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生理体液法分析肝病患者的氨基酸研究

Experimental Research on the Amino Acids in Liver Disease with Physiological Fluid Method

【作者】 李娴

【导师】 刘树业;

【作者基本信息】 天津医科大学 , 临床检验诊断学, 2010, 硕士

【摘要】 目的:(1)采用生理体液方法分析肝硬化、肝癌及慢性重型肝炎患者体液氨基酸的浓度,建立生理体液法分析氨基酸模型。(2)通过比较肝硬化、肝癌及慢性重型肝炎患者血清氨基酸代谢特点,探讨其氨基酸代谢模式。(3)通过分析肝硬化患者腹水氨基酸与血清氨基酸的变化,探讨其临床意义。方法:随机选取天津市第三中心医院体检患者60例作为对照组(N组),选取住院患者70例,其中30例为肝硬化组(A组)、20例为肝癌组(B组)、20例为慢性重型肝炎组(C组),于入院后第一天早晨空腹抽取静脉血检测肝功能、凝血功能并采用生理体液法进行氨基酸分析。10例肝硬化伴腹水患者抽取腹水采用生理体液法进行氨基酸分析。结果:(1)肝功能:与N组相比,试验组血清中白蛋白、前白蛋白浓度逐渐降低,血清谷草转氨酶、总胆汁酸、总胆红素浓度逐渐升高,C组最明显,与N组比较差异有统计学意义(P<0.05)。(2)凝血功能:与N组比较,试验组血清凝血酶原时间、活化部分凝血激酶时间及凝血酶时间逐渐延长,C组升高最明显,差异有统计学意义(P<0.05);血清纤维蛋白原浓度降低,与N组比较,差异无显著统计学意义(P>0.05)。(3)氨基酸分析结果:与N组比较,A组患者血清牛磺酸(Tau)、天门冬氨酸(Asp)、胱硫醚(Cysthi)、异亮氨酸(Ile)、精氨酸(Arg)浓度及支芳比值下降;p-丙氨酸(p-Ala)、p-氨基乙丁酸(p-Aiba)、γ-氨基乙丁酸(GABA)、α-氨基己二酸(α-AAA)、蛋氨酸(Met)、酪氨酸(Tyr)、苯丙氨酸(Phe)浓度升高,差异有统计学意义(P<0.05)。B组患者血清Asp、Cysthi、Ile、Arg、亮氨酸(Leu)、赖氨酸(Lys)浓度及支芳比值下降;Met、β-Ala、β-Aiba、GABA、α-AAA、Tyr、Phe、3甲基组氨酸(3Mehis)浓度升高,差异有统计学意义(P<0.05)。C组患者血清Tau、Asp、Cysthi、Ile、Leu、Lys、Arg、谷氨酸(Glu)、丙氨酸(Ala)、缬氨酸(Val)浓度及支芳比值下降;苏氨酸(Thr)、Met、β-Ala、β-Aiba、GABA、3Mehis、Tyr、Phe、1-甲基组氨酸(1Mehis)浓度升高,差异有统计学意义(P<0.05)。其中A组与B组比较,血清Val、Lys、Arg浓度下降,Tau、3Mehis浓度升高,差异有统计学意义(P<0.05);A组与C组比较,血清Thr、Met、Tyr、3Mehis浓度升高,Ala、Glu、α-AAA、Val、Leu及Arg浓度下降,差异有统计学意义(P<0.05);B组与C组比较,血清Thr、Met、Tyr浓度升高,Asp、Glu、Ala、Val、Cysthi及α-AAA浓度下降,差异有统计学意义(P<0.05)。(4)腹水氨基酸分析:与N组血清氨基酸比较,腹水Tau、Asp、Ser、Glu、Cysthi、Ile、Leu、α-氨基正丁酸(α-ABA)浓度降低,瓜氨酸(Cit)、胱氨酸(Cys)、et、Tyr、Phe、β-Ala、β-Aiba、GABA、3Mehis浓度升高,差异有统计学意义(P<0.05)。结论:(1)成功采用生理体液法分析氨基酸,通过分析患者血清及腹水氨基酸的变化,得到更多氨基酸代谢信息,为研究肝脏疾病的氨基酸代谢变化提供了一种理想的方法;(2)通过比较肝硬化、肝癌及慢性重型肝炎患者与健康人血清氨基酸的变化,发现其氨基酸代谢变化不同,为临床诊治提供了一定的参考意义;(3)通过比较肝硬化、肝癌及慢性重型肝炎患者之间血清氨基酸浓度的差异,发现一些氨基酸在不同疾病进程中可能起重要作用,建立完善代谢物资源数据库,可能成为今后诊断和治疗肝病的努力方向;(4)与血清氨基酸相比较,腹水中氨基酸浓度变化与血清变化相一致,它同样反映了肝脏的损害情况,为揭示肝硬化的代谢异常提供了线索。

【Abstract】 Objective:(1) we use physiological fluid method to analyze the concentration of amino acids in patients of hepatic ciirrhosis, hepatocellular carcinoma and chronic hepatitis and found a standard model of physiological fluid analysis. (2) By comparing different serum amino acids concentration of hepatic ciirrhosis, hepatocellular carcinoma and chronic hepatitis,we investigate the model of amino acids metabolism of different liver disease. (3)By analyzing the amino acid changes of ascites in patients with cirrhosis,we evaluate their clinical significance.Methods:We randomly selected Tianjin Third Central Hospital of 60 patients as a medical control group.Experiment group was dedived into hepatic cirrhosis group(A group),hepatic carcinoma group(B group) and chronic severe hepatitis group(C group). In the first morning after admission,the blood samples were collected to carry out the liver function,blood coagulation and we adopted the physiological fluid method to analyze the amino acids. The ascites of 10 cases in liver cirrhosis patients with ascites was analyzed by physiological fluid method.Results:(1)The liver function:Compared with the N group, serum albumin(Alb)、prealbumin of experimental group decreased gradually, and the serum aspartate aminotransferase, total bilirubin and total bile acid gradually increased, C group was the most significant compared with the N group (P<0.05). (2)The blood coagulation:With the N group, the serum in prothrombin time, activated partial thromboplastin time and thrombin time of experimental group gradually extended, and C group increased most significantly(P<0.05); the serum fibrinogen was decreased, and comparing with the N group, the difference was not statistically significant (P>0.05). (3)The amino acids:Compared with the N group, the serum concentration of taurine(Tau)、aspartic acid(Asp)、isoleucine(Ile)、arginine(Arg)、cystathionine(Cysthi) and BCAA/AAA ratio of A group decreased significantly (P<0.05); while the concentration of P-Alanine(β-Ala)、β-Amino isobutyric acid(β-Aiba)、γ-Amino-n-butyric acid(GABA)、α-amino adipic acid(a-AAA)、methionine(Met)、tyrosine(Tyr) and phenylalanine(Phe) increased significantly (P<0.05). We found that these amino acids(Asp、Cysthi、Ile、Arg、leucine(Leu)、 lysine(Lys))and BCAA/AAA ratio was decreased in B group(P<0.05), and the concentration of Met、β-Ala、β-Aiba、GABA、α-AAA、Tyr、Phe、3-Methylhistidine(3Mehis) was higher than N group (P<0.05). The concentration of Tau、Asp、Cysthi、ILe、Leu、Lys、Arg、glutamic acid(Glu)、alanine(Ala)、valine(Val) and BCAA/AAA ratio in C group was decreased(P<0.05); while Met、β-Ala、β-Aiba、GABA、3Mehis、Tyr、Phe、threonine(Thr)、1-Methylhistidine(1Mehis) increased significantly(P<0.05). Between A and B group, the concentration of Val、Lys and Arg decreased significantly (P<0.05), Tau and 3Mehis was increased significantly (P<0.05). While compared A and C group, serum concentration of Thr、Met、Tyr、3Mehis was increased significantly (P<0.05), Ala、Glu、α-AAA、Val、Leu and Arg was decreased significantly(P<0.05). While compared B and C group, serum concentration of Thr、Met、Tyr was increased significantly (P<0.05), the concentration of Asp、Glu、Ala、Val、Cysthi and a-AAA was decreased significantly(P<0.05). (4)The amino acids concentration in ascites:With the N group, the concentration of Tau、Asp、Ser、Glu、Cysthi、Ile、Leu、α-amino-n-butyric acid(α-ABA) was decreased, while the concentrition of citrulline(Cit)、cystine(Cys)、Met、Tyr、Phe、β-Ala、β-Aiba、GABA and 3Mehis was increased significantly(P<0.05).Conclusion:(1) We have a successful adoption of physiological fluid method in amino acid analysis, and by analyzing different amino acids in serum metabolites in various patients, we get more information about amino acids metabolism in petients. It provides an ideal method for the study of amino acid metabolism in liver disease. (2) By comparing amino acids concentration in serum of hepatic cirrhosis、hepatocellular carcinoma and chronic hepatitis patients with N group, we found they have different changes in amino acid metabolism and it provides some reference value for clinical diagnosis. (3) By comparing the difference between the serum amino acid concentrations in hepatic cirrhosis、hepatocellular carcinoma and chronic hepatitis, we found that a number of amino acids play an important role in the disease process, and establishing and improving metabolites resource database may be the direction in diagnosis and treatment of liver disease in the future. (4) Compared with the serum amino acids, the changesof amino acids in ascites and serum in hepatic ciirrhosis patients was consistent, it also reveals liver damage and provid the clues of metabolic abnormalities in hepatic cirrhosis.

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