Recent Advances and Prognosis in Idiopathic Membranous Nephropathy

被引:49
作者
Segal, Paul E. [1 ]
Choi, Michael J. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Div Nephrol, Johns Hopkins Bayview Med Ctr, Baltimore, MD 21224 USA
关键词
Proteinuria; Membranous nephropathy; Podocyte; Subepithelial deposits; BOVINE SERUM-ALBUMIN; NEPHROTIC SYNDROME; NATURAL-HISTORY; ANTIGEN; GLOMERULONEPHRITIS; GLOMERULOSCLEROSIS; AUTOANTIBODIES; ANTIBODIES; DIAGNOSIS; RECEPTOR;
D O I
10.1053/j.ackd.2012.01.007
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
Idiopathic membranous nephropathy (MN) is one of the most common causes of nephrotic syndrome. Recently, progress has been made in understanding the pathogenesis of idiopathic MN with the finding of M-type phospholipase A2 receptor (PLA2R) antibodies in the serum and immune complexes of glomeruli in the majority of adult idiopathic MN patients. In the future, the detection of M-type PLA2R antibodies may help distinguish patients with primary MN who require aggressive immunosuppressive therapy from those with secondary disease. Levels of circulating antibody to this receptor may help in monitoring disease activity and in gauging response to therapy, as changes in antibody levels may precede changes in proteinuria. The degree of renal dysfunction or change in renal function over time and the level of persistent proteinuria are key prognostic factors in the decision to initiate therapy in idiopathic MN patients. Although spontaneous remissions occur in similar to 30% of patients, partial and complete remissions help to define the clinical course of an individual patient. (C) 2012 by the National Kidney Foundation, Inc. All rights reserved.
引用
收藏
页码:114 / 119
页数:6
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