2016
DOI: 10.1016/j.metabol.2016.02.012
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Beta-2-microglobulin (B2M) expression in the urinary sediment correlates with clinical markers of kidney disease in patients with type 1 diabetes

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Cited by 27 publications
(20 citation statements)
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“…For example, in diabetic kidney, B2m contributes to diabetic tubulopathy and might not be a good RG for the kidney [51]. GAPDH has been reported to contribute to neurological disorder such as Huntington and Alzheimer diseases [52] which indicates GAPDH might not be an optimal candidate gene in hypothalamus.…”
Section: Discussionmentioning
confidence: 99%
“…For example, in diabetic kidney, B2m contributes to diabetic tubulopathy and might not be a good RG for the kidney [51]. GAPDH has been reported to contribute to neurological disorder such as Huntington and Alzheimer diseases [52] which indicates GAPDH might not be an optimal candidate gene in hypothalamus.…”
Section: Discussionmentioning
confidence: 99%
“…Several studies have shown that the phenotype of cultured GMCs caused by HG environment mimics the pathophysiological changes in diabetic nephropathy [24]. Gene variations also critically contribute to the renal dysfunction in diabetes [25, 26]. We found that high concentration DBD extract significantly inhibited GMCs proliferation at all three time-points (24, 48 and 72 h), while medium concentration DBD extract only inhibited GMCs proliferation at 72 h. Low concentration DBD extract did not seem to inhibit proliferation of GMCs.…”
Section: Discussionmentioning
confidence: 99%
“…All patients were receiving intensive insulin therapy. At the time of recruitment, urine samples were collected as previously described (5,6) and later used for gene expression analyses. Briefly, urine specimens were collected in sterile RNAse-free flasks.…”
Section: Participantsmentioning
confidence: 99%
“…Gene expression analyses were performed with 10 ng of cDNA/sample, in duplicates, with the use of Taqman assays in a StepOne plus Real-Time PCR System (ThermoFisher Scientific, Carlsbad, CA). The relative mRNA abundance was calculated using the 2-Ct method (13) and E74-Like Factor 1 (ELF1) was used as reference gene (5). Taqman assays are listed in Supplemental Table 1.…”
Section: Qrt-pcr Validationmentioning
confidence: 99%
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