1型糖尿病患者胃排空与日血糖控制的关系:一项随机试验

G. Parthasarathy, Y. Kudva, P. Low, M. Camilleri, A. Basu, A. Bharucha
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引用次数: 22

摘要

背景:在1型糖尿病(T1D)中,胃排空延迟(GE)可能容易导致胰岛素输送和葡萄糖吸收之间的不匹配。先前的研究仅部分评估了延迟GE与餐后血糖之间的关系,而不是每日血糖。目的:探讨糖尿病糖尿病患者GE紊乱与血糖控制的关系及加速GE对血糖控制的影响。设计、环境和参与者:这是一项随机安慰剂对照试验,在一家学术医疗中心对30名T1D患者进行胰岛素泵治疗。干预措施:在基线(GEbaseline)、静脉注射生理盐水或红霉素(2或3mg /kg;GEiv)和口服红霉素或安慰剂7天后(GEoral)。在整个研究过程中都提供称重餐。主要结局指标:GE和连续血糖监测(CGM)。结果:基线糖化血红蛋白为7.6%±0.8%(60±8.7 mmol/mol);迟发性GE 12例(40%);较快的GE与较高的餐后血糖相关,但较慢的GE与餐后低血糖(<70 mg/dL)无关。静脉注射红霉素(3mg /kg)而非口服红霉素加速GE。GE与血糖的关系在餐后和全天有所不同。在调整了碳水化合物摄入和胰岛素消耗后,在整个研究中,更快的GE与餐后期间更多的高血糖有关,但血糖值较低。结论:在T1D中,药物介导的GE加速增加了餐后基于cgm的血糖。相反,延迟的GE与全天更高的基于cgm的葡萄糖值相关。
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Relationship Between Gastric Emptying and Diurnal Glycemic Control in Type 1 Diabetes Mellitus: A Randomized Trial
Context: In type 1 diabetes (T1D), delayed gastric emptying (GE) may predispose to a mismatch between insulin delivery and glucose absorption. Previous studies evaluated, only partly, the relationship between delayed GE and postprandial, but not diurnal, glycemia. Objective: To assess the relationship between GE disturbances and glycemic control in T1D and the effects of accelerating GE on glycemic control. Design, Setting, and Participants: This was a randomized placebo-controlled trial in 30 patients with T1D on an insulin pump at an academic medical center. Intervention(s): GE was evaluated with a [13C]-Spirulina breath test at baseline (GEbaseline), during intravenous saline or erythromycin (2 or 3 mg/kg; GEiv), and after 7 days of oral erythromycin or placebo (GEoral). Weighed meals were provided throughout the study. Main Outcome Measure(s): These were GE and continuous glucose monitoring (CGM). Results: The baseline glycosylated hemoglobin was 7.6% ± 0.8% (60 ± 8.7 mmol/mol); 12 patients (40%) had delayed GE; faster GE was associated with a greater postprandial CGM-based glucose, but slower GE was not associated with postprandial hypoglycemia (<70 mg/dL). Intravenous (3 mg/kg) but not oral erythromycin accelerated GE. The relationship between GE and glycemia differed between the postprandial periods and the entire day. After adjusting for carbohydrate intake and insulin consumption, faster GE was associated with more hyperglycemia during the postprandial period but lower glucose values across the entire study. Conclusions: In T1D, pharmacologically mediated acceleration of GE increases postprandial CGM-based glucose. In contrast, delayed GE is associated with greater CGM-based glucose values over the entire day.
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