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Distribution of serum concentrations reported for macroenzyme aspartate aminotransferase (macro-AST)
BACKGROUND: The presence of macroenzyme (M) is often the explanation of an isolated elevation of aspartate aminotransferase (AST). Where M is identified, it is reasonable for the clinician to ask where an individual patient's result fits in with known concentrations of M. In this context, we co...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575363/ https://www.ncbi.nlm.nih.gov/pubmed/28856230 http://dx.doi.org/10.1016/j.plabm.2017.05.003 |
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author | Rubin, Asa S. Sass, David A. Stickle, Douglas F. |
author_facet | Rubin, Asa S. Sass, David A. Stickle, Douglas F. |
author_sort | Rubin, Asa S. |
collection | PubMed |
description | BACKGROUND: The presence of macroenzyme (M) is often the explanation of an isolated elevation of aspartate aminotransferase (AST). Where M is identified, it is reasonable for the clinician to ask where an individual patient's result fits in with known concentrations of M. In this context, we conducted a survey of literature to examine the distribution of reported serum concentrations of macro-AST. We also analyzed the distribution data to examine whether elevations were consistent with simple alteration of circulatory half-life (t(1/2)) of M relative to normal AST. METHODS: Distributions of M were compiled from the literature. These distributions were compared to predictions based on fixed changes in t(1/2) applied to the reference interval for AST. RESULTS: There was a bimodal distribution of literature values for M (n =51), comprised roughly of populations A (M <200 U/L; 60% of total) and B (M >200 U/L; 40% of total). The two distributions were reasonably well characterized by a simple projection to the right of the reference interval for AST according to increased t(1/2) (A: t(1/2) =3.3 days; B: t(1/2) =19.8 days) relative to AST (t(1/2) =0.7 days). CONCLUSIONS: Knowledge of distributions for M may be useful in discussion with clinicians regarding significance of M for individual patients. Distributions for M were consistent with the simplest explanation for elevated AST due strictly to an extended circulatory lifetime for M. Caveats to analysis, however, include selection within literature data mainly for patients with various co-morbidities. |
format | Online Article Text |
id | pubmed-5575363 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-55753632017-08-30 Distribution of serum concentrations reported for macroenzyme aspartate aminotransferase (macro-AST) Rubin, Asa S. Sass, David A. Stickle, Douglas F. Pract Lab Med Article BACKGROUND: The presence of macroenzyme (M) is often the explanation of an isolated elevation of aspartate aminotransferase (AST). Where M is identified, it is reasonable for the clinician to ask where an individual patient's result fits in with known concentrations of M. In this context, we conducted a survey of literature to examine the distribution of reported serum concentrations of macro-AST. We also analyzed the distribution data to examine whether elevations were consistent with simple alteration of circulatory half-life (t(1/2)) of M relative to normal AST. METHODS: Distributions of M were compiled from the literature. These distributions were compared to predictions based on fixed changes in t(1/2) applied to the reference interval for AST. RESULTS: There was a bimodal distribution of literature values for M (n =51), comprised roughly of populations A (M <200 U/L; 60% of total) and B (M >200 U/L; 40% of total). The two distributions were reasonably well characterized by a simple projection to the right of the reference interval for AST according to increased t(1/2) (A: t(1/2) =3.3 days; B: t(1/2) =19.8 days) relative to AST (t(1/2) =0.7 days). CONCLUSIONS: Knowledge of distributions for M may be useful in discussion with clinicians regarding significance of M for individual patients. Distributions for M were consistent with the simplest explanation for elevated AST due strictly to an extended circulatory lifetime for M. Caveats to analysis, however, include selection within literature data mainly for patients with various co-morbidities. Elsevier 2017-05-17 /pmc/articles/PMC5575363/ /pubmed/28856230 http://dx.doi.org/10.1016/j.plabm.2017.05.003 Text en © 2017 The Authors http://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 | Article Rubin, Asa S. Sass, David A. Stickle, Douglas F. Distribution of serum concentrations reported for macroenzyme aspartate aminotransferase (macro-AST) |
title | Distribution of serum concentrations reported for macroenzyme aspartate aminotransferase (macro-AST) |
title_full | Distribution of serum concentrations reported for macroenzyme aspartate aminotransferase (macro-AST) |
title_fullStr | Distribution of serum concentrations reported for macroenzyme aspartate aminotransferase (macro-AST) |
title_full_unstemmed | Distribution of serum concentrations reported for macroenzyme aspartate aminotransferase (macro-AST) |
title_short | Distribution of serum concentrations reported for macroenzyme aspartate aminotransferase (macro-AST) |
title_sort | distribution of serum concentrations reported for macroenzyme aspartate aminotransferase (macro-ast) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575363/ https://www.ncbi.nlm.nih.gov/pubmed/28856230 http://dx.doi.org/10.1016/j.plabm.2017.05.003 |
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