages 40-49 years: 6.26 events per 1,000 person years [HR: 1.09; 95% CI: 1.06-1.12]; ages 50-65 years: 14.9 events per 1,000 person years [HR: 1.07; 95% CI: 1.05-1.08]). Results persisted for each MACE component and in additional analyses (stratifying according to past CV disease, accounting for albuminuria at index, and using repeated eGFR measures). Conclusions: In young adults, eGFR below age-expected values were associated with an elevated risk for MACE and MACE+, warranting age-appropriate risk stratification, proactive monitoring, and timely intervention. | - |
dc.language | eng | - |
dc.relation.ispartof | Journal of the American College of Cardiology | - |
dc.subject | cardiovascular disease | - |
dc.subject | chronic | - |
dc.subject | epidemiology | - |
dc.subject | hypertension | - |
dc.subject | kidney failure | - |
dc.subject | prevention | - |
dc.title | Impaired Renal Function and Major Cardiovascular Events in Young Adults | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.jacc.2023.07.012 | - |
dc.identifier.pmid | 37730288 | - |
dc.identifier.scopus | eid_2-s2.0-85170550222 | - |
dc.identifier.volume | 82 | - |
dc.identifier.issue | 13 | - |
dc.identifier.spage | 1316 | - |
dc.identifier.epage | 1327 | - |
dc.identifier.eissn | 1558-3597 | - |