Abstract Background: Imbalance and disfuntion in regulatory T-cells (Tregs) and IL-17 producer lymphocytes (Th17) have been implicated in the pathogenesis of rheumatoid arthritis (RA). Gray scale synovial proliferation (GS), power Doppler signal (pD) and bone erosions seen on high resolution muskuloskeletal ultrasound (MSUS) are hallmarks of destructive articular disease. Objective: To evaluate the association of peripheral Tregs and Th17 with MSUS findings in RA. Methods: RA patients (1987 ACR criteria) treated with disease-modifying antirheumatic drugs (DMARDs) were included. Lymphocytes were isolated and immunophenotyped by flow cytometry to investigate regulatory FoxP3+ T cells and IL-17+ cells. MSUS (MyLab 60, Esaote, Genova, Italy, linear probe 6-18 MHz) was performed on hand joints, and a 10-joint US score was calculated for each patient. Results: Data on lymphocytes subsets were avaiable for 90 patients. The majority of patients were Caucasian women with a median disease duration of 6 years (interquartile range: 2-13 years). Mean DAS28 was 4.28 (SD ± 1.64) and mean HAQ score was 1.11 (SD ± 0.83). There was no significant correlation of 10-joint GS score (rS = 0.122, 95% CI: - 0.124 to 0.336, P = 0.254) and 10-joint pD score (rS = 0.056, 95% CI: - 0.180 to 0.273, P = 0.602) with the mean percentage of peripheral Treg cells. Also, 10-joint GS score (rS = 0.083, 95% CI: - 0.125 to 0.302, P = 0.438) and 10-joint pD score 10 (rS = - 0.060, 95% CI: - 0.271 to 0.150, P = 0.575); did not correlate to Th17 profile. No association of bone erosions on MSUS with Treg and Th17 profiles (P = 0.831 and P = 0.632, respectively) was observed. Conclusion: In this first study addressing MSUS features and lymphocytes subtypes in established RA, data did not support an association of circulating Tregs and Th17 lymphocytes with inflammatory and structural damage findings on MSUS.

Abstract High-resolution musculoskeletal ultrasound (MSUS) has been increasingly employed in daily rheumatological practice and in clinical research. In rheumatoid arthritis (RA), MSUS can be now considered a complement to physical examination. This method evaluates synovitis through gray-scale and power Doppler and it is also able to identify bone erosions. The utilization of MSUS as a marker of RA activity has received attention in recent literature. Current data account for good correlation of MSUS with classical measures of clinical activity; in some instances, MSUS appears to perform even better. Diagnosis of subclinical synovitis by MSUS might help the physician in RA management. With some variation, interobserver MSUS agreement seems excellent for erosion and good for synovitis. However, lack of MSUS score standardization is still an unmet need. In this review, we describe several MSUS scores, as well as their correlation with clinical RA activity and response to therapy. Finally, we look at the relationship of MSUS with synovial tissue inflammation and discuss future perspectives for a better interpretation and integration of this imaging method into clinical practice.

Introdução: A ultrassonografia (US) tem uso recente na reumatologia, e a confiabilidade do método em pacientes com artrite reumatoide (AR) ainda está por ser definida. Objetivo: Testar, em uma pesquisa de AR, a reprodutibilidade da US musculosquelética realizada por reumatologistas com treinamento de um ano por meio da reanálise por um reumatologista com experiência no método. Pacientes e métodos: Esse estudo transversal incluiu pacientes de AR consecutivos de nosso centro terciário. O exame US foi realizado nas articulações metacarpofalângicas, articulações interfalângicas proximais e punhos. Os parâmetros avaliados foram: presença de sinovite, sinal de power Doppler (PD), erosões ósseas e alterações cartilaginosas. Um valor Kappa entre 0,20 e 0,40 foi considerado razoável; entre 0,41 e 0,60, moderado; entre 0,61 e 0,80, bom; e acima de 0,81, excelente. Resultados: Analisamos 1380 articulações de pacientes com AR (78% mulheres, 78% caucasoides). Média de idade = 58 ± 11,56 anos, duração média da doença = 9,98 ± 7,79 anos, DAS28 média = 3,82 ± 1,53 e HAQ média = 0,91 ± 0,67. A concordância de Kappa para sinovite variou de 0,30-0,70; para sinal PD, de 0,53 até a concordância absoluta; para erosões, de 0,70-0,97; para alterações cartilaginosas, de 0,28-0,63. Conclusão: Embora tenha sido obtida concordância interobservadores boa, moderada e excelente para erosões e PD, a concordância para sinovite e alterações cartilaginosas foi me-nos substancial em nossos pacientes com AR ativa. Há necessidade de novos estudos sobre a padronização da técnica de análise, objetivando a melhora da reprodutibilidade da US musculosquelética.

Introduction: Ultrasonography (US) has a recent use in Rheumatology, and the reliability of the method in rheumatoid arthritis (RA) patients has yet to be clarified. Objective: To test, in a RA survey, the reproducibility of musculoskeletal US performed by rheumatologists with one-year training through re-analysis by a Rheumatologist experienced in the method. Patients and methods: This cross-sectional study included consecutive RA patients from our tertiary center. US exam was performed in metacarpophalangeal joints, proximal interphalangeal joints, and wrists. Presence of synovitis, power Doppler (PD) signal, bone erosions, and cartilage changes comprised the US parameters evaluated. A kappa value in-between 0.20 and 0.40 was considered fair; in-between 0.41 and 0.60 was moderate; in-between 0.61 and 0.80 was good; and above 0.81 was excellent. Results: We analyzed 1,380 joints of 60 RA patients (78% females, 78% caucasoids). Mean age was 58 ± 11.56 years, mean disease duration was 9.98 ± 7.79 years, mean DAS28 was 3.82 ± 1.53, and mean HAQ was 0.91 ± 0.67. Kappa agreement for synovitis ranged from 0.30 to 0.70; for PD signal, from 0.53 to absolute agreement; for erosions, from 0.70 to 0.97; for cartilage changes, from 0.28 to 0.63. Conclusion: Although good, moderate and excellent interobserver agreement were obtained for erosions and PD, concordance for synovitis and cartilage changes were less impressive in our patients with active RA. Further studies on standardization of scanning technique are necessary to improve musculoskeletal US reproducibility.

Recentemente, vem-se atribuindo uma influência benéfica dos antimaláricos no perfil lipídico de pacientes com lúpus eritematoso sistêmico (LES). Neste estudo transversal, avaliamos o efeito da cloroquina nos níveis de colesterol de uma população brasileira com LES. O estudo avaliou 60 pacientes, 95% dos quais, mulheres, sendo a idade média 48,7 anos (DP 13,3 anos). Em 27 casos (45%), sobrepeso ou obesidade estava presente. Trinta e quatro pacientes (56,6%) usavam cloroquina em uma dosagem padrão, enquanto 33 (55%) usavam corticosteroides. Hipercolesterolemia foi detectada em 26 pacientes (43,3%), e baixos níveis de colesterol HDL em 18 (30%). Colesterolemia normal foi observada igualmente em usuários e não usuários de antimaláricos (P > 0,20). Após ajuste para a ingestão de estatina e corticosteroide através de análise multivariada, os níveis de colesterol total e colesterol HDL não diferiram significativamente em usuários e não usuários de cloroquina (P > 0,05). A ingestão de cloroquina não se associou a um baixo índice de massa corporal (P = 0,314). Nossos achados sugerem que a ingestão de antimaláricos por si não distingue perfis lipídicos em pacientes com LES.

A benefi cial influence of antimalarials on lipid profile of systemic lupus erythematosus (SLE) patients has been recently claimed. In this cross-sectional study, we evaluated the effect of chloroquine on cholesterol levels of a Brazilian population with SLE. Sixty patients were studied, 95% females. Mean age was 48.7 years (SD 13.3 years). Overweight or obesity was documented in 27 cases (45%). Thirty-four patients (56.6%) were using chloroquine in standard dosage, while 33 (55%) were on corticosteroids. Hypercholesterolemia was present in 26 patients (43.3%), while low HDLcholesterol levels were seen in 18 cases (30%). Normal cholesterolemia was documented equally in users and non-users of antimalarials (P > 0.20). After adjustment for statin and corticosteroid intake by multivariate analysis, cholesterol and HDL-cholesterol levels did not significantly differ in users or non-users of chloroquine (P > 0.05). There was no association of chloroquine intake with low body mass index (P = 0.314). Our findings suggest that antimalarial intake by itself does not distinguish cholesterol profiles in SLE patients.