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Abstract
There is no data in the available literature on the description of juvenile idiopathic arthritis in the indigenous peoples of the North of Yakutia.
Objective: to describe the clinical characteristics, therapy, and outcomes of juvenile idiopathic arthritis (JIA) in children of indigenous peoples of the North (IPN) living in the Republic of Sakha (Yakutia).
Materials and methods: The study included data from 8 children of IPN with a diagnosis of JIA who were examined and treated in the cardiorheumatology department of the Pediatric Center of the Republican Hospital N 1 – the National Center of Medicine named after M.E. Nikolaev in 2016-2023. The methods of descriptive statistics are used in the work.
Results and discussion. Enthesitis-associated arthritis (EAA) dominates in the structure of the incidence of JIA in children with IPN (62,5%). A high frequency of HLA-B27 carriers (62,5%) was revealed. The onset of the disease is relatively late (the average age is 9,6 years). The joints of the lower extremities are mainly affected, and there is a high incidence of sacroiliitis. The severe course of the disease is characterized by low efficacy or poor tolerance of methotrexate, which required the appointment of genetically engineered biological drugs (GEBD) in 87,5% of cases.
Conclusion. In children of INP living in the Arctic and northern regions of the Republic of Sakha (Yakutia), JIA is characterized by pronounced clinical and genetic specificity: the predominance of HLA-B27-associated forms (EAA), late onset, frequent development of sacroiliitis and severe course of articular syndrome. The revealed resistance to methotrexate therapy and the high efficacy of TNF-α inhibitors justify the expediency of early administration of GEBD to achieve stable remission and prevent disability.
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