E-cadherin and periostin in early detection and progression of diabetic nephropathy: epithelial-to-mesenchymal transition

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dc.contributor.author El-Dawla, Nada M. Qamar
dc.contributor.author Sallam, Al-Aliaa M
dc.contributor.author El-Hefnawy, Mohamed H
dc.contributor.author El-Mesallamy, Hala O
dc.date.accessioned 2019-11-14T14:41:00Z
dc.date.available 2019-11-14T14:41:00Z
dc.date.issued 2019-08
dc.identifier.issn 1342-1751
dc.identifier.other https://doi.org/
dc.identifier.uri https://cutt.ly/peGPvNL
dc.description Accession Number: WOS:000475963400009 en_US
dc.description.abstract Results Concerning E-cadherin levels, in comparison to control group, there were significantly decreased in all groups (0.94, 0.52, and 0.14 ng/mL in normoalbuminuria, microalbuminuria, and macroalbuminuria groups; respectively). For periostin levels, nonsignificant increase in normoalbuminuria (0.32 ng/mL) than control group (0.3 ng/mL) was observed. There was a significant increase in other groups with the highest values in macroalbuminuria group (1.66 ng/mL). E-cadherin and periostin were correlated with each other (r = -0.353, P < 0.001). UACR was negatively correlated with E-cadherin and positively correlated with periostin. ROC curve analyses showed that the AUC to diagnose established microalbuminuria using E-cadherin was 0.998 (95% CI 0.932-1), and using periostin was 0.833 (95% CI 0.709-0.919). en_US
dc.description.uri https://www.scimagojr.com/journalsearch.php?q=19417&tip=sid&clean=0
dc.language.iso en_US en_US
dc.publisher Springer en_US
dc.relation.ispartofseries CLINICAL AND EXPERIMENTAL NEPHROLOGY;Volume: 23 Issue: 8 Pages: 1050-1057
dc.relation.uri https://cutt.ly/teDysru
dc.subject TISSUE en_US
dc.subject EXPRESSION en_US
dc.subject MECHANISMS en_US
dc.subject IDENTIFICATION en_US
dc.subject BIOMARKER en_US
dc.subject Plus:RENAL INJURY en_US
dc.subject Periostin en_US
dc.subject EMT en_US
dc.subject E-cadherin en_US
dc.subject Diabetic nephropathy en_US
dc.title E-cadherin and periostin in early detection and progression of diabetic nephropathy: epithelial-to-mesenchymal transition en_US
dc.type Article en_US
dc.identifier.doi https://doi.org/
dc.Affiliation October University for modern sciences and Arts (MSA)


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