Lupus nephritis biomarkers

被引:85
|
作者
Soliman, Samar [1 ,2 ]
Mohan, Chandra [1 ]
机构
[1] Univ Houston, Dept Biomed Engn, 3605 Cullen Blvd, Houston, TX 77204 USA
[2] Minya Univ, Fac Med, Rheumatol & Rehabil Dept, Al Minya, Egypt
关键词
Biomarkers; Cytokines; Chemokines; Proteomics; Diagnostics; Adhesion molecules; MONOCYTE CHEMOATTRACTANT PROTEIN-1; GELATINASE-ASSOCIATED LIPOCALIN; CELL-ADHESION MOLECULES; KIDNEY INJURY MOLECULE-1; ANTI-NUCLEOSOME ANTIBODIES; STRANDED DNA ANTIBODIES; RECEPTOR FAMILY-MEMBER; BETA-D-GLUCOSAMINIDASE; RENAL-DISEASE ACTIVITY; FREE LIGHT-CHAINS;
D O I
10.1016/j.clim.2016.08.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Lupus nephritis (LN), a potentially destructive outcome of SLE, is a real challenge in the management of SLE because of the difficulty in diagnosing its subclinical onset and identifying relapses before serious complications set in. Conventional clinical parameters such as proteinuria, GFR, urine sediments, anti-dsDNA and complement levels are not sensitive or specific enough for detecting ongoing disease activity in lupus kidneys and early relapse of nephritis. There has long been a need for biomarkers of disease activity in LN. Such markers ideally should be capable of predicting early sub-clinical flares and could be used to gauge response to therapy, thus obviating the need for serial renal biopsies with their possible hazardous complications. Since urine can be readily obtained, it lends itself as an obvious biological substrate. In this review, the use of urine and serum as sources of lupus nephritis biomarkers is described, and the results of biomarker discovery studies using candidate and proteomic approaches are summarized. Published by Elsevier Inc.
引用
收藏
页码:10 / 20
页数:11
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