LABORATORY BIOMARKERS FOR ANKYLOSING SPONDYLITIS

Ankylosing spondylitis (AS) is a chronic inflammatory disease from a group of spondyloarthritis (SpA), which is characterized by lesions of the sacroiliac joints and spine with the common involvement of entheses and peripheral joints in the pathological process. Advances in modern laboratory medicin...

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Main Authors: E. N. Aleksandrova, A. A. Novikov
Format: Article
Language:Russian
Published: IMA PRESS LLC 2017-03-01
Series:Научно-практическая ревматология
Subjects:
Online Access:https://rsp.mediar-press.net/rsp/article/view/2344
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author E. N. Aleksandrova
A. A. Novikov
author_facet E. N. Aleksandrova
A. A. Novikov
author_sort E. N. Aleksandrova
collection DOAJ
description Ankylosing spondylitis (AS) is a chronic inflammatory disease from a group of spondyloarthritis (SpA), which is characterized by lesions of the sacroiliac joints and spine with the common involvement of entheses and peripheral joints in the pathological process. Advances in modern laboratory medicine have contributed to a substantial expansion of the range of pathogenetic, diagnostic, and prognostic biomarkers of AS. As of now, there are key pathogenetic biomarkers of AS (therapeutic targets), which include tumor necrosis factor-α (TNF-α), interleukin 17 (IL-17), and IL-23. Among the laboratory diagnostic and prognostic biomarkers, HLA-B27 and C-reactive protein are of the greatest value in clinical practice; the former for the early diagnosis of the disease and the latter for the assessment of disease activity, the risk of radiographic progression and the efficiency of therapy. Anti-CD74 antibodies are a new biomarker that has high sensitivity and specificity values in diagnosing axial SpA at an early stage. A number of laboratory biomarkers, including calprotectin, matrix metalloproteinase-3 (MMP-3), vascular endothelial growth factor, Dickkopf-1 (Dkk-1), and C-terminal telopeptide of type II collagen (CTX II) do not well reflect disease activity, but may predict progressive structural changes in the spine and sacroiliac joints in AS. Blood calprotectin level monitoring allows the effective prediction of a response to therapy with TNF inhibitors and anti-IL-17А monoclonal antibodies. The prospects for the laboratory diagnosis of AS are associated with the clinical validation of candidate biomarkers during large-scale prospective cohort studies and with a search for new proteomic, transcriptomic and genomic markers, by using innovative molecular and cellular technologies.
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spelling doaj.art-937087b27a444cd08958d91bd71b91852023-03-22T13:45:52ZrusIMA PRESS LLCНаучно-практическая ревматология1995-44841995-44922017-03-015519610310.14412/1995-4484-2017-96-1032205LABORATORY BIOMARKERS FOR ANKYLOSING SPONDYLITISE. N. Aleksandrova0A. A. Novikov1V.A. Nasonova Research Institute of RheumatologyV.A. Nasonova Research Institute of RheumatologyAnkylosing spondylitis (AS) is a chronic inflammatory disease from a group of spondyloarthritis (SpA), which is characterized by lesions of the sacroiliac joints and spine with the common involvement of entheses and peripheral joints in the pathological process. Advances in modern laboratory medicine have contributed to a substantial expansion of the range of pathogenetic, diagnostic, and prognostic biomarkers of AS. As of now, there are key pathogenetic biomarkers of AS (therapeutic targets), which include tumor necrosis factor-α (TNF-α), interleukin 17 (IL-17), and IL-23. Among the laboratory diagnostic and prognostic biomarkers, HLA-B27 and C-reactive protein are of the greatest value in clinical practice; the former for the early diagnosis of the disease and the latter for the assessment of disease activity, the risk of radiographic progression and the efficiency of therapy. Anti-CD74 antibodies are a new biomarker that has high sensitivity and specificity values in diagnosing axial SpA at an early stage. A number of laboratory biomarkers, including calprotectin, matrix metalloproteinase-3 (MMP-3), vascular endothelial growth factor, Dickkopf-1 (Dkk-1), and C-terminal telopeptide of type II collagen (CTX II) do not well reflect disease activity, but may predict progressive structural changes in the spine and sacroiliac joints in AS. Blood calprotectin level monitoring allows the effective prediction of a response to therapy with TNF inhibitors and anti-IL-17А monoclonal antibodies. The prospects for the laboratory diagnosis of AS are associated with the clinical validation of candidate biomarkers during large-scale prospective cohort studies and with a search for new proteomic, transcriptomic and genomic markers, by using innovative molecular and cellular technologies.https://rsp.mediar-press.net/rsp/article/view/2344ankylosing spondylitisaxial spondyloarthritisgenetic polymorphismsautoantibodiesinflammation markerscytokinesangiogenic factorsbone and cartilage remodeling markers
spellingShingle E. N. Aleksandrova
A. A. Novikov
LABORATORY BIOMARKERS FOR ANKYLOSING SPONDYLITIS
Научно-практическая ревматология
ankylosing spondylitis
axial spondyloarthritis
genetic polymorphisms
autoantibodies
inflammation markers
cytokines
angiogenic factors
bone and cartilage remodeling markers
title LABORATORY BIOMARKERS FOR ANKYLOSING SPONDYLITIS
title_full LABORATORY BIOMARKERS FOR ANKYLOSING SPONDYLITIS
title_fullStr LABORATORY BIOMARKERS FOR ANKYLOSING SPONDYLITIS
title_full_unstemmed LABORATORY BIOMARKERS FOR ANKYLOSING SPONDYLITIS
title_short LABORATORY BIOMARKERS FOR ANKYLOSING SPONDYLITIS
title_sort laboratory biomarkers for ankylosing spondylitis
topic ankylosing spondylitis
axial spondyloarthritis
genetic polymorphisms
autoantibodies
inflammation markers
cytokines
angiogenic factors
bone and cartilage remodeling markers
url https://rsp.mediar-press.net/rsp/article/view/2344
work_keys_str_mv AT enaleksandrova laboratorybiomarkersforankylosingspondylitis
AT aanovikov laboratorybiomarkersforankylosingspondylitis