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Kidney thrombotic microangiopathy in lupus nephritis: Impact on treatment and prognosis

INTRODUCTION: Lupus nephritis (LN) may present with thrombotic microangiopathy (TMA) on kidney biopsy, the impact of which on outcomes is unclear. This study examined the prognostic importance of LN with TMA on kidney biopsy, including response to therapy and long-term outcomes. METHODS: We conducte...

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Autores principales: Massicotte-Azarniouch, David, Kotzen, Elizabeth, Todd, Sarah, Hu, Yichun, Hogan, Susan L., Jain, Koyal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449430/
https://www.ncbi.nlm.nih.gov/pubmed/35650019
http://dx.doi.org/10.1177/09612033221106301
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author Massicotte-Azarniouch, David
Kotzen, Elizabeth
Todd, Sarah
Hu, Yichun
Hogan, Susan L.
Jain, Koyal
author_facet Massicotte-Azarniouch, David
Kotzen, Elizabeth
Todd, Sarah
Hu, Yichun
Hogan, Susan L.
Jain, Koyal
author_sort Massicotte-Azarniouch, David
collection PubMed
description INTRODUCTION: Lupus nephritis (LN) may present with thrombotic microangiopathy (TMA) on kidney biopsy, the impact of which on outcomes is unclear. This study examined the prognostic importance of LN with TMA on kidney biopsy, including response to therapy and long-term outcomes. METHODS: We conducted a single-center, retrospective study of all cases of LN with concomitant TMA on kidney biopsy in the Glomerular Disease Collaborative Network database. Controls were individuals with LN without TMA matched to cases based on demographic and clinical variables. Outcomes were remission at 6- and 12-months, end-stage kidney disease (ESKD) and death. Logistic regression and Cox proportional hazards models were used to ascertain the risks for outcomes, with adjustment for serum creatinine and proteinuria. RESULTS: There were 17 cases and 28 controls. Cases had higher creatinine, higher proteinuria and greater chronicity on biopsy at baseline compared to controls. The rates of remission at 6-months and 12-months were similar between cases and controls (6-months 53.9% vs 46.4%, adjusted OR 2.54, 95% CI 0.48, 13.37; 12-months 53.9% vs 50.0%, adjusted OR 2.95, 95% CI 0.44, 19.78). Cases were at greater risk for ESKD in univariate analysis (HR 3.77; 95% CI 1.24, 11.41) but not when adjusting for serum creatinine and proteinuria (HR 2.20; 95% CI 0.63, 7.71). There was no significant difference in the risk of death between cases and controls. CONCLUSION: Lupus nephritis with renal TMA likely responds to therapy similarly to those without TMA; risk for ESKD is not significantly increased, although the influence of renal function and proteinuria in larger samples is needed.
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spelling pubmed-94494302022-09-08 Kidney thrombotic microangiopathy in lupus nephritis: Impact on treatment and prognosis Massicotte-Azarniouch, David Kotzen, Elizabeth Todd, Sarah Hu, Yichun Hogan, Susan L. Jain, Koyal Lupus Papers INTRODUCTION: Lupus nephritis (LN) may present with thrombotic microangiopathy (TMA) on kidney biopsy, the impact of which on outcomes is unclear. This study examined the prognostic importance of LN with TMA on kidney biopsy, including response to therapy and long-term outcomes. METHODS: We conducted a single-center, retrospective study of all cases of LN with concomitant TMA on kidney biopsy in the Glomerular Disease Collaborative Network database. Controls were individuals with LN without TMA matched to cases based on demographic and clinical variables. Outcomes were remission at 6- and 12-months, end-stage kidney disease (ESKD) and death. Logistic regression and Cox proportional hazards models were used to ascertain the risks for outcomes, with adjustment for serum creatinine and proteinuria. RESULTS: There were 17 cases and 28 controls. Cases had higher creatinine, higher proteinuria and greater chronicity on biopsy at baseline compared to controls. The rates of remission at 6-months and 12-months were similar between cases and controls (6-months 53.9% vs 46.4%, adjusted OR 2.54, 95% CI 0.48, 13.37; 12-months 53.9% vs 50.0%, adjusted OR 2.95, 95% CI 0.44, 19.78). Cases were at greater risk for ESKD in univariate analysis (HR 3.77; 95% CI 1.24, 11.41) but not when adjusting for serum creatinine and proteinuria (HR 2.20; 95% CI 0.63, 7.71). There was no significant difference in the risk of death between cases and controls. CONCLUSION: Lupus nephritis with renal TMA likely responds to therapy similarly to those without TMA; risk for ESKD is not significantly increased, although the influence of renal function and proteinuria in larger samples is needed. SAGE Publications 2022-06-01 2022-09 /pmc/articles/PMC9449430/ /pubmed/35650019 http://dx.doi.org/10.1177/09612033221106301 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Papers
Massicotte-Azarniouch, David
Kotzen, Elizabeth
Todd, Sarah
Hu, Yichun
Hogan, Susan L.
Jain, Koyal
Kidney thrombotic microangiopathy in lupus nephritis: Impact on treatment and prognosis
title Kidney thrombotic microangiopathy in lupus nephritis: Impact on treatment and prognosis
title_full Kidney thrombotic microangiopathy in lupus nephritis: Impact on treatment and prognosis
title_fullStr Kidney thrombotic microangiopathy in lupus nephritis: Impact on treatment and prognosis
title_full_unstemmed Kidney thrombotic microangiopathy in lupus nephritis: Impact on treatment and prognosis
title_short Kidney thrombotic microangiopathy in lupus nephritis: Impact on treatment and prognosis
title_sort kidney thrombotic microangiopathy in lupus nephritis: impact on treatment and prognosis
topic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449430/
https://www.ncbi.nlm.nih.gov/pubmed/35650019
http://dx.doi.org/10.1177/09612033221106301
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