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Plasma GDF15 level is elevated in psychosis and inversely correlated with severity

Accumulating evidence suggests that GDF15 is a biomarker for ageing and morbidity of many somatic disorders such as cancer and inflammatory disorders. Recently, elevated serum GDF15 level was proposed as a marker for mood disorder. However, psychosis severity was not investigated in relation to plas...

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Autores principales: Kumar, Parvin, Millischer, Vincent, Villaescusa, J. Carlos, Nilsson, Ida A. K., Östenson, Claes-Göran, Schalling, Martin, Ösby, Urban, Lavebratt, Catharina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5554200/
https://www.ncbi.nlm.nih.gov/pubmed/28801589
http://dx.doi.org/10.1038/s41598-017-07503-2
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author Kumar, Parvin
Millischer, Vincent
Villaescusa, J. Carlos
Nilsson, Ida A. K.
Östenson, Claes-Göran
Schalling, Martin
Ösby, Urban
Lavebratt, Catharina
author_facet Kumar, Parvin
Millischer, Vincent
Villaescusa, J. Carlos
Nilsson, Ida A. K.
Östenson, Claes-Göran
Schalling, Martin
Ösby, Urban
Lavebratt, Catharina
author_sort Kumar, Parvin
collection PubMed
description Accumulating evidence suggests that GDF15 is a biomarker for ageing and morbidity of many somatic disorders such as cancer and inflammatory disorders. Recently, elevated serum GDF15 level was proposed as a marker for mood disorder. However, psychosis severity was not investigated in relation to plasma GDF15 levels. In the present study we measured GDF15 levels in plasma of 120 psychosis patients compared to 120 age and gender matched healthy controls. Within the patient cohort GDF15 levels were evaluated for association with age, gender, lifestyle factors, C-reactive protein levels, psychosis severity and metabolic disorder. Psychosis patients had elevated GDF15 levels compared to controls (median(Psychosis) = 744 ng/mL, median(controls) = 516 ng/mL, p < 0.001). Within the psychosis cohort, GDF15 levels, when corrected for age, metabolic health and lifestyle factors, were negatively correlated with psychosis severity (β = −0.218, p = 0.012). While GDF15 levels were elevated in patients versus healthy controls, the negative correlation between psychosis severity and GDF15 suggests a loss of anti-inflammatory GDF15 mediated functionality in severe psychosis. Study replication in larger cohorts will be necessary to assess the potential of GDF15 as a prognostic biomarker in psychosis.
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spelling pubmed-55542002017-08-15 Plasma GDF15 level is elevated in psychosis and inversely correlated with severity Kumar, Parvin Millischer, Vincent Villaescusa, J. Carlos Nilsson, Ida A. K. Östenson, Claes-Göran Schalling, Martin Ösby, Urban Lavebratt, Catharina Sci Rep Article Accumulating evidence suggests that GDF15 is a biomarker for ageing and morbidity of many somatic disorders such as cancer and inflammatory disorders. Recently, elevated serum GDF15 level was proposed as a marker for mood disorder. However, psychosis severity was not investigated in relation to plasma GDF15 levels. In the present study we measured GDF15 levels in plasma of 120 psychosis patients compared to 120 age and gender matched healthy controls. Within the patient cohort GDF15 levels were evaluated for association with age, gender, lifestyle factors, C-reactive protein levels, psychosis severity and metabolic disorder. Psychosis patients had elevated GDF15 levels compared to controls (median(Psychosis) = 744 ng/mL, median(controls) = 516 ng/mL, p < 0.001). Within the psychosis cohort, GDF15 levels, when corrected for age, metabolic health and lifestyle factors, were negatively correlated with psychosis severity (β = −0.218, p = 0.012). While GDF15 levels were elevated in patients versus healthy controls, the negative correlation between psychosis severity and GDF15 suggests a loss of anti-inflammatory GDF15 mediated functionality in severe psychosis. Study replication in larger cohorts will be necessary to assess the potential of GDF15 as a prognostic biomarker in psychosis. Nature Publishing Group UK 2017-08-11 /pmc/articles/PMC5554200/ /pubmed/28801589 http://dx.doi.org/10.1038/s41598-017-07503-2 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kumar, Parvin
Millischer, Vincent
Villaescusa, J. Carlos
Nilsson, Ida A. K.
Östenson, Claes-Göran
Schalling, Martin
Ösby, Urban
Lavebratt, Catharina
Plasma GDF15 level is elevated in psychosis and inversely correlated with severity
title Plasma GDF15 level is elevated in psychosis and inversely correlated with severity
title_full Plasma GDF15 level is elevated in psychosis and inversely correlated with severity
title_fullStr Plasma GDF15 level is elevated in psychosis and inversely correlated with severity
title_full_unstemmed Plasma GDF15 level is elevated in psychosis and inversely correlated with severity
title_short Plasma GDF15 level is elevated in psychosis and inversely correlated with severity
title_sort plasma gdf15 level is elevated in psychosis and inversely correlated with severity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5554200/
https://www.ncbi.nlm.nih.gov/pubmed/28801589
http://dx.doi.org/10.1038/s41598-017-07503-2
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