Results 41 to 50 of about 2,423,946 (178)
Interaction between PLA2R1 and HLA-DQA1 Variants Associates with Anti-PLA2R Antibodies and Membranous Nephropathy [PDF]
Risk alleles at genome loci containing phospholipase A2 receptor 1 (PLA2R1) and HLA-DQA1 closely associate with idiopathic membranous nephropathy (IMN) in the European population, but it is unknown whether a similar association exists in the Chinese population and whether high-risk alleles promote the development of anti-PLA2R antibodies.
Jicheng, Lv +8 more
openaire +2 more sources
BackgroundThe concurrence of anti-contactin 1 (CNTN1) antibody-associated chronic inflammatory demyelinating polyneuropathy (CIDP) and membranous nephropathy (MN) has previously been reported in the literature.
Qianhui Xu +14 more
doaj +1 more source
BackgroundPrimary membranous nephritis (PMN) is an autoimmune disease induced by the deposit of antibodies (Ab) to the phospholipase receptor A2 receptor (PLA2R) on podocytes.
Hanene Gaied +9 more
core +1 more source
The Human Biomarker Navigator integrates the disease continuum, biomarker dynamics, cross‐organ biomarker networks, biomarker classification, and technology‐driven paradigms. It maps how biomarkers link multi‐system physiology and pathology across the nervous, respiratory, endocrine, circulatory, immune, digestive, urinary, reproductive, and ...
Meng‐Yao Li +29 more
wiley +1 more source
Background Idiopathic membranous nephropathy (MN) is one of the major glomerulonephritis that cause nephrotic syndrome. The phospholipase A2 receptor (PLA2R) has recently been identified as an endogenous antigen of idiopathic MN.
Rei Iio +11 more
doaj +1 more source
Serum anti-PLA2R antibodies may be present before clinical manifestations of membranous nephropathy [PDF]
Figure 1 | Phospholipase A2 antibodies (PLA2R) are present in immune deposits. First biopsy is shown. To the Editor: Antiphospholipase A2 antibodies (aPLA2R) are identified in 75% of cases of primary membranous nephropathy. A direct pathogenic action of these antibodies is not established.
Mary-Jane Guerry +3 more
openaire +1 more source
ABSTRACT Minimal change disease (MCD) frequently relapses, and infection is one of the most common clinical triggers. Arachidonic acid (AA), an inflammatory lipid mediator released during tissue injury and infection, has been implicated in podocyte injury, but its contribution to metabolic dysfunction in MCD remains unclear.
Kun Nie +10 more
wiley +1 more source
Background: The natural course of idiopathic membranous nephropathy (MN) varies, as it is known through favorable outcomes in most patients. However, one third of patients with idiopathic MN will slowly progress to end-stage renal disease (ESRD).
Timmermans S.A.M.E.G. (3683929) +5 more
core +1 more source
Anti-phospholipase A2 receptor antibodies directly induced podocyte damage in vitro
The pathogenesis of primary membranous nephropathy (MN) involves the antibodies against antigens on the cell surface of podocytes, with the majority of M-type phospholipase A2 receptor (PLA2R), and a profound podocyte dysfunction.
Juntao Yu (12294890) +4 more
core +1 more source
Persistent Haematuria Is Associated With Reduced Kidney Survival in Primary Podocytopathies
ABSTRACT Aim Haematuria is frequently present in podocytopathies, but its significance and prognostic value are not well described. This study aimed to determine the prevalence and association between persistent haematuria and kidney survival in patients with membranous nephropathy (MN), minimal change disease (MCD) and focal segmental ...
Gabriel Ștefan +3 more
wiley +1 more source

