| Literature DB >> 28814545 |
Claudia R Molins1, Laura V Ashton1,2, Gary P Wormser3, Barbara G Andre2, Ann M Hess4, Mark J Delorey1, Mark A Pilgard1, Barbara J Johnson1, Kristofor Webb2, M Nurul Islam2, Adoracion Pegalajar-Jurado1, Irida Molla3, Mollie W Jewett5, John T Belisle6.
Abstract
Lyme disease, the most commonly reported vector-borne disease in the United States, results from infection with Borrelia burgdorferi. Early clinical diagnosis of this disease is largely based on the presence of an erythematous skin lesion for individuals in high-risk regions. This, however, can be confused with other illnesses including southern tick-associated rash illness (STARI), an illness that lacks a defined etiological agent or laboratory diagnostic test, and is coprevalent with Lyme disease in portions of the eastern United States. By applying an unbiased metabolomics approach with sera retrospectively obtained from well-characterized patients, we defined biochemical and diagnostic differences between early Lyme disease and STARI. Specifically, a metabolic biosignature consisting of 261 molecular features (MFs) revealed that altered N-acyl ethanolamine and primary fatty acid amide metabolism discriminated early Lyme disease from STARI. Development of classification models with the 261-MF biosignature and testing against validation samples differentiated early Lyme disease from STARI with an accuracy of 85 to 98%. These findings revealed metabolic dissimilarity between early Lyme disease and STARI, and provide a powerful and new approach to inform patient management by objectively distinguishing early Lyme disease from an illness with nearly identical symptoms.Entities:
Mesh:
Year: 2017 PMID: 28814545 PMCID: PMC5773101 DOI: 10.1126/scitranslmed.aal2717
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956