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Total Globulin Fraction at Diagnosis Could Forecast All-Cause Mortality during the Disease Course in Patients with Antineutrophil Cytoplasmic Antibody-Associated Vasculitis
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | 박용범 | - |
| dc.contributor.author | 송정식 | - |
| dc.contributor.author | 안성수 | - |
| dc.contributor.author | 이상원 | - |
| dc.contributor.author | 하장우 | - |
| dc.date.accessioned | 2023-07-12T03:10:26Z | - |
| dc.date.available | 2023-07-12T03:10:26Z | - |
| dc.date.issued | 2023-06 | - |
| dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/195528 | - |
| dc.description.abstract | Total globulin fraction (TGF) is calculated by subtracting serum albumin levels from serum total protein levels. The present study examined whether TGF at diagnosis could forecast all-cause mortality during the disease course in patients with antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV). The present study included 283 patients with AAV. The variables at AAV diagnosis such as demographic data, AAV-specific data including the Birmingham vasculitis activity score (BVAS), five-factor score (FFS), and laboratory data including ANCA, erythrocyte sedimentation rate (ESR), and C-reactive protein (CRP) were collected. The number of deceased patients during the follow-up duration based on all-cause mortality was counted. The median age of the 283 AAV patients was 60 years, and 35.7% were men. ANCAs were detected in 228 patients, and the median TGF was 2.9. A total of 39 patients (13.8%) died within a median follow-up duration of 46.9 months. TGF at AAV diagnosis was significantly correlated with ESR and CRP rather than AAV activity. Patients with ANCA positivity exhibited a significantly higher median TGF at AAV diagnosis than those without. Patients with TGF ≥ 3.1 g/dL at AAV diagnosis exhibited a significantly lower cumulative survival rate than those without. Furthermore, in the multivariable Cox hazards model analysis, TGF ≥ 3.1 g/dL (hazard ratio 2.612) was independently associated with all-cause mortality, along with age, male sex, and body mass index. The present study is the first to demonstrate that TGF at AAV diagnosis can forecast all-cause mortality during the disease course in AAV patients. | - |
| dc.description.statementOfResponsibility | open | - |
| dc.format | application/pdf | - |
| dc.language | English | - |
| dc.publisher | MDPI AG | - |
| dc.relation.isPartOf | JOURNAL OF CLINICAL MEDICINE | - |
| dc.rights | CC BY-NC-ND 2.0 KR | - |
| dc.title | Total Globulin Fraction at Diagnosis Could Forecast All-Cause Mortality during the Disease Course in Patients with Antineutrophil Cytoplasmic Antibody-Associated Vasculitis | - |
| dc.type | Article | - |
| dc.contributor.college | College of Medicine (의과대학) | - |
| dc.contributor.department | Dept. of Internal Medicine (내과학교실) | - |
| dc.contributor.googleauthor | Jang-Woo Ha | - |
| dc.contributor.googleauthor | Sung-Soo Ahn | - |
| dc.contributor.googleauthor | Jason-Jungsik Song | - |
| dc.contributor.googleauthor | Yong-Beom Park | - |
| dc.contributor.googleauthor | Sang-Won Lee | - |
| dc.identifier.doi | 10.3390/jcm12124170 | - |
| dc.contributor.localId | A01579 | - |
| dc.contributor.localId | A02057 | - |
| dc.contributor.localId | A02233 | - |
| dc.contributor.localId | A02824 | - |
| dc.relation.journalcode | J03556 | - |
| dc.identifier.eissn | 2077-0383 | - |
| dc.identifier.pmid | 37373863 | - |
| dc.subject.keyword | antineutrophil cytoplasmic antibody | - |
| dc.subject.keyword | fraction | - |
| dc.subject.keyword | globulin | - |
| dc.subject.keyword | mortality | - |
| dc.subject.keyword | vasculitis | - |
| dc.contributor.alternativeName | Park, Yong Beom | - |
| dc.contributor.affiliatedAuthor | 박용범 | - |
| dc.contributor.affiliatedAuthor | 송정식 | - |
| dc.contributor.affiliatedAuthor | 안성수 | - |
| dc.contributor.affiliatedAuthor | 이상원 | - |
| dc.citation.volume | 12 | - |
| dc.citation.number | 12 | - |
| dc.citation.startPage | 4170 | - |
| dc.identifier.bibliographicCitation | JOURNAL OF CLINICAL MEDICINE, Vol.12(12) : 4170, 2023-06 | - |
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