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Disease modification achievement in patients with lupus nephritis in a real-life setting: mission impossible?
OBJECTIVE: A preliminary definition of disease modification (DM) in lupus nephritis (LN) was recently developed focusing on long-term remission and damage prevention, with minimal treatment-associated toxicity. We aimed to further specify aspects of DM criteria in LN, assess DM achievement in a real...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10277535/ https://www.ncbi.nlm.nih.gov/pubmed/37308249 http://dx.doi.org/10.1136/rmdopen-2023-003158 |
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author | Panagiotopoulos, Alexandros Kapsia, Eleni Michelakis, Ioannis Boletis, John Marinaki, Smaragdi Sfikakis, Petros P Tektonidou, Maria G |
author_facet | Panagiotopoulos, Alexandros Kapsia, Eleni Michelakis, Ioannis Boletis, John Marinaki, Smaragdi Sfikakis, Petros P Tektonidou, Maria G |
author_sort | Panagiotopoulos, Alexandros |
collection | PubMed |
description | OBJECTIVE: A preliminary definition of disease modification (DM) in lupus nephritis (LN) was recently developed focusing on long-term remission and damage prevention, with minimal treatment-associated toxicity. We aimed to further specify aspects of DM criteria in LN, assess DM achievement in a real-world setting and examine potential DM predictors and long-term outcomes. METHODS: We collected clinical/laboratory and histological inception cohort data from biopsy-proven LN patients (82% females) with ≥72 months follow-up at two joint academic centres. Specific criteria for 24-hour proteinuria, estimated glomerular filtration rate (eGFR), renal flares and glucocorticoids dose were set at three time frames (months 0–12, 13–60 and 72) to assess DM. In the first model, DM was achieved if patients fulfilled all four criteria at all three time frames (achievers). In the second model, the continued glucocorticoids reduction criterion was excluded. Logistic regression analyses were performed. Possible different trends in DM achievement between past and recent decades were also investigated. RESULTS: DM was achieved by 60% of patients, increased to 70% when glucocorticoids excluded from DM criteria. 24-hour proteinuria at 9 months predicted DM achievement (OR 0.72, 95% CI 0.53 to 0.97, p=0.03), but none of baseline characteristics. Among patients with >72 month follow-up, non-achievers had worse renal outcomes (flares, >30% proteinuria increase, eGFR decline) than achievers at the end of follow-up (median 138 months). Patients diagnosed between 1992 and 2005 were found to have significantly lower percentages of DM achievement and met less often the glucocorticoids dose reduction criterion in all three time frames, compared with those diagnosed between 2006 and 2016 (p=0.006 and p<0.01, respectively). CONCLUSIONS: DM was achieved by only 60% of LN patients in a real-life setting, partly due to lack of glucocorticoids dose target attainment, while DM failure was associated with worse long-term renal outcomes. This may imply limitations in the effectiveness or implementation of current LN treatments, supporting the need for novel therapeutic strategies. |
format | Online Article Text |
id | pubmed-10277535 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-102775352023-06-20 Disease modification achievement in patients with lupus nephritis in a real-life setting: mission impossible? Panagiotopoulos, Alexandros Kapsia, Eleni Michelakis, Ioannis Boletis, John Marinaki, Smaragdi Sfikakis, Petros P Tektonidou, Maria G RMD Open Connective Tissue Diseases OBJECTIVE: A preliminary definition of disease modification (DM) in lupus nephritis (LN) was recently developed focusing on long-term remission and damage prevention, with minimal treatment-associated toxicity. We aimed to further specify aspects of DM criteria in LN, assess DM achievement in a real-world setting and examine potential DM predictors and long-term outcomes. METHODS: We collected clinical/laboratory and histological inception cohort data from biopsy-proven LN patients (82% females) with ≥72 months follow-up at two joint academic centres. Specific criteria for 24-hour proteinuria, estimated glomerular filtration rate (eGFR), renal flares and glucocorticoids dose were set at three time frames (months 0–12, 13–60 and 72) to assess DM. In the first model, DM was achieved if patients fulfilled all four criteria at all three time frames (achievers). In the second model, the continued glucocorticoids reduction criterion was excluded. Logistic regression analyses were performed. Possible different trends in DM achievement between past and recent decades were also investigated. RESULTS: DM was achieved by 60% of patients, increased to 70% when glucocorticoids excluded from DM criteria. 24-hour proteinuria at 9 months predicted DM achievement (OR 0.72, 95% CI 0.53 to 0.97, p=0.03), but none of baseline characteristics. Among patients with >72 month follow-up, non-achievers had worse renal outcomes (flares, >30% proteinuria increase, eGFR decline) than achievers at the end of follow-up (median 138 months). Patients diagnosed between 1992 and 2005 were found to have significantly lower percentages of DM achievement and met less often the glucocorticoids dose reduction criterion in all three time frames, compared with those diagnosed between 2006 and 2016 (p=0.006 and p<0.01, respectively). CONCLUSIONS: DM was achieved by only 60% of LN patients in a real-life setting, partly due to lack of glucocorticoids dose target attainment, while DM failure was associated with worse long-term renal outcomes. This may imply limitations in the effectiveness or implementation of current LN treatments, supporting the need for novel therapeutic strategies. BMJ Publishing Group 2023-06-12 /pmc/articles/PMC10277535/ /pubmed/37308249 http://dx.doi.org/10.1136/rmdopen-2023-003158 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Connective Tissue Diseases Panagiotopoulos, Alexandros Kapsia, Eleni Michelakis, Ioannis Boletis, John Marinaki, Smaragdi Sfikakis, Petros P Tektonidou, Maria G Disease modification achievement in patients with lupus nephritis in a real-life setting: mission impossible? |
title | Disease modification achievement in patients with lupus nephritis in a real-life setting: mission impossible? |
title_full | Disease modification achievement in patients with lupus nephritis in a real-life setting: mission impossible? |
title_fullStr | Disease modification achievement in patients with lupus nephritis in a real-life setting: mission impossible? |
title_full_unstemmed | Disease modification achievement in patients with lupus nephritis in a real-life setting: mission impossible? |
title_short | Disease modification achievement in patients with lupus nephritis in a real-life setting: mission impossible? |
title_sort | disease modification achievement in patients with lupus nephritis in a real-life setting: mission impossible? |
topic | Connective Tissue Diseases |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10277535/ https://www.ncbi.nlm.nih.gov/pubmed/37308249 http://dx.doi.org/10.1136/rmdopen-2023-003158 |
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