2013
DOI: 10.1016/j.ejogrb.2012.10.011
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Comparison of serum and urinary nephrin levels between normal pregnancies and severe preeclampsia

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Cited by 35 publications
(30 citation statements)
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“…Several laboratories have independentlyconfirmed the urinary presence of podocytes, podocyte-specific tryptic peptides, or their respective mRNAs (9)(10)(11)(12)(13)(14)(15)(16)(17)(18)(19)(20) (Table 1), following our initial report in 2007 that the urinary excretion of viable podocytes is a highly sensitive and specific marker for preeclampsia (9). These preliminary data also reported a positive correlation between the degree of proteinuria and podocyturia, as determined by podocin staining, further suggesting that these may be mechanistically related and that podocyte loss may contribute to proteinuria in preeclampsia.…”
mentioning
confidence: 99%
“…Several laboratories have independentlyconfirmed the urinary presence of podocytes, podocyte-specific tryptic peptides, or their respective mRNAs (9)(10)(11)(12)(13)(14)(15)(16)(17)(18)(19)(20) (Table 1), following our initial report in 2007 that the urinary excretion of viable podocytes is a highly sensitive and specific marker for preeclampsia (9). These preliminary data also reported a positive correlation between the degree of proteinuria and podocyturia, as determined by podocin staining, further suggesting that these may be mechanistically related and that podocyte loss may contribute to proteinuria in preeclampsia.…”
mentioning
confidence: 99%
“…While, a significant decrease in serum nephrin level was recorded in rats pretreated with sodium selenite or taurine prior HgCl 2 . Son et al 73 observed that both serum and urine concentrations of nephrin were significantly higher in the sever preeclamptic group than in the normal pregnancy group. They explained this result as that preeclampsia is associated with renal pathologic changes as glomerular endotheliosis.…”
Section: Discussionmentioning
confidence: 98%
“…Another 10 blood experimental biomarkers (AT-1AA [31], calcyclin, copeptin [34], galectin-1 [36], Gas6 [37], HIF-1aOH [38], IGFALS [41], mammalian HtrA3 [45], NT-proBNP [47], and PTX3 [49]), and four urine ones (C5b-9 [33], nephrin [46], iodine [42], and prolactin [52]) had limited clinical evaluation information, which impeded the evaluation of their performance for the diagnosis of PE. No clinical data were found for the remaining nine blood markers, which consisted of adipsin, α enolase, ADMA, Ba, 2,3-BPGM, Fetal DNA, marinobufagenin, plasma UA [51], and soluble CD117.…”
Section: Resultsmentioning
confidence: 99%