Shin Hyun Phil, Lee Joung Il, Jung Joo-Ho, Yim Sung-Vin, Kim Hyun Jeong, Cha Jae Myung, Park Jong Beom, Joo Kwang Ro, Hwang Jae Seok, Jang Byoung-Kuk
Department of Internal Medicine, East-West Neo Medical Center, Kyung Hee University College of Medicine, Gangdong-gu, Seoul 134-090, Korea.
Dig Dis Sci. 2008 Mar;53(3):823-9. doi: 10.1007/s10620-007-9937-7. Epub 2007 Sep 1.
A common and important problem in patients with chronic hepatitis B is the progression of liver fibrosis. Matrix metalloproteinases (MMPs) play an important role in the progression of liver fibrosis. Our aim of this study was to examine the association of MMP-3 polymorphism with liver cirrhosis in Korean patients with chronic hepatitis B. Genomic DNA was extracted from 127 patients with chronic hepatitis B (CHB), 92 patients with hepatitis B virus (HBV)-related liver cirrhosis (HBV-LC), and 146 healthy subjects. MMP-3 polymorphism was determined by polymerase-chain reaction-based assays, and the association with the progression of liver cirrhosis was investigated. With regard to MMP-3 polymorphism, there was no statistical difference in genotype distributions among the three groups. However, the peripheral platelet count of the 5A carriers was significantly lower than that of the 6A homozygotes in the HBV-LV group (85.0 +/- 36.9 vs. 109.8 +/- 47.0 x 10(9)/l; P = 0.02). With MMP-3 promoter polymorphism (rs3025058), a lower peripheral blood platelet count, which was related to advanced liver cirrhosis, was observed in 5A carriers. Therefore, more studies of MMP-3 gene polymorphism with larger populations should be conducted to further understand its role in the progression of liver cirrhosis.
慢性乙型肝炎患者中一个常见且重要的问题是肝纤维化的进展。基质金属蛋白酶(MMPs)在肝纤维化进展中起重要作用。本研究的目的是检测韩国慢性乙型肝炎患者中MMP - 3基因多态性与肝硬化的关联。从127例慢性乙型肝炎(CHB)患者、92例乙型肝炎病毒(HBV)相关肝硬化(HBV - LC)患者和146名健康受试者中提取基因组DNA。通过基于聚合酶链反应的检测方法确定MMP - 3基因多态性,并研究其与肝硬化进展的关联。关于MMP - 3基因多态性,三组间基因型分布无统计学差异。然而,在HBV - LV组中,5A携带者的外周血小板计数显著低于6A纯合子(85.0±36.9 vs. 109.8±47.0×10⁹/L;P = 0.02)。在5A携带者中,观察到与晚期肝硬化相关的较低外周血血小板计数,这与MMP - 3启动子多态性(rs3025058)有关。因此,应开展更多涉及更大样本量人群的MMP - 3基因多态性研究,以进一步了解其在肝硬化进展中的作用。