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One Giant Step for Giant Cell Arteritis: Updates in Diagnosis and Treatment
PURPOSE OF REVIEW: Giant cell arteritis (GCA), a medium and large vessel vasculitis occurring in the aged, remains a formidable disease, capable of taking both vision and life, through a multitude of vascular complications. Our understanding of the spectrum of its manifestations has grown over the y...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7811148/ https://www.ncbi.nlm.nih.gov/pubmed/33488050 http://dx.doi.org/10.1007/s11940-020-00660-2 |
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author | Dinkin, Marc Johnson, Editha |
author_facet | Dinkin, Marc Johnson, Editha |
author_sort | Dinkin, Marc |
collection | PubMed |
description | PURPOSE OF REVIEW: Giant cell arteritis (GCA), a medium and large vessel vasculitis occurring in the aged, remains a formidable disease, capable of taking both vision and life, through a multitude of vascular complications. Our understanding of the spectrum of its manifestations has grown over the years, to include limb claudication, aortitis, and cardiac disease, in addition to the more classic visual complications resulting from of ischemia to branches of the external and internal carotid arteries. While a clinical presentation of headache, jaw claudication, scalp tenderness, fever and other systemic symptoms and serum markers are together highly suggestive of the disease, diagnosis can be challenging in those cases in which classic symptoms are lacking. The purpose of this review is to update the reader on advances in the diagnosis and treatment of giant cell arteritis and to review our evolving understanding of the immunological mechanism underlying the disease, which have helped guide our search for novel therapies. RECENT FINDINGS: There is increasing evidence supporting the use of Doppler ultrasound, dedicated post-contrast T1-weighted spin echo MRI of the scalp arteries and PET scan, which can together improve our diagnostic accuracy in cases in which temporal artery biopsy is either inconclusive or not feasible. Advances in our understanding of the immunological cascades underlying the disease have helped guide our search for steroid-sparing treatments for the GCA, the most important of which has been the IL-6 receptor antibody inhibitor tocilizumab, which has been shown to reduce cumulative steroid dose in a large multicenter, placebo-controlled prospective study. Other biologic agents, such as abatacept and ustekinumab have shown promise in smaller studies. SUMMARY: GCA is no longer a disease whose diagnosis is based exclusively on temporal artery biopsy and whose complications are prevented solely with the use of corticosteroids. Modern vascular imaging techniques and targeted immunologic therapies are heralding a new era for the disease, in which practitioners will hopefully be able to diagnosis it with greater accuracy and treat it with less ischemic complications and iatrogenic side effects. |
format | Online Article Text |
id | pubmed-7811148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-78111482021-01-18 One Giant Step for Giant Cell Arteritis: Updates in Diagnosis and Treatment Dinkin, Marc Johnson, Editha Curr Treat Options Neurol Cerebrovascular Disorders (D Jamieson, Section Editor) PURPOSE OF REVIEW: Giant cell arteritis (GCA), a medium and large vessel vasculitis occurring in the aged, remains a formidable disease, capable of taking both vision and life, through a multitude of vascular complications. Our understanding of the spectrum of its manifestations has grown over the years, to include limb claudication, aortitis, and cardiac disease, in addition to the more classic visual complications resulting from of ischemia to branches of the external and internal carotid arteries. While a clinical presentation of headache, jaw claudication, scalp tenderness, fever and other systemic symptoms and serum markers are together highly suggestive of the disease, diagnosis can be challenging in those cases in which classic symptoms are lacking. The purpose of this review is to update the reader on advances in the diagnosis and treatment of giant cell arteritis and to review our evolving understanding of the immunological mechanism underlying the disease, which have helped guide our search for novel therapies. RECENT FINDINGS: There is increasing evidence supporting the use of Doppler ultrasound, dedicated post-contrast T1-weighted spin echo MRI of the scalp arteries and PET scan, which can together improve our diagnostic accuracy in cases in which temporal artery biopsy is either inconclusive or not feasible. Advances in our understanding of the immunological cascades underlying the disease have helped guide our search for steroid-sparing treatments for the GCA, the most important of which has been the IL-6 receptor antibody inhibitor tocilizumab, which has been shown to reduce cumulative steroid dose in a large multicenter, placebo-controlled prospective study. Other biologic agents, such as abatacept and ustekinumab have shown promise in smaller studies. SUMMARY: GCA is no longer a disease whose diagnosis is based exclusively on temporal artery biopsy and whose complications are prevented solely with the use of corticosteroids. Modern vascular imaging techniques and targeted immunologic therapies are heralding a new era for the disease, in which practitioners will hopefully be able to diagnosis it with greater accuracy and treat it with less ischemic complications and iatrogenic side effects. Springer US 2021-01-16 2021 /pmc/articles/PMC7811148/ /pubmed/33488050 http://dx.doi.org/10.1007/s11940-020-00660-2 Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Cerebrovascular Disorders (D Jamieson, Section Editor) Dinkin, Marc Johnson, Editha One Giant Step for Giant Cell Arteritis: Updates in Diagnosis and Treatment |
title | One Giant Step for Giant Cell Arteritis: Updates in Diagnosis and Treatment |
title_full | One Giant Step for Giant Cell Arteritis: Updates in Diagnosis and Treatment |
title_fullStr | One Giant Step for Giant Cell Arteritis: Updates in Diagnosis and Treatment |
title_full_unstemmed | One Giant Step for Giant Cell Arteritis: Updates in Diagnosis and Treatment |
title_short | One Giant Step for Giant Cell Arteritis: Updates in Diagnosis and Treatment |
title_sort | one giant step for giant cell arteritis: updates in diagnosis and treatment |
topic | Cerebrovascular Disorders (D Jamieson, Section Editor) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7811148/ https://www.ncbi.nlm.nih.gov/pubmed/33488050 http://dx.doi.org/10.1007/s11940-020-00660-2 |
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