What have we learned from long-term studies in juvenile idiopathic arthritis? - Prediction, classification, transition.

被引:0
作者
Rygg, Marite [1 ,2 ]
Ramos, Filipa Oliveira [3 ,4 ]
Nordal, Ellen Berit [5 ,6 ]
机构
[1] Norwegian Univ Sci & Technol NTNU, Fac Med & Hlth Sci IKOM, Dept Clin & Mol Med, Trondheim, Norway
[2] St Olavs Univ Hosp, Dept Pediat, Trondheim, Norway
[3] Hosp Univ ULS Santa Maria, Pediat Rheumatol Unit, Lisbon, Portugal
[4] Univ Lisbon, Fac Med, Lisbon, Portugal
[5] Arctic Univ Norway UiT, Dept Clin Med, Tromso, Norway
[6] Univ Hosp North Norway UNN, Dept Pediat, Tromso, Norway
关键词
Juvenile idiopathic arthritis; Adult; Outcome; Prediction; Classification; Transition; DISEASE COURSE; FOLLOW-UP; RHEUMATOID-ARTHRITIS; SELECT CATEGORIES; YOUNG-ADULTS; COHORT; CHILDREN; CRITERIA; HEALTH; CARE;
D O I
10.1186/s12969-025-01070-x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
BackgroundResearch and management of juvenile idiopathic arthritis (JIA) are challenging due to its heterogeneous nature, chronicity, and unpredictable, multidimensional long-term outcomes.Main bodyLong-term studies have consistently shown that a majority of children with JIA reach adulthood with ongoing disease activity, on medication, or with recurrent flares. The heterogeneity is evident both between and within the present JIA categories based on The International League of Associations for Rheumatology (ILAR) JIA classification system. Several baseline predicting factors are known, but prediction modelling is only in the initial phase, and more models need to be tested in independent cohorts and possibly also supplemented with new biomarkers. Many have criticized the ILAR classification system, but new or updated classification systems have not yet been validated and proved their superiority. The lack of prediction possibilities for long-term outcomes and the limited alignment between JIA classification categories and adult rheumatic conditions are challenges for research, may limit the accessibility to treatment, and hamper a smooth transition to adult care.ConclusionWe need more prospective, long-term studies based on unselected JIA cohorts with disease onset in the biologic era that can aid decision-making for individualized early treatment, suggest intervention studies, and ensure our patients the best possible transition to adulthood and the best likelihood of optimal health and quality of life.
引用
收藏
页数:10
相关论文
共 82 条
[1]   Distinctions Between Diagnostic and Classification Criteria? [J].
Aggarwal, Rohit ;
Ringold, Sarah ;
Khanna, Dinesh ;
Neogi, Tuhina ;
Johnson, Sindhu R. ;
Miller, Amy ;
Brunner, Hermine I. ;
Ogawa, Rikke ;
Felson, David ;
Ogdie, Alexis ;
Aletaha, Daniel ;
Feldman, Brian M. .
ARTHRITIS CARE & RESEARCH, 2015, 67 (07) :891-897
[2]   Favourable social functioning and health related quality of life of patients with JIA in early adulthood [J].
Arkela-Kautiainen, M ;
Haapasaari, J ;
Kautiainen, H ;
Vilkkumaa, I ;
Mälkiä, E ;
Leirisalo-Repo, M .
ANNALS OF THE RHEUMATIC DISEASES, 2005, 64 (06) :875-880
[3]   Fatigue in young adults with juvenile idiopathic arthritis 18 years after disease onset: data from the prospective Nordic JIA cohort [J].
Arnstad, Ellen Dalen ;
Glerup, Mia ;
Rypdal, Veronika ;
Peltoniemi, Suvi ;
Fasth, Anders ;
Nielsen, Susan ;
Zak, Marek ;
Aalto, Kristiina ;
Berntson, Lillemor ;
Nordal, Ellen ;
Herlin, Troels ;
Romundstad, Pal Richard ;
Rygg, Marite .
PEDIATRIC RHEUMATOLOGY, 2021, 19 (01)
[4]   Early Self-Reported Pain in Juvenile Idiopathic Arthritis as Related to Long-Term Outcomes: Results From the Nordic Juvenile Idiopathic Arthritis Cohort Study [J].
Arnstad, Ellen Dalen ;
Rypdal, Veronika ;
Peltoniemi, Suvi ;
Herlin, Troels ;
Berntson, Lillemor ;
Fasth, Anders ;
Nielsen, Susan ;
Glerup, Mia ;
Ekelund, Maria ;
Zak, Marek ;
Aalto, Kristiina ;
Nordal, Ellen ;
Romundstad, Pal Richard ;
Rygg, Marite ;
Marhaug, Gudmund ;
Anderson-Gare, Boel ;
Pedersen, Freddy Karup ;
Lahdenne, Pekka ;
Pelkonen, Pirkko .
ARTHRITIS CARE & RESEARCH, 2019, 71 (07) :961-969
[5]   Long-Term Health-Related Quality of Life in German Patients with Juvenile Idiopathic Arthritis in Comparison to German General Population [J].
Barth, Swaantje ;
Haas, Johannes-Peter ;
Schlichtiger, Jenny ;
Molz, Johannes ;
Bisdorff, Betty ;
Michels, Hartmut ;
Huegle, Boris ;
Radon, Katja .
PLOS ONE, 2016, 11 (04)
[6]   HLA-B27 Predicts a More Chronic Disease Course in an 8-year Followup Cohort of Patients with Juvenile Idiopathic Arthritis [J].
Bemtson, Lillemor ;
Nordal, Ellen ;
Aalto, Kristiina ;
Peltoniemi, Suvi ;
Herlin, Troels ;
Zak, Marek ;
Nielsen, Susan ;
Rygg, Marite .
JOURNAL OF RHEUMATOLOGY, 2013, 40 (05) :725-731
[7]  
Berntson L, 2003, J RHEUMATOL, V30, P2275
[8]  
Berntson L, 2001, J RHEUMATOL, V28, P2737
[9]   Anti-type II collagen antibodies, anti-CCP, IgA RF and IgM RF are associated with joint damage, assessed eight years after onset of juvenile idiopathic arthritis (JIA) [J].
Berntson, Lillemor ;
Nordal, Ellen ;
Fasth, Anders ;
Aalto, Kristiina ;
Herlin, Troels ;
Nielsen, Susan ;
Rygg, Marite ;
Zak, Marek ;
Ronnelid, Johan .
PEDIATRIC RHEUMATOLOGY, 2014, 12
[10]   The risk of depression and anxiety is not increased in individuals with juvenile idiopathic arthritis - results from the south-Swedish juvenile idiopathic arthritis cohort [J].
Berthold, Elisabet ;
Dahlberg, Alma ;
Joud, Anna ;
Tyden, Helena ;
Mansson, Bengt ;
Kahn, Fredrik ;
Kahn, Robin .
PEDIATRIC RHEUMATOLOGY, 2022, 20 (01)