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Assessing the links between childhood trauma, C-reactive protein and response to antidepressant treatment in patients with affective disorders
Adverse Childhood Experiences (ACE) are a well-known risk-factor for depression. Additionally, (high-sensitive) C-reactive Protein (hsCRP) is elevated in subgroups of depressed patients and high following ACE. In this context the literature considers hsCRP and ACE to be associated with treatment res...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8429368/ https://www.ncbi.nlm.nih.gov/pubmed/33733300 http://dx.doi.org/10.1007/s00406-021-01245-z |
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author | Fischer, Kai F. Simon, Maria S. Elsner, Julie Dobmeier, Johanna Dorr, Johannes Blei, Leonie Zill, Peter Obermeier, Michael Musil, Richard |
author_facet | Fischer, Kai F. Simon, Maria S. Elsner, Julie Dobmeier, Johanna Dorr, Johannes Blei, Leonie Zill, Peter Obermeier, Michael Musil, Richard |
author_sort | Fischer, Kai F. |
collection | PubMed |
description | Adverse Childhood Experiences (ACE) are a well-known risk-factor for depression. Additionally, (high-sensitive) C-reactive Protein (hsCRP) is elevated in subgroups of depressed patients and high following ACE. In this context the literature considers hsCRP and ACE to be associated with treatment resistant depression. With the data being heterogenous, this study aimed to explore the associations of ACE, hsCRP levels and response to antidepressant treatment in uni- and bipolar depression. N = 76 patients diagnosed with uni- or bipolar depression and N = 53 healthy controls were included. Treatment was over 6 weeks in an inpatient psychiatric setting within an observatory study design. Depressive symptoms were assessed by the Montgomery-Asberg Depression Rating Scale (MADRS), ACE were assessed by the Childhood Trauma Questionnaire (CTQ); the body-mass-index (BMI) and hsCRP were measured. HsCRP levels did not differ between the study population and the healthy controls. While the depressive symptoms decreased, the hsCRP levels increased. Sexual abuse was associated with significant higher and emotional abuse with lower levels of hsCRP after 6 weeks. The baseline hsCRP levels and the ACE subgroups did not show significant associations with the treatment response in unipolar depressed patients. The long-lasting effects of specific forms of ACE may have relevant impact on inflammation, supporting hsCRP to be a suitable biomarker. With ACE and hsCRP not showing any significant associations with treatment response in the unipolar depressed subgroup, a more differentiate research concerning biomarkers and treatment regimens is needed when talking about treatment response. |
format | Online Article Text |
id | pubmed-8429368 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-84293682021-09-29 Assessing the links between childhood trauma, C-reactive protein and response to antidepressant treatment in patients with affective disorders Fischer, Kai F. Simon, Maria S. Elsner, Julie Dobmeier, Johanna Dorr, Johannes Blei, Leonie Zill, Peter Obermeier, Michael Musil, Richard Eur Arch Psychiatry Clin Neurosci Original Paper Adverse Childhood Experiences (ACE) are a well-known risk-factor for depression. Additionally, (high-sensitive) C-reactive Protein (hsCRP) is elevated in subgroups of depressed patients and high following ACE. In this context the literature considers hsCRP and ACE to be associated with treatment resistant depression. With the data being heterogenous, this study aimed to explore the associations of ACE, hsCRP levels and response to antidepressant treatment in uni- and bipolar depression. N = 76 patients diagnosed with uni- or bipolar depression and N = 53 healthy controls were included. Treatment was over 6 weeks in an inpatient psychiatric setting within an observatory study design. Depressive symptoms were assessed by the Montgomery-Asberg Depression Rating Scale (MADRS), ACE were assessed by the Childhood Trauma Questionnaire (CTQ); the body-mass-index (BMI) and hsCRP were measured. HsCRP levels did not differ between the study population and the healthy controls. While the depressive symptoms decreased, the hsCRP levels increased. Sexual abuse was associated with significant higher and emotional abuse with lower levels of hsCRP after 6 weeks. The baseline hsCRP levels and the ACE subgroups did not show significant associations with the treatment response in unipolar depressed patients. The long-lasting effects of specific forms of ACE may have relevant impact on inflammation, supporting hsCRP to be a suitable biomarker. With ACE and hsCRP not showing any significant associations with treatment response in the unipolar depressed subgroup, a more differentiate research concerning biomarkers and treatment regimens is needed when talking about treatment response. Springer Berlin Heidelberg 2021-03-17 2021 /pmc/articles/PMC8429368/ /pubmed/33733300 http://dx.doi.org/10.1007/s00406-021-01245-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Paper Fischer, Kai F. Simon, Maria S. Elsner, Julie Dobmeier, Johanna Dorr, Johannes Blei, Leonie Zill, Peter Obermeier, Michael Musil, Richard Assessing the links between childhood trauma, C-reactive protein and response to antidepressant treatment in patients with affective disorders |
title | Assessing the links between childhood trauma, C-reactive protein and response to antidepressant treatment in patients with affective disorders |
title_full | Assessing the links between childhood trauma, C-reactive protein and response to antidepressant treatment in patients with affective disorders |
title_fullStr | Assessing the links between childhood trauma, C-reactive protein and response to antidepressant treatment in patients with affective disorders |
title_full_unstemmed | Assessing the links between childhood trauma, C-reactive protein and response to antidepressant treatment in patients with affective disorders |
title_short | Assessing the links between childhood trauma, C-reactive protein and response to antidepressant treatment in patients with affective disorders |
title_sort | assessing the links between childhood trauma, c-reactive protein and response to antidepressant treatment in patients with affective disorders |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8429368/ https://www.ncbi.nlm.nih.gov/pubmed/33733300 http://dx.doi.org/10.1007/s00406-021-01245-z |
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