Zochowska D, Zegarska J, Hryniewiecka E, Samborowska E, Jazwiec R, Tszyrsznic W, Borowiec A, Dadlez M, Paczek L
Department of Immunology, Transplant Medicine, and Internal Diseases, Medical University of Warsaw, Transplantation Institute, Warsaw, Poland.
Department of Clinical Nursing, Medical University of Warsaw, Warsaw, Poland.
Transplant Proc. 2016 Jun;48(5):1836-9. doi: 10.1016/j.transproceed.2016.01.084.
6-Mercaptopurine (6-MP) and its prodrug azathioprine (AZA) are used in many autoimmune diseases and after solid-organ transplantation. Their properties are mediated by active metabolites, 6-thioguanine nucleotides (6-TGN), and 6-methylmercaptopurine (6-MMP). The most common adverse effects are myelo- and hepato-toxicity. The aim of the study was quantification of 6-TG and 6-MMP, with the use of liquid chromatography combined with tandem mass spectrometry (LC/MS/MS) in solid-organ transplant recipients.
In 33 patients, kidney transplant recipient (n = 25) and liver transplant recipient (n = 8) intra-erythrocyte concentrations of 6-TG and 6-MMP were measured with the use of LC/MS/MS.
The mean concentration of 6-TG was 205.35 ± 157.62 pmol/8 × 10(8) red blood cells (RBC); median concentration of 6-MMP was 1064.1 (35.78-11,552.9) pmol/8 × 10(8) RBC. There were no correlations between 6-TG levels and peripheral blood parameters (white blood cell count, WBC; hemoglobin, Hb concentration; PLT, blood platelet count) or alanine aminotransferase activity (AlAT) activity. Relationships between 6-MMP concentrations and peripheral blood parameters (WBC, Hb, PLT) or AlAT activity have not been found. Subgroups with leukopenia, anemia, thrombocytopenia, and liver dysfunction did not differ in concentrations of 6-TG or 6-MMP. We have observed a negative correlation between daily azathioprine dose and WBC count (r = -0.37, P = .04).
Relationships between concentrations of azathioprine metabolites and myelotoxicity or hepatotoxicity have not been confirmed. Further studies on larger groups of patients would be helpful in a more accurate understanding of the impact of azathioprine metabolites on parameters of bone marrow and liver function.
6-巯基嘌呤(6-MP)及其前体药物硫唑嘌呤(AZA)被用于多种自身免疫性疾病以及实体器官移植后。它们的特性由活性代谢产物6-硫鸟嘌呤核苷酸(6-TGN)和6-甲基巯基嘌呤(6-MMP)介导。最常见的不良反应是骨髓毒性和肝毒性。本研究的目的是利用液相色谱-串联质谱法(LC/MS/MS)对实体器官移植受者体内的6-TG和6-MMP进行定量分析。
对33例患者进行研究,其中肾移植受者25例,肝移植受者8例,采用LC/MS/MS测定红细胞内6-TG和6-MMP的浓度。
6-TG的平均浓度为205.35±157.62 pmol/8×10⁸红细胞(RBC);6-MMP的中位浓度为1064.1(35.78 - 11552.9)pmol/8×10⁸RBC。6-TG水平与外周血参数(白细胞计数、血红蛋白浓度、血小板计数)或丙氨酸转氨酶活性之间无相关性。未发现6-MMP浓度与外周血参数(白细胞、血红蛋白、血小板)或丙氨酸转氨酶活性之间存在关联。白细胞减少、贫血、血小板减少和肝功能不全亚组的6-TG或6-MMP浓度无差异。我们观察到硫唑嘌呤每日剂量与白细胞计数之间呈负相关(r = -0.37,P = 0.04)。
硫唑嘌呤代谢产物浓度与骨髓毒性或肝毒性之间的关系尚未得到证实。对更多患者群体进行进一步研究将有助于更准确地了解硫唑嘌呤代谢产物对骨髓和肝功能参数的影响。