Predictive comparison of specific depression symptoms for peripheral inflammation

Peripheral inflammation has been associated with depression but may not map uniformly onto all depression symptoms and rather be associated with specific neurovegetative symptoms. The current work aims to extend previous research by applying a benchmark comparison in a residualized random forest framework, which allows us to statistically compare depression sum scores with specific symptoms in their relation to inflammation. The analysis was run using data of 311,474 individuals from the UK Biobank. Circulating C-reactive protein, white blood cell counts, the neutrophil-to-lymphocyte ratio and the systemic immune inflammation index were used as markers of peripheral inflammation. Depressive symptoms were assessed with a self-report questionnaire. Across multiple analytic settings, we found lethargy to perform significantly better in predicting peripheral inflammation levels compared to depression sum scores. These findings point to a specific phenotype of depression in which fatigue-related symptoms are most closely tied to peripheral inflammation, underscoring the value of symptom-level approaches for biomarker discovery and precision intervention. However, overall model performance was poor, making the practical significance of these differences difficult to interpret.

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Publication Details

Journal
Brain Behavior and Immunity
Published
2026-01-05
DOI
https://doi.org/10.1016/j.bbi.2026.106258
Primary Topic
Tryptophan and brain disorders
Type
article
Field-Weighted Citation Impact
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article

Predictive comparison of specific depression symptoms for peripheral inflammation

Lennart Seizer
Brain Behavior and Immunity
Tryptophan and brain disorders
article

Predictive comparison of specific depression symptoms for peripheral inflammation

Lennart Seizer
article en

Abstract

Peripheral inflammation has been associated with depression but may not map uniformly onto all depression symptoms and rather be associated with specific neurovegetative symptoms. The current work aims to extend previous research by applying a benchmark comparison in a residualized random forest framework, which allows us to statistically compare depression sum scores with specific symptoms in their relation to inflammation. The analysis was run using data of 311,474 individuals from the UK Biobank. Circulating C-reactive protein, white blood cell counts, the neutrophil-to-lymphocyte ratio and the systemic immune inflammation index were used as markers of peripheral inflammation. Depressive symptoms were assessed with a self-report questionnaire. Across multiple analytic settings, we found lethargy to perform significantly better in predicting peripheral inflammation levels compared to depression sum scores. These findings point to a specific phenotype of depression in which fatigue-related symptoms are most closely tied to peripheral inflammation, underscoring the value of symptom-level approaches for biomarker discovery and precision intervention. However, overall model performance was poor, making the practical significance of these differences difficult to interpret.

Brain Behavior and ImmunityVol. 133
German Center for Pediatric and Adolescent Rheumatology (DE)
No poverty
Openalex Percentile: Top 92%
Tryptophan and brain disorders
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