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Estimation of Urinary Nanocrystals in Humans using Calcium Fluorophore Labeling and Nanoparticle Tracking Analysis
Published on: February 9, 2021
Epidemiological and biological associations between cardiovascular disease and kidney stone formation: A systematic
Luke Muschialli1, Ankith Mannath1, Shabbir H Moochhala2
1UCL Medical School, Faculty of Medical Sciences, UCL, London, UK.
Insights
Individuals with kidney stones (KSF) face a significantly higher risk of cardiovascular disease (CVD). This systematic review highlights the connection, suggesting KSF may be a systemic, calcium-mediated condition.
Area of Science:
- Nephrology and Cardiology
- Systemic Manifestations of Kidney Stones
- Cardiovascular Epidemiology
Background:
- Kidney stone formers (KSF) exhibit an elevated risk of developing cardiovascular disease (CVD), a link not widely recognized by clinicians.
- The precise biological mechanisms underlying this association remain inadequately understood.
Approach:
- A systematic review was conducted, searching epidemiological and biological literature.
- Analyzed data from 15 epidemiological studies encompassing over 4.2 million participants, including 230,720 KSF.
- Extracted and discussed potential biological mechanisms from 14 biological studies.
Key Points:
- KSF is associated with a 25% increased risk of coronary artery disease (CAD), a 17% increased risk of stroke/transient ischemic attacks (TIA), and a 39% increased risk of arterial disease (AD).
- Female KSFs demonstrated a disproportionately higher risk for stroke and CAD.
- Potential mechanisms include vascular calcification, oxidative stress (osteopontin), cholesterol pathology, and endothelial dysfunction.
Conclusions:
- A significant association exists between KSF and CVD.
- This connection supports viewing KSF as a systemic, calcium-mediated disease.
- Increased clinical awareness of this association is warranted.
Aims:
Previous studies find kidney stone formers (KSF) are at greater risk of developing cardiovascular disease (CVD). The underlying mechanisms are poorly understood, and many clinicians are unaware of this connection. We will: DATA SYNTHESIS: Our systematic review is registered with PROSPERO (ID CRD42021251477). We searched epidemiological and biological data. The epidemiological search generated 669 papers, narrowed down to 15. There were 4,259,869 participants (230,720 KSFs). KSF was associated with 25% higher risk of coronary artery disease (CAD) (95% confidence interval (CI): 15, 35%), 17% higher risk of stroke/transient ischemic attacks (TIA) (CI:10, 25%) and 39% higher risk of arterial disease (AD) (CI: 17 65%). Significant heterogeneity was found. Female-identifying KSFs had a higher risk of stroke (ratio = 1.10) and CAD (1.20). The biological search generated 125 papers, narrowed down to 14. Potential underlying mechanisms were extracted and discussed, including intimal/medial vascular calcification, oxidative stress via osteopontin (OPN), cholesterol-induced pathology, and endothelial dysfunction.
Conclusions:
There is a significant association between KSF and CVD, supporting the consideration of KSF as a systemic, calcium-mediated disease. Clinicians will benefit from being aware of this connection.
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