Immunological substrates of depressive symptoms in patients with severe obesity: An exploratory study

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Immunological substrates of depressive symptoms in patients with severe obesity: An exploratory study. / Stiglbauer, Victoria; Gamradt, Stefanie; Scherzer, Marie; Brasanac, Jelena; Otte, Christian; Rose, Matthias; Hofmann, Tobias; Hinkelmann, Kim; Gold, Stefan M.

in: CELL BIOCHEM FUNCT, Jahrgang 39, Nr. 3, 04.2021, S. 423-431.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Stiglbauer, V, Gamradt, S, Scherzer, M, Brasanac, J, Otte, C, Rose, M, Hofmann, T, Hinkelmann, K & Gold, SM 2021, 'Immunological substrates of depressive symptoms in patients with severe obesity: An exploratory study', CELL BIOCHEM FUNCT, Jg. 39, Nr. 3, S. 423-431. https://doi.org/10.1002/cbf.3608

APA

Stiglbauer, V., Gamradt, S., Scherzer, M., Brasanac, J., Otte, C., Rose, M., Hofmann, T., Hinkelmann, K., & Gold, S. M. (2021). Immunological substrates of depressive symptoms in patients with severe obesity: An exploratory study. CELL BIOCHEM FUNCT, 39(3), 423-431. https://doi.org/10.1002/cbf.3608

Vancouver

Bibtex

@article{4519a9f0d070433b921ba5c8b54ca26b,
title = "Immunological substrates of depressive symptoms in patients with severe obesity: An exploratory study",
abstract = "In this pilot study, we explored the immune phenotype of patients with severe obesity and comorbid depressive symptoms compared to non-depressed patients with obesity and normal-weight controls. Immune cell subsets were analysed by flow cytometry and depressive symptoms assessed using the Patient Health Questionnaire (PHQ-9). Cell frequencies were correlated with depressive symptom scores and waist-to-hip ratio (WHR). Patients with obesity and comorbid depression showed significantly lower numbers of circulating cytotoxic natural killer cells, dendritic cells and CD8+ effector memory T cells, compared to normal-weight controls. Regulatory T cells and CD4+ central memory T cells were increased compared to non-depressed patients with obesity and compared to normal-weight controls, respectively. Frequencies of cytotoxic natural killer cells and CD4+ central memory T cells significantly correlated with PHQ-9 scores, but not with WHR. Reduced numbers of dendritic cells were observed in both patient groups with obesity and correlated with PHQ-9 scores and WHR. These findings provide evidence for an altered immune composition in comorbid obesity and depression, supporting a pathobiological overlap between the two disorders.",
author = "Victoria Stiglbauer and Stefanie Gamradt and Marie Scherzer and Jelena Brasanac and Christian Otte and Matthias Rose and Tobias Hofmann and Kim Hinkelmann and Gold, {Stefan M}",
note = "{\textcopyright} 2021 The Authors. Cell Biochemistry and Function published by John Wiley & Sons Ltd.",
year = "2021",
month = apr,
doi = "10.1002/cbf.3608",
language = "English",
volume = "39",
pages = "423--431",
journal = "CELL BIOCHEM FUNCT",
issn = "0263-6484",
publisher = "John Wiley and Sons Ltd",
number = "3",

}

RIS

TY - JOUR

T1 - Immunological substrates of depressive symptoms in patients with severe obesity: An exploratory study

AU - Stiglbauer, Victoria

AU - Gamradt, Stefanie

AU - Scherzer, Marie

AU - Brasanac, Jelena

AU - Otte, Christian

AU - Rose, Matthias

AU - Hofmann, Tobias

AU - Hinkelmann, Kim

AU - Gold, Stefan M

N1 - © 2021 The Authors. Cell Biochemistry and Function published by John Wiley & Sons Ltd.

PY - 2021/4

Y1 - 2021/4

N2 - In this pilot study, we explored the immune phenotype of patients with severe obesity and comorbid depressive symptoms compared to non-depressed patients with obesity and normal-weight controls. Immune cell subsets were analysed by flow cytometry and depressive symptoms assessed using the Patient Health Questionnaire (PHQ-9). Cell frequencies were correlated with depressive symptom scores and waist-to-hip ratio (WHR). Patients with obesity and comorbid depression showed significantly lower numbers of circulating cytotoxic natural killer cells, dendritic cells and CD8+ effector memory T cells, compared to normal-weight controls. Regulatory T cells and CD4+ central memory T cells were increased compared to non-depressed patients with obesity and compared to normal-weight controls, respectively. Frequencies of cytotoxic natural killer cells and CD4+ central memory T cells significantly correlated with PHQ-9 scores, but not with WHR. Reduced numbers of dendritic cells were observed in both patient groups with obesity and correlated with PHQ-9 scores and WHR. These findings provide evidence for an altered immune composition in comorbid obesity and depression, supporting a pathobiological overlap between the two disorders.

AB - In this pilot study, we explored the immune phenotype of patients with severe obesity and comorbid depressive symptoms compared to non-depressed patients with obesity and normal-weight controls. Immune cell subsets were analysed by flow cytometry and depressive symptoms assessed using the Patient Health Questionnaire (PHQ-9). Cell frequencies were correlated with depressive symptom scores and waist-to-hip ratio (WHR). Patients with obesity and comorbid depression showed significantly lower numbers of circulating cytotoxic natural killer cells, dendritic cells and CD8+ effector memory T cells, compared to normal-weight controls. Regulatory T cells and CD4+ central memory T cells were increased compared to non-depressed patients with obesity and compared to normal-weight controls, respectively. Frequencies of cytotoxic natural killer cells and CD4+ central memory T cells significantly correlated with PHQ-9 scores, but not with WHR. Reduced numbers of dendritic cells were observed in both patient groups with obesity and correlated with PHQ-9 scores and WHR. These findings provide evidence for an altered immune composition in comorbid obesity and depression, supporting a pathobiological overlap between the two disorders.

U2 - 10.1002/cbf.3608

DO - 10.1002/cbf.3608

M3 - SCORING: Journal article

C2 - 33401342

VL - 39

SP - 423

EP - 431

JO - CELL BIOCHEM FUNCT

JF - CELL BIOCHEM FUNCT

SN - 0263-6484

IS - 3

ER -