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Effects of sodium-glucose cotransporter 2 inhibitors on urinary excretion of intact and total angiotensinogen in patients with type 2 diabetes.
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- Author(s): Yoshimoto T;Yoshimoto T; Furuki T; Furuki T; Kobori H; Kobori H; Miyakawa M; Miyakawa M; Imachi H; Imachi H; Murao K; Murao K; Nishiyama A; Nishiyama A
- Source:
Journal of investigative medicine : the official publication of the American Federation for Clinical Research [J Investig Med] 2017 Oct; Vol. 65 (7), pp. 1057-1061. Date of Electronic Publication: 2017 Jun 08.- Publication Type:
Journal Article- Language:
English - Source:
- Additional Information
- Source: Publisher: SAGE Publications Country of Publication: England NLM ID: 9501229 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1708-8267 (Electronic) Linking ISSN: 10815589 NLM ISO Abbreviation: J Investig Med Subsets: MEDLINE
- Publication Information: Publication: 2023-: [Thousand Oaks] : SAGE Publications
Original Publication: Thorofare, NJ : Slack, c1994- - Subject Terms: Sodium-Glucose Transporter 2 Inhibitors*; Angiotensinogen/*urine ; Diabetes Mellitus, Type 2/*urine; Adult ; Aged ; Aged, 80 and over ; Albuminuria/urine ; Blood Glucose ; Blood Pressure ; Creatinine/urine ; Diabetes Mellitus, Type 2/physiopathology ; Diastole ; Female ; Humans ; Male ; Middle Aged ; Sodium-Glucose Transporter 2/metabolism ; Systole
- Abstract: We conducted a descriptive case study to examine the effects of sodium-glucose cotransporter 2 (SGLT2) inhibitors on urinary angiotensinogen excretion, which represents the function of the intrarenal renin-angiotensin system, in patients with type 2 diabetes. An SGLT2 inhibitor (canagliflozin 100 mg/day, ipragliflozin 25 mg/day, dapagliflozin 5 mg/day, luseogliflozin 2.5 mg/day or tofogliflozin 20 mg/day) was administered for 1 month (n=9). ELISA kits were used to measure both urinary intact and total angiotensinogen levels. Treatment with SGLT2 inhibitors significantly decreased hemoglobin A1c, body weight, systolic blood pressure and diastolic blood pressure (8.5±1.3 to 7.5%±1.0%, 82.5±20.2 to 80.6±20.9 kg, 143±8 to 128±14 mm Hg, 78±10 to 67±9 mm Hg, p<0.05, respectively), while urinary albumin/creatinine ratio was not significantly changed (58.6±58.9 to 29.2±60.7 mg/g, p=0.16). Both total urinary angiotensinogen/creatinine ratio and intact urinary angiotensinogen/creatinine ratio tended to decrease after administration of SGLT2 inhibitors. However, these changes were not significant (p=0.19 and p=0.08, respectively). These data suggest that treatment with SGLT2 inhibitors does not activate the intrarenal renin-angiotensin system in patients with type 2 diabetes.
Competing Interests: Competing interests: None declared.
(© American Federation for Medical Research (unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.) - Comments: Comment in: J Investig Med. 2018 Feb;66(2):e4. (PMID: 29030417)
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Diabetes Care. 2015 Mar;38(3):384-93. (PMID: 25583754) - Grant Information: R01 DK072408 United States DK NIDDK NIH HHS
- Contributed Indexing: Keywords: SGLT2 inhibitor; blood pressure; type 2 diabetes; urinary albumin; urinary angiotensinogen
- Accession Number: 0 (Blood Glucose)
0 (SLC5A2 protein, human)
0 (Sodium-Glucose Transporter 2)
0 (Sodium-Glucose Transporter 2 Inhibitors)
11002-13-4 (Angiotensinogen)
AYI8EX34EU (Creatinine) - Publication Date: Date Created: 20170610 Date Completed: 20180528 Latest Revision: 20181202
- Publication Date: 20240628
- Accession Number: PMC5812257
- Accession Number: 10.1136/jim-2017-000445
- Accession Number: 28596160
- Source:
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