Hoppe Bernd, von Unruh Gerd, Laube Norbert, Hesse Albrecht, Sidhu Harmeet
University Children's Hospital Cologne, Division of Pediatric Nephrology, University of Cologne, Kerpenerstrasse 62, 50931 Cologne, Germany.
Urol Res. 2005 Nov;33(5):372-5. doi: 10.1007/s00240-005-0497-z. Epub 2005 Nov 13.
Current treatment options in patients with primary and secondary hyperoxaluria are limited and do not always lead to sufficient reduction in urinary oxalate excretion. Intestinal oxalate degrading bacteria are capable of degrading oxalate to CO(2) and formate, the latter being further metabolized and excreted via the feces. It is speculated, that both endogenously produced, as well as dietary oxalate can be significantly removed via the intestinal tract. Oxalobacter formigenes, an obligate anaerobic microbe normally found in the intestinal tract has one oxalate degrading enzyme, oxalyl-CoA decarboxylase, which is also found in Bifidobacterium lactis. Other bacteria with possible oxalate degrading potency are lactic acid bacteria, as well as Enterococcus faecalis and Eubacterium lentum. However, specific therapeutic studies on humans are scarce and, except for Oxalobacter, data are not congruent. We found the oral application of Oxalobacter successful in patients with primary hyperoxaluria. However, long-term post-treatment follow-up of 1-2 years showed that constant intestinal colonization is not achieved in most patients. In one patient with constant colonization, urinary oxalate excretion normalized over time. Short-term studies with other bacteria such as lactic acid bacteria did not show a specific reduction in urinary oxalate excretion. O. formigenes might be a promising new therapeutic tool in patients with primary and secondary hyperoxaluria.
原发性和继发性高草酸尿症患者目前的治疗选择有限,且并不总能使尿草酸排泄量充分降低。肠道草酸降解菌能够将草酸降解为二氧化碳和甲酸,后者会进一步代谢并通过粪便排出。据推测,内源性产生的草酸以及膳食草酸都可通过肠道被显著清除。产甲酸草酸杆菌是一种通常存在于肠道中的专性厌氧菌,它有一种草酸降解酶,即草酰辅酶A脱羧酶,在乳酸双歧杆菌中也能发现这种酶。其他可能具有草酸降解能力的细菌有乳酸菌、粪肠球菌和迟缓真杆菌。然而,针对人类的具体治疗研究很少,除了产甲酸草酸杆菌外,数据并不一致。我们发现,对原发性高草酸尿症患者口服产甲酸草酸杆菌是成功的。然而,1至2年的长期治疗后随访表明,大多数患者并未实现肠道的持续定植。在一名实现持续定植的患者中,尿草酸排泄量随时间推移恢复正常。对其他细菌(如乳酸菌)进行的短期研究并未显示尿草酸排泄量有特定降低。产甲酸草酸杆菌可能是原发性和继发性高草酸尿症患者一种有前景的新治疗工具。