Department of Clinical Biochemistry and Pharmacology, Tomas Bata Hospital in Zlín a. s., Zlín, Czech Republic.
Department of Biomedical sciences, Medical Faculty, University of Ostrava, Ostrava, Zábřeh, Czech Republic.
Basic Clin Pharmacol Toxicol. 2019 Mar;124(3):298-302. doi: 10.1111/bcpt.13132. Epub 2018 Oct 17.
The aim of this study was to provide evidence for the hypothesis that estimated glomerular filtration rate from serum Cystatin C (eGFRcys) is better to be determined for all elderly type 2 diabetes mellitus (T2DM) patients based on eGFRcys upward and downward reclassification rate for hypothetical metformin dose reduction by eGFRcys at the GFR decision point of 45 mL/min/1.73 m . A total of 265 consecutive T2DM elderly patients (age range 65-91 years) from outpatient diabetic clinic were included in the study. The Kidney Disease Improving Global Outcomes (KDIGO) guidelines for metformin dosing were strictly followed. Estimated glomerular filtration rate from serum creatinine (eGFRcrea) led to results of metformin eligibility. Each of the results of eGFRcrea-based eligibility was further compared to eGFRcys-based eligibility. Creatinine was measured by enzymatic method standardized against international reference material SRM 967. Cystatin C was determined by method traceable to DA ERM 471 international standard. eGFRcrea and eGFRcys were calculated according to Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equations. A downward reclassification rate was higher than upward reclassification rate (31 vs 3, respectively; P < 0.0001). The median (IQR) eGFRcrea was higher than eGFRcys (73 (58-85) vs 63 (50-75) mL/min/1.73 m , respectively; P < 0.0001). eGFRcys reclassified significant proportion of patients with T2DM from metformin eligible CKD stages to less or non-eligible stages. The downward reclassification was more frequent in patients older than 80 years (P < 0.01). Cystatin C-based eGFR selects more complicated patients, where lower doses of metformin are possibly advisable. We recommend calculating both eGFRcrea and eGFRcys for metformin dosing in elderly patients with T2DM.
本研究旨在为假设提供证据,即根据血清胱抑素 C(eGFRcys)估算的肾小球滤过率(eGFR),对于所有老年 2 型糖尿病(T2DM)患者,在肾小球滤过率(GFR)决策点 45 mL/min/1.73 m 时,通过 eGFRcys 对假设的二甲双胍剂量减少进行向上和向下重新分类的比率更好地确定 eGFRcys。本研究共纳入 265 例来自门诊糖尿病诊所的连续老年 T2DM 患者(年龄 65-91 岁)。严格遵循肾脏病改善全球结局(KDIGO)二甲双胍剂量指南。基于血清肌酐的估算肾小球滤过率(eGFRcrea)导致二甲双胍合格的结果。eGFRcrea 为基础的合格结果中的每一个结果都与 eGFRcys 为基础的合格结果进行了比较。肌酐采用国际参考物质 SRM 967 标准化的酶法测量。胱抑素 C 采用与 DA ERM 471 国际标准溯源的方法测定。eGFRcrea 和 eGFRcys 根据慢性肾脏病流行病学合作(CKD-EPI)方程计算。向下重新分类率高于向上重新分类率(分别为 31%和 3%;P<0.0001)。中位数(IQR)eGFRcrea 高于 eGFRcys(分别为 73(58-85)和 63(50-75)mL/min/1.73 m ;P<0.0001)。eGFRcys 将相当比例的 T2DM 患者从二甲双胍合格的 CKD 分期重新分类为更低或不合格的分期。80 岁以上患者的向下重新分类更为频繁(P<0.01)。基于胱抑素 C 的 eGFR 选择更复杂的患者,可能需要更低剂量的二甲双胍。我们建议为老年 T2DM 患者计算 eGFRcrea 和 eGFRcys 以确定二甲双胍的剂量。