Liu Chengcheng, Janke Laura J, Kawedia Jitesh D, Ramsey Laura B, Cai Xiangjun, Mattano Leonard A, Boyd Kelli L, Funk Amy J, Relling Mary V
Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
Department of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
PLoS One. 2016 Mar 11;11(3):e0151433. doi: 10.1371/journal.pone.0151433. eCollection 2016.
Osteonecrosis is a common dose-limiting toxicity of glucocorticoids. Data from clinical trials suggest that other medications can increase the risk of glucocorticoid-induced osteonecrosis. Here we utilized a mouse model to study the effect of asparaginase treatment on dexamethasone-induced osteonecrosis. Mice receiving asparaginase along with dexamethasone had a higher rate of osteonecrosis than those receiving only dexamethasone after 6 weeks of treatment (44% vs. 10%, P = 0.006). Similarly, epiphyseal arteriopathy, which we have shown to be an initiating event for osteonecrosis, was observed in 58% of mice receiving asparaginase and dexamethasone compared to 17% of mice receiving dexamethasone only (P = 0.007). As in the clinic, greater exposure to asparaginase was associated with greater plasma exposure to dexamethasone (P = 0.0001). This model also recapitulated other clinical risk factors for osteonecrosis, including age at start of treatment, and association with the systemic exposure to dexamethasone (P = 0.027) and asparaginase (P = 0.036). We conclude that asparaginase can potentiate the osteonecrotic effect of glucocorticoids.
骨坏死是糖皮质激素常见的剂量限制性毒性。临床试验数据表明,其他药物会增加糖皮质激素诱导的骨坏死风险。在此,我们利用小鼠模型研究天冬酰胺酶治疗对地塞米松诱导的骨坏死的影响。治疗6周后,接受天冬酰胺酶和地塞米松联合治疗的小鼠骨坏死发生率高于仅接受地塞米松治疗的小鼠(44% 对10%,P = 0.006)。同样,我们已证明骨骺动脉病是骨坏死的起始事件,接受天冬酰胺酶和地塞米松联合治疗的小鼠中58%出现骨骺动脉病,而仅接受地塞米松治疗的小鼠中这一比例为17%(P = 0.007)。与临床情况一样,天冬酰胺酶暴露量增加与地塞米松血浆暴露量增加相关(P = 0.0001)。该模型还重现了骨坏死的其他临床风险因素,包括开始治疗时的年龄,以及与地塞米松全身暴露量(P = 0.027)和天冬酰胺酶暴露量(P = 0.036)的关联。我们得出结论,天冬酰胺酶可增强糖皮质激素的骨坏死效应。