IMP脱氢酶
霉酚酸
医学
肌苷酸
肌苷
霉酚酸酯
内科学
移植
治疗药物监测
置信区间
胃肠病学
加药
不利影响
四分位间距
泌尿科
药理学
药代动力学
生物化学
化学
腺苷
核苷酸
基因
作者
Petra Glander,Johannes Waiser,Pia Hambach,Friederike Bachmann,Klemens Budde,Kai‐Uwe Eckardt,Frank Friedersdorff,Jens Gaedeke,Susanne Kron,Christine Lorkowski,Marco Mai,Hans‐H. Neumayer,Robert W. Peters,Birgit Rudolph,Danilo Schmidt,Kaiyin Wu,Lutz Liefeldt
出处
期刊:Transplantation
[Wolters Kluwer]
日期:2020-06-01
卷期号:105 (4): 916-927
被引量:10
标识
DOI:10.1097/tp.0000000000003336
摘要
Background. Mycophenolic acid (MPA) is a standard immunosuppressant in organ transplantation. A simple monitoring biomarker for MPA treatment has not been established so far. Here, we describe inosine 5′-monophosphate dehydrogenase (IMPDH) monitoring in erythrocytes and its application to kidney allograft recipients. Methods. IMPDH activity measurements were performed using a high-performance liquid chromatography assay. Based on 4203 IMPDH measurements from 1021 patients, we retrospectively explored the dynamics early after treatment start. In addition, we analyzed the influence of clinically relevant variables on IMPDH activity in a multivariate model using data from 711 stable patients. Associations between IMPDH activity and clinical events were evaluated in hospitalized patients. Results. We found that IMPDH activity reflects MPA exposure after 8 weeks of constant dosing. In addition to dosage, body mass index, renal function, and coimmunosuppression affected IMPDH activity. Significantly lower IMPDH activities were found in patients with biopsy-proven acute rejection as compared to patients without rejection (median [interquartile range]: 696 [358–1484] versus 1265 [867–1618] pmol xanthosine-5′-monophosphate/h/mg hemoglobin, P < 0.001). The highest IMPDH activities were observed in hospitalized patients with clinically evident MPA toxicity as compared to patients with hospitalization not related to MPA treatment (1548 [1021–2270] versus 1072 [707–1439] pmol xanthosine-5′-monophosphate/h/mg hemoglobin; P < 0.001). Receiver operating characteristic curve analyses underlined the usefulness of IMPDH to predict rejection episodes (area, 0.662; confidence interval, 0.584-0.740; P < 0.001) and MPA-associated adverse events (area, 0.632; confidence interval, 0.581-0.683; P < 0.001), respectively. Conclusions. IMPDH measurement in erythrocytes is a novel and useful strategy for the longitudinal monitoring of MPA treatment.
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