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Cobalamin Related Parameters and Disease Patterns in Patients with Increased Serum Cobalamin Levels

BACKGROUND: Measurement of serum cobalamin levels is routinely used to diagnose cobalamin deficiency. Surprisingly, approximately 15% of patients have high cobalamin levels and no consensus exists regarding the clinical implications. METHODS: Hospital-treated patients above 18 years of age referred...

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Detalles Bibliográficos
Autores principales: Arendt, Johan F. B., Nexo, Ebba
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3448722/
https://www.ncbi.nlm.nih.gov/pubmed/23029349
http://dx.doi.org/10.1371/journal.pone.0045979
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author Arendt, Johan F. B.
Nexo, Ebba
author_facet Arendt, Johan F. B.
Nexo, Ebba
author_sort Arendt, Johan F. B.
collection PubMed
description BACKGROUND: Measurement of serum cobalamin levels is routinely used to diagnose cobalamin deficiency. Surprisingly, approximately 15% of patients have high cobalamin levels and no consensus exists regarding the clinical implications. METHODS: Hospital-treated patients above 18 years of age referred for serum cobalamin measurement were included in groups of patients [percentage cobalamin supplemented] with low (<200 pmol/L, n = 200 [6%]), normal (200–600, n = 202 [6%]) high (601–1000, n = 217 [27%]) and very high (>1000, n = 199 [53%]) cobalamin levels. Total and cobalamin-saturated (holo) transcobalamin, total haptocorrin, soluble TC receptor, sCD320, and methylmalonic acid were analyzed. Data on diagnoses and medical prescriptions was obtained through medical files and the Aarhus University Prescription Database. RESULTS: Among patients not cobalamin supplemented median total haptocorrin and holo transcobalamin levels were markedly higher in the groups with high/very high cobalamin levels compared to groups with low/normal cobalamin levels. Median total transcobalamin and sCD320 levels were similar across the groups. A number of diagnoses were significantly associated to very high Cbl levels (odds ratio (95% confidence interval)): alcoholism (5.74 (2.76–11.96)), liver disease (8.53 (3.59–20.23)), and cancer (5.48 (2.85–10.55)). Elevated haptocorrin levels were seen in patients with alcoholism, cancer, liver-, renal-, autoimmune-, and bronchopulmonary disease. No clinical associations to sCD320 and total and holo transcobalamin levels were found. CONCLUSION: In non-supplemented patients, high cobalamin levels were associated to high haptocorrin levels, and several diagnoses, including alcoholism, liver disease and cancer. Our study emphasizes that clinicians should take high serum cobalamin levels into consideration in the diagnostic process.
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spelling pubmed-34487222012-10-01 Cobalamin Related Parameters and Disease Patterns in Patients with Increased Serum Cobalamin Levels Arendt, Johan F. B. Nexo, Ebba PLoS One Research Article BACKGROUND: Measurement of serum cobalamin levels is routinely used to diagnose cobalamin deficiency. Surprisingly, approximately 15% of patients have high cobalamin levels and no consensus exists regarding the clinical implications. METHODS: Hospital-treated patients above 18 years of age referred for serum cobalamin measurement were included in groups of patients [percentage cobalamin supplemented] with low (<200 pmol/L, n = 200 [6%]), normal (200–600, n = 202 [6%]) high (601–1000, n = 217 [27%]) and very high (>1000, n = 199 [53%]) cobalamin levels. Total and cobalamin-saturated (holo) transcobalamin, total haptocorrin, soluble TC receptor, sCD320, and methylmalonic acid were analyzed. Data on diagnoses and medical prescriptions was obtained through medical files and the Aarhus University Prescription Database. RESULTS: Among patients not cobalamin supplemented median total haptocorrin and holo transcobalamin levels were markedly higher in the groups with high/very high cobalamin levels compared to groups with low/normal cobalamin levels. Median total transcobalamin and sCD320 levels were similar across the groups. A number of diagnoses were significantly associated to very high Cbl levels (odds ratio (95% confidence interval)): alcoholism (5.74 (2.76–11.96)), liver disease (8.53 (3.59–20.23)), and cancer (5.48 (2.85–10.55)). Elevated haptocorrin levels were seen in patients with alcoholism, cancer, liver-, renal-, autoimmune-, and bronchopulmonary disease. No clinical associations to sCD320 and total and holo transcobalamin levels were found. CONCLUSION: In non-supplemented patients, high cobalamin levels were associated to high haptocorrin levels, and several diagnoses, including alcoholism, liver disease and cancer. Our study emphasizes that clinicians should take high serum cobalamin levels into consideration in the diagnostic process. Public Library of Science 2012-09-21 /pmc/articles/PMC3448722/ /pubmed/23029349 http://dx.doi.org/10.1371/journal.pone.0045979 Text en © 2012 Arendt, Nexo http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Arendt, Johan F. B.
Nexo, Ebba
Cobalamin Related Parameters and Disease Patterns in Patients with Increased Serum Cobalamin Levels
title Cobalamin Related Parameters and Disease Patterns in Patients with Increased Serum Cobalamin Levels
title_full Cobalamin Related Parameters and Disease Patterns in Patients with Increased Serum Cobalamin Levels
title_fullStr Cobalamin Related Parameters and Disease Patterns in Patients with Increased Serum Cobalamin Levels
title_full_unstemmed Cobalamin Related Parameters and Disease Patterns in Patients with Increased Serum Cobalamin Levels
title_short Cobalamin Related Parameters and Disease Patterns in Patients with Increased Serum Cobalamin Levels
title_sort cobalamin related parameters and disease patterns in patients with increased serum cobalamin levels
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3448722/
https://www.ncbi.nlm.nih.gov/pubmed/23029349
http://dx.doi.org/10.1371/journal.pone.0045979
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