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|a pubmed25n0598.xml
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|a (DE-627)NLM179487639
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|a (NLM)18471357
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a chi
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1 |
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|a Rong, Zan-Hua
|e verfasserin
|4 aut
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|a Expression and clinical implication of platelet-derived growth factor-D and platelet-derived growth factor-beta in childhood IgA nephropathy
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|c 2008
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|a Text
|b txt
|2 rdacontent
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|a ohne Hilfsmittel zu benutzen
|b n
|2 rdamedia
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|a Band
|b nc
|2 rdacarrier
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|a Date Completed 04.02.2010
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|a Date Revised 12.05.2008
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|a published: Print
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|a Citation Status MEDLINE
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|a OBJECTIVE: To investigate the clinical implication of platelet-derived growth factor (PDGF)-D and PDGF-beta in IgA nephropathy in childhood
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|a METHODS: Forty-seven children with IgA nephropathy and 26 controls were enrolled for study, and their serum, urine and renal biopsy specimens were examined. The patients were divided into control group [including serum, urine specimens of 13 healthy children and 13 renal biopsy samples of non-IgA nephropathy in children], mild proliferation (MP) group (13 patients), focal proliferation (FP) group (19 patients), and proliferation sclerosis (PS) group (15 patients). Enzyme-linked immunosorbent assay (ELISA) and immunohistochemistry were used to determine contents of PDGF-D, PDGF-beta and PDGF-B in blood, urine and renal tissues. The levels of 24-hour urinary protein excretion, serum albumin (Alb), serum blood urea nitrogen (BUN) and creatinine (Cr) were also determined
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|a RESULTS: Compared with control group, levels of PDGF-D and PDGF-B were progressively elevated in blood and urine of IgA nephropathy children with increase in severity of glomerular damage (all P<0.01). Serum as well as urinary PDGF-D and PDGF-B levels were positively correlated with 24-hour urinary protein excretion (PDGF-D blood: r=0.546, urine: r=0.760; PDGF-B blood: r=0.634, urine: r=0.577, respectively, P<0.01), while negatively correlated with serum Alb levels in IgA nephropathy patients (PDGF-D blood: r=-0.649, urine: r=-0.528; PDGF-B blood: r=-0.613, urine: r=-0.531, respectively, P<0.01). Contents of PDGF-D and PDGF-beta in renal tissue were much higher than those of control group (P<0.01). Along with the increase in severity of glomerular pathology, their contents increased gradually. PDGF-B was only significantly expressed in renal tissue in FP group and PS group
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|a CONCLUSION: PDGF-D might significantly enhance the development of mesangial proliferation and tubulointerstitial fibrosis. In comparison with PDGF-B, PDGF-D appears to reflect more sensitive to the severity and prognosis of IgA nephropathy
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|a English Abstract
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Lymphokines
|2 NLM
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|a PDGFD protein, human
|2 NLM
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|a Platelet-Derived Growth Factor
|2 NLM
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650 |
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|a Proto-Oncogene Proteins c-sis
|2 NLM
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700 |
1 |
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|a Wang, Chen
|e verfasserin
|4 aut
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700 |
1 |
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|a Hao, Jun
|e verfasserin
|4 aut
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700 |
1 |
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|a Duan, Hui-Jun
|e verfasserin
|4 aut
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773 |
0 |
8 |
|i Enthalten in
|t Zhongguo wei zhong bing ji jiu yi xue = Chinese critical care medicine = Zhongguo weizhongbing jijiuyixue
|d 1998
|g 20(2008), 5 vom: 12. Mai, Seite 275-8
|w (DE-627)NLM098227793
|x 1003-0603
|7 nnns
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773 |
1 |
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|g volume:20
|g year:2008
|g number:5
|g day:12
|g month:05
|g pages:275-8
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|a GBV_USEFLAG_A
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|a SYSFLAG_A
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|a GBV_NLM
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|a GBV_ILN_350
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|a AR
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|d 20
|j 2008
|e 5
|b 12
|c 05
|h 275-8
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