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在新诊断的肾移植患者中,霉酚酸酯治疗早期监测肌苷单磷酸脱氢酶活性和表达。

Monitoring of inosine monophosphate dehydrogenase activity and expression during the early period of mycophenolate mofetil therapy in de novo renal transplant patients.

机构信息

Clinical Pharmacokinetics in Transplantation and Autoimmune Diseases, Foundation IRCCS Policlinico S. Matteo, Pavia, Italy.

出版信息

Drug Metab Pharmacokinet. 2013;28(2):109-17. doi: 10.2133/dmpk.dmpk-12-rg-048. Epub 2012 Aug 14.

Abstract

Measurement of inosine-monophosphate dehydrogenase (IMPDH) activity or gene expression was used as a further approach in pharmacokinetics (PK)/pharmacodynamic (PD)-guided mycophenolate mofetil (MMF) therapy. Forty-four de novo kidney transplant patients were enrolled; 35 of these completed the study, and were followed for 24 weeks for clinical status, PK parameters, IMPDH activity and IMPDH1/2 gene expression. IMPDH activity and expression were measured in peripheral blood mononuclear cells before transplant and at week 2,4,12 and 24, drawn before (t0) and 2 h (t2 h) after MMF administration. No significant correlation was found between IMPDH activity/expression and PK parameters. For both genes, significant enhancement in t2 h expression was observed, then decreases towards week 24 with a trend following steroid dosages. Seven patients experienced acute rejection (AR) and exhibited significantly higher pre-transplant expression of both IMPDH1 (median 3.42 vs. 0.84; p=0.0025), and IMPDH2 genes (135 vs. 104; p=0.0218) with respect to non-rejecting patients. A significant association was also found between pre-transplant IMPDH1 mRNA and haematological complications (p=0.032). This study suggests that high steroid dosages may influence IMPDH1/2 expression, hampering their use as a PD biomarker, particularly during the early post-transplant period. The measurement of pre-transplant levels of IMPDH1/2 may contribute to prediction of individual drug responsiveness to improve the clinical management of patients in MMF therapy.

摘要

在药代动力学(PK)/药效学(PD)指导下的霉酚酸酯(MMF)治疗中,使用肌苷单磷酸脱氢酶(IMPDH)活性或基因表达的测量作为进一步的方法。招募了 44 名新诊断的肾移植患者;其中 35 名完成了研究,并在 24 周内随访临床状况、PK 参数、IMPDH 活性和 IMPDH1/2 基因表达。在移植前和第 2、4、12 和 24 周时,在接受 MMF 治疗前(t0)和 2 小时(t2 h)时,测量外周血单核细胞中的 IMPDH 活性和表达。未发现 IMPDH 活性/表达与 PK 参数之间存在显著相关性。对于这两个基因,在 t2 h 时观察到表达显著增强,然后在第 24 周时下降,并随类固醇剂量呈趋势。7 名患者发生急性排斥反应(AR),与未发生排斥反应的患者相比,IMPDH1(中位数 3.42 对 0.84;p=0.0025)和 IMPDH2 基因(135 对 104;p=0.0218)的移植前表达明显更高。还发现移植前 IMPDH1 mRNA 与血液学并发症之间存在显著相关性(p=0.032)。本研究表明,高剂量类固醇可能会影响 IMPDH1/2 的表达,使其无法用作 PD 生物标志物,特别是在移植后早期。测量移植前 IMPDH1/2 的水平可能有助于预测个体对药物的反应性,从而改善 MMF 治疗中患者的临床管理。

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