影响1型糖尿病儿童血糖管理指标及糖化血红蛋白不一致的临床因素评估-一年真实数据观察

IF 2.6
Grażyna Deja, Aleksandra Brudzińska, Łukasz Wybrańczyk, Rafal Deja, Przemysława Jarosz-Chobot
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引用次数: 0

摘要

目的:已发表的数据仍然强调GMI(从CGM报告中估计HbA1c的参数)与实验室HbA1c之间的不一致,原因尚待探讨。本研究旨在找出导致这些不一致的潜在临床因素。方法:对99例12.92岁(SD 4.03)使用CGM装置(Dexcom G6-31、Libre 2-30、Guardian 3-38)的儿童进行回顾性研究。纳入标准为:1型糖尿病,过去一年持续使用一种CGM(>70%传感器活动),每季度访问一次。每次就诊时,我们收集数据:年龄、性别、BMI、糖尿病病程、每日胰岛素剂量、CGM报告(14/90天)和实验室HbA1c。结果:我们证实了HbA1c和GMI之间的线性依赖关系——HbA1c越高,HbA1c-GMI的差异越大。HbA1c-GMI 90天不一致性分为4个阈值:48.7% 0.75。结论:一年真实数据显示,临床显著不一致(HbA1c-GMI 90 >0.5%)发生在不到30%的儿童中。在HbA1c值较高、糖尿病病程较长、血糖控制不稳定的个体中,差异更大。HbA1c-GMI 90虽然存在不同程度的差异,但比较稳定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The assessment of clinical factors influencing Glucose Management Indicator and Hba1c discordance in children with type one diabetes - one-year real-world data observation.

Objectives: Published data still highlighted discordances between GMI (parameter estimating HbA1c from CGM report) and laboratory HbA1c, with reasons yet to be explored. This study aimed: to identify potential clinical factors contributing to these discordances.

Methods: A retrospective study of 99 children aged 12.92 (SD 4.03) using CGM devices (Dexcom G6-31, Libre 2-30, Guardian 3-38) was conducted. Inclusion criteria were: type 1 diabetes, continuous use of one type of CGM (with >70% sensor activity) over the last year, quarterly visits. At each visit, we collected data: age, sex, BMI, diabetes duration, daily insulin dose, CGM report (14/90 days) and laboratory HbA1c.

Results: We confirmed linear dependency between HbA1c and GMI - higher HbA1c led to more HbA1c-GMI differences. The HbA1c-GMI 90 days discordance was categorized into four thresholds: 48.7% <0.25, 20.1% in the range 0.25-0.5, 22.4% in 0.5-0.75, and 8.7% >0.75. Children with HbA1c-GMI 90 discordance <0.5% had significantly lower HbA1c (6.80 vs 7.59%), shorter T1D duration (<5 years) and more stable HbA1c (differences <0.4 between results). The analysis of participants stability, based on comparing HbA1c-GMI 90 discordances at subsequent follow-up visits confirmed the individual variability <0.25 in two-thirds of participants. Other factors were not associated with the HbA1c-GMI discordance.

Conclusion: One-year real-world data showed that clinically significant discordances (HbA1c-GMI 90 >0.5%) occurred in less than 30% children. Higher difference is more likely in individuals with higher HbA1c values, longer diabetes duration, and less stable glycemic control. Individual discordance HbA1c-GMI 90 is rather stable, although with varying degrees of difference.

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