PMID- 34481963 OWN - NLM STAT- MEDLINE DCOM- 20211209 LR - 20211214 IS - 1878-1780 (Electronic) IS - 1262-3636 (Linking) VI - 47 IP - 5 DP - 2021 Sep TI - Canagliflozin could improve the levels of renal oxygenation in newly diagnosed type 2 diabetes patients with normal renal function. PG - 101274 LID - S1262-3636(21)00057-4 [pii] LID - 10.1016/j.diabet.2021.101274 [doi] AB - OBJECTIVE: To evaluate the effects of canagliflozin on the renal oxygen level and blood perfusion in newly diagnosed type 2 diabetes mellitus (T2DM) patients with normal renal function. METHODS: We conducted a prospective, randomised, and drug-controlled trial to determine the reno-protective effect exerted by canagliflozin in newly diagnosed T2DM patients with normal renal function using blood oxygen level-dependent magnetic resonance imaging (BOLD-MRI) and arterial spin labelling MRI (ASL-MRI). This provides an experimental basis for a first-line of defence for the prevention of diabetic nephropathy. RESULTS: Canagliflozin induced a significant decrease in body weight and diastolic blood pressure compared with glimepiride (all p < 0.05). The high baseline mean estimated glomerular filtration rate (eGFR) in both groups was indicative of a GFR level at a relatively high status that was significantly alleviated after 24 weeks of canagliflozin treatment (change from baseline, p = 0.04, and change versus glimepiride control, p = 0.048). However, neither drug regimen significantly affected renal blood perfusion. The R2* values were inversely proportional to the tissue oxygen content. Compared to the baseline, 24 weeks of canagliflozin treatment decreased the R2* values of the renal cortex and medulla by 22.3% (p = 0.005) and 29.2% (p = 0.0002) respectively, and these decreases were significantly greater than in the glimepiride control group (p = 0.0004 and p = 0.02). CONCLUSIONS: Canagliflozin improved the levels of renal oxygenation in newly diagnosed T2DM patients with normal renal function independent of changes in renal blood perfusion. CI - Published by Elsevier Masson SAS. FAU - Zhou, Saijun AU - Zhou S AD - NHC Key Laboratory of Hormones and Development, Tianjin Key Laboratory of Metabolic Diseases, Chu Hsien-I Memorial Hospital & Tianjin Institute of Endocrinology, Tianjin Medical University, Tianjin 300134, China. FAU - Zhang, YuLing AU - Zhang Y AD - The first centre Hospital of Tianjin, Tianjin 300192,China. FAU - Wang, TongDan AU - Wang T AD - NHC Key Laboratory of Hormones and Development, Tianjin Key Laboratory of Metabolic Diseases, Chu Hsien-I Memorial Hospital & Tianjin Institute of Endocrinology, Tianjin Medical University, Tianjin 300134, China. FAU - Huang, Shuai AU - Huang S AD - NHC Key Laboratory of Hormones and Development, Tianjin Key Laboratory of Metabolic Diseases, Chu Hsien-I Memorial Hospital & Tianjin Institute of Endocrinology, Tianjin Medical University, Tianjin 300134, China. FAU - Gong, Siyi AU - Gong S AD - NHC Key Laboratory of Hormones and Development, Tianjin Key Laboratory of Metabolic Diseases, Chu Hsien-I Memorial Hospital & Tianjin Institute of Endocrinology, Tianjin Medical University, Tianjin 300134, China. FAU - Wang, Junmei AU - Wang J AD - NHC Key Laboratory of Hormones and Development, Tianjin Key Laboratory of Metabolic Diseases, Chu Hsien-I Memorial Hospital & Tianjin Institute of Endocrinology, Tianjin Medical University, Tianjin 300134, China. FAU - Yu, Pei AU - Yu P AD - NHC Key Laboratory of Hormones and Development, Tianjin Key Laboratory of Metabolic Diseases, Chu Hsien-I Memorial Hospital & Tianjin Institute of Endocrinology, Tianjin Medical University, Tianjin 300134, China. Electronic address: peiyu@tmu.edu.cn. LA - eng PT - Journal Article PT - Randomized Controlled Trial DEP - 20210903 PL - France TA - Diabetes Metab JT - Diabetes & metabolism JID - 9607599 RN - 0 (Hypoglycemic Agents) RN - 0 (Pharmaceutical Preparations) RN - 0 (Sodium-Glucose Transporter 2 Inhibitors) RN - 0SAC974Z85 (Canagliflozin) RN - S88TT14065 (Oxygen) SB - IM MH - Canagliflozin/*therapeutic use MH - *Diabetes Mellitus, Type 2/complications/drug therapy MH - Humans MH - Hypoglycemic Agents/therapeutic use MH - Kidney/diagnostic imaging/physiology MH - Oxygen MH - Oxygen Saturation MH - Pharmaceutical Preparations MH - Prospective Studies MH - Sodium-Glucose Transporter 2 Inhibitors/therapeutic use OTO - NOTNLM OT - Arterial spin labelling magnetic resonance imaging (ASL-MRI) OT - Blood oxygen level-dependent MRI (BOLD-MRI) OT - Canagliflozin OT - Diabetic kidney disease OT - Sodium-glucose cotransporter-2 (SGLT-2) inhibitor OT - Type 2 diabetes COIS- Disclosure of interest The authors declare that they have no competing interest. EDAT- 2021/09/06 06:00 MHDA- 2021/12/15 06:00 CRDT- 2021/09/05 20:38 PHST- 2020/12/25 00:00 [received] PHST- 2021/08/03 00:00 [revised] PHST- 2021/08/04 00:00 [accepted] PHST- 2021/09/06 06:00 [pubmed] PHST- 2021/12/15 06:00 [medline] PHST- 2021/09/05 20:38 [entrez] AID - S1262-3636(21)00057-4 [pii] AID - 10.1016/j.diabet.2021.101274 [doi] PST - ppublish SO - Diabetes Metab. 2021 Sep;47(5):101274. doi: 10.1016/j.diabet.2021.101274. Epub 2021 Sep 3.