Diagnosis and management of cardiovascular risk in rheumatoid arthritis: main challenges and research agenda

被引:2
|
作者
Atzeni, Fabiola [1 ]
Maiani, Silvia [2 ]
Corda, Marco [3 ]
Rodriguez-Carrio, Javier [4 ,5 ]
机构
[1] Univ Messina, Dept Expt & Internal Med, Rheumatol Unit, Messina, Italy
[2] Univ Cagliari, Dept Med Sci & Publ Hlth, Clin Cardiol, Cagliari, Italy
[3] SC Cardiol UTIC, ARNAS, G Brotzu, Cagliari, Italy
[4] Univ Oviedo, Fac Med, Dept Funct Biol, Area Immunol, Oviedo, Spain
[5] Inst Invest Sanitaria Principado Asturias ISPA, Area Metab, Oviedo, Spain
关键词
Algorithms; antibodies; atherosclerosis; cardiovascular risk; imaging; inflammation; lipoproteins; rheumatoid arthritis; ENDOTHELIAL PROGENITOR CELLS; ACUTE MYOCARDIAL-INFARCTION; C-REACTIVE PROTEIN; GENERAL-POPULATION; FOLLOW-UP; SYSTEMIC INFLAMMATION; PRIMARY-CARE; DISEASE; EVENTS; ATHEROSCLEROSIS;
D O I
10.1080/1744666X.2023.2170351
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IntroductionRheumatoid arthritis (RA) exhibit a cardiovascular (CV) risk that is 1.5-2.0 times higher compared to the general population. This CV risk excess is likely caused by the involvement of chronic inflammation and immune dysregulation. Therefore, conventional algorithms and imaging techniques fail to fully account for this risk excess and provide a suboptimal risk stratification, hence limiting clinical management in this setting.Areas coveredCompelling evidence has suggested a role for adaptations of conventional algorithms (Framingham, SCORE, AHA, etc) or the development of RA-specific algorithms, as well as the use of a number of several, noninvasive imaging techniques to improve CV risk assessment in RA populations. Similarly, in-depth analyses of atherosclerosis pathogenesis in RA patients have shed new light into a plethora of soluble biomarkers (such as inflammatory cytokines, vascular remodeling mediators or autoantibodies) that may provide incremental value for CV risk stratification.Expert opinionExtensive research has demonstrated a lack of performance of chart adaptations in capturing real CV risk in RA population, as well as for RA-specific algorithms. Similarly, limitations have been detected in the use of soluble mediators. The development of a novel, RA-specific algorithm including classical and non-traditional risk factors may be advisable.
引用
收藏
页码:279 / 292
页数:14
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