Nephroprotective Effects of Dapagliflozin in Patients with Type 2 Diabetes

Objective This study analyzed changes in the estimated glomerular filtration rate calculated using cystatin C (eGFRcys) and sodium excretion in the urine after administering dapagliflozin as an add-on therapy to conventional treatment for diabetes. Methods This was a single-center, single-group, pro...

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Veröffentlicht in:Internal Medicine 2023/03/01, Vol.62(5), pp.681-688
Hauptverfasser: Iijima, Yasuhiro, Nakayama, Masafumi, Miwa, Takashi, Yakou, Fumiyoshi, Tomiyama, Hirofumi, Shikuma, Junpei, Ito, Rokuro, Tanaka, Akihiko, Manda, Naoki, Odawara, Masato
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container_issue 5
container_start_page 681
container_title Internal Medicine
container_volume 62
creator Iijima, Yasuhiro
Nakayama, Masafumi
Miwa, Takashi
Yakou, Fumiyoshi
Tomiyama, Hirofumi
Shikuma, Junpei
Ito, Rokuro
Tanaka, Akihiko
Manda, Naoki
Odawara, Masato
description Objective This study analyzed changes in the estimated glomerular filtration rate calculated using cystatin C (eGFRcys) and sodium excretion in the urine after administering dapagliflozin as an add-on therapy to conventional treatment for diabetes. Methods This was a single-center, single-group, prospective interventional study. Dapagliflozin was administered to improve the plasma glucose control in 30 subjects with type 2 diabetes mellitus (age 53±8 years old; 66.6% men). Blood and urine tests were performed before and 6 and 12 months after dapagliflozin administration. The daily sodium excretion was estimated with the Kawasaki formula using second-morning urine samples. Results The eGFRcys did not markedly differ before and 6 months after the dapagliflozin administration but was significantly increased after 12 months (p
doi_str_mv 10.2169/internalmedicine.6685-20
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Methods This was a single-center, single-group, prospective interventional study. Dapagliflozin was administered to improve the plasma glucose control in 30 subjects with type 2 diabetes mellitus (age 53±8 years old; 66.6% men). Blood and urine tests were performed before and 6 and 12 months after dapagliflozin administration. The daily sodium excretion was estimated with the Kawasaki formula using second-morning urine samples. Results The eGFRcys did not markedly differ before and 6 months after the dapagliflozin administration but was significantly increased after 12 months (p&lt;0.001), and the estimated daily sodium excretion was also significantly increased (p&lt;0.001 at 6 months and p=0.002 at 12 months). The systolic and diastolic blood pressures tended to decrease after administration. The HbA1c level after the administration of dapagliflozin tended to be lower in the T3 group, showing the smallest increase in changes in the estimated daily sodium excretion from baseline to 6 months (28.2-107.5 mEq/day), than in the combined groups of T1 (219.5-110.1 mEq/day) and T2 (101.4-28.9 mEq/day). In contrast, the eGFRcys was significantly higher in the combined groups of T1 and T2 than that in the T3 group at both 6 and 12 months (p=0.031 and p=0.007, respectively). Conclusions Add-on therapy with dapagliflozin increased the urinary sodium excretion and decreased the blood pressure even in the early phase of this therapy. Our results suggest that dapagliflozin add-on therapy may exert nephroprotective effects in subjects with type 2 diabetes mellitus.</description><identifier>ISSN: 0918-2918</identifier><identifier>EISSN: 1349-7235</identifier><identifier>DOI: 10.2169/internalmedicine.6685-20</identifier><identifier>PMID: 36858619</identifier><language>eng</language><publisher>Japan: The Japanese Society of Internal Medicine</publisher><subject>Benzhydryl Compounds ; Blood pressure ; Cystatin C ; dapagliflozin ; Diabetes ; diabetes mellitus ; Diabetes mellitus (non-insulin dependent) ; Diabetes Mellitus, Type 2 ; Excretion ; Female ; Glomerular filtration rate ; Glucosides ; Humans ; Internal medicine ; Male ; Middle Aged ; nephroprotective effects ; Original ; Prospective Studies ; Sodium ; sodium excretion ; sodium glucose cotransporter-2 ; Urine</subject><ispartof>Internal Medicine, 2023/03/01, Vol.62(5), pp.681-688</ispartof><rights>2023 by The Japanese Society of Internal Medicine</rights><rights>Copyright Japan Science and Technology Agency 2023</rights><rights>Copyright © 2023 by The Japanese Society of Internal Medicine</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c555t-bc1368ad1703a776c54838e464602f8b821a255536c38d980e920348f34fcebd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10037009/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10037009/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,1876,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36858619$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Iijima, Yasuhiro</creatorcontrib><creatorcontrib>Nakayama, Masafumi</creatorcontrib><creatorcontrib>Miwa, Takashi</creatorcontrib><creatorcontrib>Yakou, Fumiyoshi</creatorcontrib><creatorcontrib>Tomiyama, Hirofumi</creatorcontrib><creatorcontrib>Shikuma, Junpei</creatorcontrib><creatorcontrib>Ito, Rokuro</creatorcontrib><creatorcontrib>Tanaka, Akihiko</creatorcontrib><creatorcontrib>Manda, Naoki</creatorcontrib><creatorcontrib>Odawara, Masato</creatorcontrib><title>Nephroprotective Effects of Dapagliflozin in Patients with Type 2 Diabetes</title><title>Internal Medicine</title><addtitle>Intern. Med.</addtitle><description>Objective This study analyzed changes in the estimated glomerular filtration rate calculated using cystatin C (eGFRcys) and sodium excretion in the urine after administering dapagliflozin as an add-on therapy to conventional treatment for diabetes. Methods This was a single-center, single-group, prospective interventional study. Dapagliflozin was administered to improve the plasma glucose control in 30 subjects with type 2 diabetes mellitus (age 53±8 years old; 66.6% men). Blood and urine tests were performed before and 6 and 12 months after dapagliflozin administration. The daily sodium excretion was estimated with the Kawasaki formula using second-morning urine samples. Results The eGFRcys did not markedly differ before and 6 months after the dapagliflozin administration but was significantly increased after 12 months (p&lt;0.001), and the estimated daily sodium excretion was also significantly increased (p&lt;0.001 at 6 months and p=0.002 at 12 months). The systolic and diastolic blood pressures tended to decrease after administration. The HbA1c level after the administration of dapagliflozin tended to be lower in the T3 group, showing the smallest increase in changes in the estimated daily sodium excretion from baseline to 6 months (28.2-107.5 mEq/day), than in the combined groups of T1 (219.5-110.1 mEq/day) and T2 (101.4-28.9 mEq/day). In contrast, the eGFRcys was significantly higher in the combined groups of T1 and T2 than that in the T3 group at both 6 and 12 months (p=0.031 and p=0.007, respectively). Conclusions Add-on therapy with dapagliflozin increased the urinary sodium excretion and decreased the blood pressure even in the early phase of this therapy. Our results suggest that dapagliflozin add-on therapy may exert nephroprotective effects in subjects with type 2 diabetes mellitus.</description><subject>Benzhydryl Compounds</subject><subject>Blood pressure</subject><subject>Cystatin C</subject><subject>dapagliflozin</subject><subject>Diabetes</subject><subject>diabetes mellitus</subject><subject>Diabetes mellitus (non-insulin dependent)</subject><subject>Diabetes Mellitus, Type 2</subject><subject>Excretion</subject><subject>Female</subject><subject>Glomerular filtration rate</subject><subject>Glucosides</subject><subject>Humans</subject><subject>Internal medicine</subject><subject>Male</subject><subject>Middle Aged</subject><subject>nephroprotective effects</subject><subject>Original</subject><subject>Prospective Studies</subject><subject>Sodium</subject><subject>sodium excretion</subject><subject>sodium glucose cotransporter-2</subject><subject>Urine</subject><issn>0918-2918</issn><issn>1349-7235</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkdtOGzEQhi1EVdLQV0Ar9YabpT7s-nBVVRx6EAIu6LXldcaJo816azsgeHqcJo1ahGSNLc3nf2b-Qagi-IwSrj77IUMcTL-Cmbd-gDPOZVtTfIAmhDWqFpS1h2iCFZE1LeEIfUhpiTGTQtH36IgVXHKiJujnDYyLGMYYMtjsH6C6dK68UhVcdWFGM--968OzH6py7kz2MJTko8-L6v5phIpWF950kCEdo3fO9Ak-7u4p-nV1eX_-vb6-_fbj_Ot1bdu2zXVnSSlvZkRgZoTgtm0kk9DwhmPqZCcpMbSQjFsmZ0piUBSzRjrWOAvdjE3Rl63uuO6KAbY0FE2vx-hXJj7pYLz-PzP4hZ6HB02KAQJjVRROdwox_F5Dynrlk4W-NwOEddJUSMJpMY4U9NMrdBnWG-v_UFwQoRQvlNxSNoaUIrh9NwTrzcb0643pzcZ0GWyKTv6dZv_x74oKcLMFlimbOewBE7O3PbyhTHW7CbsKe9AuTNQwsBcgBrQf</recordid><startdate>20230301</startdate><enddate>20230301</enddate><creator>Iijima, Yasuhiro</creator><creator>Nakayama, Masafumi</creator><creator>Miwa, Takashi</creator><creator>Yakou, Fumiyoshi</creator><creator>Tomiyama, Hirofumi</creator><creator>Shikuma, Junpei</creator><creator>Ito, Rokuro</creator><creator>Tanaka, Akihiko</creator><creator>Manda, Naoki</creator><creator>Odawara, Masato</creator><general>The Japanese Society of Internal Medicine</general><general>Japan Science and Technology Agency</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TK</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20230301</creationdate><title>Nephroprotective Effects of Dapagliflozin in Patients with Type 2 Diabetes</title><author>Iijima, Yasuhiro ; Nakayama, Masafumi ; Miwa, Takashi ; Yakou, Fumiyoshi ; Tomiyama, Hirofumi ; Shikuma, Junpei ; Ito, Rokuro ; Tanaka, Akihiko ; Manda, Naoki ; Odawara, Masato</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c555t-bc1368ad1703a776c54838e464602f8b821a255536c38d980e920348f34fcebd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Benzhydryl Compounds</topic><topic>Blood pressure</topic><topic>Cystatin C</topic><topic>dapagliflozin</topic><topic>Diabetes</topic><topic>diabetes mellitus</topic><topic>Diabetes mellitus (non-insulin dependent)</topic><topic>Diabetes Mellitus, Type 2</topic><topic>Excretion</topic><topic>Female</topic><topic>Glomerular filtration rate</topic><topic>Glucosides</topic><topic>Humans</topic><topic>Internal medicine</topic><topic>Male</topic><topic>Middle Aged</topic><topic>nephroprotective effects</topic><topic>Original</topic><topic>Prospective Studies</topic><topic>Sodium</topic><topic>sodium excretion</topic><topic>sodium glucose cotransporter-2</topic><topic>Urine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Iijima, Yasuhiro</creatorcontrib><creatorcontrib>Nakayama, Masafumi</creatorcontrib><creatorcontrib>Miwa, Takashi</creatorcontrib><creatorcontrib>Yakou, Fumiyoshi</creatorcontrib><creatorcontrib>Tomiyama, Hirofumi</creatorcontrib><creatorcontrib>Shikuma, Junpei</creatorcontrib><creatorcontrib>Ito, Rokuro</creatorcontrib><creatorcontrib>Tanaka, Akihiko</creatorcontrib><creatorcontrib>Manda, Naoki</creatorcontrib><creatorcontrib>Odawara, Masato</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Internal Medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Iijima, Yasuhiro</au><au>Nakayama, Masafumi</au><au>Miwa, Takashi</au><au>Yakou, Fumiyoshi</au><au>Tomiyama, Hirofumi</au><au>Shikuma, Junpei</au><au>Ito, Rokuro</au><au>Tanaka, Akihiko</au><au>Manda, Naoki</au><au>Odawara, Masato</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nephroprotective Effects of Dapagliflozin in Patients with Type 2 Diabetes</atitle><jtitle>Internal Medicine</jtitle><addtitle>Intern. Med.</addtitle><date>2023-03-01</date><risdate>2023</risdate><volume>62</volume><issue>5</issue><spage>681</spage><epage>688</epage><pages>681-688</pages><artnum>6685-20</artnum><issn>0918-2918</issn><eissn>1349-7235</eissn><abstract>Objective This study analyzed changes in the estimated glomerular filtration rate calculated using cystatin C (eGFRcys) and sodium excretion in the urine after administering dapagliflozin as an add-on therapy to conventional treatment for diabetes. Methods This was a single-center, single-group, prospective interventional study. Dapagliflozin was administered to improve the plasma glucose control in 30 subjects with type 2 diabetes mellitus (age 53±8 years old; 66.6% men). Blood and urine tests were performed before and 6 and 12 months after dapagliflozin administration. The daily sodium excretion was estimated with the Kawasaki formula using second-morning urine samples. Results The eGFRcys did not markedly differ before and 6 months after the dapagliflozin administration but was significantly increased after 12 months (p&lt;0.001), and the estimated daily sodium excretion was also significantly increased (p&lt;0.001 at 6 months and p=0.002 at 12 months). The systolic and diastolic blood pressures tended to decrease after administration. The HbA1c level after the administration of dapagliflozin tended to be lower in the T3 group, showing the smallest increase in changes in the estimated daily sodium excretion from baseline to 6 months (28.2-107.5 mEq/day), than in the combined groups of T1 (219.5-110.1 mEq/day) and T2 (101.4-28.9 mEq/day). In contrast, the eGFRcys was significantly higher in the combined groups of T1 and T2 than that in the T3 group at both 6 and 12 months (p=0.031 and p=0.007, respectively). Conclusions Add-on therapy with dapagliflozin increased the urinary sodium excretion and decreased the blood pressure even in the early phase of this therapy. Our results suggest that dapagliflozin add-on therapy may exert nephroprotective effects in subjects with type 2 diabetes mellitus.</abstract><cop>Japan</cop><pub>The Japanese Society of Internal Medicine</pub><pmid>36858619</pmid><doi>10.2169/internalmedicine.6685-20</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Benzhydryl Compounds
Blood pressure
Cystatin C
dapagliflozin
Diabetes
diabetes mellitus
Diabetes mellitus (non-insulin dependent)
Diabetes Mellitus, Type 2
Excretion
Female
Glomerular filtration rate
Glucosides
Humans
Internal medicine
Male
Middle Aged
nephroprotective effects
Original
Prospective Studies
Sodium
sodium excretion
sodium glucose cotransporter-2
Urine
title Nephroprotective Effects of Dapagliflozin in Patients with Type 2 Diabetes
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