Patients with IgA nephropathy exhibit high systemic PDGF-DD levels

被引:23
作者
Boor, Peter [1 ,2 ]
Eitner, Frank [1 ]
Cohen, Clemens D. [3 ]
Lindenmeyer, Maja T. [3 ]
Mertens, Peter R. [1 ,4 ]
Ostendorf, Tammo [1 ]
Floege, Juergen [1 ]
机构
[1] Rhein Westfal TH Aachen, Div Nephrol & Immunol, Aachen, Germany
[2] Res Base Slovak Med Univ, Dept Clin & Expt Pharmacotherapy, Bratislava, Slovakia
[3] Univ Zurich, Inst Physiol & Nephrol Clin, Zurich, Switzerland
[4] Otto VonGuericke Univ Magdegurg, Dept Hypertens & Nephrol, Magdeburg, Germany
关键词
glomerulonephritis; growth factor; serum marker; GROWTH-FACTOR-D; HUMAN MONOCLONAL-ANTIBODY; RENAL-DISEASE; EXPRESSION; CR002; GLOMERULONEPHRITIS; CELLS; MICE; AB;
D O I
10.1093/ndt/gfp152
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Methods. We assessed disease activity in 72 patients with GN, established a novel PDGF-D ELISA and then determined their PDGF-DD levels. In parallel, we studied renal PDGF-DD mRNA expression by RT-PCR. Results. PDGF-DD serum levels in patients with IgA nephropathy (IgAN) were significantly higher (1.67 +/- 0.45 ng/ml) and in patients with lupus nephritis significantly lower (0.66 +/- 0.86 ng/ml) compared to healthy controls (1.17 +/- 0.46 ng/ml), while patients with focal segmental glomerulosclerosis, membranous GN and ANCA-positive vasculitis did not differ from controls. The subgroup of IgAN patients with elevated PDGF-DD levels (27% of samples) did not differ in their clinical features from those with normal PDGF-DD levels. In IgAN patients with repetitive PDGF-DD determinations, most exhibited only minor fluctuations of serum levels over time. Intrarenal PDGF-DD mRNA expression did not differ between controls and patients, suggesting an extrarenal source of the elevated PDGF-DD in IgAN. Conclusions. Serum PDGF-DD levels were specifically elevated in patients with IgAN, in particular in those with early disease, i.e. preserved renal function. Our data support the rationale for anti-PDGF-DD therapy in mesangioproliferative GN.
引用
收藏
页码:2755 / 2762
页数:8
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