Key Genetic Components of Fibrosis in Diabetic Nephropathy: An Updated Systematic Review and Meta-Analysis.
Maria TziastoudiTheoharis C TheoharidesEvdokia NikolaouMaria EfthymiadiTheodoros EleftheriadisIoannis StefanidisPublished in: International journal of molecular sciences (2022)
Renal fibrosis (RF) constitutes the common end-point of all kinds of chronic kidney disease (CKD), regardless of the initial cause of disease. The aim of the present study was to identify the key players of fibrosis in the context of diabetic nephropathy (DN). A systematic review and meta-analysis of all available genetic association studies regarding the genes that are included in signaling pathways related to RF were performed. The evaluated studies were published in English and they were included in PubMed and the GWAS Catalog. After an extensive literature review and search of the Kyoto Encyclopedia of Genes and Genomes (KEGG) database, eight signaling pathways related to RF were selected and all available genetic association studies of these genes were meta-analyzed. ACE , AGT , EDN1 , EPO , FLT4 , GREM1 , IL1B , IL6 , IL10 , IL12RB1 , NOS3 , TGFB1 , IGF2/INS/TH cluster , and VEGFA were highlighted as the key genetic components driving the fibrosis process in DN. The present systematic review and meta-analysis indicate, as key players of fibrosis in DN, sixteen genes. However, the results should be interpreted with caution because the number of studies was relatively small.
Keyphrases
- genome wide
- diabetic nephropathy
- chronic kidney disease
- dna methylation
- case control
- copy number
- genome wide identification
- bioinformatics analysis
- liver fibrosis
- end stage renal disease
- acute myeloid leukemia
- pi k akt
- gene expression
- cell proliferation
- case report
- genome wide analysis
- tyrosine kinase
- nitric oxide
- peritoneal dialysis
- nitric oxide synthase
- endoplasmic reticulum stress