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Urinary Sodium and Potassium Excretion and Risk of Cardiovascular Events
Open accessAbstract
CONTEXT: The precise relationship between sodium and potassium intake and cardiovascular (CV) risk remains uncertain, especially in patients with CV disease. OBJECTIVE: To determine the association between estimated urinary sodium and potassium excretion (surrogates for intake) and CV events in patients with established CV disease or diabetes mellitus. DESIGN, SETTING, AND PATIENTS: Observational analyses of 2 cohorts (N = 28,880) included in the ONTARGET and TRANSCEND trials (November 2001-March 2008 from initial recruitment to final follow-up). We estimated 24-hour urinary sodium and potassium excretion from a morning fasting urine sample (Kawasaki formula). We used restricted cubic spline plots to describe the association between sodium and potassium excretion and CV events and mortality, and to identify reference categories for sodium and potassium excretion. We used Cox proportional hazards multivariable models to determine the association of urinary sodium and potassium with CV events and mortality. MAIN OUTCOME MEASURES: CV death, myocardial infarction (MI), stroke, and hospitalization for congestive heart failure (CHF). RESULTS: At baseline, the mean (SD) estimated 24-hour excretion for sodium was 4.77 g (1.61); and for potassium was 2.19 g (0.57). After a median follow-up of 56 months, the composite outcome occurred in 4729 (16.4%) participants, including 2057 CV deaths, 1412 with MI, 1282 with stroke, and 1213 with hospitalization for CHF. Compared with the reference group with estimated baseline sodium excretion of 4 to 5.99 g per day (n = 14,156; 6.3% participants with CV death, 4.6% with MI, 4.2% with stroke, and 3.8% admitted to hospital with CHF), higher baseline sodium excretion was associated with an increased risk of CV death (9.7% for 7-8 g/day; hazard ratio [HR], 1.53; 95% CI, 1.26-1.86; and 11.2% for >8 g/day; HR, 1.66; 95% CI, 1.31-2.10), MI (6.8%; HR, 1.48; 95% CI, 1.11-1.98 for >8 g/day), stroke (6.6%; HR, 1.48; 95% CI, 1.09-2.01 for >8 g/day), and hospitalization for CHF (6.5%; HR, 1.51; 1.12-2.05 for >8 g/day). Lower sodium excretion was associated with an increased risk of CV death (8.6%; HR, 1.19; 95% CI, 1.02-1.39 for 2-2.99 g/day; 10.6%; HR, 1.37; 95% CI, 1.09-1.73 for <2 g/day), and hospitalization for CHF (5.2%; HR, 1.23; 95% CI, 1.01-1.49 for 2-2.99 g/day) on multivariable analysis. Compared with an estimated potassium excretion of less than 1.5 g per day (n = 2194; 6.2% with stroke), higher potassium excretion was associated with a reduced risk of stroke (4.7% [HR, 0.77; 95% CI, 0.63-0.94] for 1.5-1.99 g/day; 4.3% [HR, 0.73; 95% CI, 0.59-0.90] for 2-2.49 g/day; 3.9% [HR, 0.71; 95% CI, 0.56-0.91] for 2.5-3 g/day; and 3.5% [HR, 0.68; 95% CI, 0.49-0.92] for >3 g/day) on multivariable analysis. CONCLUSIONS: The association between estimated sodium excretion and CV events was J-shaped. Compared with baseline sodium excretion of 4 to 5.99 g per day, sodium excretion of greater than 7 g per day was associated with an increased risk of all CV events, and a sodium excretion of less than 3 g per day was associated with increased risk of CV mortality and hospitalization for CHF. Higher estimated potassium excretion was associated with a reduced risk of stroke.
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“Prospective cohort studies suggest a J-shaped association between sodium intake and CVD events, consistent across methods of sodium estimation (259–265).”
From Food Consumption and its Impact on Cardiovascular Disease: Importance of Solutions Focused on the Globalized Food System (2015) · cites this paper as [260]
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Zhang, Z., Liao, H., Zhang, X., Meng, Q., Shi, R., Feng, J., Li, X., Gou, Q., Ye, R., Hu, X., et al. (2021) · Journal of Clinical Hypertension · doi:10.1111/jch.14356 · Cited by 6
Chen, D., Tang, J., Gong, T., Mu, L., Li, J., Yu, P., Wang, H., Bu, X., Mu, L., & Mei, Y. (2022) · Clinical and Experimental Hypertension · doi:10.1080/10641963.2022.2079666 · Cited by 6
[Retracted] Association between Perceived Salt Intake and Arterial Stiffness
Jin, M., Miao, C., An, L., Guo, L., Yang, X., Zheng, M., Jiang, H., Wu, S., & Su, Q. (2022) · BioMed Research International · doi:10.1155/2022/9072082 · Cited by 6
RetractedThe Science upon Which to Base Dietary Sodium Policy
Alderman, M. H. (2014) · Advances in Nutrition · doi:10.3945/an.114.006593 · Cited by 6
Yanovski, Z., Sacks, F. M., Smith, S. C., Svetkey, L. P., Wadden, T. A., Lee, I.-M. M., Lichtenstein, A. H., Loria, C. M., Millen, B. E., Eckel, H., et al. (2014) · Cited by 6
Clinical Update on Nursing Home Medicine: 2012
Messinger‐Rapport, B. J., Cruz‐Oliver, D. M., Thomas, D. R., & Morley, J. E. (2012) · Journal of the American Medical Directors Association · doi:10.1016/j.jamda.2012.06.006 · Cited by 6
What Level of Sodium Intake Worsens Renal Outcomes?
Lipkowitz, M. S., & Wilcox, C. S. (2014) · American Journal of Hypertension · doi:10.1093/ajh/hpu067 · Cited by 6
Low dietary sodium in heart failure: a need for scientific rigour
Jun, M., & Neal, B. C. (2012) · Heart · doi:10.1136/heartjnl-2012-303266 · Cited by 6
O'Donnell, M. J., Mente, A., & Yusuf, S. (2016) · International Journal of Epidemiology · doi:10.1093/ije/dyw297 · Cited by 6
Estimating dietary sodium intake using spot urine samples
He, J., & Obst, K. M. (2017) · Journal of Hypertension · doi:10.1097/hjh.0000000000001230 · Cited by 6
Sodium Intake and Incident Atrial Fibrillation in Individuals With Vascular Disease
Johnson, L., Mente, A., Joseph, P. G., Conen, D., Benz, A. P., McIntyre, W. F., Drake, I., Engström, G., Connolly, S. J., Yusuf, S., et al. (2024) · JAMA Network Open · doi:10.1001/jamanetworkopen.2024.21589 · Cited by 6
A nutritional analysis of juices of ora-pro-nobis’s leaves and stalks
Zem, L. M., Helm, C. V., Zuffellato-Ribas, K. C., & Koehler, H. S. (2018) · Revista Eletrônica Científica da UERGS · doi:10.21674/2448-0479.43.512-524 · Cited by 5
Metadata
- Authors
- O'Donnell, M. J., Yusuf, S., Mente, A., Gao, P., Mann, J. F., Teo, K., McQueen, M., Sleight, P., Sharma, A. M., Dans, A., Probstfield, J., & Schmieder, R. E.
- Affiliations
- Hamilton General Hospital (CA)
- Corresponding author
- O'Donnell, Martin J.
- ORCID
- Venue
- JAMA
- Publisher
- American Medical Association (AMA)
- Published
- 2011-11-23
- Volume
- 306
- Issue
- 20
- Pages
- 2229-38
- ISSN
- 0002-9955 (ISSN-L)
- 0098-7484
- OpenAlex
- W2116529135
- Cited by
- 564
- References
- 52
- Citations by year
- 2026: 4 · 2025: 16 · 2024: 17 · 2023: 25 · 2022: 27 · 2021: 34 · 2020: 34 · 2019: 27 · 2018: 35 · 2017: 34 · 2016: 58 · 2015: 60 · 2014: 76 · 2013: 74 · 2012: 37
- FWCI
- 56.68
- Type
- journal article
- Language
- en
- Open access
- green
- hdl.handle.net
- Licence
- cc-by-nc-nd
- Locations
- JAMA (publishedVersion)
- PubMed (publishedVersion)
- ARAN (University of Galway Research Repository) (Ollscoil na Gaillimhe – University of Galway) (acceptedVersion, cc-by-nc-nd)
- Arrow@dit (Dublin Institute of Technology) (submittedVersion)
- ARAN (University of Galway Research Repository) (Ollscoil na Gaillimhe – University of Galway) (submittedVersion, cc-by-nc-nd)
- University of Galway Research Repository (submittedVersion, cc-by-nc)
- Research Repository UCD (University College Dublin) (cc-by-nc)
- Topics
- Health Sciences › Nursing › Nutrition and Dietetics › Sodium Intake and Health
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Blood Pressure and Hypertension Studies
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Nutritional Studies and Diet
- Keywords
- sodium excretion, potassium excretion, cardiovascular events, cardiovascular mortality, myocardial infarction, stroke, congestive heart failure, sodium intake, potassium intake, diabetes mellitus, cardiovascular disease
- MeSH terms
- Aged, Diabetes Mellitus, Female, Heart Failure, Hospitalization, Humans, Male, Middle Aged, Myocardial Infarction, Potassium, Risk, Sodium, Sodium, Dietary, Cohort Studies, Randomized Controlled Trials as Topic, Urinalysis, Stroke
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