Early arthritis in children – first results of prospective follow up
https://doi.org/10.14412/1995-4484-2007-72-80
Abstract
Objective. To perform a prospective investigation of clinico-laboratory and sonographic picture of juvenile arthritis (JA) onset, to follow up its evolution during the first years of the disease, to prove the program of appropriate treatment.
Material and methods. 128 pts with early JA (61% girls and 39% boys aged 1,5 to 16 years) were included. Disease duration varied from 2 weeks to 6 months. General health, joint status, disease activity, functional class (Steinbroker), systemic and organ disturbances, laboratory activity indices, immunologic parameters (ANF, RF) were assessed. Antibodies to cyclic citrullinated peptide (ACCP) were evaluated in 38 pts by immunofluorescence method (IFM) with commercial kits “Axis Shild Diagnostics Limited, UK”, antibodies to modified citrullinated vimentin (MCV) were assessed in 60 pts by IFM with commercial kits “Orgentec” (Germany). Pts were examined every 3 months, the main investigations were repeated after 6, 12 and 24 months. Accuracy of the diagnosis was checked at every examination.
Results. Mono- oligoarticular variant of onset was found in 68,6% polyarticular – in 21,4%, systemic – in 10% of pts. Knee and ankle joints were involved first (61% and 24% respectively), later – wrist (13%) and hand joints (17%). Morning stiffness was absent in 85% of pts. 37% of pts had ANF and 13,2% - RF. 10,5% were ACCP positive and 28,3% – MCV positive. Antibodies correlated with polyarticular variant of JA and RF. Reactive arthritis was the preliminary diagnosis in 39% and JRA – in 21% of pts at inclusion. Later Juvenile chronic arthritis was the most frequent diagnosis (73-80%). Disease modifying antirheumatic drugs were prescribed early (before 6 months) in 53% of pts. Exacerbations of the disease appeared in 1/3 of pts, more frequently – in pts with polyarthritis. After 12 months functional class 1 remained in 71,4% of pts.
Conclusion. Stabilization of pathological process or remission can be achieved in most children with early JA. Pts with polyarthritis sometimes need intensification of treatment (administration of biological agents or change of DMARD. Evaluation of ACCP and MCV can be helpful for diagnosis and prognosis of the disease. Questions of diagnosis, terminology and early verification of diagnosis need further discussion.
About the Authors
S. O. SaluginaRussian Federation
N. N. Kuzmina
Russian Federation
G. R. Movsisyan
Russian Federation
E. S. Fedorov
Russian Federation
S. V. Arsenjeva
Russian Federation
E. N. Alexandrova
Russian Federation
A. A. Novikov
Russian Federation
A. A. Baranov
Russian Federation
References
1. Насонов Е.Л. Почему необходима ранняя диагностика и лечение ревматоидного артрита? РМЖ, 2002, 10,22,1009-1012.
2. Каратеев Д.Е. Фармакотерапия раннего ревматоидного артрита. Фарматека,2006, 6[121], 2006, 92-97.
3. Шостак Н.А. Ранний ревматоидный артрит и место лефлуномида в его лечении. Фарматека,2005,7, [102],52-54.
4. Emery P. Early rheumatoid arthritis. Rheum. Dis. Clin. North Am., 2005, 31,4.
5. Bowyer S.L., Roettcher P.A., Higgins G.C. et al. Health status of patients with JRA at 1 and 5 years after diagnosis. J. Rheumatol., 2003, 30, 394-400
6. Пуринь В.И. Диагноз, лечение и прогноз хронических артритов у детей. Автореф. дисс. д.м.н, С-П., 1999.
7. Michels H., Hafner R., Morhart R. et al. Five year follow-up of a prospective cohort of juvenile chronic arthritis with recent onset. Clin. Rheumatol., 1987,6,l 2,87-92.
8. Selvaag A., Lien G., Sorskaar D. et al. Early disease course and predictors of disability in juvenile rheumatoid arthritis and juvenile spondiloarthropathy: a 3 year prospective study. J. Rheumatol., 2005, 32, 1122-1130.
9. Кузьмина Н.Н., Салугина С.О., Никишина И.П. Ювенильный артрит – XXI век – как мы сегодня понимаем терминологические и классификационные аспекты? Научно-практич. pевматол., 2006,4, 86-96.
10. Fantini F., Gerloni V., Gattinara M. et al. Remission in juvenile chronic arthritis: a cohort study of 683 consecutive cases with a mean 10 year followup. J. Rheumatol., 2003, 30(3), 579-584
11. Cassidy J.T., Petty R.E. Juvenile Rheumatoid Arthritis. In: Textbook of pediatric rheumatology. 4th Edition., 2002, 218.
12. Чемерис Н.А., Насонов Е.Л. Диагностическое значение антител к циклическому цитруллинированному пептиду при ревматоидном артрите. Клинич. мед., 2005, 8,48-54.
13. Александрова Е.Н., Чемерис Н.А., Каратеев Д.Е. и др. Антитела к циклическому цитруллинированному пептиду при ревматоидном артрите. Тер. архив, 2004, 12, 64-68.
14. Avcin T., Cimaz R., Falcini F. et al. Prevalence and clinical significance of anticyclic citrullinated peptide antibodies in juvenile idiopathic arthritis Ann. Rheum. Dis., 2002, 61,608-611.
15. Kasapcopur O., Altun S., Aslan M. et al. Diagnostic accuracy of anti-cyclic citrullinated peptide antibodies in juvenile idiopathic arthritis. Ann. Rheum. Dis.,2004, 63(12),1687-1689.
16. Boehme M., Jouquan J., Blaschek M. et al. The prevalence of anti-cyclic citrullinated peptide antibodies in JIA. J.Pediatr., 2005, 81,491-494.
17. Dejaco C., Klotz W., Larcher H. et al. Diagnostic value of antibodies against a modified citrullinated vimentin arthritis. Arthr. Res.Ther., 2006, 8,119.
18. Мовсисян Г.Р., Кузьмина Н.Н., Мач Э.С. Оценка структур тазобедренного сустава при ювенильном идиопатическом (хроническом) артрите по данным ультразвуковой томографии. Научно-практич. pевматол., 2004,3, 83-88.
19. Долгополова А.В., Бисярина В.П., Алексеев Л.С. и др. Разработка критериев ранней диагностики ювенильного ревматоидного артрита (ЮРА). Вопр. ревматизма, 1979, 4, 3-7.
Review
For citations:
Salugina S.O., Kuzmina N.N., Movsisyan G.R., Fedorov E.S., Arsenjeva S.V., Alexandrova E.N., Novikov A.A., Baranov A.A. Early arthritis in children – first results of prospective follow up. Rheumatology Science and Practice. 2007;45(4):72-80. (In Russ.) https://doi.org/10.14412/1995-4484-2007-72-80