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A new method for anti‐negative interference of calcium dobesilate in serum creatinine enzymatic analysis
BACKGROUND: Serum creatinine is a widely used biomarker for evaluating renal function. Sarcosine oxidase enzymatic (SOE) analysis is currently the most widely used method for the detection of creatinine. This method was negatively interfered with by calcium dobesilate, causing pseudo‐reduced results...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8418471/ https://www.ncbi.nlm.nih.gov/pubmed/34329518 http://dx.doi.org/10.1002/jcla.23928 |
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author | Shen, Hailan Chen, Kena Cao, Ju |
author_facet | Shen, Hailan Chen, Kena Cao, Ju |
author_sort | Shen, Hailan |
collection | PubMed |
description | BACKGROUND: Serum creatinine is a widely used biomarker for evaluating renal function. Sarcosine oxidase enzymatic (SOE) analysis is currently the most widely used method for the detection of creatinine. This method was negatively interfered with by calcium dobesilate, causing pseudo‐reduced results. The aim of this study was to explore a new method to alleviate the negative interference of this drug on creatinine detection. METHOD: We formulated eight drug concentrations and 12 creatinine concentrations from serum. The SOE method, the new method, and the Jaffe method were used for detection in five systems. Creatinine biases were analyzed under the conditions with or without the interference of calcium dobesilate, at consistent or inconsistent creatinine concentrations. Creatinine concentrations were also analyzed at three medical decision levels (MDLs). RESULTS: Calcium dobesilate had negative interference in creatinine SOE analysis. With the increase in calcium dobesilate concentrations, the negative bias increases. The new BG method showed an anti‐negative interference effect. In the Roche system, the BG method reduced the negative bias from −71.11% to −16.7%. In the Abbott system, bias was reduced from −45.15% to −2.74%. In the Beckman system, the bias was reduced from −65.36% to −7.58%. In the Siemens system, the bias was reduced from −58.62% to −7.58%. In the Mindray system, the bias was reduced from −36.29% to −6.84%. CONCLUSION: The new method alleviated the negative interference of calcium dobesilate in creatinine SOE detection. The negative bias could be reduced from −60% or −70% to less than −20%. |
format | Online Article Text |
id | pubmed-8418471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84184712021-09-08 A new method for anti‐negative interference of calcium dobesilate in serum creatinine enzymatic analysis Shen, Hailan Chen, Kena Cao, Ju J Clin Lab Anal Research Articles BACKGROUND: Serum creatinine is a widely used biomarker for evaluating renal function. Sarcosine oxidase enzymatic (SOE) analysis is currently the most widely used method for the detection of creatinine. This method was negatively interfered with by calcium dobesilate, causing pseudo‐reduced results. The aim of this study was to explore a new method to alleviate the negative interference of this drug on creatinine detection. METHOD: We formulated eight drug concentrations and 12 creatinine concentrations from serum. The SOE method, the new method, and the Jaffe method were used for detection in five systems. Creatinine biases were analyzed under the conditions with or without the interference of calcium dobesilate, at consistent or inconsistent creatinine concentrations. Creatinine concentrations were also analyzed at three medical decision levels (MDLs). RESULTS: Calcium dobesilate had negative interference in creatinine SOE analysis. With the increase in calcium dobesilate concentrations, the negative bias increases. The new BG method showed an anti‐negative interference effect. In the Roche system, the BG method reduced the negative bias from −71.11% to −16.7%. In the Abbott system, bias was reduced from −45.15% to −2.74%. In the Beckman system, the bias was reduced from −65.36% to −7.58%. In the Siemens system, the bias was reduced from −58.62% to −7.58%. In the Mindray system, the bias was reduced from −36.29% to −6.84%. CONCLUSION: The new method alleviated the negative interference of calcium dobesilate in creatinine SOE detection. The negative bias could be reduced from −60% or −70% to less than −20%. John Wiley and Sons Inc. 2021-07-30 /pmc/articles/PMC8418471/ /pubmed/34329518 http://dx.doi.org/10.1002/jcla.23928 Text en © 2021 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Shen, Hailan Chen, Kena Cao, Ju A new method for anti‐negative interference of calcium dobesilate in serum creatinine enzymatic analysis |
title | A new method for anti‐negative interference of calcium dobesilate in serum creatinine enzymatic analysis |
title_full | A new method for anti‐negative interference of calcium dobesilate in serum creatinine enzymatic analysis |
title_fullStr | A new method for anti‐negative interference of calcium dobesilate in serum creatinine enzymatic analysis |
title_full_unstemmed | A new method for anti‐negative interference of calcium dobesilate in serum creatinine enzymatic analysis |
title_short | A new method for anti‐negative interference of calcium dobesilate in serum creatinine enzymatic analysis |
title_sort | new method for anti‐negative interference of calcium dobesilate in serum creatinine enzymatic analysis |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8418471/ https://www.ncbi.nlm.nih.gov/pubmed/34329518 http://dx.doi.org/10.1002/jcla.23928 |
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