抗炎1号方治疗慢性肝病重叠巨细胞病毒感染导致胆汁淤积的疗效观察OA
Observation on the efficacy of anti-inflammatory formula No.1 in the treatment of cholestasis caused by chronic liver disease with cytomegalovirus infection
目的:阐述抗炎1号方治疗慢性肝病重叠巨细胞病毒感染的疗效及作用机制.方法:回顾性分析慢性肝病重叠巨细胞病毒感染30例使用抗炎1号方+西药治疗,30例单纯西药治疗,对比两组患者临床疗效及胆汁酸代谢组学特征.结果:两组患者慢性肝病重叠巨细胞病毒感染导致肝功能损伤患者临床症状及体征较轻,生化指标治疗前后相比,治疗组患者治疗后2周、4周总胆红素(TBil)、丙氨酸氨基转移酶(ALT)、总胆汁酸(TBA)、肿瘤坏死因子α(TNF-α)、白细胞介素6(IL-6)较对照组显著下降(P<0.01);胆汁酸代谢组学分析检测出29种物质,治疗后均较治疗前下降,其中胆酸(CA)、鹅脱氧胆酸(CDCA)差异有统计学意义(P<0.05);治疗组总有效率明显高于对照组(2x=8.523,P=0.004),两组患者在治疗过程中均未出现不良反应.结论:治疗组在改善患者临床生化指标、降低TNF-α、IL-6水平及改善胆汁酸代谢方面更佳,提示抗炎1号方治疗慢性肝病重叠巨细胞病毒感染致胆汁淤积的作用机制可能是下调了TNF-α、IL-6的表达,改善胆汁酸的组成成分,减少CA、CDCA的产生,同时改变胆汁酸组成成分,达到减轻肝脏氧化应激和炎症反应,抑制胆汁酸合成,增加胆汁分泌,改善肝损伤及促进肝细胞修复.
Objective:Elucidate the efficacy and action mechanism of anti-inflammatory formula No.1 in the treatment of chronic liver disease with cytomegalovirus infection.Methods:A retrospective analysis was conducted on 30 cases of chronic liver diseases complicated with cytomegalovirus infection who were treated with Anti-inflammatory Prescription No.1 combined with western medicine,and 30 cases who were treated with western medicine alone.The clinical efficacy and characteristics of bile acid metabolomics of the two groups were compared.Results:The clinical symptoms and signs of patients with liver function impairment caused by chronic liver diseases complicated with cytomegalovirus infection in both groups were relatively mild.When comparing the biochemical indexes before and after treatment,there was no difference in total bilirubin(TBil)before treatment between the treatment group(285.52±125.34)μmol/L)and the control group(338.28±129.19)μmol/L)(P>0.05).Two weeks and four weeks after treatment,the TBil level in the treatment group decreased significantly compared with that in the control group(P<0.01).There was no significant difference in alanine aminotransferase(ALT)before treatment between the treatment group(681.08±587.07)U/L)and the control group(670.50±924.61)U/L)(P>0.05).Two weeks and four weeks after treatment,the ALT level in the treatment group decreased compared with that in the control group(P<0.05).There was no difference in total bile acid(TBA)between the two groups before treatment.Two weeks and four weeks after treatment,the TBA level in the treatment group decreased significantly compared with that in the control group(P<0.01).There was no statistical difference in the levels of tumor necrosis factor(TNF-α)and interleukin-6(IL-6)between the two groups before treatment.After treatment,the levels of TNF-α and IL-6 in the treatment group decreased significantly compared with those in the control group(P<0.01).Bile acid metabolomics analysis detected 29 substances,all of which decreased after treatment compared with that before treatment,and cholic acid(CA)and chenodeoxycholic acid(CDCA)showed statistical significance(P<0.05).The total effective rate of the treatment group was significantly higher than that of the control group(x2=8.523,P=0.004),and no adverse reactions occurred in both groups during the treatment process.Conclusion:The treatment group for chronic liver diseases complicated with cytomegalovirus infection is better in improving the clinical biochemical indexes of patients,reducing the levels of TNF-α and IL-6,and improving bile acid metabolism.It is suggested that the mechanism of Anti-inflammatory Prescription No.1 in treating cholestasis caused by chronic liver diseases complicated with cytomegalovirus infection may be to down-regulate the expression of TNF-α and IL-6,improve the composition of bile acids,reduce the production of CA and CDCA,and change the composition of bile acids at the same time,so as to reduce the oxidative stress and inflammatory response of the liver,inhibit the synthesis of bile acids,increase bile secretion,improve liver injury,and promote the repair of liver cells.
吕锦珍;陈卓瑜;冉云;陈文林;崔玉;王锃铭;胡世平
北京中医药大学深圳医院(龙岗)(广东 深圳,518000)北京中医药大学深圳医院(龙岗)(广东 深圳,518000)北京中医药大学深圳医院(龙岗)(广东 深圳,518000)北京中医药大学深圳医院(龙岗)(广东 深圳,518000)北京中医药大学深圳医院(龙岗)(广东 深圳,518000)北京中医药大学深圳医院(龙岗)(广东 深圳,518000)北京中医药大学深圳医院(龙岗)(广东 深圳,518000)
医药卫生
胆汁淤积慢性肝病巨细胞病毒感染抗炎1号方胆汁酸代谢
cholestasischronic liver diseasecytomegalovirus infectionanti-inflammatory formula No.1bile acid metabolism
《中西医结合肝病杂志》 2026 (4)
402-406,5
国家自然科学基金面上项目(No.81973733),国家卫生健康委能力建设和继续教育中心慢病管理研究课题(No.GWJJMB202510025044),深圳市"医疗卫生三名工程"项目资助(No.SZZYSM202311018),深圳市龙岗区科技创新局(No.LGWJ2022-76)
评论