Abstract

Rheumatoid arthritis (RA) is the second most common rheumatic disease. In recent decades, there has been an active search for and study of biologically active substances involved in the pathogenesis of RA, which can serve as a starting point in designing new drugs for targeted therapy of this disease. The hepatokine fetuin-A (FA) is one of these substances.Objective: to investigate serum FA levels in patients with RA.Subjects and methods. The investigation enrolled 110 patients with RA. All the patients underwent the following set of studies: general blood test and determination of the serum levels of C-reactive protein (CRP), serum FA, rheumatoid factor, anti-cyclic citrullinated peptide (anti-CCP) antibodies, cartilage degradation products (CartiLaps), and urine creatinine. A control group consisted of 30 apparently healthy individuals whose serum FA level was determined in order to obtain reference values.Results and discussion. The normal FA level varied from 653.55 to 972.19 μg/ml. All the patients with RA were divided into two groups: 1) 23 patients with a low FA level (<653.55 μg/ml) and 2) 87 patients with a normal FA levels (≥653.55 μg/ml). The groups differed significantly in anti-CCP antibody concentrations, disease activity, radiological stages, functional classes, and the presence of complications. Patients with lower FA levels were noted to have increased CRP concentrations, erythrocyte sedimentation rate, and CartiLaps/urine creatinine ratio. The mean FA concentration was considerably and significantly lower in patients with higher DAS28 scores. Conclusion. Our investigation has revealed that there is a relationship between the levels of FA and the individual clinical manifestations of RA. The lower FA level is associated with higher disease activity and the aggressive phenotype of RA (the presence of anti-CCP antibodies, radiological stages III and IV, extra-articular manifestations and complications).

Highlights

  • ФГБНУ «Научноисследовательский институт клинической и экспериментальной ревматологии им

  • There has been an active search for and study of biologically active substances involved in the pathogenesis of RA, which can serve as a starting point in designing new drugs for targeted therapy of this disease

  • A control group consisted of 30 apparently healthy individuals whose serum FA level was determined in order to obtain reference values

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Summary

Оригинальные исследования

Папичев Е.В., Заводовский Б.В., Сивордова Л.Е., Ахвердян Ю.Р., Полякова Ю.В. ФГБНУ «Научноисследовательский институт клинической и экспериментальной ревматологии им. Цель исследования – изучить уровень ФА в сыворотке больных РА, а также его взаимосвязи с клинико-иммунологическими особенностями РА, лабораторными маркерами воспалительной активности и деструкции суставного хряща. Всем пациентам проводился следующий набор исследований: общеклинический анализ крови, определение уровня С-реактивного белка (СРБ; тест-система hs-CRP EIA, BIOMERICA, США), ФА сыворотки крови (тест-система Human Fetuin-A ELISA, BioVendor, Чехия), ревматоидного фактора (РФ), антител к циклическим цитруллинированным пептидам (АЦЦП; тест-система Anti-CCP hs ELISA-based, ORGENTEC Diagnostika GmbH, Германия), CartiLaps мочи (тест-система UrineCartilaps EIA; IDS, Германия) и креатинина мочи. Нормальный уровень ФА был рассчитан по фор- фазового ответа (СРБ и СОЭ) и дегенерации хряща муле M±2σ в группе условно здоровых лиц и составил (CartiLaps/креатинин мочи) с уровнем ФА представлена от 653,55 до 972,19 мкг/мл. 900 p=0,14 p

Средний уровень ФА у больных
III IV
Findings
Взаимосвязь уровня ФА с показателями углеводного обмена и ИМТ
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