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Serum BDNF levels and state anxiety are associated with somatic symptoms in patients with panic disorder

BACKGROUND: We aimed to explore the predictive role of serum BDNF and anxiety-related variables in changes in somatic symptoms post-escitalopram treatment in panic disorder (PD) patients. METHODS: Ninety PD patients and 99 healthy controls (HCs) were enrolled. PD patients received an 8-week escitalo...

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Autores principales: Li, Jiaxin, Li, Ru, Li, Dazhi, Zhang, Jian, Luo, Xingguang, Zhang, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10393281/
https://www.ncbi.nlm.nih.gov/pubmed/37533888
http://dx.doi.org/10.3389/fpsyt.2023.1168771
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author Li, Jiaxin
Li, Ru
Li, Dazhi
Zhang, Jian
Luo, Xingguang
Zhang, Yong
author_facet Li, Jiaxin
Li, Ru
Li, Dazhi
Zhang, Jian
Luo, Xingguang
Zhang, Yong
author_sort Li, Jiaxin
collection PubMed
description BACKGROUND: We aimed to explore the predictive role of serum BDNF and anxiety-related variables in changes in somatic symptoms post-escitalopram treatment in panic disorder (PD) patients. METHODS: Ninety PD patients and 99 healthy controls (HCs) were enrolled. PD patients received an 8-week escitalopram treatment. All patients were administered the Panic Disorder Severity Scale–Chinese Version (PDSS-CV) and State-Trait Anxiety Inventory (STAI) to assess panic and anxiety-related symptoms, respectively. Patient Health Questionnaire 15-item scale (PHQ-15) was performed to measure somatic symptoms, and the blood sample was collected to detect serum BDNF levels in all participants. We performed partial correlation analysis and multiple linear regression to explore correlates of PHQ-15 and predictors of PHQ-15 changes post-escitalopram treatment after controlling for age, gender, education levels (set as a dummy variable), the current duration, comorbid AP, and/or GAD. RESULTS: Compared to HCs, PD patients had lower serum BDNF levels and higher PHQ-15 scores that could be improved post-escitalopram treatment. Lower baseline STAI state (b = −0.07, p = 0.004), and PDSS-CV scores (b = −0.25, p = 0.007), but higher baseline serum BDNF levels (b = 0.35, p = 0.007) contributed to the prediction of PHQ-15 changes post-escitalopram treatment. CONCLUSION: State anxiety, serum BDNF levels, and panic severity could predict changes in somatic symptoms post-escitalopram treatment, our results highlighted that serum BDNF could serve as a biological indicator for improving somatic symptoms in PD patients.
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spelling pubmed-103932812023-08-02 Serum BDNF levels and state anxiety are associated with somatic symptoms in patients with panic disorder Li, Jiaxin Li, Ru Li, Dazhi Zhang, Jian Luo, Xingguang Zhang, Yong Front Psychiatry Psychiatry BACKGROUND: We aimed to explore the predictive role of serum BDNF and anxiety-related variables in changes in somatic symptoms post-escitalopram treatment in panic disorder (PD) patients. METHODS: Ninety PD patients and 99 healthy controls (HCs) were enrolled. PD patients received an 8-week escitalopram treatment. All patients were administered the Panic Disorder Severity Scale–Chinese Version (PDSS-CV) and State-Trait Anxiety Inventory (STAI) to assess panic and anxiety-related symptoms, respectively. Patient Health Questionnaire 15-item scale (PHQ-15) was performed to measure somatic symptoms, and the blood sample was collected to detect serum BDNF levels in all participants. We performed partial correlation analysis and multiple linear regression to explore correlates of PHQ-15 and predictors of PHQ-15 changes post-escitalopram treatment after controlling for age, gender, education levels (set as a dummy variable), the current duration, comorbid AP, and/or GAD. RESULTS: Compared to HCs, PD patients had lower serum BDNF levels and higher PHQ-15 scores that could be improved post-escitalopram treatment. Lower baseline STAI state (b = −0.07, p = 0.004), and PDSS-CV scores (b = −0.25, p = 0.007), but higher baseline serum BDNF levels (b = 0.35, p = 0.007) contributed to the prediction of PHQ-15 changes post-escitalopram treatment. CONCLUSION: State anxiety, serum BDNF levels, and panic severity could predict changes in somatic symptoms post-escitalopram treatment, our results highlighted that serum BDNF could serve as a biological indicator for improving somatic symptoms in PD patients. Frontiers Media S.A. 2023-07-18 /pmc/articles/PMC10393281/ /pubmed/37533888 http://dx.doi.org/10.3389/fpsyt.2023.1168771 Text en Copyright © 2023 Li, Li, Li, Zhang, Luo and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Li, Jiaxin
Li, Ru
Li, Dazhi
Zhang, Jian
Luo, Xingguang
Zhang, Yong
Serum BDNF levels and state anxiety are associated with somatic symptoms in patients with panic disorder
title Serum BDNF levels and state anxiety are associated with somatic symptoms in patients with panic disorder
title_full Serum BDNF levels and state anxiety are associated with somatic symptoms in patients with panic disorder
title_fullStr Serum BDNF levels and state anxiety are associated with somatic symptoms in patients with panic disorder
title_full_unstemmed Serum BDNF levels and state anxiety are associated with somatic symptoms in patients with panic disorder
title_short Serum BDNF levels and state anxiety are associated with somatic symptoms in patients with panic disorder
title_sort serum bdnf levels and state anxiety are associated with somatic symptoms in patients with panic disorder
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10393281/
https://www.ncbi.nlm.nih.gov/pubmed/37533888
http://dx.doi.org/10.3389/fpsyt.2023.1168771
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