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Respiratory medicine · Feb 2013
The role of vascular endothelial growth factor-D in diagnosis of lymphangioleiomyomatosis (LAM).
- Kai-Feng Xu, Peng Zhang, Xinlun Tian, Aiping Ma, Xue Li, Jiong Zhou, Ni Zeng, Yao-Song Gui, Zijian Guo, Ruie Feng, Weihong Zhang, Wei Sun, and Baiqiang Cai.
- Department of Respiratory Medicine, Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences, Beijing 100730, China. kaifeng.xu@gmail.com
- Respir Med. 2013 Feb 1; 107 (2): 263-8.
BackgroundDefinite diagnosis of lymphangioleiomyomatosis (LAM) depends on either transbronchial lung biopsy or video-assisted thoracic surgery, unless there is a history of chylothorax, kidney angiomyolipoma (AML), or tuberous sclerosis complex (TSC). Vascular endothelial growth factor-D (VEGF-D) was recently considered as a novel diagnostic marker for LAM. Herein, we evaluated diagnostic value of serum VEGF-D in LAM patients.MethodsSerum samples were obtained from 78 cases of LAM (50 definite and 28 probable LAM based on European Respiratory Society guidelines), and 40 healthy female volunteers. VEGF-D was measured using enzyme-linked immunosorbant assay according to product instruction (R&D).ResultsSerum VEGF-D was significantly increased in definite LAM group, compared with that of health control (median: 3841.9 pg/mL vs 405.5 pg/mL respectively, p < 0.001). The optimal cut-off point for definite LAM diagnosis was 850.7 pg/mL. In probable LAM group, the majority of patients (92.9%) had serum VEGF-D level over 850.7 pg/mL. The serum levels of VEGF-D in LAM patients with pulmonary cystic lesions only were lower than that in patients with any of evidences of AML, chylous effusions, adenopathy, lymphangioleiomyomas, or TSC, but higher than that in the health control. In addition, VEGF-D levels were correlated with disease severity measured as LAM CT grade, and presentations of chylous effusions and/or lymphatic involvement (p < 0.05).ConclusionSerum VEGF-D should be added to the current diagnosis algorithm to enhance definitive diagnosis for LAM.Copyright © 2012 Elsevier Ltd. All rights reserved.
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