TY - JOUR
T1 - Urine soluble triggering receptor expressed on myeloid cells-1 is a novel biomarker for active lupus nephritis
T2 - a case-control study
AU - Molad, Y.
AU - Egbaria, M.
AU - Tovar, A.
AU - Dortort Lazar, A.
AU - Pokroy Shapira, E.
AU - Oren, S.
AU - Edel, Y.
AU - Kliminski, V.
N1 - Publisher Copyright:
© 2023 Clinical and Experimental Rheumatology S.A.S.. All rights reserved.
PY - 2023/5
Y1 - 2023/5
N2 - Objective To determine the value of plasma and urine sTREM-1 levels as a biomarker of lupus nephritis (LN) as well as extra-renal systemic lupus erythematosus (SLE). Methods Consecutive adult patients with SLE attending a tertiary lupus clinic in 2016–2018 were prospectively divided into 3 groups according to SLEDAI-2K and renal-SLEDAI scores: active renal lupus (ARL), active non-renal lupus (ANL), and inactive lupus (IL). Blood and spot urine samples from each group and matched healthy subjects were analysed by means of ELISA for plasma and urine sTREM-1 levels. Results The cohort included 59 patients (mean age 41.5+2.9 years, 85% female) with SLE: 15 ARL, 14 ANL, and 30 IL. The ARL group had higher scores on the SLEDAI-2K and renal-SLEDAI, and higher urine protein/creatinine ratio than the other patient groups (p=0.0001 for all). Plasma sTREM-1 level was highest in the ANL group (p=0.0085). Urine sTREM-1 level was higher in the whole SLE cohort than the healthy controls (p=0.0249), and higher in the ARL group than the others (p=0.0044). Neither plasma nor urine sTREM-1 level was associated with non-renal SLE features. On Spearman correlation analysis, urine sTREM-1 level, but not plasma sTREM-1 level, was correlated positively with renal-SLEDAI score (r=0.34, p=0.018), inversely with serum C3 and C4 levels (r=-0.42, p=0.0027 and r=-0.28, p=0.056, respectively), and positively with proteinuria (UPCR: r=0.32, p=0.0305). Conclusion Urine sTREM-1 might serve as a potential biomarker of active renal SLE.
AB - Objective To determine the value of plasma and urine sTREM-1 levels as a biomarker of lupus nephritis (LN) as well as extra-renal systemic lupus erythematosus (SLE). Methods Consecutive adult patients with SLE attending a tertiary lupus clinic in 2016–2018 were prospectively divided into 3 groups according to SLEDAI-2K and renal-SLEDAI scores: active renal lupus (ARL), active non-renal lupus (ANL), and inactive lupus (IL). Blood and spot urine samples from each group and matched healthy subjects were analysed by means of ELISA for plasma and urine sTREM-1 levels. Results The cohort included 59 patients (mean age 41.5+2.9 years, 85% female) with SLE: 15 ARL, 14 ANL, and 30 IL. The ARL group had higher scores on the SLEDAI-2K and renal-SLEDAI, and higher urine protein/creatinine ratio than the other patient groups (p=0.0001 for all). Plasma sTREM-1 level was highest in the ANL group (p=0.0085). Urine sTREM-1 level was higher in the whole SLE cohort than the healthy controls (p=0.0249), and higher in the ARL group than the others (p=0.0044). Neither plasma nor urine sTREM-1 level was associated with non-renal SLE features. On Spearman correlation analysis, urine sTREM-1 level, but not plasma sTREM-1 level, was correlated positively with renal-SLEDAI score (r=0.34, p=0.018), inversely with serum C3 and C4 levels (r=-0.42, p=0.0027 and r=-0.28, p=0.056, respectively), and positively with proteinuria (UPCR: r=0.32, p=0.0305). Conclusion Urine sTREM-1 might serve as a potential biomarker of active renal SLE.
KW - SLE Disease Activity Index (SLEDAI)
KW - biomarker
KW - lupus nephritis
KW - systemic lupus erythematosus
KW - triggering receptor expressed on myeloid cells-1 (TREM-1)
UR - http://www.scopus.com/inward/record.url?scp=85159547370&partnerID=8YFLogxK
U2 - 10.55563/clinexprheumatol/4lvaye
DO - 10.55563/clinexprheumatol/4lvaye
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C2 - 36622114
AN - SCOPUS:85159547370
SN - 0392-856X
VL - 41
SP - 1155
EP - 1162
JO - Clinical and Experimental Rheumatology
JF - Clinical and Experimental Rheumatology
IS - 5
ER -