PMID- 30084579 OWN - NLM STAT- MEDLINE DCOM- 20190523 LR - 20190523 IS - 1565-1088 (Print) VI - 20 IP - 8 DP - 2018 Aug TI - Clinical Spectrum and Mechanism of Acute Kidney Injury in Patients with Diabetes Mellitus on SGLT-2 Inhibitors. PG - 513-516 AB - BACKGROUND: Sodium-glucose cotransporter 2 inhibitors (SGLT2i) (such as canagliflozin, empagliflozin, and dapagliflozin) are widely used to treat patients with type 2 diabetes mellitus (T2DM) to improve glycemic, cardiovascular and renal outcomes. However, based on post-marketing data, a warning label was added regarding possible occurrence of acute kidney injury (AKI). OBJECTIVES: To describe the clinical presentation of T2DM patients treated with SGLT2i who were evaluated for AKI at our institution and to discuss the potential pathophysiologic mechanisms. METHODS: A retrospective study of a computerized database was conducted of patients with T2DM who were hospitalized or evaluated for AKI while receiving SGLT2i, including descriptions of clinical and laboratory characteristics, at our institution. RESULTS: We identified seven patients in whom AKI occurred 7-365 days after initiation of SGLT2i. In all cases, renin-angiotensin-aldosterone system blockers had also been prescribed. In five patients, another concomitant nephrotoxic agent (injection of contrast-product, use of nonsteroidal anti-inflammatory drugs or cox-2 inhibitors) or occurrence of an acute medical event potentially associated with AKI (diarrhea, sepsis) was identified. In two patients, only the initiation of SGLT2i was evident. The mechanisms by which AKI occurs under SGLT2i are discussed with regard to the associated potential triggers: altered trans-glomerular filtration or, alternatively, kidney medullary hypoxia. CONCLUSIONS: SGLT2i are usually safe and provide multiple benefits for patients with T2DM. However, during particular medical circumstances, and in association with usual co-medications, particularly if baseline glomerular filtration rate is decreased, patients treated with SGLT2i may be at risk of AKI, thus warranting caution when prescribed. FAU - Perlman, Amichai AU - Perlman A AD - Department of Medicine, Hadassah-Hebrew University Medical Center, Mount Scopus, Jerusalem, Israel. FAU - Heyman, Samuel N AU - Heyman SN AD - Department of Medicine, Hadassah-Hebrew University Medical Center, Mount Scopus, Jerusalem, Israel. FAU - Stokar, Joshua AU - Stokar J AD - Department of Medicine, Hadassah-Hebrew University Medical Center, Mount Scopus, Jerusalem, Israel. FAU - Darmon, David AU - Darmon D AD - Department of Medicine, Hadassah-Hebrew University Medical Center, Mount Scopus, Jerusalem, Israel. FAU - Muszkat, Mordechai AU - Muszkat M AD - Department of Medicine, Hadassah-Hebrew University Medical Center, Mount Scopus, Jerusalem, Israel. FAU - Szalat, Auryan AU - Szalat A AD - Department of Medicine, Hadassah-Hebrew University Medical Center, Mount Scopus, Jerusalem, Israel. LA - eng PT - Journal Article PL - Israel TA - Isr Med Assoc J JT - The Israel Medical Association journal : IMAJ JID - 100930740 RN - 0 (Hypoglycemic Agents) RN - 0 (Sodium-Glucose Transporter 2 Inhibitors) SB - IM MH - Acute Kidney Injury/*chemically induced MH - Aged MH - Diabetes Mellitus, Type 2/*drug therapy MH - Female MH - Humans MH - Hypoglycemic Agents/*adverse effects MH - Kidney/drug effects/physiopathology MH - Kidney Function Tests MH - Male MH - Middle Aged MH - Retrospective Studies MH - Risk Factors MH - Sodium-Glucose Transporter 2 Inhibitors/*adverse effects EDAT- 2018/08/08 06:00 MHDA- 2019/05/24 06:00 CRDT- 2018/08/08 06:00 PHST- 2018/08/08 06:00 [entrez] PHST- 2018/08/08 06:00 [pubmed] PHST- 2019/05/24 06:00 [medline] PST - ppublish SO - Isr Med Assoc J. 2018 Aug;20(8):513-516.