| Literature DB >> 30663011 |
Junki Morino1, Keiji Hirai2, Shohei Kaneko1, Saori Minato1, Katsunori Yanai1, Yuko Mutsuyoshi1, Hiroki Ishii1, Momoko Matsuyama1, Taisuke Kitano1, Mitsutoshi Shindo1, Akinori Aomatsu1, Haruhisa Miyazawa1, Kiyonori Ito1, Yuichiro Ueda1, Taro Hoshino1, Susumu Ookawara1, Kazuo Hara3, Yoshiyuki Morishita1.
Abstract
We herein report two cases of advanced stage rapidly progressive diabetic nephropathy that were effectively treated with combination therapy including renin-angiotensin-aldosterone system (RAS) blocker [angiotensin II receptor blocker (ARB)], glucagon-like peptide-1 (GLP-1) receptor agonist and sodium glucose transporter-2 (SGLT-2) inhibitor. A 30-year-old woman with advanced stage diabetic nephropathy [estimated glomerular filtration rate (eGFR): 20.7 mL/min/1.73 m2; proteinuria: 13.2 g/gCr], showing a rapidly progressive pattern (annual eGFR change: - 60.0 mL/min/1.73 m2/year), had improvement in proteinuria (5.9 g/gCr) and eGFR change (+ 4.3 mL/min/1.73 m2 over 15 weeks) after administration of ARB (irbesartan 25 mg/day), GLP-1 receptor agonist (liraglutide 0.3 mg/day) and SGLT-2 inhibitor (canagliflozin 50 mg/day). A 59-year-old man with advanced stage diabetic nephropathy (eGFR: 32.4 mL/min/1.73 m2; proteinuria: 8.90 g/gCr), showing a rapidly progressive pattern (annual eGFR change: - 21.2 mL/min/1.73 m2/year), had an improvement in proteinuria (0.02 g/gCr) and annual eGFR change (+ 0.1 mL/min/1.73 m2/year) after combination therapy with ARB (olmesartan 40 mg/day), GLP-1 receptor agonist (liraglutide 0.9 mg/day) and SGLT-2 inhibitor (tofogliflozin 10 mg/day). These results suggest that this triple combination therapy has renoprotective effects on advanced stage rapidly progressive diabetic nephropathy.Entities:
Keywords: Angiotensin II receptor blocker; Glucagon-like peptide-1 receptor agonist; Rapidly progressive diabetic nephropathy; Sodium glucose transporter-2 inhibitor
Year: 2019 PMID: 30663011 PMCID: PMC6450986 DOI: 10.1007/s13730-019-00379-3
Source DB: PubMed Journal: CEN Case Rep ISSN: 2192-4449