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Author Spotlight: Developing a Bedside Protocol for Kidney and Genitourinary Ultrasonography
Published on: June 21, 2024
Nephrolithiasis: A Red Flag for Cardiovascular Risk
Alessia Gambaro1, Gianmarco Lombardi2, Chiara Caletti2
1Division of Cardiology, Department of Medicine, University of Verona, 37126 Verona, Italy.
Insights
Nephrolithiasis (kidney stones) is linked to cardiovascular disease due to shared metabolic risk factors. Kidney stones may signal underlying atherosclerosis and heart disease risk.
Area of Science:
- Nephrology
- Cardiology
- Metabolic Diseases
- Public Health
Background:
- Nephrolithiasis (kidney stones) shares common risk factors with cardiovascular (CV) disease.
- Metabolic syndrome (MS) and habits promoting kidney stones also contribute to CV disease development.
- Oxidative stress, endothelial dysfunction, and arterial stiffness link these conditions.
Purpose of the Study:
- To explore the association between nephrolithiasis and cardiovascular morbidities.
- To highlight shared pathogenic mechanisms.
- To emphasize the importance of evaluating cardiometabolic risk in kidney stone patients.
Main Methods:
- Review of epidemiological evidence.
- Analysis of shared risk factors and pathophysiological pathways.
- Discussion of the 'calcification paradox' in osteoporosis and nephrolithiasis.
Main Results:
- Metabolic derangements and MS are common to both conditions.
- Systemic metabolic acidosis in stone formers may contribute to osteoporosis and CV calcifications.
- Kidney stones can be an early indicator of silent atherosclerosis.
Conclusions:
- Nephrolithiasis and cardiovascular disease share underlying metabolic and inflammatory pathways.
- Osteoporosis/osteopenia may be an independent risk factor for CV calcifications.
- Routine cardiometabolic risk assessment in kidney stone patients is crucial for preventing severe CV complications.
Abstract:
Epidemiological evidence shows that nephrolithiasis is associated with cardiovascular (CV) morbidities. The association between nephrolithiasis and CV disease is not surprising because both diseases share conditions that facilitate their development. Metabolic conditions, encompassed in the definition of metabolic syndrome (MS), and habits that promote nephrolithiasis by altering urine composition also promote clinical manifestations of CV disease. By inducing oxidative stress, these conditions cause endothelial dysfunction and increased arterial stiffness, which are both well-known predictors of CV disease. Furthermore, the subtle systemic metabolic acidosis observed in stone formers with CV disease may have a pathogenic role by increasing bone turnover and leading to reduced mineral content and osteoporosis/osteopenia. Heart valves and/or coronary artery and aortic calcifications are frequently associated with reduced mineral density. This is known as the 'calcification paradox' in osteoporosis and has also been observed in subjects with calcium nephrolithiasis. Evidence supports the hypothesis that osteoporosis/osteopenia is an independent risk factor for the development of CV calcifications. In the long term, episodes of renal stones may occur from the onset of metabolic derangements/MS to arterial stiffness/atherosclerosis and CV morbidities. These episodes should be considered a warning sign of an ongoing and silent atherosclerotic process. The evaluation of cardiometabolic risk factors and MS components should be routine in the assessment of renal stone formers. This would allow for treatment and prevention of the development of CV complications, which are much more severe for the patient and for public health.
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