| Literature DB >> 31849225 |
Hyou-Arm Joung1,2,3, Zachary S Ballard1,2,3, Jing Wu1,4, Derek K Tseng1, Hailemariam Teshome5, Linghao Zhang6, Elizabeth J Horn7, Paul M Arnaboldi8, Raymond J Dattwyler8, Omai B Garner9, Dino Di Carlo2,3,6, Aydogan Ozcan1,2,3,10.
Abstract
Caused by the tick-borne spirochete Borrelia burgdorferi, Lyme disease (LD) is the most common vector-borne infectious disease in North America and Europe. Though timely diagnosis and treatment are effective in preventing disease progression, current tests are insensitive in early stage LD, with a sensitivity of <50%. Additionally, the serological testing currently recommended by the U.S. Center for Disease Control has high costs (>$400/test) and extended sample-to-answer timelines (>24 h). To address these challenges, we created a cost-effective and rapid point-of-care (POC) test for early-stage LD that assays for antibodies specific to seven Borrelia antigens and a synthetic peptide in a paper-based multiplexed vertical flow assay (xVFA). We trained a deep-learning-based diagnostic algorithm to select an optimal subset of antigen/peptide targets and then blindly tested our xVFA using human samples (N(+) = 42, N(-) = 54), achieving an area-under-the-curve (AUC), sensitivity, and specificity of 0.950, 90.5%, and 87.0%, respectively, outperforming previous LD POC tests. With batch-specific standardization and threshold tuning, the specificity of our blind-testing performance improved to 96.3%, with an AUC and sensitivity of 0.963 and 85.7%, respectively.Entities:
Keywords: Lyme disease; machine learning; multiplexed immunoassay; paper-based immunoassay; point-of-care testing
Year: 2019 PMID: 31849225 DOI: 10.1021/acsnano.9b08151
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881