Table 8.
Different conditions | Structure change in THP molecule |
---|---|
Pregnancy | Increased glycosylation |
Familial juvenile hyperuricemic nephropathy | Mutations in THP genes |
Autosomal medullary cystic kidney disease 2 | Mutations in THP genes |
Tubulointerstitial nephritis in SLE | Decease in THP excretion |
Allograft renal rejection | Reduced mannose residues Reduced Siaα[2,3]Gal/Gal NAc and β[1,4]Glc NAc |
Glomerulonephritis | Increased IgG, IgM, and IgA depositions in urine casts |
Interstitial cystitis | Reduced high-molecular weight sialylated oligosaccharides |
Different urinary diseases | |
Urinary tract infections, glomerulonephritis, or interstitial nephritis | Decreased N-acetylglucosamine and N-acetylgalactosamine |
Bartter’s syndrome | Decreased N-acetylglucosamine and less-sialylated chains |
Abbreviation: SLE, systemic lupus erythematosus.