Gene polymorphism and risk of idiopathic membranous nephropathy

Life Sci. 2019 Jul 15:229:124-131. doi: 10.1016/j.lfs.2019.05.010. Epub 2019 May 7.

Abstract

Membranous nephropathy (MN) is the most common primary glomerular disease (PGD) in the world. Currently, MN still lacks specific diagnostic markers and effective treatment strategy. It is speculated that the occurrence of MN is mainly related to environmental and genetic factors. The pathological manifestations of MN patients are diverse, significant differences in response to treatment options, and more reports on young MN patients suggest the importance of genes in the pathogenesis and diagnosis of MN. We will propose a novel perspective on the important role of genes in the pathogenesis of MN baced on the latest research.

Keywords: Gene; Gene marker; HLA; MN; PLA2R; THSD7A.

Publication types

  • Review

MeSH terms

  • Biomarkers / analysis*
  • Glomerulonephritis, Membranous / genetics*
  • Glomerulonephritis, Membranous / pathology*
  • Humans
  • Polymorphism, Single Nucleotide*
  • Prognosis

Substances

  • Biomarkers