Pilot Randomized Double-Blind Trial of Treatment ofMycobacterium ulceransDisease (Buruli Ulcer) with Topical Nitrogen Oxides
Open Access
- 1 August 2004
- journal article
- clinical trial
- Published by American Society for Microbiology in Antimicrobial Agents and Chemotherapy
- Vol. 48 (8) , 2866-2870
- https://doi.org/10.1128/aac.48.8.2866-2870.2004
Abstract
Mycobacterium ulcerans disease (Buruli ulcer) is a serious ulcerating skin disease which is common in many tropical countries. Standard treatment, by extensive excision and skin grafting, is not available in rural communities where the disease is common. We evaluated the efficacy and safety of treatment with topical nitrogen oxides. Thirty-seven patients with a clinical diagnosis of Buruli ulcer caused by M. ulcerans disease were randomly assigned to one of two groups. In one group, two creams containing sodium nitrite (6%, wt/wt) or citric acid monohydrate (9%, wt/wt) were applied daily for 6 weeks, while the other group received a placebo. In the second 6 weeks, both groups received the nitrogen oxide-generating combination of creams. Treatment was continued for another 4 weeks for patients whose ulcers were not healed after 12 weeks. The ulcer surface area was monitored by weekly tracings made by assessors blinded to the treatment. In the first 6 weeks, patients on sodium nitrite and citric acid monohydrate (group I, active treatment) showed a rapid decrease in ulcer size from 28.6 ± 5.6 cm2 (mean ± standard error) to 12.6 ± 3.2 cm2, a decrease significantly greater than that in group II (from 15.3 ± 3.1 to 11.7 ± 3.7 cm2; P = 0.03). Five ulcers in the placebo group enlarged during this period, compared with one in the active group. In the second 6 weeks (both groups on active treatment), the rates of healing were similar for the two groups and there was a significant reduction in ulcer size in group II (previously on placebo) compared to the first 6 weeks. Yellow pigmentation of the skin, which disappeared 3 days after treatment was stopped, was the only side effect to date. We conclude that creams releasing nitrogen oxides increase the healing rate of ulcers caused by M. ulcerans infection with minimal adverse events. This is the first controlled trial of any form of therapy which demonstrates efficacy in treating this disease.Keywords
This publication has 26 references indexed in Scilit:
- In Vitro Killing ofMycobacterium ulceransby Acidified NitriteAntimicrobial Agents and Chemotherapy, 2004
- Nitric oxide, skin growth and differentiation: more questions than answers?Clinical and Experimental Dermatology, 1999
- Inducible nitric oxide synthase: what difference does it make?Journal of Clinical Investigation, 1997
- Perspectives series: host/pathogen interactions. Mechanisms of nitric oxide-related antimicrobial activity.Journal of Clinical Investigation, 1997
- Homocysteine Antagonism of Nitric Oxide-Related Cytostasis in Salmonella typhimurium Science, 1996
- Altered immune responses in mice lacking inducible nitric oxide synthaseNature, 1995
- Interleukin‐4 and interleukin‐10 inhibit nitric oxide‐dependent macrophage killing of Candida albicansEuropean Journal of Immunology, 1993
- Reactive nitrogen intermediates and antimicrobial activity: Role of nitriteFree Radical Biology & Medicine, 1993
- Resistance to Leishmania major infection correlates with the induction of nitric oxide synthase in murine macrophagesEuropean Journal of Immunology, 1991
- A CONTROLLED TRIAL OF THE TREATMENT OF MYCOBACTERIUM ULCERANS INFECTION WITH CLOFAZIMINEThe Lancet, 1973