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High-throughput nuclear magnetic resonance measurement of citrate in serum and plasma in the clinical laboratory

OBJECTIVES: Despite reports highlighting citrate association with different diseases, serum citrate is scarcely used for diagnosis. Existing methods to quantify citrate are limited by their complexity and practicality of implementation. A simple and rapid NMR-based method to measure circulating citr...

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Autores principales: Garcia, Erwin, Connelly, Margery A., Matyus, Steven P., Otvos, James D., Shalaurova, Irina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8042410/
https://www.ncbi.nlm.nih.gov/pubmed/33869707
http://dx.doi.org/10.1016/j.plabm.2021.e00213
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author Garcia, Erwin
Connelly, Margery A.
Matyus, Steven P.
Otvos, James D.
Shalaurova, Irina
author_facet Garcia, Erwin
Connelly, Margery A.
Matyus, Steven P.
Otvos, James D.
Shalaurova, Irina
author_sort Garcia, Erwin
collection PubMed
description OBJECTIVES: Despite reports highlighting citrate association with different diseases, serum citrate is scarcely used for diagnosis. Existing methods to quantify citrate are limited by their complexity and practicality of implementation. A simple and rapid NMR-based method to measure circulating citrate is described here, and its analytical performance evaluated. DESIGN: and Methods: Citrate was quantified from NMR spectra using a non-negative linear least squares deconvolution algorithm. The analytical characteristics of the assay were evaluated using CLSI guidelines. To determine if the assay has adequate sensitivity to measure clinically relevant concentrations of citrate, the assay was used to quantify citrate in apparently healthy adults (n ​= ​553), and in the general population (n ​= ​133,576). RESULTS: The LOQ for the assay was determined to be 1.48 ​mg/dL. Linearity was demonstrated over a wide range of concentrations (1.40–4.46 ​mg/dL). Coefficients of variation (%CV) for intra- and inter-assay precision ranged from 5.8–9.3 and 5.2–9.6%, respectively. Substances tested did not elicit interference with assay results. Specimen type comparison revealed <1% bias between serum and plasma samples, except for heparin plasma (3% bias). Stability was demonstrated up to 8 days at room temperature and longer at lower temperatures. In a cohort of apparently healthy adults, the reference interval was <1.48–2.97 ​mg/dL. Slightly higher values were observed in the general population. CONCLUSIONS: The newly developed NMR-based assay exhibits analytical characteristics that allow the accurate quantification of clinically relevant citrate concentrations. The assay provides a simple and fast means to analyze samples for research and clinical studies.
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spelling pubmed-80424102021-04-15 High-throughput nuclear magnetic resonance measurement of citrate in serum and plasma in the clinical laboratory Garcia, Erwin Connelly, Margery A. Matyus, Steven P. Otvos, James D. Shalaurova, Irina Pract Lab Med Research Article OBJECTIVES: Despite reports highlighting citrate association with different diseases, serum citrate is scarcely used for diagnosis. Existing methods to quantify citrate are limited by their complexity and practicality of implementation. A simple and rapid NMR-based method to measure circulating citrate is described here, and its analytical performance evaluated. DESIGN: and Methods: Citrate was quantified from NMR spectra using a non-negative linear least squares deconvolution algorithm. The analytical characteristics of the assay were evaluated using CLSI guidelines. To determine if the assay has adequate sensitivity to measure clinically relevant concentrations of citrate, the assay was used to quantify citrate in apparently healthy adults (n ​= ​553), and in the general population (n ​= ​133,576). RESULTS: The LOQ for the assay was determined to be 1.48 ​mg/dL. Linearity was demonstrated over a wide range of concentrations (1.40–4.46 ​mg/dL). Coefficients of variation (%CV) for intra- and inter-assay precision ranged from 5.8–9.3 and 5.2–9.6%, respectively. Substances tested did not elicit interference with assay results. Specimen type comparison revealed <1% bias between serum and plasma samples, except for heparin plasma (3% bias). Stability was demonstrated up to 8 days at room temperature and longer at lower temperatures. In a cohort of apparently healthy adults, the reference interval was <1.48–2.97 ​mg/dL. Slightly higher values were observed in the general population. CONCLUSIONS: The newly developed NMR-based assay exhibits analytical characteristics that allow the accurate quantification of clinically relevant citrate concentrations. The assay provides a simple and fast means to analyze samples for research and clinical studies. Elsevier 2021-03-18 /pmc/articles/PMC8042410/ /pubmed/33869707 http://dx.doi.org/10.1016/j.plabm.2021.e00213 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Garcia, Erwin
Connelly, Margery A.
Matyus, Steven P.
Otvos, James D.
Shalaurova, Irina
High-throughput nuclear magnetic resonance measurement of citrate in serum and plasma in the clinical laboratory
title High-throughput nuclear magnetic resonance measurement of citrate in serum and plasma in the clinical laboratory
title_full High-throughput nuclear magnetic resonance measurement of citrate in serum and plasma in the clinical laboratory
title_fullStr High-throughput nuclear magnetic resonance measurement of citrate in serum and plasma in the clinical laboratory
title_full_unstemmed High-throughput nuclear magnetic resonance measurement of citrate in serum and plasma in the clinical laboratory
title_short High-throughput nuclear magnetic resonance measurement of citrate in serum and plasma in the clinical laboratory
title_sort high-throughput nuclear magnetic resonance measurement of citrate in serum and plasma in the clinical laboratory
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8042410/
https://www.ncbi.nlm.nih.gov/pubmed/33869707
http://dx.doi.org/10.1016/j.plabm.2021.e00213
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