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促红细胞生成素治疗对未接受血液透析的糖尿病合并慢性肾脏病患者糖化血红蛋白A(1c)的类效应。

Class effect of erythropoietin therapy on hemoglobin A(1c) in a patient with diabetes mellitus and chronic kidney disease not undergoing hemodialysis.

作者信息

Brown Jamie N, Kemp Debra W, Brice Kira R

机构信息

Department of Pharmacy, Durham Veterans Affairs Medical Center, Durham, North Carolina 27705, USA.

出版信息

Pharmacotherapy. 2009 Apr;29(4):468-72. doi: 10.1592/phco.29.4.468.

Abstract

In patients with diabetes mellitus, hemoglobin A(1c) (A1C) is commonly interpreted as a measure of long-term glycemic control, reflecting a mean glucose level over the previous 2-3 months. Although some reports suggest that treatment with recombinant erythropoietin may affect A1C values in patients undergoing hemodialysis, we know of no evidence to support this interaction in patients with chronic renal insufficiency who are not undergoing hemodialysis. In addition, we know of no evidence specific to the treatment effect of epoetin alfa and/or darbepoetin alfa on A1C. We describe a 64-year-old man with diabetes, chronic kidney disease, and anemia who was treated consecutively with epoetin alfa and darbepoetin alfa and experienced a temporal reduction in A1C level to a nadir of 4.4%. Throughout approximately 3 years of treatment with these erythropoietin analogs, the patient's total daily dose of insulin was reduced in response to his decreasing A1C values, despite elevated blood glucose levels and the absence of patient-reported hypoglycemic events. Five months after the patient's erythropoietin therapy was discontinued, his A1C value increased to 8.8%, leading us to conclude that management of the insulin dose may have been different without the falsely lowered A1C levels. Use of the Naranjo adverse drug reaction probability scale indicated a probable association between this patient's reduced A1C levels and erythropoietin therapy. This case demonstrates that both epoetin alfa and darbepoetin alfa may artificially lower A1C levels in a patient with diabetes who is not undergoing dialysis, and therefore this finding can be interpreted as a class effect. Clinicians should be aware of factors that affect A1C values, specifically erythrocyte life span. In patients receiving erythropoietin, therapeutic decisions should be based on A1C and glucose levels, as well as patient symptoms suggestive of hypo- or hyperglycemia, to avoid therapy changes that could complicate disease management.

摘要

在糖尿病患者中,糖化血红蛋白A1C(A1C)通常被视为长期血糖控制的指标,反映过去2 - 3个月的平均血糖水平。尽管一些报告表明,重组促红细胞生成素治疗可能会影响接受血液透析患者的A1C值,但我们尚未发现证据支持未接受血液透析的慢性肾功能不全患者存在这种相互作用。此外,我们也没有发现有关促红细胞生成素α和/或达比加群酯对A1C治疗效果的具体证据。我们描述了一名64岁患有糖尿病、慢性肾病和贫血的男性患者,他先后接受了促红细胞生成素α和达比加群酯治疗,A1C水平暂时降至最低点4.4%。在使用这些促红细胞生成素类似物治疗的大约3年时间里,尽管血糖水平升高且患者未报告有低血糖事件,但随着A1C值的下降,患者的每日胰岛素总剂量也相应减少。在患者停用促红细胞生成素治疗5个月后,其A1C值升至8.8%,这使我们得出结论,如果没有A1C水平的虚假降低,胰岛素剂量的管理可能会有所不同。使用Naranjo药物不良反应概率量表表明,该患者A1C水平降低与促红细胞生成素治疗之间可能存在关联。该病例表明,促红细胞生成素α和达比加群酯均可人为降低未接受透析的糖尿病患者的A1C水平,因此这一发现可被视为一种类效应。临床医生应了解影响A1C值的因素,特别是红细胞寿命。在接受促红细胞生成素治疗的患者中,治疗决策应基于A1C和血糖水平,以及提示低血糖或高血糖的患者症状,以避免可能使疾病管理复杂化的治疗改变。

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