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Paul, Katharina ; Kretzschmar, Daniel ; Yilmaz, Atilla ; Bärthlein, Barbara ; Titze, Stephanie ; Wolf, Gunter ; Busch, Martin

Circulating dendritic cell precursors in chronic kidney disease: a cross-sectional study

Paul, Katharina, Kretzschmar, Daniel, Yilmaz, Atilla, Bärthlein, Barbara, Titze, Stephanie, Wolf, Gunter und Busch, Martin (2013) Circulating dendritic cell precursors in chronic kidney disease: a cross-sectional study. BMC nephrology 14, S. 274.

Veröffentlichungsdatum dieses Volltextes: 07 Aug 2014 13:09
Artikel
DOI zum Zitieren dieses Dokuments: 10.5283/epub.30562


Zusammenfassung

BACKGROUND: Dendritic cells (DC) are professional antigen-presenting cells in the immune system. They patrol the blood as circulating dendritic cell precursors (DCP). Decreased blood DCP count has been shown to be related to atherosclerotic plaque burden. Since chronic kidney disease (CKD) is associated with chronic inflammation and increased cardiovascular risk, the aim of our study was to ...

BACKGROUND:
Dendritic cells (DC) are professional antigen-presenting cells in the immune system. They patrol the blood as circulating dendritic cell precursors (DCP). Decreased blood DCP count has been shown to be related to atherosclerotic plaque burden. Since chronic kidney disease (CKD) is associated with chronic inflammation and increased cardiovascular risk, the aim of our study was to investigate a potential effect of CKD on circulating DCP numbers especially in patients with a history of cardiovascular disease.
METHODS:
The number of circulating myeloid (mDCP), plasmacytoid (pDCP), and total DCP (tDCP) was analysed by flow cytometry in 245 patients with CKD stage 3 (with and without known cardiovascular events) and 85 coronary healthy controls. In addition, data were compared with a historical group of 130 patients with known coronary artery disease (CAD).
RESULTS:
Compared to controls, patients with CKD 3 revealed a significant decrease in circulating mDCP (-29%), pDCP (-43%), and tDCP (-38%) (P < 0.001, respectively). Compared with CAD-patients, the decrease in circulating DCP in CKD was comparable or even more pronounced indicating a potential role for DCP in cardiovascular risk potentiation due to CKD.
CONCLUSIONS:
Based on previous findings in CAD, the marked decrease of DCP in CKD implicates a potential role for DCP as a mediator of cardiovascular disease. Whether DCP in CKD may act as new cardiovascular biomarkers needs to be established in future prospective trials.



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Details

DokumentenartArtikel
Titel eines Journals oder einer ZeitschriftBMC nephrology
Verlag:BMC
Band:14
Seitenbereich:S. 274
DatumDezember 2013
Zusätzliche Informationen (Öffentlich)authors on behalf of the GCKD-Study Investigators
InstitutionenMedizin > Institut für Funktionelle Genomik > Lehrstuhl für Funktionelle Genomik (Prof. Oefner)
Identifikationsnummer
WertTyp
21862458PubMed-ID
10.1186/1471-2369-14-274DOI
Klassifikation
NotationArt
AdultMESH
AgedMESH
Aged, 80 and overMESH
Blood Cell Count/statistics & numerical dataMESH
CausalityMESH
ComorbidityMESH
Coronary Artery Disease/pathologyMESH
Cross-Sectional StudiesMESH
Dendritic Cells/pathologyMESH
FemaleMESH
Germany/epidemiologyMESH
Hematopoietic Stem Cells/pathologyMESH
HumansMESH
MaleMESH
Middle AgedMESH
PrevalenceMESH
Renal Insufficiency, Chronic/pathologyMESH
Risk FactorsMESH
Young AdultMESH
Dewey-Dezimal-Klassifikation500 Naturwissenschaften und Mathematik > 500 Naturwissenschaften
500 Naturwissenschaften und Mathematik > 570 Biowissenschaften, Biologie
600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin
StatusVeröffentlicht
BegutachtetJa, diese Version wurde begutachtet
An der Universität Regensburg entstandenZum Teil
URN der UB Regensburgurn:nbn:de:bvb:355-epub-305625
Dokumenten-ID30562

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