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Chinese Archives of General Surgery(Electronic Edition) ›› 2013, Vol. 07 ›› Issue (02): 86-90. doi: 10.3877/cma.j.issn.1647-0793.2013.02.002

Special Issue:

• Original Article • Previous Articles     Next Articles

Expression and clinical significance of YKL-40 protein in human splenomegaly of portal hypertension

Dong WANG1, Xi-lin DU1, Rui DONG1, Ji-kai YIN1, Li ZANG1, Xue JIANG1, Jian-guo LU1,()   

  1. 1. Department of General Surgery, the Second Affiliated Hospital of the Fourth Military Medical University, Xi'an 710038, China
  • Received:2013-03-18 Online:2013-04-01 Published:2013-04-01
  • Contact: Jian-guo LU
  • About author:
    Corresponding author: LU Jian-guo,Email:

Abstract:

Objective

To investigate the expression and clinical significance of YKL-40 protein in human splenomegaly tissue of portal hypertension.

Methods

Immunohistochemical method was used to detect the expression of YKL-40 in spleen of portal hypertension. Masson trichrome staining method was used to detect the fibrosis degrees of spleens associated with portal hypertension.

Results

Expression of YKL-40 in enlarged spleens of portal hypertension was significantly higher than that in normal spleen (P < 0.05), and its expression was significantly associated with Child-Pugh Classification (P < 0.05). Furthermore, the statistical correlation between overexpression of YKL-40 and Free Portal Pressure (FPP) was found(R = 0.499, P < 0.01). Masson trichrome staining showed that a considerable amount of fibrosis extending to the entire splenic parenchyma was found in portal hypertension patients, compared with normal people(P < 0.05). Additionally, expression of YKL-40 was correlated with fibrosis area of spleen (correlation coefficient was 0.857, P < 0.01).

Conclusions

Expression of YKL-40 in enlarged spleens of portal hypertension was significantly higher than that in normal spleen, and statistical correlation between YKL-40 with FPP and Child-Pugh Classification are found. The expression of YKL-40 is correlated with fibrosis area of spleen. YKL-40 may play an important role in molecular mechanism involved in fibrosis development of splenomegaly associated with portal hypertension.

Key words: YKL-40, Splenomegaly, Portal hypertension, Fibrosis

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