基于慢性乙型肝炎合并代谢相关脂肪性肝病非靶向代谢谱的胆汁酸代谢分析OA
Analysis of bile acid metabolism based on non-targeted metabolic profile of chronic hepatitis B combined with metabolic dysfunction-associated fatty liver disease
目的:分析慢性乙型肝炎(CHB)合并代谢相关脂肪性肝病(MAFLD)患者血清代谢组学中胆汁酸(BA)相对水平的差异.方法:选取于2020年11月至2021年7月就诊的未经抗病毒治疗的28例CHB患者(CHB组)、16例健康志愿者(HC组)、25例MAFLD患者(MAFLD组)和42例CHB合并MAFLD组患者(CHB+MAFLD组),收集4组受试者的一般临床资料和血清样本,采用液相色谱-质谱联用技术对血清进行非靶向代谢组学分析,筛选出差异代谢物,并从BA角度分析患者肝脏炎症与肝纤维化特点.结果:在不同疾病组之间,BA组成的变化均不相同.在4组人群中存在5种差异的BA,分别为脱氧胆酸(DCA)、甘氨胆酸(GCA)、甘氨鹅脱氧胆酸(GCDCA)、牛磺胆酸(TCA)和鹅脱氧胆酸(CDCA);CHB+MAFLD组较CHB组、MAFLD组及HC组CDCA相对水平显著升高.结论:CHB合并MAFLD患者与健康志愿者、CHB患者、MAFLD患者在血清CDCA相对水平存在显著性差异,CDCA可作为CHB合并MAFLD的肝纤维化潜在标志物.
Objective:To analyze the differences in relative levels of bile acids in serum metabolomics of patients with chronic hepatitis B(CHB)complicated with metabolic dysfunction-associated fatty liver disease(MAFLD)Methods:From November 2020 to July 2021,28 patients with CHB 16 healthy controls,25 patients with MAFLD and 42 patients with CHB combined with MAFLD were selected from the Department of Infection,Tongji Hospital,Tongji Medical College,Huazhong University of Science and Technology without antiviral treatment Patients were divided into four groups:MAFLD group,healthy control group(HC group)and CHB combined with MAFLD group(CHB+MAFLD group).General clinical data and serum samples were collected from the four groups of subjects,and non-targeted metabolomics analysis was performed on the serum using liquid chromatography-mass spectrometry(LC-MS)technology to screen for differential metabolites.The characteristics of liver inflammation and fibrosis in patients were analyzed from the perspective of bile acids.Results:The changes in bile acid composition vary among different disease groups.There are five different bile acids in the four groups,namely deoxycholic acid(DCA),glycocholic acid(GCA),glycodeoxycholic acid(GCDCA),taurocholic acid(TCA),and chenodeoxycholic acid(CDCA);The CHB+MAFLD group showed a significant increase in the relative level of CDCA compared to the CHB group,MAFLD group,and HC group.Conclusion:There is a significant difference in the relative levels of serum CDCA between CHB+MAFLD patients and healthy volunteers,patients with CHB,MAFLD.CDCA may serve as a potential biomarker for liver fibrosis in patients with CHB combined with MAFLD.
王凯;汪鹏;胡雪;王洪武;宁琴
华中科技大学同济医学院附属同济医院感染科,人畜共患传染病重症诊治全国重点实验室(湖北 武汉,430030)华中科技大学同济医学院附属同济医院感染科,人畜共患传染病重症诊治全国重点实验室(湖北 武汉,430030)华中科技大学同济医学院附属同济医院感染科,人畜共患传染病重症诊治全国重点实验室(湖北 武汉,430030)华中科技大学同济医学院附属同济医院感染科,人畜共患传染病重症诊治全国重点实验室(湖北 武汉,430030)华中科技大学同济医学院附属同济医院感染科,人畜共患传染病重症诊治全国重点实验室(湖北 武汉,430030)
医药卫生
慢性乙型肝炎代谢相关脂肪性肝病代谢组学胆汁酸肝纤维化
chronic hepatitis Bmetabolic dysfunction-associated fatty liver diseasemetabolomicsbile acidshepatic fibrosis
《中西医结合肝病杂志》 2026 (2)
133-138,6
国家自然科学基金(No.82170596)
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