单独使用HbA1c可以安全地指导非洲青年1型糖尿病患者的胰岛素治疗吗?

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2023-01-01 Epub Date: 2023-04-24 DOI:10.1155/2023/1179830
Thereza Piloya-Were, Lucy W Mungai, Antoinette Moran, Lauren M Yauch, Nicholas Christakis, Lin Zhang, Robert McCarter, Stuart Chalew
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引用次数: 0

摘要

介绍HbA1c与平均血糖(MBG)的关系是糖尿病管理的重要指南,但不同种族之间可能有所不同。在非洲,患者的血糖信息有限或不可用,管理主要由HbA1c指导。我们试图确定来自非非洲人群的参考数据是否能够根据东非患者的HbA1c对MBG进行适当的估计。方法。我们研究了在肯尼亚和乌干达的一组患有1型糖尿病的东非青年中通过连续血糖监测获得的HbA1c与MBG的关系(n = 54)与从A1c衍生的平均葡萄糖(ADAG)和葡萄糖管理指标(GMI)研究获得的数据进行比较。一个自我认同的白人(欧洲血统)青年群体(n = 89)患有1型糖尿病,3-18 岁,居住在美国洛杉矶新奥尔良大都会区(NOLA),使用CGM作为额外参考进行研究。后果非洲队列的回归方程为MBG(mg/dL) = 32 + 16.73 × HbA1c(%),r = 0.55,p<0.0001。一般来说,使用非非洲参考资料大大高估了东非人口HbA1c的MBG。例如,HbA1c = 9%(74.9 mmol/mol)对应于MBG = 183 mg/dL(10.1 mmol/L),但212 mg/dL(11.7 mmol/L),237 mg/dL(13.1 mmol/L),使用GMI和249 mg/dL(13.8 mmol/L)。研究前一年,非洲患者中严重低血糖的发生率为21%。生成了东非患者HbA1c与MBG的对照表。结论。使用非非洲来源的参考数据根据HbA1c估计MBG通常会导致东非患者对MBG的高估。当管理主要基于在缺乏相应葡萄糖数据的情况下实现目标HbA1c时,这可能会使东非和其他非洲患者面临更高的低血糖风险。
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Can HbA1c Alone Be Safely Used to Guide Insulin Therapy in African Youth with Type 1 Diabetes?

Introduction: The relationship of HbA1c versus the mean blood glucose (MBG) is an important guide for diabetes management but may differ between ethnic groups. In Africa, the patient's glucose information is limited or unavailable and the management is largely guided by HbA1c. We sought to determine if the reference data derived from the non-African populations led to an appropriate estimation of MBG from HbA1c for the East African patients.

Methods: We examined the relationship of HbA1c versus MBG obtained by the continuous glucose monitoring in a group of East African youth having type 1 diabetes in Kenya and Uganda (n = 54) compared with the data obtained from A1c-derived average glucose (ADAG) and glucose management indicator (GMI) studies. A self-identified White (European heritage) population of youth (n = 89) with type 1 diabetes, 3-18 years old, living in New Orleans, LA, USA metropolitan area (NOLA), was studied using CGM as an additional reference.

Results: The regression equation for the African cohort was MBG (mg/dL) = 32.0 + 16.73 × HbA1c (%), r = 0.55, p < 0.0001. In general, the use of the non-African references considerably overestimated MBG from HbA1c for the East African population. For example, an HbA1c = 9% (74.9 mmol/mol) corresponded to an MBG = 183 mg/dL (10.1 mmol/L) in the East African group, but 212 mg/dL (11.7 mmol/L) using ADAG, 237 mg/dL (13.1 mmol/L) using GMI and 249 mg/dL (13.8 mmol/L) using NOLA reference. The reported occurrence of serious hypoglycemia among the African patients in the year prior to the study was 21%. A reference table of HbA1c versus MBG from the East African patients was generated.

Conclusions: The use of non-African-derived reference data to estimate MBG from HbA1c generally led to the overestimation of MBG in the East African patients. This may put the East African and other African patients at higher risk for hypoglycemia when the management is primarily based on achieving target HbA1c in the absence of the corresponding glucose data.

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