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Management of Neuropsychiatric Systemic Lupus Erythematosus: Current Approaches and Future Perspectives
Neuropsychiatric systemic lupus erythematosus (NPSLE) is a generic definition referring to a series of neurological and psychiatric symptoms directly related to systemic lupus erythematosus (SLE). NPSLE includes heterogeneous and rare neuropsychiatric (NP) manifestations involving both the central a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4791452/ https://www.ncbi.nlm.nih.gov/pubmed/26809245 http://dx.doi.org/10.1007/s40265-015-0534-3 |
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author | Magro-Checa, César Zirkzee, Elisabeth J. Huizinga, Tom W. Steup-Beekman, Gerda M. |
author_facet | Magro-Checa, César Zirkzee, Elisabeth J. Huizinga, Tom W. Steup-Beekman, Gerda M. |
author_sort | Magro-Checa, César |
collection | PubMed |
description | Neuropsychiatric systemic lupus erythematosus (NPSLE) is a generic definition referring to a series of neurological and psychiatric symptoms directly related to systemic lupus erythematosus (SLE). NPSLE includes heterogeneous and rare neuropsychiatric (NP) manifestations involving both the central and peripheral nervous system. Due to the lack of a gold standard, the attribution of NP symptoms to SLE represents a clinical challenge that obligates the strict exclusion of any other potential cause. In the acute setting, management of these patients does not differ from other non-SLE subjects presenting with the same NP manifestation. Afterwards, an individualized therapeutic strategy, depending on the presenting manifestation and severity of symptoms, must be started. Clinical trials in NPSLE are scarce and most of the data are extracted from case series and case reports. High-dose glucocorticoids and intravenous cyclophosphamide remain the cornerstone for patients with severe symptoms that are thought to reflect inflammation or an underlying autoimmune process. Rituximab, intravenous immunoglobulins, or plasmapheresis may be used if response is not achieved. When patients present with mild to moderate NP manifestations, or when maintenance therapy is warranted, azathioprine and mycophenolate may be considered. When symptoms are thought to reflect a thrombotic underlying process, anticoagulation and antiplatelet agents are the mainstay of therapy, especially if antiphospholipid antibodies or antiphospholipid syndrome are present. Recent trials on SLE using new biologicals, based on newly understood SLE mechanisms, have shown promising results. Based on what we currently know about its pathogenesis, it is tempting to speculate how these new therapies may affect the management of NPSLE patients. This article provides a comprehensive and critical review of the literature on the epidemiology, pathophysiology, diagnosis, and management of NPSLE. We describe the most common pharmacological treatments used in NPSLE, based on both a literature search and our expert opinion. The extent to which new drugs in the advanced development of SLE, or the blockade of new targets, may impact future treatment of NPSLE will also be discussed. |
format | Online Article Text |
id | pubmed-4791452 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-47914522016-04-09 Management of Neuropsychiatric Systemic Lupus Erythematosus: Current Approaches and Future Perspectives Magro-Checa, César Zirkzee, Elisabeth J. Huizinga, Tom W. Steup-Beekman, Gerda M. Drugs Review Article Neuropsychiatric systemic lupus erythematosus (NPSLE) is a generic definition referring to a series of neurological and psychiatric symptoms directly related to systemic lupus erythematosus (SLE). NPSLE includes heterogeneous and rare neuropsychiatric (NP) manifestations involving both the central and peripheral nervous system. Due to the lack of a gold standard, the attribution of NP symptoms to SLE represents a clinical challenge that obligates the strict exclusion of any other potential cause. In the acute setting, management of these patients does not differ from other non-SLE subjects presenting with the same NP manifestation. Afterwards, an individualized therapeutic strategy, depending on the presenting manifestation and severity of symptoms, must be started. Clinical trials in NPSLE are scarce and most of the data are extracted from case series and case reports. High-dose glucocorticoids and intravenous cyclophosphamide remain the cornerstone for patients with severe symptoms that are thought to reflect inflammation or an underlying autoimmune process. Rituximab, intravenous immunoglobulins, or plasmapheresis may be used if response is not achieved. When patients present with mild to moderate NP manifestations, or when maintenance therapy is warranted, azathioprine and mycophenolate may be considered. When symptoms are thought to reflect a thrombotic underlying process, anticoagulation and antiplatelet agents are the mainstay of therapy, especially if antiphospholipid antibodies or antiphospholipid syndrome are present. Recent trials on SLE using new biologicals, based on newly understood SLE mechanisms, have shown promising results. Based on what we currently know about its pathogenesis, it is tempting to speculate how these new therapies may affect the management of NPSLE patients. This article provides a comprehensive and critical review of the literature on the epidemiology, pathophysiology, diagnosis, and management of NPSLE. We describe the most common pharmacological treatments used in NPSLE, based on both a literature search and our expert opinion. The extent to which new drugs in the advanced development of SLE, or the blockade of new targets, may impact future treatment of NPSLE will also be discussed. Springer International Publishing 2016-01-26 2016 /pmc/articles/PMC4791452/ /pubmed/26809245 http://dx.doi.org/10.1007/s40265-015-0534-3 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Review Article Magro-Checa, César Zirkzee, Elisabeth J. Huizinga, Tom W. Steup-Beekman, Gerda M. Management of Neuropsychiatric Systemic Lupus Erythematosus: Current Approaches and Future Perspectives |
title | Management of Neuropsychiatric Systemic Lupus Erythematosus: Current Approaches and Future Perspectives |
title_full | Management of Neuropsychiatric Systemic Lupus Erythematosus: Current Approaches and Future Perspectives |
title_fullStr | Management of Neuropsychiatric Systemic Lupus Erythematosus: Current Approaches and Future Perspectives |
title_full_unstemmed | Management of Neuropsychiatric Systemic Lupus Erythematosus: Current Approaches and Future Perspectives |
title_short | Management of Neuropsychiatric Systemic Lupus Erythematosus: Current Approaches and Future Perspectives |
title_sort | management of neuropsychiatric systemic lupus erythematosus: current approaches and future perspectives |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4791452/ https://www.ncbi.nlm.nih.gov/pubmed/26809245 http://dx.doi.org/10.1007/s40265-015-0534-3 |
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