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Allopurinol reverses mercaptopurine-induced hypoglycemia in patients with acute lymphoblastic leukemia

机译:别嘌呤醇逆转巯基嘌呤诱发的急性淋巴细胞白血病患者的低血糖

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摘要

Fasting hypoglycemia is a known complication of mercaptopurine (6MP) maintenance therapy for acute lymphoblastic leukemia (ALL). It is associated with high levels of the methylated metabolite 6-methyl-mercaptopurine (6MMP). Symptoms of hypoglycemia include morning tremulousness, nausea and vomiting. We have previously shown that switching 6MP dosing from evening to morning resolved hypoglycemia by reducing 6MMP; however, the reduction of 6MMP was only transient, potentially resulting in return of hypoglycemia. In children and adults with Crohn’s disease, co-prescribing allopurinol with 6MP blocks the activity of thiopurine methytransferase (TPMT), reducing 6MMP and improving its tolerance. As a consequence of inhibiting TPMT, 6MP is shunted toward the production of 6-thioguanine nucleotide (6TGN), which will result in pancytopenia if the dose of 6MP is not reduced. We demonstrate that allopurinol with a reduced dose of 6MP in two patients with ALL and 6MMP-associated hypoglycemia resulted in a complete and sustained suppression of 6MMP and rapid reversal of hypoglycemia and its symptoms.
机译:空腹低血糖是巯基嘌呤(6MP)维持治疗急性淋巴细胞白血病(ALL)的已知并发症。它与高水平的甲基化代谢物6-甲基巯基嘌呤(6MMP)相关。低血糖的症状包括晨颤,恶心和呕吐。我们以前的研究表明,将6MP剂量从晚上改为早上可以通过降低6MMP来解决低血糖症。然而,6MMP的降低只是短暂的,可能导致低血糖症的复发。在患有克罗恩氏病的儿童和成人中,将别嘌呤醇与6MP并用会阻断硫嘌呤甲基转移酶(TPMT)的活性,降低6MMP并提高其耐受性。作为抑制TPMT的结果,6MP被分流产生6-硫鸟嘌呤核苷酸(6TGN),如果不减少6MP的剂量将导致全血细胞减少。我们证明,在两名ALL和6MMP相关的低血糖患者中,降低剂量的6MP别嘌呤醇导致对6MMP的完全和持续抑制,并迅速逆转低血糖症及其症状。

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