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Exploratory urinary metabolomics of type 1 leprosy reactions

Authors :
Pratibha Thapa
Annemieke Geluk
Karin Dijkman
Saraswoti Khadge
Chhatra B. Kunwar
Oleg A. Mayboroda
Rico J. E. Derks
Susan J. F. van den Eeden
Deanna A. Hagge
Anouk van Hooij
Source :
International Journal of Infectious Diseases, Vol 45, Iss C, Pp 46-52 (2016)
Publication Year :
2016
Publisher :
Elsevier BV, 2016.

Abstract

Summary Background Leprosy is an infectious disease caused by Mycobacterium leprae that affects the skin and nerves. Although curable with multidrug therapy, leprosy is complicated by acute inflammatory episodes called reactions, which are the major causes of irreversible neuropathy in leprosy that occur before, during, and even after treatment. Early diagnosis and prompt treatment of reactions reduces the risk of permanent disability. Methods This exploratory study investigated whether urinary metabolic profiles could be identified that correlate with early signs of reversal reactions (RR). A prospective cohort of leprosy patients with and without reactions and endemic controls was recruited in Nepal. Urine-derived metabolic profiles were measured longitudinally. Thus, a conventional area of biomarker identification for leprosy was extended to non-invasive urine testing. Results It was found that the urinary metabolome could be used to discriminate endemic controls from untreated patients with mycobacterial disease. Moreover, metabolic signatures in the urine of patients developing RR were clearly different before RR onset compared to those at RR diagnosis. Conclusions This study indicates that urinary metabolic profiles are promising host biomarkers for the detection of intra-individual changes during acute inflammation in leprosy and could contribute to early treatment and prevention of tissue damage.

Details

ISSN :
12019712
Volume :
45
Database :
OpenAIRE
Journal :
International Journal of Infectious Diseases
Accession number :
edsair.doi.dedup.....7a34da87286377f1f60ace6f17d0bf8a
Full Text :
https://doi.org/10.1016/j.ijid.2016.02.012