Department of Gastroenterology, Juntendo University Nerima Hospital, Tokyo, Japan.
Department of Cellular and Molecular Function Analysis, Kanazawa University Graduate School of Medical Sciences, Ishikawa, Japan.
PLoS One. 2018 Apr 30;13(4):e0196747. doi: 10.1371/journal.pone.0196747. eCollection 2018.
Paritaprevir inhibits organic anion-transporting polypeptide (OATP)1B1 and OATP1B3, which transport bilirubin. Hyperbilirubinemia is an adverse event reported during hepatitis C treatment. Gadoxetic acid is also transported by OATP1B1/1B3. We evaluated whether the enhancement effect in gadoxetic acid-enhanced magnetic resonance (MR) imaging could predict the plasma concentration of paritaprevir and might anticipate the development of hyperbilirubinemia.
This prospective study evaluated 27 patients with hepatitis C who underwent gadoxetic acid-enhanced MR imaging prior to treatment with ombitasvir, paritaprevir, and ritonavir. The contrast enhancement index (CEI), a measure of liver enhancement during the hepatobiliary phase, was assessed. Plasma trough concentrations, and concentrations at 2, 4, and 6 h after dosing were determined 7 d after the start of treatment.
Seven patients (26%) developed hyperbilirubinemia (≥ 1.6 mg/dl). Paritaprevir trough concentration (Ctrough) was significantly higher in patients with hyperbilirubinemia than in those without (p = 0.022). We found an inverse relationship between CEI and Ctrough (r = 0.612, p = 0.001), while there was not a significantly weak inverse relationship between AUC0-6 h and CEI (r = -0.338, p = 0.085). The partial correlation coefficient between CEI and Ctrough was -0.425 (p = 0.034), while excluding the effects of albumin and the FIB-4 index. Receiver operating characteristic (ROC) curve analysis showed that the CEI was relatively accurate in predicting hyperbilirubinemia, with area under the ROC of 0.882. Multivariate analysis showed that the CEI < 1.61 was the only independent predictor related to the development of hyperbilirubinemia, with an odds ratio of 9.08 (95% confidence interval 1.05-78.86, p = 0.046).
Hepatic enhancement with gadoxetic acid was independently related to paritaprevir concentration and was an independent pretreatment factor in predicting hyperbilirubinemia. Gadoxetic acid-enhanced MR imaging can therefore be useful in determining the risk of paritaprevir-induced hyperbilirubinemia.
帕立瑞韦抑制有机阴离子转运多肽(OATP)1B1 和 OATP1B3,而这两种转运蛋白负责转运胆红素。在丙型肝炎治疗期间,高胆红素血症是一种不良事件。钆塞酸也是由 OATP1B1/1B3 转运的。我们评估了在 gadoxetic 酸增强磁共振成像中的增强效应是否可以预测帕立瑞韦的血浆浓度,并预测高胆红素血症的发生。
本前瞻性研究评估了 27 例丙型肝炎患者,这些患者在接受 ombitasvir、帕立瑞韦和利托那韦治疗前进行了 gadoxetic 酸增强磁共振成像。评估了在肝胆期期间肝增强的对比增强指数(CEI)。在治疗开始后 7 天,测定治疗后第 2、4 和 6 小时的血药谷浓度和浓度。
7 例患者(26%)发生高胆红素血症(≥ 1.6mg/dl)。高胆红素血症患者的帕立瑞韦血药谷浓度(Ctrough)显著高于无高胆红素血症患者(p = 0.022)。我们发现 CEI 与 Ctrough 呈负相关(r = 0.612,p = 0.001),而 AUC0-6 h 与 CEI 之间不存在显著的弱负相关(r = -0.338,p = 0.085)。CEI 与 Ctrough 的偏相关系数为 -0.425(p = 0.034),而排除白蛋白和 FIB-4 指数的影响。受试者工作特征(ROC)曲线分析表明,CEI 预测高胆红素血症相对准确,ROC 曲线下面积为 0.882。多变量分析表明,CEI<1.61 是与高胆红素血症发生相关的唯一独立预测因子,其优势比为 9.08(95%置信区间 1.05-78.86,p = 0.046)。
gadoxetic 酸的肝增强与帕立瑞韦浓度独立相关,是预测高胆红素血症的独立预处理因素。因此,gadoxetic 酸增强磁共振成像可用于确定帕立瑞韦引起的高胆红素血症的风险。