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Estimating the within‐subject (CV(I)) and between‐subject (CV(G)) biological variation of serum tryptase

BACKGROUND: Tryptase is used as a biomarker to support the diagnosis of anaphylaxis and hematologic diseases. In the event of a mast cell activation during anaphylaxis, a temporary increase in the concentration of tryptase may be seen. On the basis of clinical studies, an increase of 2 µg/L + 20% fr...

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Autores principales: Skarbø, Birthe R., Vinnes, Erik W., Wentzel‐Larsen, Tore, Sylte, Marit S., Apelseth, Torunn O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8959422/
https://www.ncbi.nlm.nih.gov/pubmed/34904391
http://dx.doi.org/10.1002/iid3.578
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author Skarbø, Birthe R.
Vinnes, Erik W.
Wentzel‐Larsen, Tore
Sylte, Marit S.
Apelseth, Torunn O.
author_facet Skarbø, Birthe R.
Vinnes, Erik W.
Wentzel‐Larsen, Tore
Sylte, Marit S.
Apelseth, Torunn O.
author_sort Skarbø, Birthe R.
collection PubMed
description BACKGROUND: Tryptase is used as a biomarker to support the diagnosis of anaphylaxis and hematologic diseases. In the event of a mast cell activation during anaphylaxis, a temporary increase in the concentration of tryptase may be seen. On the basis of clinical studies, an increase of 2 µg/L + 20% from basis level has been proposed as significant. To evaluate the increase in tryptase levels, the within‐subject (CV(I)) and between‐subject (CV(G)) biological variations should be known. This study was conducted to estimate the biological variation of tryptase and to identify the reference change value (RCV). METHODS: Blood samples were collected from healthy volunteers once a week consecutively over a 10‐week period. Tryptase was measured by the use of a fluoroenzyme immunoassay (ImmunoCAP(TM); Thermo Fisher Scientific), and linear mixed‐effects models were used to calculate the biological variation and RCV for both nontransformed and log‐transformed tryptase. RESULTS: Fourteen presumably healthy young adults (six males and eight females, age 23–35 years) were included. The CV(I) was 5.6% and the CV(G) was 31.5% (nontransformed data). Log‐transformed data showed similar results. The analytical variation (CV(A)) was 6.3% and the RCV was 23.5%. CONCLUSIONS: Young healthy adults without ongoing allergic reactions show low within‐subject biological variation. Higher biological variation was observed between subjects.
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spelling pubmed-89594222022-04-04 Estimating the within‐subject (CV(I)) and between‐subject (CV(G)) biological variation of serum tryptase Skarbø, Birthe R. Vinnes, Erik W. Wentzel‐Larsen, Tore Sylte, Marit S. Apelseth, Torunn O. Immun Inflamm Dis Review Articles BACKGROUND: Tryptase is used as a biomarker to support the diagnosis of anaphylaxis and hematologic diseases. In the event of a mast cell activation during anaphylaxis, a temporary increase in the concentration of tryptase may be seen. On the basis of clinical studies, an increase of 2 µg/L + 20% from basis level has been proposed as significant. To evaluate the increase in tryptase levels, the within‐subject (CV(I)) and between‐subject (CV(G)) biological variations should be known. This study was conducted to estimate the biological variation of tryptase and to identify the reference change value (RCV). METHODS: Blood samples were collected from healthy volunteers once a week consecutively over a 10‐week period. Tryptase was measured by the use of a fluoroenzyme immunoassay (ImmunoCAP(TM); Thermo Fisher Scientific), and linear mixed‐effects models were used to calculate the biological variation and RCV for both nontransformed and log‐transformed tryptase. RESULTS: Fourteen presumably healthy young adults (six males and eight females, age 23–35 years) were included. The CV(I) was 5.6% and the CV(G) was 31.5% (nontransformed data). Log‐transformed data showed similar results. The analytical variation (CV(A)) was 6.3% and the RCV was 23.5%. CONCLUSIONS: Young healthy adults without ongoing allergic reactions show low within‐subject biological variation. Higher biological variation was observed between subjects. John Wiley and Sons Inc. 2021-12-13 /pmc/articles/PMC8959422/ /pubmed/34904391 http://dx.doi.org/10.1002/iid3.578 Text en © 2021 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd. 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 Review Articles
Skarbø, Birthe R.
Vinnes, Erik W.
Wentzel‐Larsen, Tore
Sylte, Marit S.
Apelseth, Torunn O.
Estimating the within‐subject (CV(I)) and between‐subject (CV(G)) biological variation of serum tryptase
title Estimating the within‐subject (CV(I)) and between‐subject (CV(G)) biological variation of serum tryptase
title_full Estimating the within‐subject (CV(I)) and between‐subject (CV(G)) biological variation of serum tryptase
title_fullStr Estimating the within‐subject (CV(I)) and between‐subject (CV(G)) biological variation of serum tryptase
title_full_unstemmed Estimating the within‐subject (CV(I)) and between‐subject (CV(G)) biological variation of serum tryptase
title_short Estimating the within‐subject (CV(I)) and between‐subject (CV(G)) biological variation of serum tryptase
title_sort estimating the within‐subject (cv(i)) and between‐subject (cv(g)) biological variation of serum tryptase
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8959422/
https://www.ncbi.nlm.nih.gov/pubmed/34904391
http://dx.doi.org/10.1002/iid3.578
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