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Clinico-Laboratory Features and Associated Factors of Lupus Mesenteric Vasculitis

INTRODUCTION: Lupus mesenteric vasculitis (LMV) is a rare but potentially life-threatening clinical entity in systemic lupus erythematosus (SLE) patients. OBJECTIVE: The present study was initiated to explore the clinical features and associated factors of LMV in SLE patients. METHODS: We conducted...

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Autores principales: Wang, Hongxu, Gao, Qing, Liao, Guanyi, Ren, Sirui, You, Wenxian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8217476/
https://www.ncbi.nlm.nih.gov/pubmed/34050908
http://dx.doi.org/10.1007/s40744-021-00323-x
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author Wang, Hongxu
Gao, Qing
Liao, Guanyi
Ren, Sirui
You, Wenxian
author_facet Wang, Hongxu
Gao, Qing
Liao, Guanyi
Ren, Sirui
You, Wenxian
author_sort Wang, Hongxu
collection PubMed
description INTRODUCTION: Lupus mesenteric vasculitis (LMV) is a rare but potentially life-threatening clinical entity in systemic lupus erythematosus (SLE) patients. OBJECTIVE: The present study was initiated to explore the clinical features and associated factors of LMV in SLE patients. METHODS: We conducted a retrospective study on 50 cases of SLE patients with lupus mesenteric vasculitis (LMV) from January 2010 to December 2019 and 89 cases of non-LMV-SLE patients with similar demographic and comorbidities were included as control. All the data regarding clinical features, laboratory findings, and treatment were reviewed independently by two experts in the field. Both univariate and multivariate logistic regression analyses were employed to identify the associated factors of LMV. RESULTS: The incidence of LMV was 2.9% among hospitalized SLE patients in the current study. The most frequent symptom and physical sign of LMV were respectively abdominal pain (48, 96%) and abdominal tenderness (45, 90%). Through univariate and subsequent multivariate analysis, oral ulcer (OR, 4.25; P = 0.024), urinary tract involvement (OR, 5.23; P = 0.021), and elevated D-dimer (OR, 1.121; P = 0.008) were demonstrated to be positively associated with LMV, while percentage of lymphocytes (OR, 0.928; P = 0.004) and complement 3 (OR, 0.048; P = 0.008) were negatively correlated with LMV. CONCLUSIONS: Oral ulcer, urinary tract involvement, reduced percentage of lymphocytes and complement 3, elevated D-dimer could be associated factors for LMV in SLE patients.
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spelling pubmed-82174762021-07-01 Clinico-Laboratory Features and Associated Factors of Lupus Mesenteric Vasculitis Wang, Hongxu Gao, Qing Liao, Guanyi Ren, Sirui You, Wenxian Rheumatol Ther Original Research INTRODUCTION: Lupus mesenteric vasculitis (LMV) is a rare but potentially life-threatening clinical entity in systemic lupus erythematosus (SLE) patients. OBJECTIVE: The present study was initiated to explore the clinical features and associated factors of LMV in SLE patients. METHODS: We conducted a retrospective study on 50 cases of SLE patients with lupus mesenteric vasculitis (LMV) from January 2010 to December 2019 and 89 cases of non-LMV-SLE patients with similar demographic and comorbidities were included as control. All the data regarding clinical features, laboratory findings, and treatment were reviewed independently by two experts in the field. Both univariate and multivariate logistic regression analyses were employed to identify the associated factors of LMV. RESULTS: The incidence of LMV was 2.9% among hospitalized SLE patients in the current study. The most frequent symptom and physical sign of LMV were respectively abdominal pain (48, 96%) and abdominal tenderness (45, 90%). Through univariate and subsequent multivariate analysis, oral ulcer (OR, 4.25; P = 0.024), urinary tract involvement (OR, 5.23; P = 0.021), and elevated D-dimer (OR, 1.121; P = 0.008) were demonstrated to be positively associated with LMV, while percentage of lymphocytes (OR, 0.928; P = 0.004) and complement 3 (OR, 0.048; P = 0.008) were negatively correlated with LMV. CONCLUSIONS: Oral ulcer, urinary tract involvement, reduced percentage of lymphocytes and complement 3, elevated D-dimer could be associated factors for LMV in SLE patients. Springer Healthcare 2021-05-29 /pmc/articles/PMC8217476/ /pubmed/34050908 http://dx.doi.org/10.1007/s40744-021-00323-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Research
Wang, Hongxu
Gao, Qing
Liao, Guanyi
Ren, Sirui
You, Wenxian
Clinico-Laboratory Features and Associated Factors of Lupus Mesenteric Vasculitis
title Clinico-Laboratory Features and Associated Factors of Lupus Mesenteric Vasculitis
title_full Clinico-Laboratory Features and Associated Factors of Lupus Mesenteric Vasculitis
title_fullStr Clinico-Laboratory Features and Associated Factors of Lupus Mesenteric Vasculitis
title_full_unstemmed Clinico-Laboratory Features and Associated Factors of Lupus Mesenteric Vasculitis
title_short Clinico-Laboratory Features and Associated Factors of Lupus Mesenteric Vasculitis
title_sort clinico-laboratory features and associated factors of lupus mesenteric vasculitis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8217476/
https://www.ncbi.nlm.nih.gov/pubmed/34050908
http://dx.doi.org/10.1007/s40744-021-00323-x
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