Panko N, Tsiura O, Shevchenko N, Zimnytska T
1V.N. Karazin Kharkiv National University, Department of Pediatrics No2; Kharkiv, Ukraine.
1V.N. Karazin Kharkiv National University, Department of Pediatrics No2; 2SI "Institute of Children and Adolescences Health Care of National Academy of Medical Sciences", Kharkiv, Ukraine.
Georgian Med News. 2020 Jul-Aug(304-305):95-99.
The aim of the research was to determine liver lesion in patients with Oligoarticular and RF-negative Polyarticular forms of JIA by noninvasive methods depending on duration of Methotrexate treatment. The study included 42 patients with Rheumatoid factor (RF) negative oligo- and polyarticular joints forms of JIA from 3 to 18 years old. They were investigated by measurement of alanine aminotransferase (ALAT), aspartate aminotransferase (ASAT), haptoglobin, triglycerides, gamma glutamine transferase (GGT), apolipoprotein-A (Apo-A), a2-macroglobulin, cholesterine levels. The equation for calculating the FibroTest score regression coefficient had been done according U.S. patent 6.631.330. Student -Fisher Test, Mann - Whitney U-test were used for the statistical processing. In spite of MTX treatment progression of JIA was determined according assessment of joints functional class and radiological stage (p<0.05). Increased level of ALAT was prominent (40%) in children taken MTX for 1-5 years in comparison with other studied patients (p<0.05). 17 % of children who took MTX longer than 5 years had increased GGT content. Metabolic liver function was not changed because levels of Apo-A, haptoglobin, total bilirubin, cholesterine were within normal limits due to all stages of MTX taking. The increased level of a2-macroglobulin as a predictor of liver fibrosis was determined in all studying groups with the average frequency 36 % and it did not correspond to the duration of MTX treatment. According FibroTest score regression 14% of patients had liver fibrosis F1, which did not depend on duration of MTX treatment. According to our findings, patients using MTX for JIA management had joint damage progresses despite usage of MTX. Hepatic cytolysis is most frequently appeared within 15 years of MTX taking. Risk of liver fibrosis does not depend on duration of MTX treatment.
该研究的目的是通过非侵入性方法,根据甲氨蝶呤治疗时间来确定少关节型和类风湿因子阴性多关节型幼年特发性关节炎(JIA)患者的肝脏病变情况。该研究纳入了42例年龄在3至18岁之间的类风湿因子(RF)阴性的少关节型和多关节型JIA患者。对他们进行了丙氨酸转氨酶(ALAT)、天冬氨酸转氨酶(ASAT)、触珠蛋白、甘油三酯、γ-谷氨酰胺转移酶(GGT)、载脂蛋白A(Apo-A)、α2-巨球蛋白、胆固醇水平的检测。根据美国专利6,631,330进行了计算FibroTest评分回归系数的公式运算。采用Student -Fisher检验、Mann - Whitney U检验进行统计处理。尽管进行了甲氨蝶呤治疗,但根据关节功能分级和放射学分期评估仍确定JIA有进展(p<0.05)。与其他研究患者相比,服用甲氨蝶呤1至5年的儿童中,ALAT水平升高显著(40%)(p<0.05)。服用甲氨蝶呤超过5年的儿童中有17%的GGT含量升高。由于在甲氨蝶呤治疗的各个阶段,Apo-A、触珠蛋白、总胆红素、胆固醇水平均在正常范围内,所以代谢性肝功能未发生改变。在所有研究组中均确定α2-巨球蛋白水平升高作为肝纤维化的预测指标,平均发生率为36%,且与甲氨蝶呤治疗时间无关。根据FibroTest评分回归,14%的患者有F1级肝纤维化,这与甲氨蝶呤治疗时间无关。根据我们的研究结果,使用甲氨蝶呤治疗JIA的患者尽管使用了甲氨蝶呤,但关节损伤仍有进展。肝细胞溶解最常出现在服用甲氨蝶呤的15年内。肝纤维化风险与甲氨蝶呤治疗时间无关。