Cystatin C measurement leads to lower metformin dosage in elderly type 2 diabetic patients
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Observational Study
PubMed
30218617
PubMed Central
PMC7379635
DOI
10.1111/bcpt.13132
Knihovny.cz E-resources
- Keywords
- creatinine, cystatin C, estimated glomerular filtration rate, glomerular filtration, metformin,
- MeSH
- Renal Insufficiency, Chronic blood physiopathology MeSH
- Cystatin C blood MeSH
- Diabetes Mellitus, Type 2 blood drug therapy physiopathology MeSH
- Glomerular Filtration Rate physiology MeSH
- Hypoglycemic Agents administration & dosage MeSH
- Creatinine blood MeSH
- Humans MeSH
- Metformin administration & dosage MeSH
- Retrospective Studies MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Age Factors MeSH
- Dose-Response Relationship, Drug MeSH
- Check Tag
- Humans MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Publication type
- Journal Article MeSH
- Observational Study MeSH
- Names of Substances
- Cystatin C MeSH
- Hypoglycemic Agents MeSH
- Creatinine MeSH
- Metformin MeSH
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 m2 . 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 m2 , 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.
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