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Abstract Number: 592

Analysis Of Relationship Between Clinical Manifestations and Autoantibody Profile In ISN/RPS Class V Lupus Nephritis

Masanori Hanaoka, Takahisa Gono, Yasushi Kawaguchi, Hisashi Yamanaka, Yasuhiro Katsumata, Kae Takagi, Hirotaka Kaneko, Hisae Ichida, Yuko Ota, Hidenaga Kawasumi, Sayumi Baba, Yuko Okamoto and Sayuri Kataoka, Institute of Rheumatology, Tokyo Women's Medical University, Tokyo, Japan

Meeting: 2013 ACR/ARHP Annual Meeting

Keywords: Autoantibodies and lupus nephritis

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Session Information

Title: Systemic Lupus Erythematosus - Clinical Aspects I - Renal, Malignancy, Cardiovascular Disease

Session Type: Abstract Submissions (ACR)

Background/Purpose: Clinical manifestations, pathohistology and treatment strategy are different between International Society of Nephrology/Renal Pathology Society (ISN /RPS) class III/IV and class V Lupus Nephritis (LN). However, it has remained unknown what factors contribute to differences of pathophysiology between ISN/RPS class III/IV LN and class V LN. Moreover, in some patients with class V LN, responses to treatment such as corticosteroid or immunosuppressive agents are refractory. Predictors for treatment response have remained unknown in class V LN. The aim of this study is to clarify the differences of autoantibody profile between ISN/RPS class III/IV LN and class V LN. We also investigate associations between clinical manifestations and each autoantibody in class V LN.

Methods: 55 LN patients were consecutively enrolled and underwent renal biopsy in this study. These patients were divided into two subsets, 31 patients with ISN/RPS class III/IV LN subset and 22 patients with class V LN subset. Combined class III/IV+ V LN cases were excluded in this study. Clinical manifestations, autoantibodies positivity (anti-dsDNA, anti-SS-A, anti-U1-snRNP, Anti-Sm and anti-ribosomal P) were compared between two subsets. In addition, we analyzed the relationship between clinical manifestation and each autoantibody in class V LN subset. 

Results: Disease duration was significantly longer in class III/IV LN than class V LN (P = 0.01). Anti-dsDNA titer was significantly higher in class III/IV LN than class V LN (P < 0.01). The frequency of anti-Sm and anti-ribosomal P positivity was higher in class V LN than class III/IV LN (43% vs 20% and 50% vs 25%, respectively), although there were no significant differences. The frequency of both anti-dsDNA positive and anti-U1snRNP negative was significantly higher in class III/IV LN than class V LN (54.1% vs 19.1%, P = 0.03). In contrary, the frequency of both anti-dsDNA negative and anti-U1snRNP positive was significantly higher in class V LN than class III/IV LN (33% vs 0%, P < 0.01). 

Among class V LN subset, complement levels were lower and renal remission rate was higher in anti-dsDNA-positive class V LN subset than anti-dsDNA-negative class V LN subset. SLEDAI score was significantly higher (P = 0.02) and 24hr proteinuria was higher in anti-Sm-positive class V LN subset than anti-Sm-negative class V LN subset. Rash and arthritis was higher in anti-ribosomal P-positive class V LN subset than anti-ribosomal P-negative class V LN subset.

Conclusion: Anti-U1snRNP is associated with complication of class V LN. Lower complement level and anti-dsDNA positivity are the predictive markers for renal remission in class V LN.


Disclosure:

M. Hanaoka,
None;

T. Gono,
None;

Y. Kawaguchi,
None;

H. Yamanaka,
None;

Y. Katsumata,
None;

K. Takagi,
None;

H. Kaneko,
None;

H. Ichida,
None;

Y. Ota,
None;

H. Kawasumi,
None;

S. Baba,
None;

Y. Okamoto,
None;

S. Kataoka,
None.

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