Recent Progress in Deciphering the Etiopathogenesis of Primary Membranous Nephropathy
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Recent Progress in Deciphering the Etiopathogenesis of Primary Membranous Nephropathy. / Kronbichler, Andreas; Oh, Jun; Meijers, Björn; Mayer, Gert; Shin, Jae Il.
In: BIOMED RES INT , Vol. 2017, 17.08.2017, p. 1936372.Research output: SCORING: Contribution to journal › SCORING: Review article › Research
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TY - JOUR
T1 - Recent Progress in Deciphering the Etiopathogenesis of Primary Membranous Nephropathy
AU - Kronbichler, Andreas
AU - Oh, Jun
AU - Meijers, Björn
AU - Mayer, Gert
AU - Shin, Jae Il
PY - 2017/8/17
Y1 - 2017/8/17
N2 - Primary membranous nephropathy (MN) is the leading cause of nephrotic syndrome in adults. Discovery of several antibodies has contributed to an increased understanding of MN. Antibodies against the M-type phospholipase A2 receptor (PLA2R) are present in 50-100% with primary MN and are associated with a lower frequency of spontaneous remission. High levels are linked with a higher probability of treatment resistance, higher proteinuria, and impaired renal function, as well as a more rapid decline of kidney function during follow-up. Immunologic remission precedes reduction of proteinuria by months. Pretransplant evaluation of PLA2R antibodies is warranted to predict recurrence of disease following renal transplantation. Several risk alleles related to the PLA2R1 gene and within the HLA loci have been identified, whereas epitope spreading of PLA2R may predict treatment response. More recently, thrombospondin type 1 domain-containing 7A (THSD7A) antibodies have been discovered in primary MN. Several other rare antigens have been described, including antibodies against neutral endopeptidase as a cause of antenatal MN and circulating cationic bovine serum albumin as an antigen with implications in childhood MN. This review focuses on the progress with a special focus on diagnostic accuracy, predictive value, and treatment implications of the established and proposed antigens.
AB - Primary membranous nephropathy (MN) is the leading cause of nephrotic syndrome in adults. Discovery of several antibodies has contributed to an increased understanding of MN. Antibodies against the M-type phospholipase A2 receptor (PLA2R) are present in 50-100% with primary MN and are associated with a lower frequency of spontaneous remission. High levels are linked with a higher probability of treatment resistance, higher proteinuria, and impaired renal function, as well as a more rapid decline of kidney function during follow-up. Immunologic remission precedes reduction of proteinuria by months. Pretransplant evaluation of PLA2R antibodies is warranted to predict recurrence of disease following renal transplantation. Several risk alleles related to the PLA2R1 gene and within the HLA loci have been identified, whereas epitope spreading of PLA2R may predict treatment response. More recently, thrombospondin type 1 domain-containing 7A (THSD7A) antibodies have been discovered in primary MN. Several other rare antigens have been described, including antibodies against neutral endopeptidase as a cause of antenatal MN and circulating cationic bovine serum albumin as an antigen with implications in childhood MN. This review focuses on the progress with a special focus on diagnostic accuracy, predictive value, and treatment implications of the established and proposed antigens.
KW - Journal Article
KW - Review
U2 - 10.1155/2017/1936372
DO - 10.1155/2017/1936372
M3 - SCORING: Review article
C2 - 28904948
VL - 2017
SP - 1936372
JO - BIOMED RES INT
JF - BIOMED RES INT
SN - 2314-6133
ER -