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Effects of Intensive Therapy and Antecedent Hypoglycemia on Counterregulatory Responses to Hypoglycemia in Type 2 Diabetes

机译:强化治疗和先行低血糖对2型糖尿病低血糖反调节反应的影响

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摘要

>OBJECTIVE—The physiology of counterregulatory responses during hypoglycemia in intensively treated type 2 diabetic subjects is largely unknown. Therefore, the specific aims of the study tested the hypothesis that 1) 6 months of intensive therapy to lower A1C <7.0% would blunt autonomic nervous system (ANS) responses to hypoglycemia, and 2) antecedent hypoglycemia will result in counterregulatory failure during subsequent hypoglycemia in patients with suboptimal and good glycemic control.>RESEARCH DESIGN AND METHODS—Fifteen type 2 diabetic patients (8 men/7 women) underwent 6-month combination therapy of metformin, glipizide XL, and acarbose to lower A1C to 6.7% and 2-day repeated hypoglycemic clamp studies before and after intensive therapy. A control group of eight nondiabetic subjects participated in a single 2-day repeated hypoglycemic clamp study.>RESULTS—Six-month therapy reduced A1C from 10.2 ± 0.5 to 6.7 ± 0.3%. Rates of hypoglycemia increased to 3.2 episodes per patient/month by study end. Hypoglycemia (3.3 ± 0.1 mmol/l) and insulinemia (1,722 ± 198 pmol/l) were similar during all clamp studies. Intensive therapy reduced (P < 0.05) ANS and metabolic counterregulatory responses during hypoglycemia. Antecedent hypoglycemia produced widespread blunting (P < 0.05) of neuroendocrine, ANS, and metabolic counterregulatory responses during subsequent hypoglycemia before and after intensive therapy in type 2 diabetic patients and in nondiabetic control subjects.>CONCLUSIONS—Intensive oral combination therapy and antecedent hypoglycemia both blunt physiological defenses against subsequent hypoglycemia in type 2 diabetes. Prior hypoglycemia of only 3.3 ± 0.1 mmol/l can result in counterregulatory failure in type 2 diabetic patients with suboptimal control and can further impair physiological defenses against hypoglycemia in intensively treated type 2 diabetes.
机译:>目标— 在强化治疗的2型糖尿病患者中,低血糖期间抗调节反应的生理机制尚不清楚。因此,该研究的特定目的检验了以下假设:1)6个月的强化治疗以降低A1C <7.0%将使自主神经系统(ANS)对低血糖的反应变钝,并且2)先前的低血糖会导致随后的低血糖过程中的调节失灵>研究设计与方法— 15名2型糖尿病患者(8名男性/ 7名女性)接受了二甲双胍,格列吡嗪XL和阿卡波糖6个月联合治疗以降低A1C强化治疗前后分别进行了6.7%和2天的重复降糖钳研究。八个非糖尿病受试者的对照组参加了为期2天的重复降糖钳研究。>结果— 六个月的治疗使A1C从10.2±0.5降低到6.7±0.3%。到研究结束时,低血糖发生率增加至每位患者/月3.2次发作。在所有钳夹研究中,低血糖(3.3±0.1 mmol / l)和胰岛素血症(1,722±198 pmol / l)相似。低血糖期间强化治疗可降低(P <0.05)ANS和代谢反调节反应。在2型糖尿病患者和非糖尿病对照组中,强化治疗前后,继发性低血糖期间,先前的低血糖症会导致广泛的神经内分泌,ANS和代谢反调节反应减弱(P <0.05)。>结论-治疗和先前的低血糖症均对2型糖尿病患者随后发生的低血糖症具有钝化的生理防御作用。先前的低血糖仅3.3±0.1 mmol / l会导致控制欠佳的2型糖尿病患者的反调节功能衰竭,并可能进一步削弱强化治疗的2型糖尿病对低血糖的生理防御能力。

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