LUPUS ANTICOAGULANT IN SYSTEMIC LUPUS-ERYTHEMATOSUS - A CLINICAL AND RENAL PATHOLOGICAL-STUDY

被引:59
作者
FARRUGIA, E
TORRES, VE
GASTINEAU, D
MICHET, CJ
HOLLEY, KE
机构
[1] MAYO CLIN & MAYO FDN,DIV NEPHROL,200 1ST ST SW,ROCHESTER,MN 55905
[2] MAYO CLIN & MAYO FDN,DIV NEPHROL & INTERNAL MED,ROCHESTER,MN 55905
[3] MAYO CLIN & MAYO FDN,DIV HEMATOL & INTERNAL MED,ROCHESTER,MN 55905
[4] MAYO CLIN & MAYO FDN,DIV RHEUMATOL & INTERNAL MED,ROCHESTER,MN 55905
[5] MAYO CLIN & MAYO FDN,MED PATHOL SECT,ROCHESTER,MN 55905
关键词
SYSTEMIC LUPUS ERYTHEMATOSUS; LUPUS ANTICOAGULANT; RENAL THROMBOTIC MICROANGIOPATHY;
D O I
10.1016/S0272-6386(12)70258-5
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Circulating lupus anticoagulant (LA) is associated with thrombosis in large and small vessels. To determine how often the presence of LA is associated with thrombosis within the renal microcirculation, 33 patients with systemic lupus erythematosus (SLE), renal dysfunction, and LA were identified over a 25-year period (LA group) and 32 patients with renal SLE but with normal gross coagulation screen were matched for age, sex, and biopsy timing (C group). Prevalences of serositis, neuropsychiatric illness, leukopenia, thrombocytopenia, hemolysis, anti-DS-DNA elevation, and complement reduction were similar. Arthritis was less and biologic false-positive (BFP) syphilis serology more common in LA. More LA patients had thrombotic events (LA 39% v C 13%; P = 0.014); bleeding episodes, including postbiopsy, were similar. At biopsy, hypertension (LA 55%, C 41 %), serum creatinine (mean ± SD: LA 186 ± 168 μmol/ L [2.1 ± 1.9 mg/dL] v C 150 ± 168 μmol/L [1.7 ± 1.9 mg/dL]) and proteinurla (LA 2.6 ± 3.1 g/24 h v C 3.1 ± 2.7) were similar. Lesions by World Health Organization (WHO) class, activity, and chronicity indices, as well as immunofluorescence (IF) and electron microscopy (EM) findings, were not significantly different. Occlusive glomerular, arteriolar, and arterial fibrin thrombi, along with varying degrees of renal thrombotic microangiopathy, were seen in five of 33 patients with LA, but zero of 32 C patients (P = 0.053); three of these five patients died soon after biopsy. Overall, mortality was not different between LA and C. We conclude that the majority of patients with SLE, renal dysfunction, and LA exhibit renal morphologic findings indistinguishable from patients without LA. However, a significant minority of LA patients have thrombotic microangiopathy in their biopsy, which is accompanied by a worse prognosis. © 1992, National Kidney Foundation. All rights reserved. All rights reserved.
引用
收藏
页码:463 / 471
页数:9
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