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Urine soluble triggering receptor expressed on myeloid cells-1 is a novel biomarker for active lupus nephritis: a case-control study


1, 2, 3, 4, 5, 6, 7, 8

 

  1. Institute of Rheumatology and Laboratory of Inflammation Research, Felsenstein Medical Research Center, Petah Tikva; Rabin Medical Center, Beilinson Hospital, Petah Tikva; and Sackler Faculty of Medicine, Tel Aviv University, Israel. ymolad@clalit.org.il
  2. Rabin Medical Center, Beilinson Hospital, Petah Tikva, and Department of Medicine B, Ha’emek Medical Center, Faculty of Medicine, Israel Institute of Technology, Afula, Israel.
  3. Sackler Faculty of Medicine, Tel Aviv University, and Department of Pathology, Rabin Medical Center, Beilinson Hospital, Petah Tikva, Israel.
  4. Rabin Medical Center, Beilinson Hospital, Petah Tikva, and Sackler Faculty of Medicine, Tel Aviv University, Israel.
  5. Rabin Medical Center, Beilinson Hospital, Petah Tikva, and Sackler Faculty of Medicine, Tel Aviv University, Israel.
  6. Rabin Medical Center, Beilinson Hospital, Petah Tikva, and Sackler Faculty of Medicine, Tel Aviv University, Israel.
  7. Rabin Medical Center, Beilinson Hospital, Petah Tikva, and Department of Medicine B, Assuta Ashdod University Medical Center, Ben-Gurion University of the Negev, Ashdod, Israel.
  8. Laboratory of Inflammation Research, Felsenstein Medical Research Center, Rabin Medical Center, Petah Tikva, and Sackler Faculty of Medicine, Tel Aviv University, Israel.

CER15761
2023 Vol.41, N°5
PI 1155, PF 1162
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PMID: 36622114 [PubMed]

Received: 10/04/2022
Accepted : 26/09/2022
In Press: 04/01/2023
Published: 03/05/2023

Abstract

OBJECTIVES:
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).
CONCLUSIONS:
Urine sTREM-1 might serve as a potential biomarker of active renal SLE.

DOI: https://doi.org/10.55563/clinexprheumatol/4lvaye

Rheumatology Article