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Clinical comparisons between previously diagnosed SLE and newly diagnosed SLE by kidney biopsy
BACKGROUND: Lupus nephritis is a type of major organ involvement in systemic lupus erythematosus (SLE) patients that leads to higher rates of morbidity and mortality and may present initially in 28% of SLE patients. However, there are limited data available on clinical differences or predictors for...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709425/ https://www.ncbi.nlm.nih.gov/pubmed/33261666 http://dx.doi.org/10.1186/s13317-020-00140-2 |
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author | Tonsawan, Pantipa Sawanyawisuth, Kittisak |
author_facet | Tonsawan, Pantipa Sawanyawisuth, Kittisak |
author_sort | Tonsawan, Pantipa |
collection | PubMed |
description | BACKGROUND: Lupus nephritis is a type of major organ involvement in systemic lupus erythematosus (SLE) patients that leads to higher rates of morbidity and mortality and may present initially in 28% of SLE patients. However, there are limited data available on clinical differences or predictors for biopsy-proven lupus nephritis in established versus newly diagnosed SLE cases. METHODS: Adult patients undergoing kidney biopsy for the first time with a diagnosis of lupus nephritis were eligible for inclusion. Patients were categorized into two groups: those with previously diagnosed SLE and those with newly diagnosed SLE by kidney biopsy. Factors associated with newly diagnosed SLE were determined using logistic regression analysis. RESULTS: There were 68 patients diagnosed with lupus nephritis by kidney biopsy. Of those, 31 cases (45.58%) were newly diagnosed. The newly diagnosed SLE group was significantly older (36.87 vs 30.95 years) and had a lower proportion of females (74.19% vs 91.89%) than the previously diagnosed group. A new-onset hypertension was the only factor independently associated with newly diagnosed SLE by kidney biopsy. The adjusted odds ratio (95% CI) was 5.152 (1.046, 25.363). CONCLUSIONS: Nearly half of the biopsy-proven lupus nephritis cases in this study were patients with newly diagnosed SLE. Patients with previously diagnosed SLE and newly diagnosed SLE by kidney biopsy had clinical differences. |
format | Online Article Text |
id | pubmed-7709425 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77094252020-12-02 Clinical comparisons between previously diagnosed SLE and newly diagnosed SLE by kidney biopsy Tonsawan, Pantipa Sawanyawisuth, Kittisak Auto Immun Highlights Original Research BACKGROUND: Lupus nephritis is a type of major organ involvement in systemic lupus erythematosus (SLE) patients that leads to higher rates of morbidity and mortality and may present initially in 28% of SLE patients. However, there are limited data available on clinical differences or predictors for biopsy-proven lupus nephritis in established versus newly diagnosed SLE cases. METHODS: Adult patients undergoing kidney biopsy for the first time with a diagnosis of lupus nephritis were eligible for inclusion. Patients were categorized into two groups: those with previously diagnosed SLE and those with newly diagnosed SLE by kidney biopsy. Factors associated with newly diagnosed SLE were determined using logistic regression analysis. RESULTS: There were 68 patients diagnosed with lupus nephritis by kidney biopsy. Of those, 31 cases (45.58%) were newly diagnosed. The newly diagnosed SLE group was significantly older (36.87 vs 30.95 years) and had a lower proportion of females (74.19% vs 91.89%) than the previously diagnosed group. A new-onset hypertension was the only factor independently associated with newly diagnosed SLE by kidney biopsy. The adjusted odds ratio (95% CI) was 5.152 (1.046, 25.363). CONCLUSIONS: Nearly half of the biopsy-proven lupus nephritis cases in this study were patients with newly diagnosed SLE. Patients with previously diagnosed SLE and newly diagnosed SLE by kidney biopsy had clinical differences. BioMed Central 2020-12-02 /pmc/articles/PMC7709425/ /pubmed/33261666 http://dx.doi.org/10.1186/s13317-020-00140-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits 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/4.0/. |
spellingShingle | Original Research Tonsawan, Pantipa Sawanyawisuth, Kittisak Clinical comparisons between previously diagnosed SLE and newly diagnosed SLE by kidney biopsy |
title | Clinical comparisons between previously diagnosed SLE and newly diagnosed SLE by kidney biopsy |
title_full | Clinical comparisons between previously diagnosed SLE and newly diagnosed SLE by kidney biopsy |
title_fullStr | Clinical comparisons between previously diagnosed SLE and newly diagnosed SLE by kidney biopsy |
title_full_unstemmed | Clinical comparisons between previously diagnosed SLE and newly diagnosed SLE by kidney biopsy |
title_short | Clinical comparisons between previously diagnosed SLE and newly diagnosed SLE by kidney biopsy |
title_sort | clinical comparisons between previously diagnosed sle and newly diagnosed sle by kidney biopsy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709425/ https://www.ncbi.nlm.nih.gov/pubmed/33261666 http://dx.doi.org/10.1186/s13317-020-00140-2 |
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