MMP-2 and MMP-9 Serum Levels Change but their Gene Promoter Polymorphisms are not Associated with Late Phase I/R Injury or Rejection after Orthotopic Liver Transplantation

W. Hove, B. D. Rooij, B. Hoek, J. Kuyvenhoven, M. Meijer, M. V. D. Berg, J. J. Reijden, W. Verduyn, J. Dubbeld, D. Hommes, C. Lamers, H. Verspaget
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引用次数: 4

Abstract

Introduction. Matrix metalloproteinases (MMPs) are involved in connective tissue remodeling processes asso- ciated with chronic liver disease and complications after orthotopic liver transplantation (OLT). Genetic variations in the promoter region of the MMP-2 and MMP-9 genes are thought to contribute not only to their transcription rate but may also have predisposing clinical impact. Methods. MMP-2 and MMP-9 gene promoter polymorphisms were analyzed in 109 patients who underwent an OLT. The relationship between these MMP polymorphisms in the donor and recipient DNA with the development of ische- mia/reperfusion (I/R) injury and rejection after OLT was evaluated. In addition, serum MMP-2 and MMP-9 levels were determined to illustrate potential phenotypical consequences in these patients. Results. The MMP-2 and -9 genotypes of the donor and recipient or a donor/recipient mismatch and chimerism were not associated with the development of late phase I/R injury or rejection in the OLT patients, although serological differences in the MMP levels did occur. The MMP-2 and -9 genotype distribution did also not have a major impact on the respective serum levels in patients that underwent an OLT. Conclusions. MMP-2 and MMP-9 gene polymorphisms do not seem to contribute to late phase I/R injury or rejection after liver transplantation. Serological changes in the MMP-2 and MMP-9 levels appear to occur independent of the MMP genotype after transplantation of the liver.
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血清中MMP-2和MMP-9水平改变,但其基因启动子多态性与原位肝移植后晚期I/R期损伤或排斥反应无关
介绍。基质金属蛋白酶(MMPs)参与与慢性肝病和原位肝移植(OLT)后并发症相关的结缔组织重塑过程。MMP-2和MMP-9基因启动子区域的遗传变异被认为不仅有助于它们的转录率,而且可能具有易感性的临床影响。方法。对109例OLT患者的MMP-2和MMP-9基因启动子多态性进行了分析。评估供体和受体DNA中这些MMP多态性与OLT后缺血/再灌注(I/R)损伤和排斥反应的关系。此外,测定血清MMP-2和MMP-9水平,以说明这些患者的潜在表型后果。结果。供体和受体的MMP-2和-9基因型或供体/受体错配和嵌合与OLT患者晚期I/R期损伤或排斥反应的发展无关,尽管MMP水平确实存在血清学差异。MMP-2和-9基因型分布对接受OLT患者各自的血清水平也没有重大影响。结论。MMP-2和MMP-9基因多态性似乎与肝移植后晚期I/R期损伤或排斥反应无关。肝脏移植后,血清中MMP-2和MMP-9水平的变化似乎与MMP基因型无关。
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