Lúpus Eritematoso Sistêmico: o que o clínico precisa saber
Palavras-chave:
Lúpus eritematoso sistêmico, critérios de classificação, desfechos, autoanticorposResumo
Lúpus eritematoso sistêmico (lúpus) é uma doença crônica, autoimune, sistêmica, caracterizada pela sua heterogeneidade clínica, curso imprevisível e períodos de agudização. Novos critérios de classificação elaborados pela associação entre a Liga Europeia Contra o Reumatismo (EULAR) e o Colégio Americano de Reumatologia (ACR) foram publicados em 2019 e permitem a sua detecção precoce e mais precisa. Vários endótipos da doença têm sido reconhecidos ao longo dos anos. Há progressiva identificação de casos leves na sua apresentação, mas quase 50% destes progride para formas mais graves. As metas de tratamento incluem a sobrevivência do paciente a longo prazo, prevenção de agudização e da instalação de danos crônicos irreversíveis, além de otimização de qualidade de vida relacionada à saúde. O tratamento se caracteriza pela terapia imunossupressora de alta intensidade para controlar a atividade da doença, seguido por um período mais longo de terapia menos intensiva para consolidar a resposta e evitar recaídas. O manejo das morbidades associadas, especialmente infecções e aterosclerose, é de suma importância. Novos agentes imunossupressores sintéticos ou biológicos – utilizados isoladamente ou em combinação, ou sequencialmente, melhoraram as chances de se alcançar as metas terapêuticas tanto a curto prazo quanto a longo prazo, incluindo minimização de uso de glicocorticoide.
Referências
Bertsias GK, Salmon JE, Boumpas DT. Therapeutic opportunities in systemic lupus erythematosus: state of the art and prospects for the new decade. Ann Rheum Dis 2010; 69:1603-11.
Smith CD, Cyr M. The history of lupus erythematosus from Hippocrates to Osler. Rheum Dis Clin North Am 1988; 14:1-14.
Mallavarapu RK, Grimsley EW. The history of lupus erythematosus. South Med J 2007; 100:896-8.
Gergianaki I, Fanouriakis A, Repa A, et al. Epidemiology and burden of systemic lupus erythematosus in a southern European population: data from the community-based lupus Registry of Crete, Greece. Ann Rheum Dis 2017; 76:1992-2000.
Nikolopoulos DS, Kostopoulou M, Pieta A, et al. Transition to severe phenotype in systemic lupus erythematosus initially presenting with non-severe disease: implications for the management of early disease. Lupus Sci Med 2020; 7.
Carter EE, Barr SG, Clarke AE. The global burden of SLE: prevalence, health disparities and socioeconomic impact. Nat Rev Rheumatol 2016; 12:605-20.
Kuo C-F, Grainge MJ, Valdes AM, et al. Familial aggregation of systemic lupus erythematosus and coaggregation of autoimmune diseases in affected families. JAMA Intern Med 2015; 175:1518.
Bertsias GK, Pamfil C, Fanouriakis A, et al. Diagnostic criteria for systemic lupus erythematosus: has the time come? Nat Rev Rheumatol 2013; 9:687-94.
Hochberg MC. Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus. Arthritis Rheum 1997; 40: 1725.
Petri M, Orbai A-M, Alarcón GS, et al. Derivation and validation of the systemic lupus international collaborating clinics classification criteria for systemic lupus erythematosus. Arthritis Rheum 2012; 64:2677-86.
Zen M, Iaccarino L, Gatto M, et al. Prolonged remission in Caucasian patients with SLE: prevalence and outcomes. Ann Rheum Dis 2015; 74:2117-22.
Tselios K, Gladman DD, Touma Z, et al. Disease course patterns in systemic lupus erythematosus. Lupus 2019; 28:114-22.
Adamichou C, Nikolopoulos D, Genitsaridi I, et al. In an early SLE cohort the ACR1997, SLICC-2012 and EULAR/ACR-2019 criteria classify non-overlapping groups of patients: use of all three criteria ensures optimal capture for clinical studies while their modification earlier classification and treatment. Ann Rheum Dis 2020; 79:232-41.
Zen M, Iaccarino L, Gatto M, et al. Lupus low disease activity state is associated with a decrease in damage progression in Caucasian patients with SLE, but overlaps with remission. Ann Rheum Dis 2018; 77:104-10.
Mikdashi J, Nived O. Measuring disease activity in adults with systemic lupus erythematosus: the challenges of administrative burden and responsiveness to patient concerns in clinical research. Arthritis Res Ther 2015; 17:183.
Gladman DD, Ibañez D, Urowitz MB. Systemic lupus erythematosus disease activity index 2000. J Rheumatol 2002; 29:288-91.
Jesus D, Matos A, Henriques C, et al. Derivation and validation of the SLE disease activity score (SLE-DAS): a new SLE continuous measure with high sensitivity for changes in disease activity. Ann Rheum Dis 2019; 78:365-71.
Fanouriakis A, et al. Update οn the diagnosis and management of systemic lupus erythematosus. Ann Rheum Dis 2021; 80:14-25.
Fanouriakis A, Kostopoulou M, Alunno A, et al. 2019 update of the EULAR recommendations for the management of systemic lupus erythematosus. Ann Rheum Dis 2019; 78:736-45.
Kostopoulou M, Nikolopoulos D, Parodis I, et al. Cardiovascular disease in systemic lupus erythematosus: recent data on epidemiology, risk factors and prevention. Curr Vasc Pharmacol 2020; 18:549-65.
Tselios K, Gladman DD, Su J, et al. Impact of the newherpes esthiomenos. American College of Cardiology/ American heart association definition of hypertension on atherosclerotic vascular events in systemic lupus erythematosus. Ann Rheum Dis 2020; 79:612-7.
Whelton PK, Carey RM, Aronow WS, et al. 2017 ACC/AHA/AAPA/ABC/ACPM/AGS/ APhA/ASH/ASPC/NMA/PCNA guideline for the prevention, detection, evaluation, and management of high blood pressure in adults. J Am Coll Cardiol 2018; 71: e127-248.
Tektonidou MG, Lewandowski LB, Hu J, et al. Survival in adults and children with systemic lupus erythematosus: a systematic review and Bayesian meta-analysis of studies from 1950 to 2016. Ann Rheum Dis 2017; 76:2009-16.