ArticleBMC psychiatry2025
Comparison of clinical features and inflammatory factors between patients with bipolar depression and unipolar depression.
Article in BMC psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.
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Who cites it
6 citing papers in PubMed, 2 syntheses or guidelines pooled it.
- Complete blood count-based inflammatory ratios in people with bipolar disorder: a systematic review and meta-analysis of neutrophil-to-lymphocyte, monocyte-to-lymphocyte, and platelet-to-lymphocyte ratios.European psychiatry : the journal of the Association of European Psychiatrists · 2026Pooled it
- Serum Brain-derived Neurotrophic Factor Levels as a Biomarker of Treatment Response in Patients With Depression: Systematic Review and Meta-analysis.Actas espanolas de psiquiatria · 2025Pooled it
- Complete Blood-Count-Derived Inflammatory Markers Across Acute Mood Episodes.Alpha psychiatry · 2026Article
- Depression among married individuals: new evidence in Türkiye.Frontiers in psychiatry · 2026Article
- Antidepressant Effects ofFoods (Basel, Switzerland) · 2025Article
- Association between the Alpha-1-acid glycoprotein concentrations and depression in US adult women: a cross-sectional study from NHANES 2021-2023.Frontiers in psychiatry · 2025Article
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Authors and funding
14 authors.
Funding
Abstract
backgroundThis study aims to compare the differences in clinical features and inflammatory factors between unipolar depression and bipolar depression, and to investigate potential clinical characteristics and peripheral blood biomarkers that could be used to differentiate between these two conditions. Furthermore, the study seeks to establish a predictive model.
methodsInpatients from the Shanghai Mental Health Center, admitted between June 2022 and June 2024, were selected as study participants. Based on diagnosis records, 274 patients were assigned to the unipolar depression group, and 128 patients to the bipolar depression group. A total of 128 patients were matched between the two groups using the propensity score matching method. Demographic data, clinical characteristics, and biological indicators were compared between the two groups. The biological markers assessed included neutrophil/lymphocyte ratio (NLR), monocyte/lymphocyte ratio (MLR), platelet/lymphocyte ratio (PLR), C-reactive protein (CRP), serum triiodothyronine (T3), thyroxine (T4), free thyroid hormones (fT3, fT4), thyroid-stimulating hormone (TSH), complement 3 (C3), complement 4 (C4), immunoglobulin A (IgA), immunoglobulin G (IgG), and immunoglobulin M (IgM). Binomial logistic regression analysis was employed to control for confounding factors and to explore the predictors of bipolar depression. Receiver operating characteristic (ROC) curve analysis was performed to evaluate the predictive value of clinical features and biological markers for bipolar depression.
resultsStatistically significant differences were observed between the unipolar depression and bipolar depression groups with respect to life events (χ² = 15.397, P = 0.000), CRP (Z = 6.717, P = 0.000), TSH (Z = 1.988, P = 0.047), C3 (Z = 5.682, P = 0.000), C4 (Z = 4.216, P = 0.000), and IgM (Z = 2.304, P = 0.021). Logistic regression analysis indicated that life events (OR = 4.552, 95% CI = 2.238-9.257), CRP (OR = 13.886, 95% CI = 5.290-36.452), and IgM (OR = 0.561, 95% CI = 0.325-0.970) were associated with bipolar depression. ROC curve analysis revealed that the area under the curve (AUC) for the logistic regression model predicting bipolar depression was 0.806, with a sensitivity of 61.7% and a specificity of 85.9%.
conclusionsCompared to unipolar depression, bipolar depression was associated with the absence of life events, elevated CRP levels, and reduced IgM levels. The combined diagnostic model proved more effective in distinguishing bipolar depression from unipolar depression.
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