Effects of sodium-glucose cotransporter 2 inhibitors on urinary excretion of intact and total angiotensinogen in patients with type 2 diabetes
URI | http://shark.lib.kagawa-u.ac.jp/kuir/metadata/28445 | ||||||
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Title |
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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Description |
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. KEYWORDS: SGLT2 inhibitor; blood pressure; type 2 diabetes; urinary albumin; urinary angiotensinogen (医博甲674) |
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Publication Title |
Journal of Investigative Medicine
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Publication Title Alternative |
J Investig Med.
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Volume |
65
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Issue |
7
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Start Page |
1057
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End Page |
1061
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Publisher |
American Federation for Medical Research
Lippincott, Williams & Wilkins
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Published Date |
2017-06-08
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ISSN |
1081-5589
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NCID |
AA11166929
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PMID |
28596160
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DOI |
10.1136/jim-2017-000445
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Resource Type |
Thesis or Dissertation
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Language |
eng
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Relation |
PMCID: PMC5812257
出版社版DOIリンク(URL): https://doi.org/10.1136/jim-2017-000445
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Resource URL |
https://doi.org/10.1136/jim-2017-000445
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5812257/
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Rights |
Copyright © 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.
This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/
DOI: https://doi.org/10.1136/jim-2017-000445
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Text Version |
ETD
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Grant ID |
博甲第674号
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Grant Date |
2017-09-27
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Degree Name |
博士(医学)
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Grantor |
香川大学
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Set |
香川大学
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