The plasma level changes of VEGF and soluble VEGF receptor-1 are associated with high-altitude pulmonary edema

  • Zhang Shukun
    Department of Pathology, Weihai Municipal Hospital Department of Pathology, Qinghai Provincial People's Hospital
  • Liu Juanli
    Department of Internal Medicine, Qinghai Provincial People's Hospital
  • Jiang Dongmei
    Institute for Neurological diseases, Qinghai Provincial People's Hospital
  • Wuren Tana
    Research Centre for High Altitude Medicine, Qinghai University Medical College
  • Ma Siqing
    Department of Intensive Care Unit, Qinghai Provincial People's Hospital
  • Du Yansheng
    Department of Neurology, Indiana University School of Medicine
  • Yi Xin
    Department of Neurology, Indiana University School of Medicine
  • Wu Shizheng
    Department of Neurology, Qinghai Provincial People's Hospital

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タイトル別名
  • The plasma level changes of VEGF and soluble VEGF receptor‐1 are associated with high‐altitude pulmonary edema

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<p>Hypoxia‐induced plasma levels of VEGF and sFlt‐1 are responsible for increased vascular permeability occurred in both brain and pulmonary edema. Currently, it remains unclear the exact roles of VEGF and sFlt‐1 in High Altitude Pulmonary Edema (HAPE) pathogenesis. In this study, plasma levels of VEGF and sFlt‐1 from 10 HAPE and 10 non‐HAPE subjects were measured and compared. The results showed that plasma levels of both VEGF and sFlt‐1 in HAPE patients were significantly increased as compared to the non‐HAPE group. Interestingly, increased plasma levels of these two protein factors were markedly reduced after treatments. As compared to VEGF, sFlt‐1 was much more affected by hypoxia and treatments, suggesting this factor was a key factor contributed to HAPE pathogenesis. Importantly, the ratio of sFlt‐1 and VEGF in group of either non‐HAPE or HAPE after recovery was significantly lower than the ratio in HAPE patients prior to treatments. Our findings suggested that sFlt‐1 was a key factor that involved in HAPE pathogenesis and the sFlt‐1/VEGF ratio could be used as a sensitive diagnostic marker for HAPE. J. Med. Invest. 65:64‐68, February, 2018</p>

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