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SLCO1B1突变致1例甲氨蝶呤清除延迟患儿的药学监护 被引量:3
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作者 湛敏 张洲 +3 位作者 李学娟 吴越 魏红 陈泽彬 《儿科药学杂志》 CAS 2016年第9期34-37,共4页
目的:分析甲氨蝶呤清除延迟的影响因素,使临床更加合理地使用甲氨蝶呤(MTX)、减少不良反应的发生。方法:对1例发生MTX排泄延迟、出现胃肠道黏膜损伤症状并继发鼠伤寒沙门菌感染的急性淋巴细胞性白血病(ALL)高危患儿的生理病理因素、合... 目的:分析甲氨蝶呤清除延迟的影响因素,使临床更加合理地使用甲氨蝶呤(MTX)、减少不良反应的发生。方法:对1例发生MTX排泄延迟、出现胃肠道黏膜损伤症状并继发鼠伤寒沙门菌感染的急性淋巴细胞性白血病(ALL)高危患儿的生理病理因素、合并用药情况进行分析,并通过测序法分析SLCO1B1多态性,探讨影响MTX清除延迟的相关因素。结果:根据MTX血药浓度,临床药师判断该患儿Block-1时发生了MTX早期清除延迟,Block-2时发生早期和晚期清除延迟。另结合相关文献,临床药师选择SLCO1B1的3个SNP位点进行测序分析,发现患儿为SLCO1B1c.521、c.1865+4846和c.1865+248 3个位点的突变纯合子。SLCO1B1突变和合并使用奥美拉唑可能是导致患儿发生MTX早期清除延迟的原因;腹水可能是导致其发生晚期清除延迟的原因。结论:临床医师在使用MTX治疗ALL患儿时,应综合考虑患儿的生理病理因素和遗传因素等,如有条件,可同时检测相关基因型,根据基因型和肾脏清除率等制定合适的治疗方案或采取一定的预防措施,同时尽量避免选择会导致患儿甲氨蝶呤排泄延迟的相关药物,以减少MTX不良反应的发生。 展开更多
关键词 甲氨蝶呤 清除延迟 SLCO1B1多态性 腹水
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脂肪负荷餐后健康老年男性雄激素水平的改变
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作者 林秀瑾 田少华 《中华老年心脑血管病杂志》 CAS 2004年第3期159-159,共1页
关键词 脂肪负荷餐后 健康老年男性 雄激素 甘油三酯 脂蛋白 IRL清除延迟 动脉粥样硬化
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Risk factors for delayed methotrexate elimination in pediatric patients with hematological malignancies: a retrospective analysis
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作者 Miao Li Xiaoyan Kong Shumei Wang 《Journal of Chinese Pharmaceutical Sciences》 CAS CSCD 2022年第10期746-754,共9页
Delayed elimination of methotrexate(MTX) is a major clinical concern in patients receiving high-dose MTX(HD-MTX) therapy. In the present study, we aimed to retrospectively explore the factors associated with MTX conce... Delayed elimination of methotrexate(MTX) is a major clinical concern in patients receiving high-dose MTX(HD-MTX) therapy. In the present study, we aimed to retrospectively explore the factors associated with MTX concentrations and elimination delay in pediatric patients with hematological malignancies. Cycles of HD-MTX therapy were categorized into the normal elimination group and delayed elimination group according to the serum MTX concentrations at 24(C) or 42 h(C) after the start of MTX therapy. Clinical characteristics associated with MTX concentrations and elimination delay were assessed by χ^(2) test, Fisher’s exact test, Mann-Whitney test, or Spearman’s correlation coefficient. Generalized Estimating Equations(GEE) were used to adjust for the clustering effects of multiple cycles in one patient and confounders. A total of 43 patients with 138 cycles of HD-MTX chemotherapy were included and evaluated in the current study. Dose, white blood cells(WBC), hemoglobin(HB), and blood urea nitrogen(BUN) were significantly correlated with MTX C(all P < 0.05). No significant correlations were noticed between baseline characteristics and MTX C. Delayed MTX elimination was observed in 34(24.6%) courses. Dose, WBC, HB, BUN, and concurrent infection were the significant risk factors for delayed MTX elimination(all P < 0.05). Our study identified several risk factors associated with MTX levels and elimination, which might be used to recognize patients with a high risk of delayed MTX elimination. However, the findings need to be confirmed in further large-scale studies. 展开更多
关键词 METHOTREXATE Elimination delay Therapeutic drug monitoring
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