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Federal government websites often end in. The site is secure. Preview improvements coming to the PMC website in October Learn More or Try it out now. Diabetic macular edema DME is a sight-threatening complication of diabetes. Consequently, studying the proteome of DME may provide novel insights into underlying molecular mechanisms. Control samples were obtained before cataract surgery.
Significantly changed proteins were identified using a permutation-based calculation, with a false discovery rate of 0. A human donor eye with DME and a control eye were used for immunofluorescence. A total of proteins were differentially expressed in the DME.
Regulated proteins were involved in complement activation, glycolysis, extracellular matrix interaction, and cholesterol metabolism.
Ceruloplasmin and complement component C8 correlated with central subfield thickness CST. LBP was correlated with vascular endothelial growth factor. The proteins involved in desmosomal integrity, including desmocollin-1 and desmoglein-1, were downregulated in DME and correlated negatively with CST.