A new integral enthesial-comorbididity index of psoriatic arthritis activity

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Abstract

Aim. To develop an integral index of psoriatic arthritis (PsA) activity.

Materials and methods. 117 patients with PsA (M/F – 63/54) were included. Patients’ age 44±11 years, psoriasis (Ps) duration – 213±153 months, PsA duration – 73.4±78.5 months. Patients underwent standard clinical examination of PsA activity: tender (out of 68) and swollen (out of 66) joint counts (TJC, SJC), LEI, tenderness of the plantar fascia (PF), skin lesion severity (BSA), presence of nail Ps, body mass index (BMI), erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), DAPSA, FACIT-F. Parametric and nonparametric statistic methods, correlation and ROC analysis were used.

Results. Mean DAPSA was 38±21, TJC – 14.2±10.6, SJC – 10.6±8.3, ESR – 30.5±29.5 mm/h, CRP – 23.3±29 mg/l, LEI – 1.2±1.5, FACIT-F – 32±11, BMI – 27.4±6.2 kg/m2. The following significant positive correlations were revealed: between DAPSA and BMI, patients’ age, ESR, PsA and Ps duration, TJC, SJC, LEI, presence of PF enthesitis, skin lesion severity, presence of nail Ps. A negative correlation between FACIT-F and male sex was found. Based on the predictive model of parameters, the Entesial-Comorbid Index of PsA (ECIPsA) was created: 3.81×LEI+13.72×PF+0.54×Age-0.25×FACIT-F+7.36×BSA+7.94×PsA duration+5.5×Nail Ps+0.32×BMI-3.52, namely LEI – Leeds Enthesial Index; PF – pain in the PF; patient’s age; FACIT-F – fatigue scale; BSA<3%=0, ≥3%=1; PsA duration≤2 years=0, >2 years=1; presence of nail Ps=1, absence=0; ECIPsA≥28 corresponds with high PsA activity according to DAPSA≥28. ROC analysis of sensitivity and specificity of the prognostic model demonstrated high correctness of the index: the area under the ROC curve was 0.768, 95% confidence interval (0.624–0.913).

Conclusion. The new PsA activity index corresponds to the existing ones and takes into consideration the clinical heterogeneity and comorbidity of the disease.

About the authors

Yulia L. Korsakova

Nasonova Research Institute of Rheumatology

Author for correspondence.
Email: yulkorsakova@bk.ru
ORCID iD: 0000-0001-5968-2403

кандидат медицинских наук, старший научный сотрудник лаборатории псориатического артрита

Russian Federation, Moscow

Tatiana V. Korotaeva

Nasonova Research Institute of Rheumatology

Email: yulkorsakova@bk.ru
ORCID iD: 0000-0003-0579-1131

доктор медицинских наук, начальник отд. Спондилоартритов

Russian Federation, Moscow

Elena Yu. Loginova

Nasonova Research Institute of Rheumatology

Email: yulkorsakova@bk.ru
ORCID iD: 0000-0001-6875-4552

кандидат медицинских наук, старший научный сотрудник лаборатории псориатического

Russian Federation, Moscow

Elena E. Gubar

Nasonova Research Institute of Rheumatology

Email: yulkorsakova@bk.ru
ORCID iD: 0000-0001-5015-7143

кандидат медицинских наук, научный сотрудник лаборатории псориатического артрита

Russian Federation, Moscow

Lyubov D. Vorobyeva

Nasonova Research Institute of Rheumatology

Email: yulkorsakova@bk.ru
ORCID iD: 0000-0001-8626-8419

кандидат медицинских наук, младший научный сотрудник лаборатории псориатического артрита

Russian Federation, Moscow

Svetlana I. Glukhova

Nasonova Research Institute of Rheumatology

Email: yulkorsakova@bk.ru
ORCID iD: 0000-0002-4285-0869

кандидат физ.-мат. наук, старший научный сотрудник лаборатории эволюции ревматоидного артрита

Russian Federation, Moscow

Evgeny L. Nasonov

Nasonova Research Institute of Rheumatology; Sechenov First Moscow State Medical University (Sechenov University)

Email: yulkorsakova@bk.ru
ORCID iD: 0000-0002-1598-8360

академик РАН, доктор медицинских наук, профессор научный рук. ФГБНУ «НИИ ревматологии имени В.А. Насоновой», заведующий кафедрой ревматологии ФГБОУ ВО СибГМУ

Russian Federation, Moscow; Moscow

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