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Circadian, Week-to-Week, and Physical Exercise-Induced Variation of Serum Microfibrillar-Associated Protein 4

Serum microfibrillar-associated protein 4 (sMFAP4) has been investigated as a biomarker for various diseases and is demonstrated to show significant gradual increase with severity of liver fibrosis. Ideal biomarkers used for disease diagnosis or prognosis should display deviating levels in affected...

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Autores principales: Sækmose, Susanne Gjørup, Holst, René, Lottenburger, Tine, Ytting, Henriette, Nielsen, Hans Jørgen, Junker, Peter, Schlosser, Anders, Sorensen, Grith Lykke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8127734/
https://www.ncbi.nlm.nih.gov/pubmed/34035648
http://dx.doi.org/10.1177/11772719211016359
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author Sækmose, Susanne Gjørup
Holst, René
Lottenburger, Tine
Ytting, Henriette
Nielsen, Hans Jørgen
Junker, Peter
Schlosser, Anders
Sorensen, Grith Lykke
author_facet Sækmose, Susanne Gjørup
Holst, René
Lottenburger, Tine
Ytting, Henriette
Nielsen, Hans Jørgen
Junker, Peter
Schlosser, Anders
Sorensen, Grith Lykke
author_sort Sækmose, Susanne Gjørup
collection PubMed
description Serum microfibrillar-associated protein 4 (sMFAP4) has been investigated as a biomarker for various diseases and is demonstrated to show significant gradual increase with severity of liver fibrosis. Ideal biomarkers used for disease diagnosis or prognosis should display deviating levels in affected individuals only and be robust to factors unrelated to the disease. Here we show the impact of normal physiological variation of sMFAP4 by characterizing the circadian variation, week-to-week variation, and physical exercise-induced levels. Serum samples from 3 groups of healthy volunteers were drawn: 7 times during a 24-hour period, 5 times during a 3-week period, and before and after a standardized physical exercise challenge. sMFAP4 was determined by AlphaLISA. Statistical analysis was performed using mixed effects modeling of repeated measurements. Circadian variation of sMFAP4 was demonstrated, with time of peak and nadir values depending on age and gender. For males, the peak values were observed during nighttime whereas for females, peak values were observed in the morning. Individual sMFAP4 levels remained stable over a period of 3 weeks and physical exercise inferred a mild negative influence. In conclusion, the circadian sMFAP4 variation was significant, and the levels could be influenced by physical activity. However, these variations were of limited magnitude relative to previously observed disease-induced levels in support of the biomarker potential of sMFAP4.
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spelling pubmed-81277342021-05-24 Circadian, Week-to-Week, and Physical Exercise-Induced Variation of Serum Microfibrillar-Associated Protein 4 Sækmose, Susanne Gjørup Holst, René Lottenburger, Tine Ytting, Henriette Nielsen, Hans Jørgen Junker, Peter Schlosser, Anders Sorensen, Grith Lykke Biomark Insights Original Research Serum microfibrillar-associated protein 4 (sMFAP4) has been investigated as a biomarker for various diseases and is demonstrated to show significant gradual increase with severity of liver fibrosis. Ideal biomarkers used for disease diagnosis or prognosis should display deviating levels in affected individuals only and be robust to factors unrelated to the disease. Here we show the impact of normal physiological variation of sMFAP4 by characterizing the circadian variation, week-to-week variation, and physical exercise-induced levels. Serum samples from 3 groups of healthy volunteers were drawn: 7 times during a 24-hour period, 5 times during a 3-week period, and before and after a standardized physical exercise challenge. sMFAP4 was determined by AlphaLISA. Statistical analysis was performed using mixed effects modeling of repeated measurements. Circadian variation of sMFAP4 was demonstrated, with time of peak and nadir values depending on age and gender. For males, the peak values were observed during nighttime whereas for females, peak values were observed in the morning. Individual sMFAP4 levels remained stable over a period of 3 weeks and physical exercise inferred a mild negative influence. In conclusion, the circadian sMFAP4 variation was significant, and the levels could be influenced by physical activity. However, these variations were of limited magnitude relative to previously observed disease-induced levels in support of the biomarker potential of sMFAP4. SAGE Publications 2021-05-14 /pmc/articles/PMC8127734/ /pubmed/34035648 http://dx.doi.org/10.1177/11772719211016359 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Sækmose, Susanne Gjørup
Holst, René
Lottenburger, Tine
Ytting, Henriette
Nielsen, Hans Jørgen
Junker, Peter
Schlosser, Anders
Sorensen, Grith Lykke
Circadian, Week-to-Week, and Physical Exercise-Induced Variation of Serum Microfibrillar-Associated Protein 4
title Circadian, Week-to-Week, and Physical Exercise-Induced Variation of Serum Microfibrillar-Associated Protein 4
title_full Circadian, Week-to-Week, and Physical Exercise-Induced Variation of Serum Microfibrillar-Associated Protein 4
title_fullStr Circadian, Week-to-Week, and Physical Exercise-Induced Variation of Serum Microfibrillar-Associated Protein 4
title_full_unstemmed Circadian, Week-to-Week, and Physical Exercise-Induced Variation of Serum Microfibrillar-Associated Protein 4
title_short Circadian, Week-to-Week, and Physical Exercise-Induced Variation of Serum Microfibrillar-Associated Protein 4
title_sort circadian, week-to-week, and physical exercise-induced variation of serum microfibrillar-associated protein 4
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8127734/
https://www.ncbi.nlm.nih.gov/pubmed/34035648
http://dx.doi.org/10.1177/11772719211016359
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