Please use this identifier to cite or link to this item: https://doi.org/10.1186/s12967-019-1783-9
Title: Mathematical models of amino acid panel for assisting diagnosis of children acute leukemia
Authors: Liu Z.
Zhou T.
Han X.
Lang T.
Liu S.
Zhang P.
Liu H.
Wan K.
Yu J.
Zhang L.
Chen L.
Beuerman R.W. 
Peng B.
Zhou L. 
Zou L.
Keywords: alanine
arginine
aspartic acid
citrulline
glutamic acid
glutamine
glycine
histidine
leucine
methionine
ornithine
phenylalanine
serine
threonine
tryptophan
tyrosine
valine
acute leukemia
algorithm
amino acid blood level
area under the curve
Article
blood sampling
cancer diagnosis
clinical evaluation
cohort analysis
controlled study
diagnostic procedure
diagnostic test accuracy study
dried blood spot testing
human
human cell
liquid chromatography-mass spectrometry
major clinical study
mathematical model
measurement accuracy
prospective study
random forest
receiver operating characteristic
sensitivity and specificity
support vector machine
validation study
Issue Date: 2019
Citation: Liu Z., Zhou T., Han X., Lang T., Liu S., Zhang P., Liu H., Wan K., Yu J., Zhang L., Chen L., Beuerman R.W., Peng B., Zhou L., Zou L. (2019). Mathematical models of amino acid panel for assisting diagnosis of children acute leukemia. Journal of Translational Medicine 17 (1) : 38. ScholarBank@NUS Repository. https://doi.org/10.1186/s12967-019-1783-9
Abstract: Background: The altered concentrations of amino acids were found in the bone marrow or blood of leukemia patients. Metabolomics technology combining mathematical model of biomarkers could be used for assisting the diagnosis of pediatric acute leukemia (AL). Methods: The concentrations of 17 amino acids was measured by targeted liquid chromatograph-tandem mass spectrometry in periphery blood collected using dried blood spots. After evaluation, the mathematical models were further evaluated by prospective clinical validation cohort for AL diagnosis. Results: The concentrations of 13 in 17 amino acids were statistically different between the periphery blood dried serum dots measured by targeted LC-MS/MS. The receiver operating characteristic analysis for the models of amino acid panel showed that the area under curve for AL diagnosis were 0.848, 0.834 and 0.856 by SVM, RF and XGBoost. The Kappa values in further prospectively evaluated clinical cohort were 0.697, 0.703 and 0.789 (p > 0.05) respectively, and the accuracies for the models were 84.86%, 85.20% and 89.46% respectively with further clinical validation. Conclusions: The established mathematical model is a faster, cheaper and more convenient way than conventional methods, and no significant difference on the effect of diagnosis comparing with conventional methods. The mathematical model can be clinically useful for assisting pediatric AL diagnosis. © 2019 The Author(s).
Source Title: Journal of Translational Medicine
URI: https://scholarbank.nus.edu.sg/handle/10635/175341
ISSN: 1479-5876
DOI: 10.1186/s12967-019-1783-9
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