Abstract

Background:Axial spondyloarthritis (axSpA) is a chronic inflammatory condition affecting mainly axial skeleton. The disease usually starts in early adulthood and cause considerable impact on physical function, work ability and quality of life (QoL). With the introduction of tumour necrosis factor inhibitors (TNFi) significant improvement in articular and extra-articular manifestations of disease was shown in randomized controlled trials and several registries. However, there is limited data about the effects of TNFi therapy on QoL and the relationship between inflammation and QoL in cohort studies before.Objectives:To evaluate the influence of TNFi agents on different aspects of QoL which might be a significant determinant of patient burden in axSpA patients in parallel with disease activity.Methods:In total 83 TNFi naïve axSpA patients (62.7% male; mean age 40.6 ± 12 years) according to the ASAS criteria were included in this prospective observational cohort study between 2014-2018. Demographic and disease related characteristics were collected at baseline. Disease activity (BASDAI, ASDAS-CRP), function (BASFI) and QoL (SF-36 and ASQoL) were evaluated at baseline and 24thand 52ndweeks of follow-up. The changes in disease activity, function and QoL were assessed with Wilcoxon test and relationship between changes in QoL and activity on week 24 was evaluated by Spearman’s correlation analysis.Results:Baseline disease related characteristics, disease activity and QoL scores were presented in table 1. Both disease activity and QoL were significantly improved at 24thand 52thweeks (Figure 1). The change of SF-36 subscales and summary scores at weeks 24 were correlated with the change in disease activity and function (Table 2). The SF-36 scale and summary scores were found to be similar at 24 and 52 weeks of TNFi treatment (Figure 2).Conclusion:The results of the present study suggest that TNFi treatment have a substantial influence on QoL in parallel to the control of disease activity at 24thweeks of treatment and this effect was sustained at 52 weeks not only randomized controlled trials but also real life experience.Table 1.Demographic and clinical features in patients with axial spondyloarthritis at baselineParametersDuration of disease, years*9 (10)Ever smoking, n(%)36 (43.4)Body mass index, kg/m2 *26 (4.9)HLA-B27 positivity, n(%)39/57 (68)Peripheral arthritis, n(%)39 (47)BASFI*5.1 (2.3)BASDAI*5.8 (1.7)ASQOL*12 (8)ASDAS-CRP*3.6 (1.1)PCS*32.5 (7.9)MCS*37.3 (10.9)*All parameters presented as mean (SD)Table 2.Correlation with changing of disease activity scores and quality of life parameters at 24 weeksΔBASDAIΔBASFIΔASDAS-CRPΔASQOLprprPrprΔPCS<0.001-.60<0.001-.43<0.001-.45.002-.39ΔMCS.001-.42.012-.31.019-.29<0.001-.50ΔPF<0.001-.48<0.001-.52.008-.31.021-.28ΔRP<0.001-.48.028-.25.001-.38.002-.35ΔBP<0.001-.60.004-.33<0.001-.45<0.001-.46ΔGH<0.001-.58.026-.27<0.001-.45<0.001-.54ΔVT<0.001-.48.001-.39.004-.33.003-.34ΔSF.001-.38.064-.21.098-.19.008-.31ΔRE.003-.34.013-.28.012-.29.004-.34ΔMH.003-.34.016-.28.044-.23<0.001-.43BASDAI Bath Ankylosing Spondylitis Activity Index; BASFI Bath Ankylosing Spondylitis Functional Index; ASDAS-CRP Ankylosing Spondylitis Disease Activity Score with CRP; ASQOL Ankylosing Spondylitis Quality of Life Questionnaire; PCS Physical Component Summary Sscore; MCS Mental Component Summary Score.; PF Physical Functioning; RP Role Physical; BP Bodily Pain; GH General Health; VT vitality; SF Social Functioning; RE Role Emotional; MH Mental HealthΔ Changing according to basal values at week 24Figure 1.Improvement in disease activity and quality of life during the follow-up timeFigure 2.Mean change in Short Form 36 scores for patients with axial spondyloarthritis following anti-TNF therapyDisclosure of Interests:None declared

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