Looking ahead: giant-cellarteritis in 10 years time

被引:12
作者
Bond, Milena [3 ]
Tomelleri, Alessandro [4 ]
Buttgereit, Frank [5 ]
Matteson, Eric L. [6 ]
Dejaco, Christian [1 ,2 ]
机构
[1] Hosp Brunico SABES ASDAA, Dept Rheumatol, Via Osped 11, I-39031 Brunico, Italy
[2] Med Univ Graz, Dept Rheumatol & Immunol, Auenbruggerpl 15, A-8036 Graz, Austria
[3] Hosp Brunico SABES ASDAA, Dept Rheumatol, Brunico, Italy
[4] IRCCS San Raffaele Hosp, Unit Immunol Rheumatol Allergy & Rare Dis, Milan, Italy
[5] Charite Univ Med Berlin, Dept Rheumatol & Clin Immunol, Berlin, Germany
[6] Mayo Clin Coll Med & Sci, Div Rheumatol, Rochester, MN USA
基金
英国科研创新办公室;
关键词
biomarkers; future; giant-cell arteritis; imaging; treatment; SEVERE ISCHEMIC COMPLICATIONS; TREAT-TO-TARGET; CELL ARTERITIS; POLYMYALGIA-RHEUMATICA; OLMSTED COUNTY; DOUBLE-BLIND; TOCILIZUMAB; TRIAL; ASSOCIATION; INFECTIONS;
D O I
10.1177/1759720X221096366
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although great improvements have been achieved in the fields of diagnosing and treating patients with giant-cell arteritis (GCA1 in the last decades, several questions remain unanswered. The progressive increase in the number of older people, together with growing awareness of the disease and use of advanced diagnostic tools by healthcare professionals, foretells a possible increase in both prevalence and number of newly diagnosed patients with GCA in the coming years. A thorough clarification of pathogenetic mechanisms and a better definition of clinical subsets are the first steps toward a better understanding of the disease and, subsequently, toward a better use of existing and future therapeutic options. Examination of the role of different imaging techniques for GCA diagnosing and monitoring, optimization, and personalization of glucocorticoids and other immunosuppressive agents, further development and introduction of novel drugs, identification of prognostic factors for long-term outcomes and management of treatment discontinuation will be the central topics of the research agenda in years to come.
引用
收藏
页数:20
相关论文
共 148 条
[1]  
AbbVie, 2021, REPORT NO NCT0497296
[2]  
acrabstracts, ACR M ABSTRACTS
[3]   Immunosenescence and Its Hallmarks: How to Oppose Aging Strategically? A Review of Potential Options for Therapeutic Intervention [J].
Aiello, Anna ;
Farzaneh, Farzin ;
Candore, Giuseppina ;
Caruso, Calogero ;
Davinelli, Sergio ;
Gambino, Caterina Maria ;
Ligotti, Mattia Emanuela ;
Zareian, Nahid ;
Accardi, Giulia .
FRONTIERS IN IMMUNOLOGY, 2019, 10
[4]   Relapses in Patients With Giant Cell Arteritis Prevalence, Characteristics, and Associated Clinical Findings in a Longitudinally Followed Cohort of 106 Patients [J].
Alba, Marco A. ;
Garcia-Martinez, Ana ;
Prieto-Gonzalez, Sergio ;
Tavera-Bahillo, Itziar ;
Corbera-Bellalta, Marc ;
Planas-Rigol, Ester ;
Espigol-Frigole, Georgina ;
Butjosa, Montserrat ;
Hernandez-Rodriguez, Jose ;
Cid, Maria C. .
MEDICINE, 2014, 93 (05) :194-201
[5]   Increased risk of cardiovascular disease in giant cell arteritis: a general population-based study [J].
Amiri, Neda ;
De Vera, Mary ;
Choi, Hyon K. ;
Sayre, Eric C. ;
Avina-Zubieta, J. Antonio .
RHEUMATOLOGY, 2016, 55 (01) :33-40
[6]   Real-life analysis of the causes of death in patients consecutively followed for giant cell arteritis in a French centre of expertise [J].
Antonini, Luca ;
Dumont, Anael ;
Lavergne, Amandine ;
Castan, Paul ;
Barakat, Clivia ;
Gallou, Sophie ;
Sultan, Audrey ;
Deshayes, Samuel ;
Aouba, Achille ;
de Boysson, Hubert .
RHEUMATOLOGY, 2021, 60 (11) :5080-5088
[7]  
ard, ANN RHEUM DIS
[8]  
Bari Syed Farhan, 2013, BMJ Case Rep, V2013, DOI 10.1136/bcr-2013-010423
[9]   High incidence of severe ischaemic complications in patients with giant cell arteritis irrespective of platelet count and size, and platelet inhibition [J].
Berger, C. T. ;
Wolbers, M. ;
Meyer, P. ;
Daikeler, T. ;
Hess, C. .
RHEUMATOLOGY, 2009, 48 (03) :258-261
[10]   Update on the epidemiology, risk factors, and outcomes of systemic vasculitides [J].
Berti, Alvise ;
Dejaco, Christian .
BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY, 2018, 32 (02) :271-294