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The management of patients with enteric hyperoxaluria
1Litholink® Corporation, Laboratory Corporation of America® Holdings, 2250 W Campbell Park Dr., Chicago, IL, 60612, USA. asplinj@labcorp.com.
Enteric hyperoxaluria, caused by fat malabsorption, increases oxalate absorption and kidney stone risk. Treatments focus on diet, oxalate binders, and bile acid sequestrants.
Area of Science:
- Nephrology
- Gastroenterology
- Urology
Background:
- Enteric hyperoxaluria commonly follows intestinal surgery causing fat malabsorption.
- This leads to increased oxalate absorption, exceeding 100 mg/d, raising risks of kidney stones and oxalate nephropathy.
- Fat malabsorption reduces calcium available for oxalate binding and increases colonic permeability.
Purpose of the Study:
- To summarize the current understanding and management of enteric hyperoxaluria.
- To discuss the mechanisms of oxalate hyper-absorption in the context of fat malabsorption.
- To review current and potential future therapeutic strategies.
Main Methods:
- Literature review of studies on enteric hyperoxaluria, fat malabsorption, and oxalate nephropathy.
- Analysis of the pathophysiology linking intestinal conditions to hyperoxaluria.
- Evaluation of dietary, pharmacological, and probiotic interventions.
Main Results:
- Enteric hyperoxaluria results from increased intestinal oxalate absorption due to fat malabsorption.
- Reduced dietary calcium binding and increased colonic permeability contribute to hyperoxaluria.
- Current therapies include dietary modifications, calcium salts, and bile acid sequestrants.
Conclusions:
- Enteric hyperoxaluria is a significant complication of fat malabsorption requiring targeted management.
- Dietary interventions and oral oxalate binders are primary treatments.
- Further research into probiotics for oxalate degradation is ongoing.
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