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Je něco špatně v tomto záznamu ?
Molecular diagnostics identifies risks for graft dysfunction despite borderline histologic changes
P. Hrubá, I. Brabcová, F. Gueler, Z. Krejčík, V. Stránecký, E. Svobodová, J. Malušková, W. Gwinner, E. Honsová, A. Lodererová, R. Oberbauer, R. Zachoval, O. Viklický,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, multicentrická studie, pozorovací studie, práce podpořená grantem, validační studie
Grantová podpora
NT11227
MZ0
CEP - Centrální evidence projektů
NT14102
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Plný text - Článek
Zdroj
Zdroj
NLK
Freely Accessible Science Journals
od 1972
ProQuest Central
od 2000-01-01 do 2015-12-31
Open Access Digital Library
od 1972-01-01
Nursing & Allied Health Database (ProQuest)
od 2000-01-01 do 2015-12-31
Health & Medicine (ProQuest)
od 2000-01-01 do 2015-12-31
PubMed
26176825
DOI
10.1038/ki.2015.211
Knihovny.cz E-zdroje
- MeSH
- asymptomatické nemoci MeSH
- biopsie MeSH
- časná diagnóza MeSH
- časové faktory MeSH
- diagnostické techniky molekulární * MeSH
- dospělí MeSH
- fenotyp MeSH
- genetická predispozice k nemoci MeSH
- genetické markery * MeSH
- hodnocení rizik MeSH
- ledviny patologie patofyziologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- polymerázová řetězová reakce MeSH
- prediktivní hodnota testů MeSH
- regulace genové exprese MeSH
- rejekce štěpu genetika patologie patofyziologie MeSH
- reprodukovatelnost výsledků MeSH
- retrospektivní studie MeSH
- rizikové faktory MeSH
- sekvenční analýza hybridizací s uspořádaným souborem oligonukleotidů MeSH
- senioři MeSH
- stanovení celkové genové exprese MeSH
- transplantace ledvin škodlivé účinky MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- pozorovací studie MeSH
- práce podpořená grantem MeSH
- validační studie MeSH
The significance of borderline changes in kidney allograft biopsies is widely debated. To help resolve this, we studied differences in intrarenal gene expression patterns between early clinical and 3-month protocol biopsies, all of which had borderline histologic changes. The gene expression profiles in training set of patients by microarray analysis and data were validated in a larger cohort using RT-qPCR. There was greater expression of immunity- and inflammation-related genes in the early clinical biopsies compared to the 3-month protocol biopsies with borderline changes. In early clinically manifested borderline changes, graft deterioration within 24 months due to chronic rejection was associated with increased activation of immune, defense, and inflammatory processes. Regression modeling identified higher donor age and expression of macrophage receptor CLEC5A as risk factors for progression. In the 3-month protocol biopsies with borderline changes, graft dysfunction was associated with increased expression of fibrinogen complex transcripts. The discrimination power of fibrinogen was confirmed by cross-validation on two independent cohorts. Thus, our study highlights variations in gene expression between clinical and subclinical borderline changes despite similar histological findings. The data also support a recommendation for frequent patient monitoring, especially in those with borderline changes who received grafts from older donors.
Department of Immunogenetics Institute for Clinical and Experimental Medicine Prague Czech Republic
Department of Nephrology and Dialysis Medical University Vienna Vienna Austria
Department of Nephrology Hannover Medical School Hannover Germany
Department of Urology Thomayer's Hospital Prague Czech Republic
Institute of Hematology and Blood Transfusion Prague Czech Republic
Transplant Laboratory Institute for Clinical and Experimental Medicine Prague Czech Republic
Citace poskytuje Crossref.org
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