丙型肝炎患者胆红素与其他肝脏生物标志物的因果关系

P. Banerjee, A. Goswami, Shreya Bhunia, Sudipta Basu
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引用次数: 1

摘要

背景:肝脏是人体功能最广泛的器官之一。但肝脏发生的任何一种紊乱都可能导致肝脏疾病。最常见的肝脏感染之一是由丙型肝炎病毒(HCV)引起的丙型肝炎。众所周知,肝脏是人体最大的固体器官,也被称为外分泌腺,因为它将胆汁分泌到肠道中。目的:本研究的目的是利用先进的回归技术评估胆红素与各肝脏生物标志物的因果关系。方法:采用联合广义线性模型(JGLM)和广义可加模型(GAM)两种先进的回归技术。对于模型的选择,我们检查了AIC值、GCV评分和调整后的r方,并显示了Q-Q图、残差与拟合图等不同的诊断图。结果:胆红素是一种人类肝脏疾病的生物标志物,是一种在胆汁中发现的棕黄色物质,当肝脏中旧的红细胞分解时产生。胆红素与谷氨酸转氨酶(AST)、肌酐(CREA)、γ -谷氨酰转肽酶(GGT)、蛋白质(PROT)、碱性磷酸酶(ALP)*白蛋白(ALB)呈正相关(p值<0.05),与胆碱酯酶(CHE)*胆固醇(CHOL)呈正相关(p值=0.0591)。而与年龄、性别、碱性磷酸酶(ALP)、丙氨酸转氨酶(ALT)、胆碱酯酶(CHE)、胆固醇(CHOL)、白蛋白(ALB)、肌酐(CREA)* γ -谷氨酰转肽酶(GGT)呈负相关(p值< 0.05)。此外,胆红素与AST、CREA、GGT、(CREA*GGT)、(CHE*CHOL)呈正相关,而与Sex、ALT、CHE、CHOL呈负相关。此外,在GAM下,ALB作为非参数平滑项具有高度正显著性(p值< 0.001)。结论:JGLM和GAM先进回归模型均能解释丙型肝炎患者胆红素与其他肝脏疾病生物标志物的相关性。
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Determination of Causal Relationship Between Bilirubin and Other Liver Biomarker in Case of Hepatitis C
Background: Liver works as one of the most versatile organs in the human body. But any kind of disturbance occurs in the liver may cause the liver disease. One of the most common liver infections is hepatitis C which is caused by the Hepatitis C Virus (HCV). It is well known that liver is the largest solid organ in the human body and also it is called the exocrine gland as it secretes bile into the intestine. Aim: The aim of this study is to evaluate the causal relationship of Bilirubin with each liver biomarker using the advanced regression techniques. Methods: We use two advanced regression techniques, namely Joint Generalized Linear Model (JGLM) and Generalized Additive Model (GAM). For model selection, we check the AIC value, GCV score and adjusted R–square as well as the different diagnostic plots like Q–Q plot, Residual vs. Fitted plot etc. are displayed. Results: Bilirubin, a human liver disease biomarker, is a brownish yellow substance found in bile and it is produced in the liver when the old red blood cells break down. The present study reveals that Bilirubin is positively associated (p-value<0.05) with Aspartate Aminotransferase (AST), Creatinine (CREA), Gamma-Glutamyl Transpeptidase (GGT), Protein (PROT), Alkaline Phosphatase (ALP)*Albumin (ALB) and marginally associated with Choline Esterase (CHE)* Cholesterol (CHOL) (p-value=0.0591). While it is negatively associated (p-value < 0.05) with Age, Sex, Alkaline Phosphatase (ALP), Alanine Aminotransferase (ALT), Choline Esterase (CHE), Cholesterol (CHOL), Albumin (ALB), Creatinine (CREA)*Gamma-Glutamyl Transpeptidase (GGT) under JGLM. Besides of that, Bilirubin is positively associated with AST, CREA, GGT, (CREA*GGT), (CHE*CHOL) whereas it is negatively associated with Sex, ALT, CHE, CHOL. Also, ALB is highly positively significant as a non–parametric smoothing term (p-value < 0.001) under GAM. Conclusion: Both the advanced regression models JGLM and GAM explain the association between Bilirubin with other liver diseases biomarker in case of Hepatitis C.
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