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
{"title":"Association between B cell activating factor (BAFF) 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","doi":"10.47626/1516-4446-2025-4228","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>B-cell activating factor (BAFF) and a proliferation-inducing ligand (APRIL) are cytokines that play critical roles in maturation, homeostasis, and differentiation of B cells, and are associated with mental disorders. The link between inflammation and depression is well-established. Patients undergoing hemodialysis (HD), who commonly experience depression, exhibit a state of immune dysfunction. We hypothesize that BAFF and APRIL may influence future depressive symptoms in HD patients.</p><p><strong>Methods: </strong>We enrolled 72 HD patients without baseline depressive symptoms. Participants' depressive symptoms were assessed annually over two years using the BDI-II. The participants were measured for plasma BAFF, APRIL, and tumor necrosis factor (TNF)-α levels. To evaluate their impact on the development of depressive symptoms, we performed Cox regression and Kaplan-Meier analysis.</p><p><strong>Results: </strong>Depressive symptoms were observed in 31 (43.1%) subjects. In both univariate and multivariate Cox regression analyses, a 1 SD increase in BAFF was significantly associated with increased risk of future depressive symptoms with hazard ratio of 1.44 (95%CI 1.03-2.00) and 1.70 (95%CI 1.04-2.78), respectively. Higher BAFF groups exhibited a significantly greater incidence of depressive symptoms over two years (p = 0.048).</p><p><strong>Conclusion: </strong>Elevated plasma BAFF levels were significantly associated with the development of depressive symptoms in HD patients.</p>","PeriodicalId":520767,"journal":{"name":"Revista brasileira de psiquiatria (Sao Paulo, Brazil : 1999)","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-07-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revista brasileira de psiquiatria (Sao Paulo, Brazil : 1999)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.47626/1516-4446-2025-4228","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: B-cell activating factor (BAFF) and a proliferation-inducing ligand (APRIL) are cytokines that play critical roles in maturation, homeostasis, and differentiation of B cells, and are associated with mental disorders. The link between inflammation and depression is well-established. Patients undergoing hemodialysis (HD), who commonly experience depression, exhibit a state of immune dysfunction. We hypothesize that BAFF and APRIL may influence future depressive symptoms in HD patients.
Methods: We enrolled 72 HD patients without baseline depressive symptoms. Participants' depressive symptoms were assessed annually over two years using the BDI-II. The participants were measured for plasma BAFF, APRIL, and tumor necrosis factor (TNF)-α levels. To evaluate their impact on the development of depressive symptoms, we performed Cox regression and Kaplan-Meier analysis.
Results: Depressive symptoms were observed in 31 (43.1%) subjects. In both univariate and multivariate Cox regression analyses, a 1 SD increase in BAFF was significantly associated with increased risk of future depressive symptoms with hazard ratio of 1.44 (95%CI 1.03-2.00) and 1.70 (95%CI 1.04-2.78), respectively. Higher BAFF groups exhibited a significantly greater incidence of depressive symptoms over two years (p = 0.048).
Conclusion: Elevated plasma BAFF levels were significantly associated with the development of depressive symptoms in HD patients.