Bomholt Tobias, Kofod Dea, Nørgaard Kirsten, Rossing Peter, Feldt-Rasmussen Bo, Hornum Mads
Department of Nephrology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Steno Diabetes Center Copenhagen, Herlev, Denmark.
Nephron. 2023;147(2):91-96. doi: 10.1159/000525676. Epub 2022 Jul 13.
Hemoglobin A1c (HbA1c) is an unreliable glycemic marker in the dialysis population, and alternative methods of glycemic monitoring should be considered. Continuous glucose monitoring (CGM) measures interstitial glucose, an indirect measure of plasma glucose, and allows for estimating mean sensor glucose, glucose variability, and time in ranges. Thus, CGM provides a more nuanced picture of glycemic variables than HbA1c, which only informs about average glucose and not variation in glucose or hypoglycemia.
In non-dialysis patients with type 1 and type 2 diabetes, CGM metrics are increasingly used to estimate glycemic control and are associated with improvements in glucose levels. Although a clear link has not yet been established between some CGM variables and the development of late diabetic complications, CGM use could be an important step forward in improving glycemic control in patients receiving dialysis. The ability to detect and prevent hypoglycemia while optimizing glucose levels could be particularly valuable. However, long-term CGM use has not been evaluated in the dialysis population, and the practical burden and cost associated with CGM use may be a limitation. We discuss the strengths and limitations of using CGM in the dialysis population with type 1 and type 2 diabetes.
CGM circumvents the pitfalls of HbA1c in dialysis patients and provides detailed measures of the mean sensor glucose, glucose variability, and time in ranges. Guidelines recommend a minimum of 50% time spent in the target range (3.9-10.0 mmol/L) and less than 1% below range (<3.9 mmol/L) for patients receiving dialysis but remain to be evaluated in the dialysis population. CGM can be a valuable tool in reducing overall glucose levels and variations while detecting hypoglycemia, but the practical burden of CGM use and cost may be a limitation.
糖化血红蛋白(HbA1c)在透析人群中是不可靠的血糖标志物,应考虑采用其他血糖监测方法。连续血糖监测(CGM)测量组织间液葡萄糖,这是血浆葡萄糖的间接测量方法,可用于估算平均传感器葡萄糖水平、血糖变异性和血糖处于目标范围的时间。因此,与仅反映平均血糖水平而不反映血糖波动或低血糖情况的HbA1c相比,CGM能更细致地呈现血糖变量情况。
在1型和2型糖尿病非透析患者中,CGM指标越来越多地用于评估血糖控制情况,且与血糖水平改善相关。尽管某些CGM变量与糖尿病晚期并发症的发生之间尚未建立明确联系,但CGM的应用可能是改善透析患者血糖控制的重要进展。在优化血糖水平的同时检测和预防低血糖的能力可能特别有价值。然而,尚未在透析人群中评估CGM的长期使用情况,且使用CGM的实际负担和成本可能是一个限制因素。我们讨论了在1型和2型糖尿病透析人群中使用CGM的优势和局限性。
CGM避免了HbA1c在透析患者中的缺陷,并提供了平均传感器葡萄糖水平、血糖变异性和血糖处于目标范围时间的详细测量结果。指南建议透析患者至少50%的时间血糖处于目标范围(3.9 - 10.0 mmol/L),低于范围(<3.9 mmol/L)的时间少于1%,但这仍有待在透析人群中进行评估。CGM在降低总体血糖水平和波动以及检测低血糖方面可能是一个有价值的工具,但使用CGM的实际负担和成本可能是一个限制因素。