Application of Epidemiology and Biostatistics to Malaria Diagnosis in Returning Travellers

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dc.contributor.advisorPillai, Dylan
dc.contributor.authorCheaveau, James
dc.contributor.committeememberDeardon, Rob
dc.contributor.committeememberGregson, Dan
dc.date2019-11-15
dc.date.accessioned2019-07-05T18:15:27Z
dc.date.available2019-07-05T18:15:27Z
dc.date.issued2019-07-04
dc.description.abstractToday, malaria elimination is back on the agenda but for this to be feasible, there must be a coordinated global effort utilizing all available tools. Portable, sensitive diagnostics with a low limit of detection are required to detect the malaria reservoir, and novel antimalarials are required to combat the threat of artemisinin resistance. Returning travellers are a good population in which to investigate malaria physiology and diagnostics because there is a good supply of study participants and an abundance of easily available data. In Canada, a combination of microscopy and rapid diagnostic tests are used to diagnose malaria, but these lack sensitivity and require repeated testing to rule out the condition. A prospective diagnostic trial of the illumigene Malaria, loop-mediated isothermal amplification (LAMP) assay, manufactured by Meridian Bioscience was conducted in symptomatic returning travellers between June 2017 and January 2018. After discrepant resolution with RT-PCR, LAMP had a sensitivity of 100% (95% CI; 95.8-100) and a specificity of 100% (95% CI; 98.7-100). In symptomatic returning travellers, LAMP has the potential to replace traditional malaria diagnostics, allowing for malaria to be ruled out in a timely manner. It is unclear if uncomplicated malaria causes deranged liver enzymes, which has implications for antimalarial drug development. A retrospective cohort study was evaluated in returning travellers (n=4548) who underwent a malaria test and had liver enzymes measured within 31 days from 2010-2017. After adjusting for gender, age, and use of hepatotoxic medications, returning travellers testing positive for malaria had higher odds of having an abnormal TB [(OR: 12.64, 95% CI: 6.32 – 25.29), p<0.001] but not ALP [(OR: 0.32, 95% CI: 0.09 – 1.10), p=0.072], ALT [(OR: 1.01, 95% CI: 0.54 – 1.89), p=0.978] or AST [(OR: 1.26, 95% CI: 0.22 – 7.37), p=0.794], compared to those who tested negative. This is most likely to be due to haemolysis, which normalizes following treatment. LAMP can be used in the diagnosis of malaria in returning travellers, and it may have a role in malaria elimination. Uncomplicated malaria does not appear to cause raised aminotransferases in returning travellers, and consideration must be given to this in antimalarial drug development.en_US
dc.identifier.citationCheaveau, J. (2019). Application of Epidemiology and Biostatistics to Malaria Diagnosis in Returning Travellers (Master's thesis, University of Calgary, Calgary, Canada). Retrieved from https://prism.ucalgary.ca.en_US
dc.identifier.doihttp://dx.doi.org/10.11575/PRISM/36709
dc.identifier.urihttp://hdl.handle.net/1880/110589
dc.language.isoengen_US
dc.publisher.facultyCumming School of Medicineen_US
dc.publisher.institutionUniversity of Calgaryen
dc.rightsUniversity of Calgary graduate students retain copyright ownership and moral rights for their thesis. You may use this material in any way that is permitted by the Copyright Act or through licensing that has been assigned to the document. For uses that are not allowable under copyright legislation or licensing, you are required to seek permission.en_US
dc.subjectMalariaen_US
dc.subjectDiagnosticsen_US
dc.subjectLiver enzymesen_US
dc.subjectReturning Travellersen_US
dc.subjectLoop-mediated isothermal amplificationen_US
dc.subjectLAMPen_US
dc.subject.classificationMicrobiologyen_US
dc.subject.classificationMedicine and Surgeryen_US
dc.subject.classificationPublic Healthen_US
dc.titleApplication of Epidemiology and Biostatistics to Malaria Diagnosis in Returning Travellersen_US
dc.typemaster thesisen_US
thesis.degree.disciplineMedicine – Microbiology & Infectious Diseasesen_US
thesis.degree.grantorUniversity of Calgaryen_US
thesis.degree.nameMaster of Science (MSc)en_US
ucalgary.item.requestcopytrueen_US
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