Original Article

J Rheum Dis 2015; 22(6): 346-355

Published online December 31, 2015

© Korean College of Rheumatology

Depression and Quality of Life in Patients with Systemic Lupus Erythematosus

Sung Hae Chang1, Ja Hyun Cho2, Na Hee Shin2, Hye Jin Oh3, Byoong Yong Choi4, Myeong Jae Yoon3, Eun Young Lee3, Eun Bong Lee3, Yun Jong Lee5, Tae Jin Lee2, Bong Jin Hahm6, Young Wook Song3,7

1Department of Internal Medicine, Soonchunhyang University Cheonan Hospital, Cheonan, 2Graduate School of Public Health, Seoul National University, 3Division of Rheumatology, Department of Internal Medicine, Seoul National University Hospital, 4Department of Internal Medicine, Seoul Medical Center, Seoul, 5Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, 6Department of Neuropsychiatry, Seoul National University Hospital, 7Department of Molecular Medicine and Biopharmaceutical Sciences, Graduate School of Convergence Science and Technology, Medical Research Center, Seoul National University, Seoul, Korea

Correspondence to : Yeong Wook Song

Received: April 7, 2015; Revised: July 4, 2015; Accepted: July 6, 2015

Abstract

Objective. The objective of this study is to examine the prevalence of depression and its related factors including quality of life, brain-derived neurotrophic factor (BDNF), and vitamin D in patients with systemic lupus erythematosus (SLE). Methods. Depression was assessed using the center for epidemiologic studies depression (CES-D) scale. Disease activity, disease-related organ damage, the EuroQol-5 dimensions (EQ-5D), sociodemographic features, and laboratory tests including serum vitamin D level were surveyed. Serum BDNF was measured using an enzyme-linked immunosorbent assay. Results. Depression was observed in 22.8% of 180 SLE patients (n=41). Patients with marital status of single/divorced/separated/widowed, a higher patient global assessment (PGA) score, and extreme pain/discomfort showed significant association with depression. The EQ-5D index showed negative correlation with CES-D score (r=?0.56, p<0.05). In each EQ-5D dimension, depression showed significant association with moderate to severe problems in self-care and usual activities, and extreme pain/discomfort. Serum BDNF levels were not associated with depression (p=0.75) but associated with SLE disease activity index (SLEDAI; r=?0.21, p<0.05). Serum vitamin D levels were not associated with depression (p=0.60) but showed negative correlation with SLEDAI (r=?0.23, p<0.05) and mean glucocorticoid dose over the previous 3 months (r=?0.21, p<0.05) after adjustment for use of vitamin D supplement. Conclusion. Depression was prevalent in patients with SLE and was associated with low quality of life, and a higher PGA but not with SLEDAI. Serum BDNF and vitamin D levels were not associated with depression but showed negative correlation with SLEDAI. (J Rheum Dis 2015;22:346-355)

Keywords Systemic lupus erythematosus, Depression, Quality of life, Brain-derived neurotrophic factor, Vitamin D

Article

Original Article

J Rheum Dis 2015; 22(6): 346-355

Published online December 31, 2015

Copyright © Korean College of Rheumatology.

Depression and Quality of Life in Patients with Systemic Lupus Erythematosus

Sung Hae Chang1, Ja Hyun Cho2, Na Hee Shin2, Hye Jin Oh3, Byoong Yong Choi4, Myeong Jae Yoon3, Eun Young Lee3, Eun Bong Lee3, Yun Jong Lee5, Tae Jin Lee2, Bong Jin Hahm6, Young Wook Song3,7

1Department of Internal Medicine, Soonchunhyang University Cheonan Hospital, Cheonan, 2Graduate School of Public Health, Seoul National University, 3Division of Rheumatology, Department of Internal Medicine, Seoul National University Hospital, 4Department of Internal Medicine, Seoul Medical Center, Seoul, 5Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, 6Department of Neuropsychiatry, Seoul National University Hospital, 7Department of Molecular Medicine and Biopharmaceutical Sciences, Graduate School of Convergence Science and Technology, Medical Research Center, Seoul National University, Seoul, Korea

Correspondence to:Yeong Wook Song

Received: April 7, 2015; Revised: July 4, 2015; Accepted: July 6, 2015

Abstract

Objective. The objective of this study is to examine the prevalence of depression and its related factors including quality of life, brain-derived neurotrophic factor (BDNF), and vitamin D in patients with systemic lupus erythematosus (SLE). Methods. Depression was assessed using the center for epidemiologic studies depression (CES-D) scale. Disease activity, disease-related organ damage, the EuroQol-5 dimensions (EQ-5D), sociodemographic features, and laboratory tests including serum vitamin D level were surveyed. Serum BDNF was measured using an enzyme-linked immunosorbent assay. Results. Depression was observed in 22.8% of 180 SLE patients (n=41). Patients with marital status of single/divorced/separated/widowed, a higher patient global assessment (PGA) score, and extreme pain/discomfort showed significant association with depression. The EQ-5D index showed negative correlation with CES-D score (r=?0.56, p<0.05). In each EQ-5D dimension, depression showed significant association with moderate to severe problems in self-care and usual activities, and extreme pain/discomfort. Serum BDNF levels were not associated with depression (p=0.75) but associated with SLE disease activity index (SLEDAI; r=?0.21, p<0.05). Serum vitamin D levels were not associated with depression (p=0.60) but showed negative correlation with SLEDAI (r=?0.23, p<0.05) and mean glucocorticoid dose over the previous 3 months (r=?0.21, p<0.05) after adjustment for use of vitamin D supplement. Conclusion. Depression was prevalent in patients with SLE and was associated with low quality of life, and a higher PGA but not with SLEDAI. Serum BDNF and vitamin D levels were not associated with depression but showed negative correlation with SLEDAI. (J Rheum Dis 2015;22:346-355)

Keywords: Systemic lupus erythematosus, Depression, Quality of life, Brain-derived neurotrophic factor, Vitamin D

JRD
Oct 01, 2024 Vol.31 No.4, pp. 191~263
COVER PICTURE
Ancestry-driven pathways for SLE-risk SNP-associated genes. The ancestry-driven key signaling pathways in Asians, Europeans, and African Americans were analyzed by enrichr (https://maayanlab.cloud/Enrichr/#libraries) using non-HLA SNP-associated genes. SLE: systemic lupus erythematosus, SNP: single-nucleotide polymorphism, JAK–STAT: janus kinase–signal transducers and activators of transcription, IFN: interferon gamma. (J Rheum Dis 2024;31:200-211)

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