9 results on '"Song, Y. W."'
Search Results
2. Characteristics of pleural effusions in systemic lupus erythematosus: differential diagnosis of lupus pleuritis
- Author
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Choi, B Y, primary, Yoon, M J, additional, Shin, K, additional, Lee, Y J, additional, and Song, Y W, additional
- Published
- 2014
- Full Text
- View/download PDF
3. Characteristics of pleural effusions in systemic lupus erythematosus: differential diagnosis of lupus pleuritis.
- Author
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Choi BY, Yoon MJ, Shin K, Lee YJ, and Song YW
- Subjects
- Adult, Diagnosis, Differential, Female, Humans, Lupus Erythematosus, Systemic diagnosis, Male, Middle Aged, Pleurisy diagnosis, Prospective Studies, Young Adult, Lupus Erythematosus, Systemic complications, Pleurisy etiology
- Abstract
We investigated the clinical characteristics of pleural effusion in systemic lupus erythematosus (SLE). A prospective analysis of 17 SLE patients with pleural effusion (seven lupus pleuritis, eight transudative effusions and two parapneumonic effusions) was performed. Thirty non-SLE patients with pleural effusion were recruited as controls. A pleural fluid ANA titer ≥1:160 was found in 8/17 (47.1%) SLE patients and none of the 30 non-SLE patients (p = 0.0001). Pleural fluid to serum C3 ratios were significantly lower in SLE than in non-SLE (median (minimum-maximum) 0.29 (0.03-0.43) versus 0.52 (0.26-0.73), p = 0.0002). Among SLE patients, pleural fluid ANA titers ≥1:160 were more frequently found in patients with lupus pleuritis than in those with pleural effusion from causes other than lupus itself (85.7% versus 20.0%, p = 0.0152). Serum CRP levels were significantly increased in patients with lupus pleuritis compared with SLE patients with transudative pleural effusion (2.30 (0.30-5.66) versus 0.7 (0.12-1.47) mg/dl, p = 0.0062). In conclusion, pleural fluid ANA titer and serum CRP levels are significantly increased in lupus pleuritis., (© The Author(s) 2015 Reprints and permissions: sagepub.co.uk/journalsPermissions.nav.)
- Published
- 2015
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- View/download PDF
4. Bone marrow analysis of immune cells and apoptosis in patients with systemic lupus erythematosus.
- Author
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Park JW, Moon SY, Lee JH, Park JK, Lee DS, Jung KC, Song YW, and Lee EB
- Subjects
- Adolescent, Adult, Antibodies, Antinuclear blood, Biomarkers analysis, Biomarkers blood, Case-Control Studies, DNA immunology, Dendritic Cells immunology, Dendritic Cells pathology, Female, Humans, Immunohistochemistry, Interleukin-6 analysis, Lupus Erythematosus, Systemic blood, Male, Middle Aged, Plasma Cells immunology, Plasma Cells pathology, Predictive Value of Tests, Severity of Illness Index, Young Adult, Apoptosis, Bone Marrow Cells immunology, Bone Marrow Cells pathology, Bone Marrow Examination, Lupus Erythematosus, Systemic immunology, Lupus Erythematosus, Systemic pathology
- Abstract
Objectives: To examine the immune cell profile in the bone marrow of systemic lupus erythematosus (SLE) patients and to assess its clinical relevance., Methods: Sixteen bone marrow samples from 14 SLE patients were compared with seven healthy control samples. The numbers of immune cells and apoptotic cells in the bone marrow were examined by immunohistochemistry. The association between immune cell subsets and clinical features was investigated., Results: CD4+ T cells, macrophages and plasma cells were more common in the bone marrow of SLE patients than in healthy controls (p=0.001, p=0.004 and p<0.001, respectively). Greater numbers of CD4+ T cells and macrophages were associated with high-grade bone marrow damage. The percentage of apoptotic cells in bone marrow of SLE patients was significantly higher than that in controls (p<0.001) and was positively correlated with the number of plasmacytoid dendritic cells (p=0.013). Increased number of plasma cells along with high interleukin-6 expression was correlated with anti-double stranded DNA antibody levels and the SLE disease activity index (p=0.031 and 0.013, respectively)., Conclusion: Bone marrow from SLE patients showed a distinct immune cell profile and increased apoptosis. This, coupled with a correlation with disease activity, suggests that the bone marrow may play a critical role in the pathogenesis of SLE., (© The Author(s) 2014 Reprints and permissions: sagepub.co.uk/journalsPermissions.nav.)
- Published
- 2014
- Full Text
- View/download PDF
5. Costs of illness and quality of life in patients with systemic lupus erythematosus in South Korea.
- Author
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Cho JH, Chang SH, Shin NH, Choi BY, Oh HJ, Yoon MJ, Lee EY, Lee EB, Lee TJ, and Song YW
- Subjects
- Adult, Depression complications, Female, Humans, Kidney Diseases complications, Lupus Erythematosus, Systemic complications, Lupus Erythematosus, Systemic therapy, Male, Republic of Korea, Cost of Illness, Lupus Erythematosus, Systemic economics, Quality of Life
- Abstract
Objective: To assess the costs of illness, health-related quality of life (HRQOL) and their associated factors in patients with systemic lupus erythematosus (SLE) in South Korea., Method: Two hundred and one patients with SLE were enrolled at the Rheumatology clinic of Seoul National University Hospital. Direct, indirect and total costs and HRQOL were measured using hospital electronic data and face-to-face interview. Socio-demographic and clinical factors associated with cost of illness and HRQOL were analyzed using multiple regression and multivariate logistic regression., Results: The average total cost of illness was estimated to be KRW 9.82 million (US $ 8993) per year, of which 41.6% was accounted for by direct costs and 58.4% by indirect costs. In multivariate regression, patients with renal involvement and those with depression incurred an average increment in annual total costs of 37.6% (p = 0.050) and 49.1% (p = 0.024), respectively, and an average increment in annual direct costs of 26.4% (p = 0.050) and 43.3% (p = 0.002), respectively, compared with patients without renal involvement and depression, respectively. In addition, disease damage was positively associated with an average increment in annual total and direct costs (55.3%, p = 0.006; 33.3%, p = 0.013, respectively), and the occurrence of indirect costs (OR 2.21, 1.09-4.88). There was no significant difference in HRQOL between patients with and without renal involvement (0.655 vs. 0.693, p = 0.203) CONCLUSION: Renal involvement, depression, and disease damage were major factors associated with higher total and medical costs for patients with SLE in South Korea. Effective treatment of renal disorders and depression may reduce the high economic burden of SLE., (© The Author(s) 2014 Reprints and permissions: sagepub.co.uk/journalsPermissions.nav.)
- Published
- 2014
- Full Text
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6. Adenosine A2A receptor polymorphisms in Korean patients with systemic sclerosis.
- Author
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Park JA, Pak JJ, Kim J, Lee EY, Lee YJ, Song YW, and Lee EB
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- Adult, Case-Control Studies, Exons, Female, Gene Frequency, Genetic Predisposition to Disease, Humans, Male, Middle Aged, Phenotype, Promoter Regions, Genetic, Republic of Korea epidemiology, Scleroderma, Systemic ethnology, Asian People genetics, Polymorphism, Single Nucleotide, Receptor, Adenosine A2A genetics, Scleroderma, Systemic genetics
- Abstract
Adenosine A2A receptor (ADORA2A) regulates inflammation, promotes tissue repair and collagen production by human dermal fibroblasts. We investigated the genetic polymorphisms of ADORA2A in susceptibility to systemic sclerosis (SSc). We genotyped 142 Korean SSc patients and 150 controls for polymorphisms of -1751A/C (rs5996696) and 1976C/T (rs5751876), to cover the promoter and all exon sequences of ADORA2A in Koreans, using TaqMan fluorogenic 5' nuclease assay and single base primer extension assay. Neither -1751A/C nor 1976C/T polymorphism showed difference in the distribution of alleles or genotypes between patients and controls with allele frequency of 89.9% v 91.0% for -1751A (p=0.64) and 56.5% v 54.0% for 1976C (p=0.55). Our findings suggest that the role of ADORA2A in SSc may not be genetically related.
- Published
- 2011
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7. Renal expression of galectin-3 in systemic lupus erythematosus patients with nephritis.
- Author
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Kang EH, Moon KC, Lee EY, Lee YJ, Lee EB, Ahn C, and Song YW
- Subjects
- Adult, Antibodies, Antinuclear, Complement C3 metabolism, Complement C4 metabolism, DNA metabolism, Enzyme-Linked Immunosorbent Assay, Female, Galectin 3 metabolism, Humans, Immunohistochemistry, Kidney Glomerulus pathology, Lupus Nephritis metabolism, Male, Young Adult, Galectin 3 genetics, Gene Expression, Kidney Glomerulus metabolism, Lupus Erythematosus, Systemic genetics, Lupus Nephritis genetics
- Abstract
The aim of the study is to characterize the expression pattern of galectin-3 (Gal-3) in renal tissues of patients with systemic lupus erythematosus (SLE) nephritis and to determine whether tissue and serum Gal-3 are associated with SLE nephritis. Gal-3 expressions were examined with immunohistochemistry in renal biopsy specimens of 88 patients with SLE nephritis and in five normal specimens. Activity and chronicity indexes and glomerular Gal-3 expressions were analysed in each specimen. Serum Gal-3 levels were measured using enzyme-linked immunosorbent assays in 20 patients with SLE, including 11 with nephritis, and in 50 healthy controls. Glomerular Gal-3 expression was observed in 81.8% (72/88) of patients with SLE nephritis but not in 5 controls. Gal-3 staining was attributed mainly to its cellular expression rather than its deposition, and Gal-3 expression levels were correlated with histologic activity indexes, anti-dsDNA titers, and complement 3 and 4 levels. Serum Gal-3 levels were higher in patients with SLE, particularly in those with nephritis, than in healthy controls, and correlated with anti-dsDNA titers. In conclusion, glomerular Gal-3 expression in renal tissue and serum Gal-3 levels were elevated in patients with SLE nephritis versus healthy controls; moreover, they reflected disease activity. These findings suggest that Gal-3 might contribute to the inflammatory process in SLE.
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- 2009
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8. Flow cytometric assessment of anti-neuronal antibodies in central nervous system involvement of systemic lupus erythematosus and other autoimmune diseases.
- Author
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Kang EH, Shen GQ, Morris R, Metzger A, Lee EY, Lee YJ, Lee EB, and Song YW
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- Adult, Cell Line, Tumor, Cerebrovascular Disorders immunology, Confusion immunology, Epilepsy immunology, Female, Headache Disorders immunology, Humans, Lupus Erythematosus, Systemic complications, Lupus Vasculitis, Central Nervous System complications, Male, Meningitis, Aseptic immunology, Middle Aged, Psychotic Disorders immunology, Rheumatic Diseases complications, Up-Regulation, Autoantibodies blood, Autoantibodies cerebrospinal fluid, Flow Cytometry, Lupus Erythematosus, Systemic immunology, Lupus Vasculitis, Central Nervous System immunology, Neurons immunology, Rheumatic Diseases immunology
- Abstract
The objective of this study is to evaluate the association between anti-neuronal antibody (anti-NA) and central nervous system (CNS) manifestations of systemic lupus erythematosus (SLE) and other rheumatic diseases using a flow cytometric method. Anti-NA was measured by flow cytometry in serum and cerebrospinal fluid (CSF) samples from patients with SLE (n=44 for serum, n=17 for CSF), other rheumatic diseases (n=64 for serum, n=21 for CSF) and from healthy controls (n=65 for serum, n=18 for CSF). Serum anti-NA was more frequently observed in SLE (31.8%, 14/44) than in other rheumatic diseases (4.7%, 3/64, P<0.001) or in healthy controls (0%, 0/65, P<0.00001). In SLE patients, the frequency of serum anti-NA was significantly higher in CNS-SLE (76.5%, 13/17) than in non CNS-SLE (3.7%, 1/27, P<0.000001). CSF anti-NA was detected in 88.2% (15/17) of CNS-SLE and was more frequently detected in CNS-SLE (15/17, 88.2%) than in other rheumatic diseases with CNS involvement (1/21, 4.8%, P<0.000001) or in healthy controls (0/18, P<0.000001). In conclusion, serum anti-NA was more frequently found in CNS-SLE than in non CNS-SLE, other rheumatic diseases or in healthy controls. The frequency of CSF anti-NA in CNS-SLE was significantly higher than in other rheumatic diseases with CNS involvement or in healthy controls.
- Published
- 2008
- Full Text
- View/download PDF
9. Takayasu's arteritis concurrent with Marfan syndrome--a case report.
- Author
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Baek HJ, Shin KC, Lee YJ, Kang SW, Lee EB, and Song YW
- Subjects
- Adult, Aorta, Thoracic pathology, Aortic Aneurysm, Thoracic complications, Aortic Aneurysm, Thoracic genetics, Aortic Aneurysm, Thoracic immunology, Aortography, Autoantibodies blood, Chromosomes, Human, Pair 15, Extracellular Matrix Proteins genetics, Extracellular Matrix Proteins immunology, Female, Fibrillins, Humans, Magnetic Resonance Imaging, Marfan Syndrome genetics, Marfan Syndrome immunology, Microfilament Proteins genetics, Microfilament Proteins immunology, Phenotype, Takayasu Arteritis genetics, Takayasu Arteritis immunology, Marfan Syndrome complications, Takayasu Arteritis complications
- Abstract
Marfan syndrome (MS) is a dominantly inherited connective tissue disorder characterized by arachnodactyly, tall stature, the presence of aortic aneurysm, and lens dislocation. Takayasu's arteritis (TA) is a chronic vasculitis that primarily affects the aorta and its branches. The authors report the first case of TA in a patient with MS. The simultaneous presence of TA and MS could be a coincidence, however; the pathogenesis of TA might be linked with autoimmunity induced by abnormal extracellular matrix protein derived from the genetic mutations in MS.
- Published
- 2000
- Full Text
- View/download PDF
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