Division of Endocrinology, Diabetes and Metabolism, Johns Hopkins University, Baltimore, Maryland, USA.
Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Diabetes Technol Ther. 2021 Apr;23(4):253-258. doi: 10.1089/dia.2020.0501. Epub 2020 Dec 1.
There can be marked discordance between laboratory and estimated (using the glucose management indicator [GMI]) glycated hemoglobin (HbA1c) from continuous glucose monitoring (CGM). This may cause errors in diabetes management. This study evaluates discordance between laboratory and CGM-estimated HbA1c (eA1C). We performed a retrospective review of patients with diabetes who use CGM. The patients were seen at the University of Washington (UW) Diabetes Care Center from 2012 to 2019. We used UW's Institute of Translational Health Sciences to extract eligible encounters from the electronic medical record. We required that patients use CGM and that HbA1c and sensor data be obtained fewer than 4 weeks apart. There were no exclusion criteria. We calculated HbA1c-GMI discordance for each subject and assessed for any impact of comorbidities. We defined HbA1c-GMI discordance as absolute difference between laboratory and eA1C. This study included 641 separate office encounters. Ninety-one percent of patients had type 1 diabetes. Most patients had diabetes for greater than 20 years. The mean duration of CGM wear was 24.5 ± 8 days. Only 11% of patients had HbA1c-GMI discordance <0.1%, but 50% and 22% had differences ≥0.5% and ≥1%. There was increased discordance with advanced chronic kidney disease (estimated glomerular filtration rate <60). We found substantial discordance between laboratory and eA1C in a real-world setting. Clinicians need be aware that HbA1c may not as accurately reflect mean glucose as previously appreciated.
实验室检测的糖化血红蛋白 (HbA1c) 与(使用血糖管理指标 [GMI])连续血糖监测 (CGM) 估算的 HbA1c 之间可能存在显著差异。这可能导致糖尿病管理中的错误。本研究评估了实验室和 CGM 估算的 HbA1c(eA1C)之间的差异。
我们对使用 CGM 的糖尿病患者进行了回顾性研究。这些患者于 2012 年至 2019 年在华盛顿大学 (UW) 糖尿病护理中心就诊。我们使用 UW 的转化健康科学研究所从电子病历中提取合格的就诊记录。我们要求患者使用 CGM,且 HbA1c 和传感器数据的获取时间间隔少于 4 周。无排除标准。我们计算了每位患者的 HbA1c-GMI 差异,并评估了合并症的任何影响。我们将 HbA1c-GMI 差异定义为实验室和 eA1C 之间的绝对差异。
本研究共包括 641 次独立的门诊就诊。91%的患者患有 1 型糖尿病。大多数患者患有糖尿病超过 20 年。CGM 佩戴的平均时间为 24.5±8 天。只有 11%的患者的 HbA1c-GMI 差异<0.1%,但 50%和 22%的患者差异分别≥0.5%和≥1%。随着慢性肾脏病(估计肾小球滤过率<60)的进展,差异更大。
我们在真实环境中发现实验室检测的 HbA1c 与 eA1C 之间存在显著差异。临床医生需要意识到,HbA1c 可能不像之前认为的那样准确地反映平均血糖。