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Cited 22 time in webofscience Cited 22 time in scopus
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Predictive inflammatory biomarkers for change in suicidal ideation in major depressive disorder and panic disorder: A 12-week follow-up study

Authors
Choi, Kwan WooJang, Eun HyeKim, Ah YoungKim, HyewonPark, Mi JinByun, SangwonFava, MaurizioMischoulon, DavidPapakostas, George, IYu, Han YoungJeon, Hong Jin
Issue Date
Jan-2021
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Suicide; Major depressive disorder; Panic disorder; Tumor necrosis factor alpha; Interleukin-6
Citation
Journal of Psychiatric Research, v.133, pp 73 - 81
Pages
9
Indexed
SCIE
SSCI
SCOPUS
Journal Title
Journal of Psychiatric Research
Volume
133
Start Page
73
End Page
81
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/52098
DOI
10.1016/j.jpsychires.2020.12.011
ISSN
0022-3956
1879-1379
Abstract
Previous studies have investigated the role of inflammatory markers in suicidality of patients with major depressive disorder (MDD) or panic disorder (PD). However, few studies have investigated associations between serum inflammatory cytokine levels and suicidality. We hypothesized that MDD and PD status might be significantly associated with serum inflammatory cytokines and that we could predict levels of improvement in suicide ideation intensity using serum inflammatory biomarkers in patients with MDD and PD. For this study, 41 patients with MDD, 52 patients with PD, and 59 healthy control (HC) subjects were enrolled. Psychological measurements and serum inflammatory markers such as interleukin (IL)-6, -10, interferon (IFN)-gamma, tumor necrosis factor (TNE)-alpha, and C reactive protein (CRP) were examined. A total of five visits were completed during 12 weeks. After controlling for confounding factors, log-transformed IL-6 (ln_IL-6) at baseline (MDD: 0.297 +/- 0.626; PD: 0.342 +/- 0.723; HC: -0.121 +/- 0.858; p = 0.007, >0.0017, 0.05/30) and mean ln_IL-6 (MDD: 0.395 +/- 0.550, PD: 0.249 +/- 0.544, HC: -0.139 +/- 0.622, p = 0.002, >0.0017, 0.05/30) levels were trends towards significantly higher in patients with MDD and PD than in HC. In MDD patients, a higher level of basal ln_TNF-alpha was a significant predictor of Delta SSI (changes in SSI scores between baseline and week 12) even after controlling for changes of depression symptoms and baseline SSI scores (standardized beta = 0.541, p = 0.002 < 0.0028, 0.05/18). In conclusion, we could predict Delta SSI using baseline inflammatory biomarkers for patients with MDD.
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