1型糖尿病合并乳糜泻患者的连续血糖监测(CGM)和代谢控制

F. Amaro, Maria Alessandra Saltarelli, M. Primavera, Marina Cerruto, S. Tumini
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引用次数: 0

摘要

1型糖尿病(T1D)和乳糜泻(CD)之间的关系是众所周知的。对37例1 ~ 18岁合并T1D和CD的患者进行代谢控制评价。对照组包括37名仅患有糖尿病的患者。通过检查专用在线平台上提供的医疗记录和CMG报告,获得了与所有患者代谢控制有关的所有数据。血糖变异性用变异系数(CV)和血糖值标准差(SD)表示。CV计算公式为:CV (%) = 100 × SD(每日血糖)/Mean(每日血糖)。T1D和CD患者的餐前快速胰岛素显著降低。如果我们只考虑使用CGM的患者,也会出现同样的减少。在没有CGM的患者中,基础胰岛素、餐前胰岛素和总胰岛素的剂量没有差异。两组使用CGM的患者代谢控制指标重叠。相反,没有CGM的糖尿病和乳糜泻患者血糖变异性指标和HbA1c水平升高。最后,无CGM的T1D和CD患者的目标血糖值百分比和>250 mg/dL血糖值百分比分别显著降低和升高。通过这项研究,我们想证明CGM是否可以改善合并T1D和CD患者的代谢控制。我们的数据显示,不使用CGM的T1D和CD患者的代谢控制更差。相反,使用CGM的患者,无论是否伴有乳糜泻,都可以通过调整餐前胰岛素剂量来达到相同的血糖目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Continuous Glucose Monitoring (CGM) and Metabolic Control in a Cohort of Patients with Type 1 Diabetes and Coeliac Disease
The association between type 1 diabetes (T1D) and coeliac disease (CD) is well known. Metabolic control of thirty-seven patients aged between 1 and 18 years, with coexisting T1D and CD were evaluated. The control group includes 37 patients affected only by diabetes. All data relating to the metabolic control of all patients were acquired through examination of medical records and CMG reports available on dedicated online platforms. Glucose variability was expressed as Coefficient of Variation (CV) and Standard Deviation of blood glucose values (SD). The formula used for CV computation is: CV (%) = 100 × SD (daily glycemia)/Mean (daily glycemia). Patients with T1D and CD showed a significant reduction in rapid pre-prandial insulin. The same reduction was present if we consider only patients using CGM. In patients without CGM, there was no difference in the doses of basal, pre-prandial and total insulin. Indicators of metabolic control were overlapping between the two groups in patients who used CGM. On the contrary, diabetic and coeliac patients without CGM had increased levels of glycaemic variability indicators and HbA1c. Finally, the percentage of target glycaemic values and >250 mg/dL glycaemic values were significantly decreased and increased, respectively in T1D and CD patients without CGM. With this study we wanted to demonstrate if CGM could improve metabolic control of patients with coexisting T1D and CD. Our data show a worse metabolic control in patients with T1D and CD who did not use CGM. Instead, patients who use CGM, regardless of the concomitant CD, manage to achieve the same glycaemic targets through an adjustment of titration of pre-prandial insulin doses.
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