Method development and validation using liquid chromatography-mass spectrometry to quantify thyroid hormones rT3, T3, T4, and TSH

dc.contributor.authorSephesu, Liezel
dc.contributor.supervisorLegg-E’Silva, Derryn
dc.contributor.supervisorKhambule, Lungile
dc.date.accessioned2025-10-13T08:23:57Z
dc.date.issued2024
dc.descriptionA research report submitted in fulfillment of the requirements for the Master of Science in Medicine, in the Faculty of Health Sciences, School of Pathology, University of the Witwatersrand, Johannesburg, 2024
dc.description.abstractThe thyroid gland produces three hormones namely: triiodothyronine (T3), thyroxine (T4) and Calcitonin. These play an important role in metabolism and development in the body. In addition to the thyroid hormones is reverse T3 (rT3), produced from the deiodination of T4. The production of these thyroid hormones is regulated by the Hypothalamus-Pituitary-Thyroid-Axis via thyrotropin releasing hormone (TRH) and thyroid stimulating hormone (TSH). Even with this regulation, thyroid hormone imbalances can occur in the body. Immunoassays (IA), the method used routinely for thyroid hormone measurement, can be affected by abnormal concentrations of albumin and other serum proteins leading to erroneous results. Furthermore, IAs have also been shown to be inaccurate at lower concentrations, causing possible misdiagnosis and health complications. Thus, alternative methods to measure thyroid hormone levels like liquid chromatography-tandem mass spectrometry (LC-MS/MS) are recommended as this method is not prone to interferences and has a better measuring range, particularly at the lower ranges. In the current study, an LC-MS/MS method for measuring free T3 (FT3), free T4 (FT4) and rT3, using commercially available standards was optimised and validated. The method was subsequently used to analyse 200 remnant samples previously measured by IA and the results from the two methods were compared. Samples with low thyroid hormone levels were prioritised when collecting remnant samples but the entire clinical measuring range was included. The correlation between the two methods was only seen at low concentrations (2-5 pmol/L for FT3 and 10-20 pmol/L for FT4). It was observed that more patients (40.5%) were diagnosed as being euthyroid using the IA method of measurement versus euthyroid sick syndrome diagnosis by LC-MS/MS (72.5%).
dc.description.submitterMM2025
dc.facultyFaculty of Health Sciences
dc.identifier0000-0001-7305-9108
dc.identifier.citationSephesu, Liezel. (2024). Method development and validation using liquid chromatography-mass spectrometry to quantify thyroid hormones rT3, T3, T4, and TSH [Master`s dissertation, University of the Witwatersrand, Johannesburg]. WIReDSpace. https://hdl.handle.net/10539/46950
dc.identifier.urihttps://hdl.handle.net/10539/46950
dc.language.isoen
dc.publisherUniversity of the Witwatersrand, Johannesburg
dc.rights© 2024 University of the Witwatersrand, Johannesburg. All rights reserved. The copyright in this work vests in the University of the Witwatersrand, Johannesburg. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of University of the Witwatersrand, Johannesburg.
dc.rights.holderUniversity of the Witwatersrand, Johannesburg
dc.schoolSchool of Pathology
dc.subjectUCTD
dc.subjectrT3
dc.subjectT3
dc.subjectT4
dc.subjectand TSH
dc.subjectliquid chromatography-mass
dc.subjectthyroid hormones
dc.subject.primarysdgSDG-3: Good health and well-being
dc.titleMethod development and validation using liquid chromatography-mass spectrometry to quantify thyroid hormones rT3, T3, T4, and TSH
dc.typeDissertation

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