甲氨蝶呤治疗青少年特发性关节炎的成纤维细胞生长因子和肝细胞生长因子

O. Pavlova
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引用次数: 2

摘要

甲氨蝶呤(MTX)是世界范围内治疗青少年特发性关节炎(JIA)的基石。尽管人们对纤维化的分子机制以及MTX的消除和纤维化指标进行了大量的研究,但对青少年的研究还不够。目的是通过测定成纤维细胞生长因子和肝细胞生长因子的含量,研究甲氨蝶呤治疗青少年特发性关节炎患者肝脏纤维化过程发展的分子-细胞机制激活动力学。材料与方法:68例青少年特发性关节炎患儿入组研究。男生25例(36.8%),女生43例(63.2%)。根据甲氨蝶呤累积剂量(CD)将患儿分为4组。分析肝功能指标(天冬氨酸转氨酶(AST) (U/L)、丙氨酰转氨酶(ALT) (U/L)、乳酸脱氢酶(LDH) (U/L)、脂联素(μg / ml)、BFGF (pg / ml)、HGF (pg / ml)、肝纤维化指标APRI和FIB-4评分。结果。甲氨蝶呤联合甲氨蝶呤治疗对肝脏有积极作用。当CD MTX达到1克和3克时,需要研究肝脏状态。当达到1克的CD MTX时,涉及刺激肝脏再生的调节机制。当CD MTX达到3克时,肝脏状况可能恶化,未来可能导致不可逆的肝纤维化过程。结论:甲氨蝶呤治疗对控制青少年可能出现的肝脏疾病具有重要意义。监测肝纤维化过程在JIA治疗的所有阶段都是适当的,但当MTX累积剂量达到1和3克时最可取
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Fibroblast growth factor and hepatocyte growth factor in adolescents with juvenile idiopathic arthritis treated with methotrexate
Methotrexate (MTX) is a cornerstone of therapy worldwide for juvenile idiopathic arthritis (JIA). Despite the fact that fibrosis molecular mechanisms as well as MTX elimination and fibrosis indexes were studied a lot there is still not enough information for adolescence. The aim was to study dynamics of molecular-cellular mechanisms activation of fibrotic processes development in the liver in adolescents with juvenile idiopathic arthritis treated with methotrexate by determining the content of fibroblast growth factor and hepatocyte growth factor. Materials and methods: A total of 68 children with juvenile idiopathic arthritis, were enrolled in the study. 25 boys (36.8 %) and 43 girls (63.2 %) were examined. Children were divided into four groups in accordance with cumulative dose (CD) of methotrexate. The following data were analyzed: liver function tests (aspartate aminotransferase (AST) (U/L), alanylaminotransferase (ALT) (U/L)), lactate dehydrogenase (LDH) (U/L), adiponectin (μg / ml), BFGF (pg / ml), HGF (pg / ml), liver fibrosis indexes APRI and FIB-4 Score. Results. Positive effect of JIA treatment with MTX on the liver is noted. When CD MTX reaches 1 and3 grams, liver state studying is needed. When the CD MTX of1 gram is reached, regulatory mechanisms are involved that provoke liver regeneration. When the CD MTX reaches3 grams, the liver condition may deteriorate, which in the future can lead to irreversible processes of liver fibrosis. Conclusions : Thus, it is important to control possible liver disorders in adolescence treated with MTX. Monitoring the processes of liver fibrosis is appropriate at all stages of JIA treatment, but it is most advisable when the MTX cumulative dose is reaching 1 and3 grams
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