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Novel Management and Screening Approaches for Haematological Complications of Gaucher’s Disease

PURPOSE: Gaucher disease (GD) is the most common lysosomal storage disorder. The principal manifestations for its diagnosis and further monitoring include haematological manifestations such as anaemia, thrombocytopaenia, spleen enlargement, and bleeding disorders, among others. This review aims to s...

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Autores principales: Giraldo, Pilar, Andrade-Campos, Marcio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8665828/
https://www.ncbi.nlm.nih.gov/pubmed/34908889
http://dx.doi.org/10.2147/JBM.S279756
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author Giraldo, Pilar
Andrade-Campos, Marcio
author_facet Giraldo, Pilar
Andrade-Campos, Marcio
author_sort Giraldo, Pilar
collection PubMed
description PURPOSE: Gaucher disease (GD) is the most common lysosomal storage disorder. The principal manifestations for its diagnosis and further monitoring include haematological manifestations such as anaemia, thrombocytopaenia, spleen enlargement, and bleeding disorders, among others. This review aims to summarise and update the role of haematological complications in GD diagnosis and follow-up, describe their management strategies, and to use these indicators as part of the diagnostic approach. MATERIALS AND METHODS: A systematic review following the recommendations of PRISMA-P 2020 was carried out. Publications indexed in the databases PubMed, Embase, Science Open, Mendeley, and Web of Science were electronically searched by three independent reviewers, and publications up to June 2021 were accessed. A total of 246 publications were initially listed, of which 129 were included for further review and analysis. Case reports were considered if they were representative of a relevant hematologic complication. RESULTS: From the first review dated in 1974 to the latest publication in 2021, including different populations confirmed that the haematological manifestations such as thrombocytopaenia and splenomegaly at diagnosis of GD type 1 are the most frequent features of the disease. The incorporation of haematological parameters to diagnosis strategies increases their cost-effectiveness. Hematologic parameters are part of the scoring system for disease assessment and the evaluation of therapeutic outcomes, providing reliable and accessible data to improve the management of GD. However, cytopaenia, underlying coagulation disorders, and platelet dysfunction need to be addressed, especially during pregnancy or surgery. Long-term haematological complications include the risk of neoplasia and immune impairment, an area of unmet need that is currently under research. CONCLUSION: Haematological features are key for GD suspicion, diagnosis, and management. Normalization of hematological parameters is achieved with the treatment; however, there are unmet needs such as the underlying inflammatory status and the long-term risk of hematologic neoplasia.
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spelling pubmed-86658282021-12-13 Novel Management and Screening Approaches for Haematological Complications of Gaucher’s Disease Giraldo, Pilar Andrade-Campos, Marcio J Blood Med Review PURPOSE: Gaucher disease (GD) is the most common lysosomal storage disorder. The principal manifestations for its diagnosis and further monitoring include haematological manifestations such as anaemia, thrombocytopaenia, spleen enlargement, and bleeding disorders, among others. This review aims to summarise and update the role of haematological complications in GD diagnosis and follow-up, describe their management strategies, and to use these indicators as part of the diagnostic approach. MATERIALS AND METHODS: A systematic review following the recommendations of PRISMA-P 2020 was carried out. Publications indexed in the databases PubMed, Embase, Science Open, Mendeley, and Web of Science were electronically searched by three independent reviewers, and publications up to June 2021 were accessed. A total of 246 publications were initially listed, of which 129 were included for further review and analysis. Case reports were considered if they were representative of a relevant hematologic complication. RESULTS: From the first review dated in 1974 to the latest publication in 2021, including different populations confirmed that the haematological manifestations such as thrombocytopaenia and splenomegaly at diagnosis of GD type 1 are the most frequent features of the disease. The incorporation of haematological parameters to diagnosis strategies increases their cost-effectiveness. Hematologic parameters are part of the scoring system for disease assessment and the evaluation of therapeutic outcomes, providing reliable and accessible data to improve the management of GD. However, cytopaenia, underlying coagulation disorders, and platelet dysfunction need to be addressed, especially during pregnancy or surgery. Long-term haematological complications include the risk of neoplasia and immune impairment, an area of unmet need that is currently under research. CONCLUSION: Haematological features are key for GD suspicion, diagnosis, and management. Normalization of hematological parameters is achieved with the treatment; however, there are unmet needs such as the underlying inflammatory status and the long-term risk of hematologic neoplasia. Dove 2021-12-07 /pmc/articles/PMC8665828/ /pubmed/34908889 http://dx.doi.org/10.2147/JBM.S279756 Text en © 2021 Giraldo and Andrade-Campos. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
Giraldo, Pilar
Andrade-Campos, Marcio
Novel Management and Screening Approaches for Haematological Complications of Gaucher’s Disease
title Novel Management and Screening Approaches for Haematological Complications of Gaucher’s Disease
title_full Novel Management and Screening Approaches for Haematological Complications of Gaucher’s Disease
title_fullStr Novel Management and Screening Approaches for Haematological Complications of Gaucher’s Disease
title_full_unstemmed Novel Management and Screening Approaches for Haematological Complications of Gaucher’s Disease
title_short Novel Management and Screening Approaches for Haematological Complications of Gaucher’s Disease
title_sort novel management and screening approaches for haematological complications of gaucher’s disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8665828/
https://www.ncbi.nlm.nih.gov/pubmed/34908889
http://dx.doi.org/10.2147/JBM.S279756
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