Potentiated clinoptilolite : artificially enhanced aluminosilicate reduces symptoms associated with endoscopically negative gastroesophageal reflux disease and nonsteroidal anti-inflammatory drug induced gastritis

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dc.contributor.author Potgieter, Wilna
dc.contributor.author Samuels, Caroline Selma
dc.contributor.author Snyman, Jacques Rene
dc.date.accessioned 2014-08-12T05:46:23Z
dc.date.available 2014-08-12T05:46:23Z
dc.date.issued 2014-07
dc.description.abstract PURPOSE : The cation exchanger, a potentiated clinoptilolite (Absorbatox™ 2.4D), is a synthetically enhanced aluminosilicate. The aim of this study was to evaluate the possible benefits of a potentiated clinoptilolite as a gastroprotective agent in reducing the severity of clinical symptoms and signs associated with 1) endoscopically negative gastroesophageal reflux disease (ENGORD) and 2) nonsteroidal anti-inflammatory drug (NSAID) medication. METHODS AND PATIENTS : Two randomized, double-blind, placebo-controlled, pilot studies, the ENGORD and NSAID studies, were conducted. After initial negative gastroscopy, a total of 25 patients suffering from ENGORD were randomized to receive either placebo capsules or 750 mg Absorbatox twice daily for 14 days. The NSAID study recruited 23 healthy patients who received orally either 1,500 mg Absorbatox or placebo three times daily, plus 500 mg naproxen twice daily. Patients underwent gastroscopic evaluation of their stomach linings prior to and on day 14 of the study. Gastric biopsies were obtained and evaluated via the upgraded Sydney system, whereas visible gastric events and status of the gastric mucosa were evaluated via a 0–3 rating scale. During both studies, patients recorded gastric symptoms in a daily symptom diary. RESULTS : In the ENGORD study, patients who received the potentiated clinoptilolite reported a significant reduction (P#0.05) in severity of symptoms including reduction in heartburn (44%), discomfort (54%), and pain (56%). Symptom-free days improved by 41% compared to the group who received placebo (not significant). This was over and above the benefits seen with the proton pump inhibitor. In the NSAID study, the reduction in gastric symptom severity was echoed in the group who received the potentiated clinoptilolite. Treatment with the potentiated clinoptilolite resulted in significant prevention (P#0.05) of mucosal erosion severity as graded by the gastroenterologist. CONCLUSION : Absorbatox is a nonabsorbable aluminosilicate with potential gastroprotective benefits as it protected against ENGORD symptoms and NSAID-induced gastric events. The exact mechanism of action is not clear but may be due to its binding to hydrogen ions and biologically active amines and nitrates. en_US
dc.description.librarian hb2014 en_US
dc.description.uri http://www.dovepress.com en_US
dc.identifier.citation Potgieter, W, Samuels, CS & Snyman, JR 2014, 'Potentiated clinoptilolite : artificially enhanced aluminosilicate reduces symptoms associated with endoscopically negative gastroesophageal reflux disease and nonsteroidal anti-inflammatory drug induced gastritis', Clinical and Experimental Gastroenterology, vol. 7, no. 1, pp. 215-220. en_US
dc.identifier.issn 1178-7023 (online)
dc.identifier.other http://dx.doi.org/10.2147/CEG.S51222
dc.identifier.uri http://hdl.handle.net/2263/41164
dc.language.iso en en_US
dc.publisher Dove Medical Press en_US
dc.rights © 2014 Potgieter et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License. en_US
dc.subject Cation exchanger en_US
dc.subject Gastro-protective agent en_US
dc.subject Endoscopy en_US
dc.subject Zeolite en_US
dc.subject Endoscopically negative gastroesophageal reflux disease (ENGORD) en_US
dc.subject Nonsteroidal anti-inflammatory drug (NSAID) en_US
dc.title Potentiated clinoptilolite : artificially enhanced aluminosilicate reduces symptoms associated with endoscopically negative gastroesophageal reflux disease and nonsteroidal anti-inflammatory drug induced gastritis en_US
dc.type Article en_US


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