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Development and validation of a nomogram based on lymphocyte subsets to distinguish bipolar depression from major depressive disorder

OBJECTIVE: Bipolar depression (BD) and major depressive disorder (MDD) are both common affective disorders. The common depression episodes make it difficult to distinguish between them, even for experienced clinicians. Failure to properly diagnose them in a timely manner leads to inappropriate treat...

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Autores principales: Su, Liming, Shuai, Yibing, Mou, Shaoqi, Shen, Yue, Shen, Xinhua, Shen, Zhongxia, Zhang, Xiaomei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9583168/
https://www.ncbi.nlm.nih.gov/pubmed/36276314
http://dx.doi.org/10.3389/fpsyt.2022.1017888
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author Su, Liming
Shuai, Yibing
Mou, Shaoqi
Shen, Yue
Shen, Xinhua
Shen, Zhongxia
Zhang, Xiaomei
author_facet Su, Liming
Shuai, Yibing
Mou, Shaoqi
Shen, Yue
Shen, Xinhua
Shen, Zhongxia
Zhang, Xiaomei
author_sort Su, Liming
collection PubMed
description OBJECTIVE: Bipolar depression (BD) and major depressive disorder (MDD) are both common affective disorders. The common depression episodes make it difficult to distinguish between them, even for experienced clinicians. Failure to properly diagnose them in a timely manner leads to inappropriate treatment strategies. Therefore, it is important to distinguish between BD and MDD. The aim of this study was to develop and validate a nomogram model that distinguishes BD from MDD based on the characteristics of lymphocyte subsets. MATERIALS AND METHODS: A prospective cross-sectional study was performed. Blood samples were obtained from participants who met the inclusion criteria. The least absolute shrinkage and selection operator (LASSO) regression model was used for factor selection. A differential diagnosis nomogram for BD and MDD was developed using multivariable logistic regression and the area under the curve (AUC) with 95% confidence interval (CI) was calculated, as well as the internal validation using a bootstrap algorithm with 1,000 repetitions. Calibration curve and decision curve analysis (DCA) were used to evaluate the calibration and clinical utility of the nomogram, respectively. RESULTS: A total of 166 participants who were diagnosed with BD (83 cases) or MDD (83 cases), as well as 101 healthy controls (HCs) between June 2018 and January 2022 were enrolled in this study. CD19(+) B cells, CD3(+) T cells, CD3(–)CD16/56(+) NK cells, and total lymphocyte counts were strong predictors of the diagnosis of BD and MDD and were included in the differential diagnosis nomogram. The AUC of the nomogram and internal validation were 0.922 (95%; CI, 0.879–0.965), and 0.911 (95% CI, 0.838–0.844), respectively. The calibration curve used to discriminate BD from MDD showed optimal agreement between the nomogram and the actual diagnosis. The results of DCA showed that the net clinical benefit was significant. CONCLUSION: This is an easy-to-use, repeatable, and economical nomogram for differential diagnosis that can help clinicians in the individual diagnosis of BD and MDD patients, reduce the risk of misdiagnosis, facilitate the formulation of appropriate treatment strategies and intervention plans.
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spelling pubmed-95831682022-10-21 Development and validation of a nomogram based on lymphocyte subsets to distinguish bipolar depression from major depressive disorder Su, Liming Shuai, Yibing Mou, Shaoqi Shen, Yue Shen, Xinhua Shen, Zhongxia Zhang, Xiaomei Front Psychiatry Psychiatry OBJECTIVE: Bipolar depression (BD) and major depressive disorder (MDD) are both common affective disorders. The common depression episodes make it difficult to distinguish between them, even for experienced clinicians. Failure to properly diagnose them in a timely manner leads to inappropriate treatment strategies. Therefore, it is important to distinguish between BD and MDD. The aim of this study was to develop and validate a nomogram model that distinguishes BD from MDD based on the characteristics of lymphocyte subsets. MATERIALS AND METHODS: A prospective cross-sectional study was performed. Blood samples were obtained from participants who met the inclusion criteria. The least absolute shrinkage and selection operator (LASSO) regression model was used for factor selection. A differential diagnosis nomogram for BD and MDD was developed using multivariable logistic regression and the area under the curve (AUC) with 95% confidence interval (CI) was calculated, as well as the internal validation using a bootstrap algorithm with 1,000 repetitions. Calibration curve and decision curve analysis (DCA) were used to evaluate the calibration and clinical utility of the nomogram, respectively. RESULTS: A total of 166 participants who were diagnosed with BD (83 cases) or MDD (83 cases), as well as 101 healthy controls (HCs) between June 2018 and January 2022 were enrolled in this study. CD19(+) B cells, CD3(+) T cells, CD3(–)CD16/56(+) NK cells, and total lymphocyte counts were strong predictors of the diagnosis of BD and MDD and were included in the differential diagnosis nomogram. The AUC of the nomogram and internal validation were 0.922 (95%; CI, 0.879–0.965), and 0.911 (95% CI, 0.838–0.844), respectively. The calibration curve used to discriminate BD from MDD showed optimal agreement between the nomogram and the actual diagnosis. The results of DCA showed that the net clinical benefit was significant. CONCLUSION: This is an easy-to-use, repeatable, and economical nomogram for differential diagnosis that can help clinicians in the individual diagnosis of BD and MDD patients, reduce the risk of misdiagnosis, facilitate the formulation of appropriate treatment strategies and intervention plans. Frontiers Media S.A. 2022-10-06 /pmc/articles/PMC9583168/ /pubmed/36276314 http://dx.doi.org/10.3389/fpsyt.2022.1017888 Text en Copyright © 2022 Su, Shuai, Mou, Shen, Shen, Shen 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
Su, Liming
Shuai, Yibing
Mou, Shaoqi
Shen, Yue
Shen, Xinhua
Shen, Zhongxia
Zhang, Xiaomei
Development and validation of a nomogram based on lymphocyte subsets to distinguish bipolar depression from major depressive disorder
title Development and validation of a nomogram based on lymphocyte subsets to distinguish bipolar depression from major depressive disorder
title_full Development and validation of a nomogram based on lymphocyte subsets to distinguish bipolar depression from major depressive disorder
title_fullStr Development and validation of a nomogram based on lymphocyte subsets to distinguish bipolar depression from major depressive disorder
title_full_unstemmed Development and validation of a nomogram based on lymphocyte subsets to distinguish bipolar depression from major depressive disorder
title_short Development and validation of a nomogram based on lymphocyte subsets to distinguish bipolar depression from major depressive disorder
title_sort development and validation of a nomogram based on lymphocyte subsets to distinguish bipolar depression from major depressive disorder
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9583168/
https://www.ncbi.nlm.nih.gov/pubmed/36276314
http://dx.doi.org/10.3389/fpsyt.2022.1017888
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