Intestinal Oxalobacter formigenes colonization in calcium oxalate stone formers and its relation to urinary oxalate
- PMID: 12803990
- DOI: 10.1089/089277903321618743
Intestinal Oxalobacter formigenes colonization in calcium oxalate stone formers and its relation to urinary oxalate
Abstract
Background and purpose: Oxalobacter formigenes is an anaerobic commensal colonic bacterium capable of degrading oxalate through the enzyme oxalyl-CoA decarboxylase. It has been theorized that individuals who lack this bacterium have higher intestinal oxalate absorption, leading to a higher urinary oxalate concentration and an increased risk of calcium oxalate urolithiasis. We performed a prospective, controlled study to evaluate O. formigenes colonization in calcium oxalate stone formers and to correlate colonization with urinary oxalate and other standard urinary stone risk factors.
Patients and methods: Thirty-five first-time calcium oxalate stone formers were compared with 10 control subjects having no history of urolithiasis and a normal renal ultrasound scan. All subjects underwent standard metabolic testing by submitting serum and 24-hour urine specimens. In addition, all subjects submitted stool samples for culture and detection of O. formigenes by Xentr(ix) O. formigenes Monitor.
Results: Intestinal Oxalobacter was detected in only 26% of the stone formers compared with 60% of the controls (p < 0.05). Overall, the average urinary oxalate excretion by the two groups was similar (38.6 mg/day v 40.8 mg/day). Among stone formers, however, there were statistically higher urinary oxalate concentrations in O. formigenes-negative patients compared with those testing positive (41.7 mg/day v 29.4 mg/day) (p = 0.03). Furthermore, all 10 stone formers with hyperoxaluria (>44 mg/day) tested negative for O. formigenes (p < 0.05).
Conclusions: Calcium oxalate stone formers have a low rate of colonization with O. formigenes. Among stone formers, absence of intestinal Oxalobacter correlates with higher urinary oxalate concentration and an increased risk of hyperoxaluria. Introduction of the Oxalobacter bacterium or an analog of its enzyme oxalyl-CoA decarboxylase into the intestinal tract may be a treatment for calcium oxalate stone disease.
Similar articles
-
The role of Oxalobacter formigenes colonization in calcium oxalate stone disease.Kidney Int. 2013 Jun;83(6):1144-9. doi: 10.1038/ki.2013.104. Epub 2013 Mar 27. Kidney Int. 2013. PMID: 23536130
-
Urinary oxalate levels and the enteric bacterium Oxalobacter formigenes in patients with calcium oxalate urolithiasis.Eur Urol. 2003 Oct;44(4):475-81. doi: 10.1016/s0302-2838(03)00318-x. Eur Urol. 2003. PMID: 14499684
-
Intestinal colonization with Oxalobacter formigenes and its relation to urinary oxalate excretion in pediatric patients with idiopathic calcium urolithiasis.Arch Med Res. 2009 Jul;40(5):369-73. doi: 10.1016/j.arcmed.2009.05.004. Arch Med Res. 2009. PMID: 19766900
-
Gut-inhabiting bacterium Oxalobacter formigenes: role in calcium oxalate urolithiasis.J Endourol. 2004 Jun;18(5):418-24. doi: 10.1089/0892779041271706. J Endourol. 2004. PMID: 15253809 Review.
-
A critical analysis of the role of gut Oxalobacter formigenes in oxalate stone disease.BJU Int. 2009 Jan;103(1):18-21. doi: 10.1111/j.1464-410X.2008.08122.x. Epub 2008 Nov 18. BJU Int. 2009. PMID: 19021605 Review.
Cited by
-
Genomic characterization of the uncultured Bacteroidales family S24-7 inhabiting the guts of homeothermic animals.Microbiome. 2016 Jul 7;4(1):36. doi: 10.1186/s40168-016-0181-2. Microbiome. 2016. PMID: 27388460 Free PMC article.
-
Evidence for net renal tubule oxalate secretion in patients with calcium kidney stones.Am J Physiol Renal Physiol. 2011 Feb;300(2):F311-8. doi: 10.1152/ajprenal.00411.2010. Epub 2010 Dec 1. Am J Physiol Renal Physiol. 2011. PMID: 21123489 Free PMC article.
-
Sleep and circadian rhythm disturbance in kidney stone disease: a narrative review.Front Endocrinol (Lausanne). 2023 Nov 27;14:1293685. doi: 10.3389/fendo.2023.1293685. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 38089624 Free PMC article. Review.
-
Acute probiotic ingestion reduces gastrointestinal oxalate absorption in healthy subjects.Urol Res. 2012 Jun;40(3):191-6. doi: 10.1007/s00240-011-0421-7. Epub 2011 Aug 28. Urol Res. 2012. PMID: 21874572
-
Deficient butyrate metabolism in the intestinal microbiome is a potential risk factor for recurrent kidney stone disease.Urolithiasis. 2024 Feb 28;52(1):38. doi: 10.1007/s00240-024-01534-x. Urolithiasis. 2024. PMID: 38413462
MeSH terms
Substances
LinkOut - more resources
Full Text Sources