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Urine Galectin-3 binding protein reflects nephritis activity in systemic lupus erythematosus

Faustini, Francesca (författare)
Division of Rheumatology, Department of Medicine Solna, Karolinska University Hospital, 59562Karolinska Institute, Stockholm, Sweden.
Idborg, Helena (författare)
Karolinska Institutet
Fuzzi, Enrico (författare)
Division of Rheumatology, Department of Medicine Solna, Karolinska University Hospital, 59562Karolinska Institute, Stockholm, Sweden.
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Larsson, Anders (författare)
Uppsala universitet,Klinisk kemi
Lie, Wen-Rong (författare)
EMD Millipore Corporation, St Louis, MO, USA.
Pötzsch, Sven (författare)
2792Merck KGaA, Darmstadt, Germany.
Okitsu, Shinji L (författare)
189697EMD Serono Research and Development Institute, Billerica, MA, USA.
Svenungsson, Elisabet (författare)
Karolinska Institutet
Gunnarsson, Iva (författare)
Karolinska Institutet
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Karolinska Institutet Division of Rheumatology, Department of Medicine Solna, Karolinska University Hospital, 59562Karolinska Institute, Stockholm, Sweden (creator_code:org_t)
2022-12-12
2023
Engelska.
Ingår i: Lupus. - : Sage Publications. - 0961-2033 .- 1477-0962. ; 32:2, s. 252-262
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • BACKGROUND: Lupus nephritis (LN) is a major and severe organ involvement in systemic lupus erythematosus (SLE), whose diagnosis and treatment necessitate to perform kidney biopsy, which is an invasive procedure. Non-invasive urine biomarkers are an active area of investigation to support LN diagnosis and management.OBJECTIVE: To investigate the role of urinary galectin-3 binding protein (u-Gal-3BP) as a candidate biomarker of renal disease in biopsy proven LN.PATIENTS AND METHODS: Levels of u-Gal-3BP were investigated in a cross-sectional fashion by ELISA in 270 subjects: 86 LN patients, 63 active SLE patients with no kidney involvement, 73 SLE patients with inactive disease and 48 age and sex-matched population-based controls (PBC). Moreover, urine samples were analysed separately by ELISA for additional markers of kidney pathology: neutrophil gelatinase-associated lipocalin (NGAL), osteopontin (OPN), kidney injury molecule-1 (KIM-1) and galectin-3 (Gal-3). The concentrations of all studied molecules were normalized to urine creatinine levels. In 10 patients, post-treatment levels of the biomarkers were measured.RESULTS: Normalized u-Gal-3BP levels were higher in LN patients compared to the other groups (p < .0001). Comparing different LN classes, u-Gal-3BP levels were higher among patients with proliferative (class III/IV) and membranous (class V) as compared to mesangial (class II) forms (p = .04). In proliferative forms, u-Gal-3BP levels correlated with the activity index in renal biopsies (r = 0.42, p = .004). Moreover, in a subset of 10 patients with repeated kidney biopsy and urine sampling before and after induction treatment, a significant decrease of u-Gal-3BP was observed (p = .03). Among the other markers, KIM-1 was also able to discriminate LN from the other groups, while NGAL, OPN and Gal-3 could not in this cohort.CONCLUSION: Given its ability to discriminate LN patients from active non-renal and inactive SLE patients, the observed correlation with the activity index in renal biopsies, and its levels declining following treatment, u-Gal-3BP shows promise as a non-invasive urinary biomarker to help detecting and to monitor renal involvement in SLE patients and should be validated in larger cohorts.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Reumatologi och inflammation (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Rheumatology and Autoimmunity (hsv//eng)

Nyckelord

Galectin-3 binding protein
Systemic lupus erythematous
lupus nephritis
urinarybiomarkers

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