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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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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. |
format | Online Article Text |
id | pubmed-5554200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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