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Serum levels of soluble vascular endothelial growth factor receptor‐2 in patients with systemic sclerosis
Author(s) -
Jinnin M.,
Makino T.,
Kajihara I.,
Honda N.,
Makino K.,
Ogata A.,
Ihn H.
Publication year - 2010
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1111/j.1365-2133.2009.09567.x
Subject(s) - microangiopathy , pathogenesis , medicine , vascular endothelial growth factor , fibrosis , thrombotic microangiopathy , real time polymerase chain reaction , biomarker , scleroderma (fungus) , connective tissue disease , endocrinology , vascular disease , disease , pathology , autoimmune disease , biology , vegf receptors , diabetes mellitus , gene , biochemistry , inoculation
Summary Background  Although vascular endothelial growth factor (VEGF)‐A/VEGF receptor 2 (KDR) signalling may play a major role in the microangiopathy of systemic sclerosis (SSc), serum levels of soluble KDR (sKDR) in this disease have not yet been determined. Objectives  To evaluate the possibility that serum sKDR levels can be a specific disease marker of SSc. Methods  Serum sKDR levels of 42 patients with SSc, 10 patients with Raynaud’s phenomenon (RP) and 22 healthy controls were measured with specific enzyme‐linked immunosorbent assays. Quantitative real‐time polymerase chain reaction (PCR) was performed to determine KDR mRNA levels. Results  In females, the serum sKDR levels were significantly higher in patients with SSc, especially limited cutaneous SSc, than in patients with RP or healthy controls. Quantitative real‐time PCR with RNA from skin sections revealed that KDR mRNA levels were also increased in the skin of patients with SSc with elevated serum sKDR levels. A significantly lower prevalence of pulmonary fibrosis, higher percentage vital capacity, and a higher incidence of telangiectasia were seen in female patients with SSc with elevated serum sKDR levels than those with normal levels. Conclusions  These results suggest that the skin can be one of the sources of elevated serum sKDR levels, and that serum sKDR levels are useful for diagnosis and may be a marker of microangiopathy in patients with SSc, especially females. The VEGF‐A/KDR signalling system may be involved in the pathogenesis of the disease.

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