Session Information
Date: Monday, November 9, 2015
Title: Systemic Lupus Erythematosus - Human Etiology and Pathogenesis Poster II
Session Type: ACR Poster Session B
Session Time: 9:00AM-11:00AM
Background/Purpose:
Systemic Lupus Erythematosis is a systemic autoimmune disease characterised by involvement of multiple organ systems Lupus nephritis (LN) is a severe and frequent manifestation of systemic lupus erythematosis (SLE). Its pathogenesis has not been fully elucidated but immune complexes are considered to contribute to the inflammatory pathology in LN.
The aim of the study to assess the potential role of HMGB1 (high-mobility group box proteins) in SLE and whether urinary and serum levels of HMGB1 reflect renal inflammation and correlate with disease activity,
Methods:
In a Case control study 61 Systemic lupus patients fulfilling the classification criteria for the diagnosis of SLE ( divided in 4 groups )selected from Internal Medicine Department, Kasr Al-Aini Hospital, Cairo University after ethical committee approval and getting written informed consent from each patient.
Group 1: 21 patients with lupus nephritis ,Group 2: 21 patients with lupus activity without nephritis .Group 3: 19 patients without activity as estimated by SLEDAI < 4 ,Group 4:included 13 healthy volunteers age and sex matched.
Participants were subjected to: Detailed medical history., Complete physical examination. disease activity scoring using SLEDAI.
Laboratory investigations: Complete blood count. ,Kidney function tests , Urine analysis,ESR,ANA,,Anti dsDNA. ,C3, C4 levels. plasma and urinary levels of HMGB1 assessed by ELISA
Study of HMGB1 in renal biopsy from 21 patients with active lupus nephritis The activity index (AI) and chronicity index (CI) were calculated for each specimen with maximum scores of 24 for the AI and 12 for the CI.
Cellular distribution of HMGB1 was determined in the kidney by counting one hundred nuclei (glomerular, tubular, and stromal) in three bright field pictures and scoring both HMGB1-positive (brown) and HMGB1-negative (blue) nuclei
Results:
Plasma and urinary HMGB1 were in lupus with activity however significantly elevated in patients with active LN compared to patients without active nephritis(p<0.037). and control(p<0.001).Plasma and urinary HMGB1 and renal tissue levels HMGB1 levels correlated with SLEDAI differentiating SLE without nephritis from SLE with nephritis using ROC curve a higher sensitivity and specificity of HMGB1 in lupus nephritis compared with other groups 95.1% and 100% respectively Similarly, renal tissue of active LN patients showed strong expression of HMGB1 at cytoplasmic and extracellular sites suggesting active release of HMGB1
Conclusion:
The present study demonstrates increase in plasma, urine, renal tissue HMGB1 levels in SLE patients, in particular in those with active LN. Increase in HMGB1 levels correlated to SLE activity index (SLEDAI). Thus we suggest that HMGB1 may play an important role in renal pathology in SLE patients and HMGB1 blocking may be of future interest in development new treatment strategies for lupus nephritis
To cite this abstract in AMA style:
Badawy A, Salam R, Fouad H, Bassam A, Lashen S. HMGB1 Early Marker in Lupus Nephritis [abstract]. Arthritis Rheumatol. 2015; 67 (suppl 10). https://acrabstracts.org/abstract/hmgb1-early-marker-in-lupus-nephritis/. Accessed .« Back to 2015 ACR/ARHP Annual Meeting
ACR Meeting Abstracts - https://acrabstracts.org/abstract/hmgb1-early-marker-in-lupus-nephritis/