Key result
Glucose-lowering agents require dose reduction or are contraindicated in the ≈25% of type 2 diabetes patients with stage 3-5 chronic kidney disease due to pharmacokinetic and safety risks.
Dose adjustments or contraindications are necessary for most oral antidiabetic agents in patients with CKD due to altered pharmacokinetics and safety risks.
Clinicians must verify renal dosing in T2D with stage 3-5 CKD; extends pharmacokinetic synthesis but leaves comparative outcomes open.
INTRODUCTION: People with chronic kidney disease (CKD) of stages 3 - 5 (creatinine clearance < 60 ml/min) represent ≈ 25% of patients with type 2 diabetes mellitus (T2DM), but the problem is underrecognized or neglected in clinical practice. However, most oral antidiabetic agents have limitations in case of renal impairment (RI), either because they require a dose adjustment or because they are contraindicated for safety reasons. AREAS COVERED: The author performed an extensive literature search to analyze the influence of RI on the pharmacokinetics (PK) of glucose-lowering agents and the potential consequences for clinical practice. EXPERT OPINION: As a result of PK interferences and for safety reasons, the daily dose should be reduced according to glomerular filtration rate (GFR) or even the drug is contraindicated in presence of severe CKD. This is the case for metformin (risk of lactic acidosis) and for many sulfonylureas (risk of hypoglycemia). At present, however, the exact GFR cutoff for metformin use is controversial. New antidiabetic agents are better tolerated in case of CKD, although clinical experience remains quite limited for most of them. The dose of DPP-4 inhibitors should be reduced (except for linagliptin), whereas both the efficacy and safety of SGLT2 inhibitors are questionable in presence of CKD.
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André Scheen (2013) conducted a review in Type 2 diabetes mellitus with chronic kidney disease. Glucose-lowering agents was evaluated. Glucose-lowering agents require dose reduction or are contraindicated in the ≈25% of type 2 diabetes patients with stage 3-5 chronic kidney disease due to pharmacokinetic and safety risks.
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