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Published on: February 9, 2021
Topiramate increases biochemical risk of nephrolithiasis
Edmund J Lamb1, Paul E Stevens, Lina Nashef
1Department of Clinical Biochemistry, East Kent Hospitals NHS Trust, Kent and Canterbury Hospital, Canterbury, CT1 3NG, UK. edmund.lamb@ekht.nhs.uk
Abstract:
The incidence of renal stone disease in patients receiving topiramate (Topamax) is 2-4 times that expected in the background population. This has been attributed to a weak carbonic anhydrase inhibitor effect, but published data are scant. Following three cases of renal stones in patients receiving topiramate, we evaluated biochemical risk for nephrolithiasis in eight further unselected patients. Most patients demonstrated inadequate urinary acidification and hypocitraturia; in some cases citrate was undetectable. Several patients also had other risk factors for nephrolithiasis, including increased urinary sodium, calcium and oxalate excretion. The biochemical changes induced by topiramate appear highly penetrant. Experience with this drug is relatively short-lived and it is being prescribed for long-term use in (often) relatively young patients. This report highlights the significantly increased metabolic risk of stone formation in patients receiving topiramate.
Insights
Topiramate (Topamax) significantly increases the risk of kidney stones by altering urine chemistry. Patients on this medication show inadequate acidification and low citrate, raising metabolic risk for nephrolithiasis.
Area of Science:
- Nephrology
- Pharmacology
- Urology
Background:
- Topiramate (Topamax) is associated with a 2-4 fold increased incidence of renal stone disease.
- This effect is hypothesized to be due to its weak carbonic anhydrase inhibitor properties, though data are limited.
Observation:
- Three cases of renal stones in patients on topiramate prompted further investigation.
- Biochemical risk factors for nephrolithiasis were evaluated in eight additional unselected patients receiving topiramate.
Findings:
- Most patients exhibited inadequate urinary acidification and hypocitraturia, with undetectable citrate in some cases.
- Several patients also presented with other risk factors, including elevated urinary sodium, calcium, and oxalate.
- The biochemical alterations induced by topiramate appear to be highly prevalent in patients.
Implications:
- Topiramate significantly increases the metabolic risk for kidney stone formation.
- Given its long-term use in younger populations, these findings highlight a critical safety concern.
- Further research and clinical monitoring are warranted for patients on long-term topiramate therapy.
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