Monitoring Lupus Nephritis Through Urinary Extracellular Vesicles
NCT ID: NCT06642402
Last Updated: 2025-09-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
40 participants
OBSERVATIONAL
2024-11-15
2030-05-01
Brief Summary
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Detailed Description
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Hypothesis: The primary objective of this prospective study is to investigate the utility of urinary exosomes as non-invasive biomarkers for monitoring the activity and progression of lupus nephritis.
Methods: SLE patients, fulfilling the 2019 EULAR/ACR classification criteria, referred to kidney biopsy, will be recruited from Department of Rheumatology and Department of Nephrology at Odense University Hospital. Detailed demographic and clinical data including age, sex, ethnicity, medicine, duration of SLE activity, SLE damage and laboratory results will be collected from each patient. Activity of SLE at the time of biopsy will be evaluated using SLE disease activity index 2000 (SLEDAI-2K). SLE damage will be evaluated in accordance with the SLICC damage index. Spot-urine samples will be collected, added protease-inhibitors and frozen at -80 degree. UEVs will be isolated using polyethylene glycol (PEG) precipitation, the concentration of uEV will be determined and protein accessed using western blotting and/or PCR. Glomerular specific uEVs will be isolated and previous developed tests will be applied to detect the membrane attack complex (MAC)/C5b-9 complex. uEVs from plasma/serum will be isolated to test for correlation with uEVs. Kidney biopsies will be histological analyzed at Department of Pathology by experienced nephropathologists according to existing clinical guidelines. Differences in uEV cargo between SLE patients with and without lupus nephritis will be analyzed using appropriate statistical tests. Correlations between uEV biomarkers, histological differences on the kidney biopsy and disease activity will be evaluated using Pearson's correlation analysis.
Perspective: This prospective study aims to establish urinary extracellular vesicles as potential non-invasive biomarkers for monitoring lupus nephritis in SLE patients. The findings from this research may lead to the development of more efficient and patient-friendly approaches for LN management, enabling timely interventions and improved renal outcomes in SLE patients.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Systemic lupus erythomatosus with lupus nephritis
SLE patients with kidney involvement
Kidney biopsy
Patient refered to kidney biopsy independent of the presented study
Urinary extracellular vesicle testing
Urinary extracellular vesicles will be isolated and tested for complement activation and other markers of kidney disease
Autoimmunity in plasma
Expected autoimmunity in plasma isolated from blood samples
Systemic lupus erythomatosus without lupus nephritis
SLE patients, fulfilling the 2019 EULAR/ACR classification criteria with no sign of kidney disease
Urinary extracellular vesicle testing
Urinary extracellular vesicles will be isolated and tested for complement activation and other markers of kidney disease
Autoimmunity in plasma
Expected autoimmunity in plasma isolated from blood samples
Healthy controls
Healthy controls
Urinary extracellular vesicle testing
Urinary extracellular vesicles will be isolated and tested for complement activation and other markers of kidney disease
Biopsy controls
A biopsy control group with no predictive complement activation referred to biopsy
Kidney biopsy
Patient refered to kidney biopsy independent of the presented study
Urinary extracellular vesicle testing
Urinary extracellular vesicles will be isolated and tested for complement activation and other markers of kidney disease
Interventions
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Kidney biopsy
Patient refered to kidney biopsy independent of the presented study
Urinary extracellular vesicle testing
Urinary extracellular vesicles will be isolated and tested for complement activation and other markers of kidney disease
Autoimmunity in plasma
Expected autoimmunity in plasma isolated from blood samples
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Fulfilling the 2019 EULAR/ACR classification criteria
* Positive autoantibodies, medical history and obejctive examination compatible with SLE
* Referred to kidney biopsy
* \> 18 years old
* Fulfilling the 2019 EULAR/ACR classification criteria
* Positive autoantibodies, medical history and obejctive examination compatible with SLE
* Normal plasma creatinine
* Urine albumine/creatinine \< 100 mg/g
* \> 18 years old
* No known kidney disease
* \> 18 years old
* Negative autoantibiodies and immunoglobulines
* Referred to kidney biopsy
Exclusion Criteria
* Significant comorbidity, which is considered to potentially impact the outcome
SLE patients with no sign of kidney disease
* Lack of ability or willingness to provide informed consent
* Significant comorbidity, which is considered to potentially impact the outcome
Healthy controls:
* Lack of ability or willingness to provide informed consent
* Urine albumin-creatinine ratio \> 100 mg/g or proteinuria \> 100 mg/day
* Postive autoantibodies
* Significant comorbidity, which is considered to potentially impact the outcome
Biopsy control:
* Lack of ability or willingness to provide informed consent
* Significant comorbidity, which is considered to potentially impact the outcome
18 Years
ALL
Yes
Sponsors
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University of Southern Denmark
OTHER
Odense University Hospital
OTHER
Kolding Sygehus
OTHER
Responsible Party
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Principal Investigators
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Anne F Christensen, Chief of Medicine, MD, phd
Role: STUDY_CHAIR
Sygehus Lillebaelt, Kolding Hospitl
Locations
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Kolding Hospital
Kolding, , Denmark
Department of Nephrology
Odense, , Denmark
Department of Rheumatology
Odense, , Denmark
Univesity of Southern Denmark
Odense, , Denmark
Countries
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Central Contacts
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Facility Contacts
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michael Aarup, MD, consultant
Role: primary
Other Identifiers
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SLELNuEV
Identifier Type: -
Identifier Source: org_study_id
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