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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12710/28594
Title: The clinical value of enthesitis in the early diagnosis of psoriatic arthritis
Authors: Melnic, Nicolae
Issue Date: 2024
Publisher: Instituţia Publică Universitatea de Stat de Medicină şi Farmacie „Nicolae Testemiţanu” din Republica Moldova
Citation: MELNIC, Nicolae. The clinical value of enthesitis in the early diagnosis of psoriatic arthritis. In: MedEspera: the 10th Intern. Medical Congress for Stud. and Young Doctors, 24-27 April 2024: abstract book. Chișinău, 2024, p. 175. ISBN 978-9975-3544-2-4.
Abstract: Introduction. Joint diseases are one of the most common chronic diseases of society, and one of the most common is psoriatic arthritis (PsA), which is differentiated by a high incidence of enthesitis. Aim of study. Appreciation of ligamentous and muscular damage through enthesopathy in patients with psoriatic arthritis. Methods and materials. The study included 50 patients diagnosed with PsA (according to CASPAR criteria): group 1 – duration of disease <2 years (n = 24), group 2 – >2 years (n = 26); age 18-65 (51.0±3.4) years. For the evaluation of enthesitis MASES score (Maastricht Ankylosing Spondylitis Enthesitis Score) was applied. Results. Following the study, it was established that the frequency of the anatomica land clinical features of the joint syndrome was different in patients with early PsA and those with late PsA, in early PsA, unlike the late one, the oligoarticular variant was attested (41.7% and 15.3%, respectively), and less often – the spondyloarticular variant (8.3% and 19.2%), the polyarticular variant (33.3% and 38.4%), and the distal one (16.7% and 15.3%,) was found with the same frequency in both cases, while the osteolytic variant was observed only in the late stage of PsA (1.15%). Enthesities, by the MASES method, were determined with approximately the same frequency both in the early PsA group and in the group of patients with late PsA, in 10 (41.6%) and 11 (45.8%) patients, respectively (p>0.05). The mean values of MASES were higher in the late PsA group than in the early PsA 4.03±0.8 and 2.6±0.5 (p = 0.0032). In patients with early PsA, MASES was associated with the number of painful joints (r = 0.31 p = 0.03), the number of swollen joints (r = 0.29 p = 0.04), the BASDAI score (r = 0.34 p = 0.02 ) and BASFI (r = 0.39 p = 0.02), as well as the index score DAS28 (r= 0.31 p = 0.03). In patients with a longer evolution of the disease, the correlation of the MASES index only with the BASFI index was verified (r = 0.35 p = 0.02). The objectification of enthesitis was performed by musculoskeletal USG, the average value of the GUESS score in the late PsA group was 3.6 ± 0.3 compared to early 2.43 ± 0.2 (p = 0.02). Conclusion. The early stage of PsA is characterized by a marked heterogeneity of its manifestations with the particularities of the joint syndrome and damage to the tendons and ligaments – oligoarticular and polyarticular variants of the joint syndrome are more frequently attested. Enthesitis is a characteristic manifestation of early PsA, it was found in 40% of patients, and the ultrasonographic examination of the calcaneal region confirmed it more frequently than the clinical data (69% and 31%). the most common is psoriatic arthritis (PsA), which i s differentiated by a high incidence of enthesitis. Aim of study. Appreciation of ligamentous and muscular damage through enthe sopathy in patients with psoriatic arthritis. Methods and materials. The study included 50 patients diagnosed with PsA (according to CASPAR criteria): group 1 – duration of disease <2 years ( n = 24), group 2 – >2 years (n = 26); age 18-65 (51.0±3.4) years. For the evaluation of enthesitis MASES score (Maastricht Ankylosing Spondylitis Enthesitis Score) was applied. Results. Following the study, it was established that the frequency of the anatomica land clinical features of the joint syndrome was different in patient s with early PsA and those with late PsA, in early PsA, unlike the late one, the oligoarticular variant was attested (41.7% and 15.3%, respectively), and less often – the spondyloarticular varia nt (8.3% and 19.2%), the polyarticular variant (33.3% and 38.4%), and the distal one (16.7% and 15.3%,) was found with the same frequency in both cases, while the osteolytic variant was observed only in the late stage of PsA (1.15%). Enthesities, by the MASES method, were determined w ith approximately the same frequency both in the early PsA group and in the group of pa tients with late PsA, in 10 (41.6%) and 11 (45.8%) patients, respectively (p>0.05). The mean values o f MASES were higher in the late PsA group than in the early PsA 4.03±0.8 and 2.6±0.5 (p = 0.0032). In patients with early PsA, MASES was associated with the number of painful joints ( r = 0.31 p = 0.03), the number of swollen joints (r = 0.29 p = 0.04), the BASDAI score (r = 0.34 p = 0 .02 ) and BASFI (r = 0.39 p = 0.02), as well as the index score DAS28 (r= 0.31 p = 0.03). In patie nts with a longer evolution of the disease, the correlation of the MASES index only with the BASFI index was verified (r = 0.35 p = 0.02). The objectification of enthesitis was performed by musculoskeletal USG, the average value of the GUESS score in the late PsA group was 3.6 ± 0. 3 compared to early 2.43 ± 0.2 (p = 0.02). Conclusion. The early stage of PsA is characterized by a marked heter ogeneity of its manifestations with the particularities of the joint sy ndrome and damage to the tendons and ligaments – oligoarticular and polyarticular variants of the joint syndrome are more frequently attested. Enthesitis is a characteristic manifestatio n of early PsA, it was found in 40% of patients, and the ultrasonographic examination of the calcaneal reg ion confirmed it more frequently than the clinical data (69% and 31%).
metadata.dc.relation.ispartof: MedEspera: The 10th International Medical Congress for Students and Young Doctors, 24-27 April 2024, Chișinău, Republic of Moldova
URI: https://medespera.md/en/books?page=10
http://repository.usmf.md/handle/20.500.12710/28594
ISBN: 978-9975-3544-2-4
Appears in Collections:MedEspera 2024

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