Hayashi Akinori, Takano Koji, Kawai Sayuki, Shichiri Masayoshi
Department of Endocrinology, Diabetes and Metabolism, Kitasato University School of Medicine, Kanagawa 252-0374, Japan.
Endocr J. 2016;63(2):187-91. doi: 10.1507/endocrj.EJ15-0523. Epub 2015 Nov 7.
Diabetes mellitus complicated with insulin antibodies is rare in clinical practice but usually difficult to control. A high amount of insulin antibodies, especially with low affinity and high binding capacity, leads to unstable glycemic control characterized by hyperglycemia unresponsive to large volume of insulin and unanticipated hypoglycemia. There are several treatment options, such as changing insulin preparation, immunosupression with glucocorticoids, and plasmapheresis, most of which are of limited efficacy. Sodium-glucose cotransporter 2 (SGLT2) inhibitors are a novel class of drug which decrease renal glucose reabsorption and lowers plasma glucose level independent of insulin action. We report here a case with diabetes complicated with insulin antibodies who was effectively controlled by an SGLT2 inhibitor. A 47-year-old man with type 2 diabetes treated with insulin had very poor glycemic control characterized by postprandial hyperglycemia unresponsive to insulin therapy and repetitive hypoglycemia due to insulin antibodies. Treatment with ipragliflozin, an SGLT2 inhibitor, improved HbA1c from 8.4% to 6.0% and glycated albumin from 29.4% to 17.9%. Continuous glucose monitoring revealed improvement of glycemic profile (average glucose level from 212 mg/dL to 99 mg/dL and glycemic standard deviation from 92 mg/dL to 14 mg/dL) with disappearance of hypoglycemic events. This treatment further ameliorated the characteristics of insulin antibodies and resulted in reduced insulin requirement. SGLT2 inhibitors may offer an effective treatment option for managing the poor glycemic control in diabetes complicated with insulin antibodies.
糖尿病合并胰岛素抗体在临床实践中较为罕见,但通常难以控制。大量的胰岛素抗体,尤其是低亲和力和高结合能力的抗体,会导致血糖控制不稳定,其特征为对大量胰岛素无反应的高血糖和意外低血糖。有几种治疗选择,如更换胰岛素制剂、使用糖皮质激素进行免疫抑制和血浆置换,其中大多数疗效有限。钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂是一类新型药物,可减少肾脏对葡萄糖的重吸收并降低血浆葡萄糖水平,且不依赖胰岛素作用。我们在此报告一例糖尿病合并胰岛素抗体患者,其通过SGLT2抑制剂得到有效控制。一名47岁的2型糖尿病男性,接受胰岛素治疗,血糖控制极差,表现为餐后高血糖对胰岛素治疗无反应,且因胰岛素抗体导致反复低血糖。使用SGLT2抑制剂依帕列净治疗后,糖化血红蛋白从8.4%改善至6.0%,糖化白蛋白从29.4%降至17.9%。持续葡萄糖监测显示血糖谱得到改善(平均血糖水平从212mg/dL降至99mg/dL,血糖标准差从92mg/dL降至14mg/dL),低血糖事件消失。该治疗进一步改善了胰岛素抗体的特征,并减少了胰岛素需求。SGLT2抑制剂可能为治疗糖尿病合并胰岛素抗体时血糖控制不佳提供一种有效的治疗选择。