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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タイトル |
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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ファイル |
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内容記述 |
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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著者 |
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掲載誌 |
Journal of Investigative Medicine
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掲載誌(別表記) |
J Investig Med.
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巻 |
65
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号 |
7
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開始ページ |
1057
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終了ページ |
1061
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出版者 |
American Federation for Medical Research
Lippincott, Williams & Wilkins
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出版年月日 |
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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資料タイプ |
学位論文
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言語 |
英語
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関連情報 |
PMCID: PMC5812257
出版社版DOIリンク(URL): https://doi.org/10.1136/jim-2017-000445
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関連情報URL |
https://doi.org/10.1136/jim-2017-000445
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5812257/
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権利関係 |
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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版 |
博士論文(全文を含む)
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学位授与番号 |
博甲第674号
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学位授与年月日 |
2017-09-27
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学位名 |
博士(医学)
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学位授与機関 |
香川大学
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区分 |
香川大学
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