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Pediatric Origins of Nephrolithiasis-Associated Atherosclerosis
Kirsten Kusumi1, Sally Smith2, Evan Barr-Beare3
1Division of Nephrology, Department of Pediatrics, Nationwide Children's Hospital/The Ohio State University, Columbus, OH.
Insights
Kidney stones in children may signal early signs of atherosclerosis, a hardening of the arteries. Specific urine proteins like osteopontin and fibronectin 1 are linked to this increased vascular risk.
Area of Science:
- Pediatric Nephrology
- Cardiovascular Research
- Vascular Biology
Background:
- Nephrolithiasis (kidney stones) is increasingly diagnosed in children.
- Atherosclerosis, a condition typically associated with adults, may have origins in childhood.
- Understanding the link between pediatric kidney stones and vascular disease is crucial for long-term health.
Purpose of the Study:
- To investigate if atherosclerosis associated with kidney stones begins in childhood.
- To explore the relationship between kidney stones and specific atherosclerosis-related proteins in pediatric patients.
Main Methods:
- A study compared children aged 12-17 with and without kidney stones.
- Carotid artery intima-media thickness (cIMT) was measured using ultrasound.
- Urine levels of fibronectin 1, macrophage scavenger receptor 1, osteopontin, and vascular cell adhesion molecule 1 were analyzed.
Main Results:
- Children with kidney stones exhibited increased cIMT, indicating early atherosclerosis.
- Urine osteopontin and fibronectin 1 levels were significant predictors of cIMT.
- These findings suggest a pediatric origin for nephrolithiasis-associated atherosclerosis.
Conclusions:
- Preliminary evidence suggests that atherosclerosis linked to kidney stones can originate in childhood.
- The study identifies potential molecular reasons for the association between kidney stones and vascular disease.
- Further research is warranted to confirm these pediatric origins and explore preventative strategies.
Objectives:
To determine if nephrolithiasis-associated atherosclerosis has pediatric origins and to consider possible association between kidney stones and atherosclerosis-related proteins.
Study Design:
We matched children aged 12-17 years with kidney stones and without kidney stones. Carotid artery intima-media thickness (cIMT) was measured by ultrasound. Participants' urine was investigated by enzyme-linked immunosorbent assay for the atherosclerosis-related proteins fibronectin 1, macrophage scavenger receptor 1, osteopontin, and vascular cell adhesion molecule 1 levels, and normalized to urine creatinine levels.
Results:
Subjects with nephrolithiasis had higher cIMT in the right common carotid artery and overall mean measurement. Urine osteopontin and fibronectin 1 were significant predictors of cIMT.
Conclusions:
We have provided initial preliminary evidence that nephrolithiasis-associated atherosclerosis has pediatric origins and performed studies that begin to identify potential reasons for the association of nephrolithiasis and vascular disease.
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