# Association between B-cell activating factor and future depressive symptoms in hemodialysis patients

**Authors:** Dong-Young Lee, Woojin Jang, Beom Kim, Jae-Hon Lee, Young Lee, Yu Ho Lee, Shin Young Ahn, Jin Sug Kim, Yang Gyun Kim, Hyeon Seok Hwang, Ju-Young Moon, Jae-Hong Ryoo, Kayla M. Teopiz, Rodrigo B. Mansur, Joshua D. Rosenblat, Roger S. McIntyre

PMC · DOI: 10.47626/1516-4446-2025-4228 · Brazilian Journal of Psychiatry · 2025-12-18

## TL;DR

Higher levels of B-cell activating factor (BAFF) in hemodialysis patients are linked to a greater risk of developing depressive symptoms over time.

## Contribution

This study identifies BAFF as a novel biomarker for predicting future depressive symptoms in hemodialysis patients.

## Key findings

- A 1 SD increase in BAFF was associated with a 44% higher risk of depressive symptoms in univariate analysis.
- Higher BAFF levels correlated with a 70% increased risk in multivariate analysis.
- Patients with elevated BAFF had a significantly greater incidence of depressive symptoms over 2 years.

## Abstract

B-cell activating factor (BAFF) and a proliferation-inducing ligand (APRIL) are cytokines that play critical roles in the maturation, homeostasis, and differentiation of B-cells. Both cytokines have also been associated with mental disorders. The link between inflammation and depression is well-established. Patients undergoing hemodialysis who also experience depressive symptoms exhibit a state of immune dysfunction. We hypothesized that BAFF and APRIL levels would influence future depressive symptoms in hemodialysis patients.

We enrolled 72 hemodialysis patients without baseline depressive symptoms. Depressive symptoms were assessed annually for 2 years using the Beck Depression Inventory-II. The participants were measured for plasma BAFF, APRIL, and tumor necrosis factor-α levels. To evaluate the impact of these levels on the development of depressive symptoms, we performed Cox regression and Kaplan-Meier analysis.

Depressive symptoms were observed in 31 (43.1%) patients. In both univariate and multivariate Cox regression analyses, a 1 SD increase in BAFF was significantly associated with an increased risk of future depressive symptoms, with hazard ratios of 1.44 (95%CI 1.03-2.00) and 1.70 (95%CI 1.04-2.78), respectively. Higher BAFF groups had a significantly greater incidence of depressive symptoms over 2 years (p = 0.048).

Elevated plasma BAFF levels were significantly associated with the development of depressive symptoms in hemodialysis patients.

## Linked entities

- **Proteins:** TNFSF13B (TNF superfamily member 13b), TNFSF13 (TNF superfamily member 13)
- **Diseases:** depression (MONDO:0002050)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, TNFSF13B (TNF superfamily member 13b) [NCBI Gene 10673] {aka BAFF, BLYS, CD257, TALL-1, TALL1, THANK}
- **Diseases:** Depressive symptoms (MESH:D003866), mental disorders (MESH:D001523), immune dysfunction (MESH:D007154), inflammation (MESH:D007249)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC12880556/full.md

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Source: https://tomesphere.com/paper/PMC12880556