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dc.contributor.authorMason, Shayne
dc.contributor.authorReinecke, Carolus J.
dc.contributor.authorSolomons, Regan
dc.date.accessioned2018-06-06T13:26:06Z
dc.date.available2018-06-06T13:26:06Z
dc.date.issued2017
dc.identifier.citationMason, S. et al. 2017. Cerebrospinal fluid amino acid profiling of pediatric cases with tuberculous meningitis. Frontiers in neuroscience, 11: Article no 534. [https://doi.org/10.3389/fnins.2017.00534]en_US
dc.identifier.issn1662-4548
dc.identifier.issn1662-453X (Online)
dc.identifier.urihttp://hdl.handle.net/10394/27347
dc.identifier.urihttps://doi.org/10.3389/fnins.2017.00534
dc.identifier.urihttps://www.frontiersin.org/articles/10.3389/fnins.2017.00534/full
dc.description.abstractBackground: In Africa, tuberculosis is generally regarded as persisting as one of the most devastating infectious diseases. The pediatric population is particularly vulnerable, with infection of the brain in the form of tuberculous meningitis (TBM) being the most severe manifestation. TBM is often difficult to diagnose in its early stages because of its non-specific clinical presentation. Of particular concern is that late diagnosis, and subsequent delayed treatment, leads to high risk of long-term neurological sequelae, and even death. Using advanced technology and scientific expertise, we are intent on further describing the biochemistry behind this devastating neuroinflammatory disease, with the goal of improving upon its early diagnosis. Method: We used the highly sensitive analytical platform of gas chromatography-mass spectrometry (GC-MS) to analyze amino acid profiles of cerebrospinal fluid (CSF) collected from a cohort of 33 South African pediatric TBM cases, compared to 34 controls. Results: Through the use of a stringent quality assurance procedure and various statistical techniques, we were able to confidently identify five amino acids as being significantly elevated in TBM cases, namely, alanine, asparagine, glycine, lysine, and proline. We found also in an earlier untargeted metabolomics investigation that alanine can be attributed to increased CSF lactate levels, and lysine as a marker of lipid peroxidation. Alanine, like glycine, is an inhibitory neurotransmitter in the brain. Asparagine, as with proline, is linked to the glutamate-glutamine cycle. Asparagine is associated with the removal of increased nitrites in the brain, whereas elevated proline coincides with the classic biochemical marker of increased CSF protein in TBM. All five discriminatory amino acids are linked to ammonia due to increased nitrites in TBM. Conclusion: A large amount of untapped biochemical information is present in CSF of TBM cases, of which amino acid profiling through GC-MS has potential in aiding in earlier diagnosis, and hence crucial earlier treatmenten_US
dc.language.isoenen_US
dc.publisherFrontiers Mediaen_US
dc.subjectGas chromatography-mass spectrometry (GC-MS)en_US
dc.subjectTuberculous meningitis (TBM)en_US
dc.subjectPediatricen_US
dc.subjectCerebrospinal fluid (CSF)en_US
dc.subjectAmino acid profilingen_US
dc.titleCerebrospinal fluid amino acid profiling of pediatric cases with tuberculous meningitisen_US
dc.typeArticleen_US
dc.contributor.researchID10055037 - Reinecke, Carolus Johannes
dc.contributor.researchID21487855 - Mason, Shayne William


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