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Serum Lipoprotein Profiles and Response to Pegylated Interferon Plus Ribavirin Combination Therapy in Patients With Chronic HCV Genotype 1b Infection

机译:慢性HCV基因型1b感染患者的血清脂蛋白谱和聚乙二醇干扰素加利巴韦林联合治疗的反应

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Background: Abnormal serum lipid profiles have been noted in patients with chronic hepatitis C virus (HCV) infection. Moreover, many reports suggest that serum lipoprotein profiles are more profoundly distorted in patients with HCV G1b infection who have an unfavorable response to pegylated interferon (peg-IFN) plus ribavirin (RBV) combination therapy. However, after the discovery of single nucleotide polymorphisms near the IL28B gene (rs8099917 and rs12979860) as potent predictive factors affecting the response to peg-IFN plus RBV, lipid factors are thought to be confounding factors. Objectives: To re-examine the significance of lipoprotein profiles on virological response to peg-IFN plus RBV combination therapy in patients with chronic HCV G1b infection, we examined cholesterol and triglyceride concentrations in each lipoprotein fraction separated by high performance liquid chromatography. Patients and Methods: Lipoprotein profiles were examined using fasting sera from 108 patients infected with HCV G1b who had chronic hepatitis, as determined by liver biopsy. Results of lipoprotein profiles and clinical data, including IL28B genotype and amino acid substitution at aa70 of HCV G1b, were compared between patients with a sustained virological response (SVR) and non-SVR or a non-virological response (NVR) and virological responses other than NVR (non-NVR). In addition, significant predictive factors independently associated with virological response to peg-IFNα-2b plus RBV were determined by logistic regression analysis. Results: An increased ratio of cholesterol/triglyceride in very low-density lipoprotein (odds ratio (OR) 3.03; 95% confidence interval (CI) 1.01-9.44) along with a major genotype of rs8099917 (OR 9.09; 95% CI 2.94-33.33), were independent predictive factors for SVR. In contrast, lipid factors were not elucidated as independent predictive factors for NVR. Conclusions: Examination of the fasting lipid profile has clinical importance in predicting the efficacy of peg-IFN-α-2b plus RBV combination therapy for patients with HCV G1b even after the discovery of the IL28 genotype as a potent predictive factor.
机译:背景:慢性丙型肝炎病毒(HCV)感染患者的血脂异常。此外,许多报告表明,在对聚乙二醇化干扰素(peg-IFN)加利巴韦林(RBV)联合治疗反应不良的HCV G1b感染患者中,血清脂蛋白分布会更严重变形。但是,在发现IL28B基因附近的单核苷酸多态性(rs8099917和rs12979860)作为影响对peg-IFN加RBV应答的有效预测因素后,脂质因子被认为是混杂因素。目的:为了重新检查脂蛋白谱对慢性HCV G1b感染患者对peg-IFN加RBV联合治疗的病毒学应答的意义,我们通过高效液相色谱法检测了每个脂蛋白组分中胆固醇和甘油三酯的浓度。患者和方法:通过肝活检确定,使用空腹血清检查了108名感染了HCV G1b的慢性肝炎患者的脂蛋白谱。比较了具有持续病毒学应答(SVR)和非SVR或非病毒学应答(NVR)和其他病毒学应答的患者之间脂蛋白谱和临床数据的结果,包括HCV G1b的aa70的IL28B基因型和氨基酸取代比NVR(非NVR)大。另外,通过logistic回归分析确定了与对peg-IFNα-2b加RBV的病毒学应答独立相关的重要预测因素。结果:极低密度脂蛋白中胆固醇/甘油三酯的比例增加(奇数比(OR)3.03; 95%置信区间(CI)1.01-9.44),以及主要基因型rs8099917(OR 9.09; 95%CI 2.94- 33.33)是SVR的独立预测因素。相比之下,脂质因子并未阐明为NVR的独立预测因子。结论:空腹血脂检查对预测peg-IFN-α-2b加RBV联合疗法对HCV G1b患者的疗效具有重要的临床意义,即使发现IL28基因型为有效的预测因子也是如此。

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