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Renal and Cardiovascular Effects of SGLT2 Inhibition in Combination With Loop Diuretics in Patients With Type 2 Diabetes and Chronic Heart Failure: The RECEDE-CHF Trial
BACKGROUND:SGLT2 (sodium-glucose cotransporter-2) inhibitors improve heart failure–associated outcomes in patients with type 2 diabetes. In patients with heart failure, SGLT2 inhibitors will likely be coprescribed with a loop diuretic, but this combined effect is not well-defined. Our aim was to ass...
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Published in: | Circulation (New York, N.Y.) N.Y.), 2020-11, Vol.142 (18), p.1713-1724 |
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creator | Mordi, Natalie A. Mordi, Ify R. Singh, Jagdeep S. McCrimmon, Rory J. Struthers, Allan D. Lang, Chim C. |
description | BACKGROUND:SGLT2 (sodium-glucose cotransporter-2) inhibitors improve heart failure–associated outcomes in patients with type 2 diabetes. In patients with heart failure, SGLT2 inhibitors will likely be coprescribed with a loop diuretic, but this combined effect is not well-defined. Our aim was to assess the diuretic and natriuretic effect of empagliflozin in combination with loop diuretics.
METHODS:The RECEDE-CHF trial (SGLT2 Inhibition in Combination With Diuretics in Heart Failure) was a randomized, double-blind, placebo-controlled, crossover trial of patients with type 2 diabetes and heart failure with reduced ejection fraction taking regular loop diuretic who were randomized to empagliflozin 25 mg once daily or placebo for 6 weeks with a 2-week washout period. The primary outcome was change in 24-hour urinary volume from baseline to week 6.
RESULTS:Twenty-three participants (mean age, 69.8 years; 73.9% male; mean furosemide dose, 49.6±31.3 mg/d; mean HbA1c, 7.9±3.8%) were recruited. Compared with placebo, empagliflozin caused a significant increase in 24-hour urinary volume at both day 3 (mean difference, 535 mL [95% CI, 133–936]; P=0.005) and week 6 (mean difference, 545 mL [95% CI, 136–954]; P=0.005) after adjustment for treatment order, baseline 24-hour urine volume, and percentage change in loop diuretic dose. At 6 weeks, empagliflozin did not cause a significant change in 24-hour urinary sodium (mean difference, −7.85 mmol/L [95% CI, −2.43 to 6.73]; P=0.57). Empagliflozin caused a nonsignificant increase in fractional excretion of sodium at day 3, which was absent at week 6 (mean difference day 3, 0.30% [95% CI, −0.03 to 0.63]; P=0.09; week 6, 0.11% [95% CI, −0.22 to 0.44]; P>0.99), and a significant increase in electrolyte-free water clearance at week 6 (mean difference, 312 mL [95% CI, 26–598]; P=0.026) compared with placebo. Empagliflozin also caused significant reductions in body weight and serum urate at week 6.
CONCLUSIONS:Empagliflozin caused a significant increase in 24-hour urine volume without an increase in urinary sodium when used in combination with loop diuretic.
REGISTRATION:URLhttps://www.clinicaltrials.gov; Unique IdentifierNCT03226457. |
doi_str_mv | 10.1161/CIRCULATIONAHA.120.048739 |
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METHODS:The RECEDE-CHF trial (SGLT2 Inhibition in Combination With Diuretics in Heart Failure) was a randomized, double-blind, placebo-controlled, crossover trial of patients with type 2 diabetes and heart failure with reduced ejection fraction taking regular loop diuretic who were randomized to empagliflozin 25 mg once daily or placebo for 6 weeks with a 2-week washout period. The primary outcome was change in 24-hour urinary volume from baseline to week 6.
RESULTS:Twenty-three participants (mean age, 69.8 years; 73.9% male; mean furosemide dose, 49.6±31.3 mg/d; mean HbA1c, 7.9±3.8%) were recruited. Compared with placebo, empagliflozin caused a significant increase in 24-hour urinary volume at both day 3 (mean difference, 535 mL [95% CI, 133–936]; P=0.005) and week 6 (mean difference, 545 mL [95% CI, 136–954]; P=0.005) after adjustment for treatment order, baseline 24-hour urine volume, and percentage change in loop diuretic dose. At 6 weeks, empagliflozin did not cause a significant change in 24-hour urinary sodium (mean difference, −7.85 mmol/L [95% CI, −2.43 to 6.73]; P=0.57). Empagliflozin caused a nonsignificant increase in fractional excretion of sodium at day 3, which was absent at week 6 (mean difference day 3, 0.30% [95% CI, −0.03 to 0.63]; P=0.09; week 6, 0.11% [95% CI, −0.22 to 0.44]; P>0.99), and a significant increase in electrolyte-free water clearance at week 6 (mean difference, 312 mL [95% CI, 26–598]; P=0.026) compared with placebo. Empagliflozin also caused significant reductions in body weight and serum urate at week 6.
CONCLUSIONS:Empagliflozin caused a significant increase in 24-hour urine volume without an increase in urinary sodium when used in combination with loop diuretic.
REGISTRATION:URLhttps://www.clinicaltrials.gov; Unique IdentifierNCT03226457.</description><identifier>ISSN: 0009-7322</identifier><identifier>EISSN: 1524-4539</identifier><identifier>DOI: 10.1161/CIRCULATIONAHA.120.048739</identifier><identifier>PMID: 32865004</identifier><language>eng</language><publisher>United States: by the American College of Cardiology Foundation and the American Heart Association, Inc</publisher><subject>Original s</subject><ispartof>Circulation (New York, N.Y.), 2020-11, Vol.142 (18), p.1713-1724</ispartof><rights>by the American College of Cardiology Foundation and the American Heart Association, Inc.</rights><rights>2020 by the American College of Cardiology Foundation and the American Heart Association, Inc.</rights><rights>2020 The Authors. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4719-ec89558b471fff9f5c06c86164c5a37c989f021631ace5dc83210be39bb45fae3</citedby><cites>FETCH-LOGICAL-c4719-ec89558b471fff9f5c06c86164c5a37c989f021631ace5dc83210be39bb45fae3</cites><orcidid>0000-0002-7358-9712 ; 0000-0002-4530-3078 ; 0000-0002-3957-1981</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32865004$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mordi, Natalie A.</creatorcontrib><creatorcontrib>Mordi, Ify R.</creatorcontrib><creatorcontrib>Singh, Jagdeep S.</creatorcontrib><creatorcontrib>McCrimmon, Rory J.</creatorcontrib><creatorcontrib>Struthers, Allan D.</creatorcontrib><creatorcontrib>Lang, Chim C.</creatorcontrib><title>Renal and Cardiovascular Effects of SGLT2 Inhibition in Combination With Loop Diuretics in Patients With Type 2 Diabetes and Chronic Heart Failure: The RECEDE-CHF Trial</title><title>Circulation (New York, N.Y.)</title><addtitle>Circulation</addtitle><description>BACKGROUND:SGLT2 (sodium-glucose cotransporter-2) inhibitors improve heart failure–associated outcomes in patients with type 2 diabetes. In patients with heart failure, SGLT2 inhibitors will likely be coprescribed with a loop diuretic, but this combined effect is not well-defined. Our aim was to assess the diuretic and natriuretic effect of empagliflozin in combination with loop diuretics.
METHODS:The RECEDE-CHF trial (SGLT2 Inhibition in Combination With Diuretics in Heart Failure) was a randomized, double-blind, placebo-controlled, crossover trial of patients with type 2 diabetes and heart failure with reduced ejection fraction taking regular loop diuretic who were randomized to empagliflozin 25 mg once daily or placebo for 6 weeks with a 2-week washout period. The primary outcome was change in 24-hour urinary volume from baseline to week 6.
RESULTS:Twenty-three participants (mean age, 69.8 years; 73.9% male; mean furosemide dose, 49.6±31.3 mg/d; mean HbA1c, 7.9±3.8%) were recruited. Compared with placebo, empagliflozin caused a significant increase in 24-hour urinary volume at both day 3 (mean difference, 535 mL [95% CI, 133–936]; P=0.005) and week 6 (mean difference, 545 mL [95% CI, 136–954]; P=0.005) after adjustment for treatment order, baseline 24-hour urine volume, and percentage change in loop diuretic dose. At 6 weeks, empagliflozin did not cause a significant change in 24-hour urinary sodium (mean difference, −7.85 mmol/L [95% CI, −2.43 to 6.73]; P=0.57). Empagliflozin caused a nonsignificant increase in fractional excretion of sodium at day 3, which was absent at week 6 (mean difference day 3, 0.30% [95% CI, −0.03 to 0.63]; P=0.09; week 6, 0.11% [95% CI, −0.22 to 0.44]; P>0.99), and a significant increase in electrolyte-free water clearance at week 6 (mean difference, 312 mL [95% CI, 26–598]; P=0.026) compared with placebo. Empagliflozin also caused significant reductions in body weight and serum urate at week 6.
CONCLUSIONS:Empagliflozin caused a significant increase in 24-hour urine volume without an increase in urinary sodium when used in combination with loop diuretic.
REGISTRATION:URLhttps://www.clinicaltrials.gov; Unique IdentifierNCT03226457.</description><subject>Original s</subject><issn>0009-7322</issn><issn>1524-4539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqNUt1u0zAUjhATK4NXQOaOm3T-TWIkkKqsXStVDJVMXFqOaxODGxc72bQ34jFx1zGxG8SVfc75fmx_zrK3CE4RKtB5vdrU1-tZs7r6NFvOpgjDKaRVSfizbIIYpjllhD_PJhBCnpcE49PsZYzfU1mQkr3ITgmuCgYhnWS_NrqXDsh-C2oZttbfyKhGJwOYG6PVEIE34MvlusFg1Xe2tYP1PbA9qP2utb28L7_aoQNr7_fgwo5BD1bFA-Rzmuo-SdzPm7u9BjghZKsHHY-WXfC9VWCpZRjAQlqX6O9B02mwmdfzi3leLxegCVa6V9mJkS7q1w_rWXa9mDf1Ml9fXa7q2TpXtEQ816rijFVtKowx3DAFC1UVqKCKSVIqXnEDMSoIkkqzraoIRrDVhLctZUZqcpZ9POrux3antypdIEgn9sHuZLgTXlrxdNLbTnzzN6JkPD17kQTePQgE_3PUcRA7G5V2Tvbaj1FgSirOC0hxgvIjVAUfY9Dm0QZBcUhaPE1apKTFMenEffP3OR-Zf6JNgA9HwK13gw7xhxtvdRCdlm7o_suA_oOf_hIkEJU5hhgilPb5oUXJb5wYylo</recordid><startdate>20201103</startdate><enddate>20201103</enddate><creator>Mordi, Natalie A.</creator><creator>Mordi, Ify R.</creator><creator>Singh, Jagdeep S.</creator><creator>McCrimmon, Rory J.</creator><creator>Struthers, Allan D.</creator><creator>Lang, Chim C.</creator><general>by the American College of Cardiology Foundation and the American Heart Association, Inc</general><general>Lippincott Williams & Wilkins</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-7358-9712</orcidid><orcidid>https://orcid.org/0000-0002-4530-3078</orcidid><orcidid>https://orcid.org/0000-0002-3957-1981</orcidid></search><sort><creationdate>20201103</creationdate><title>Renal and Cardiovascular Effects of SGLT2 Inhibition in Combination With Loop Diuretics in Patients With Type 2 Diabetes and Chronic Heart Failure: The RECEDE-CHF Trial</title><author>Mordi, Natalie A. ; Mordi, Ify R. ; Singh, Jagdeep S. ; McCrimmon, Rory J. ; Struthers, Allan D. ; Lang, Chim C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4719-ec89558b471fff9f5c06c86164c5a37c989f021631ace5dc83210be39bb45fae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Original s</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mordi, Natalie A.</creatorcontrib><creatorcontrib>Mordi, Ify R.</creatorcontrib><creatorcontrib>Singh, Jagdeep S.</creatorcontrib><creatorcontrib>McCrimmon, Rory J.</creatorcontrib><creatorcontrib>Struthers, Allan D.</creatorcontrib><creatorcontrib>Lang, Chim C.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Circulation (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mordi, Natalie A.</au><au>Mordi, Ify R.</au><au>Singh, Jagdeep S.</au><au>McCrimmon, Rory J.</au><au>Struthers, Allan D.</au><au>Lang, Chim C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Renal and Cardiovascular Effects of SGLT2 Inhibition in Combination With Loop Diuretics in Patients With Type 2 Diabetes and Chronic Heart Failure: The RECEDE-CHF Trial</atitle><jtitle>Circulation (New York, N.Y.)</jtitle><addtitle>Circulation</addtitle><date>2020-11-03</date><risdate>2020</risdate><volume>142</volume><issue>18</issue><spage>1713</spage><epage>1724</epage><pages>1713-1724</pages><issn>0009-7322</issn><eissn>1524-4539</eissn><abstract>BACKGROUND:SGLT2 (sodium-glucose cotransporter-2) inhibitors improve heart failure–associated outcomes in patients with type 2 diabetes. In patients with heart failure, SGLT2 inhibitors will likely be coprescribed with a loop diuretic, but this combined effect is not well-defined. Our aim was to assess the diuretic and natriuretic effect of empagliflozin in combination with loop diuretics.
METHODS:The RECEDE-CHF trial (SGLT2 Inhibition in Combination With Diuretics in Heart Failure) was a randomized, double-blind, placebo-controlled, crossover trial of patients with type 2 diabetes and heart failure with reduced ejection fraction taking regular loop diuretic who were randomized to empagliflozin 25 mg once daily or placebo for 6 weeks with a 2-week washout period. The primary outcome was change in 24-hour urinary volume from baseline to week 6.
RESULTS:Twenty-three participants (mean age, 69.8 years; 73.9% male; mean furosemide dose, 49.6±31.3 mg/d; mean HbA1c, 7.9±3.8%) were recruited. Compared with placebo, empagliflozin caused a significant increase in 24-hour urinary volume at both day 3 (mean difference, 535 mL [95% CI, 133–936]; P=0.005) and week 6 (mean difference, 545 mL [95% CI, 136–954]; P=0.005) after adjustment for treatment order, baseline 24-hour urine volume, and percentage change in loop diuretic dose. At 6 weeks, empagliflozin did not cause a significant change in 24-hour urinary sodium (mean difference, −7.85 mmol/L [95% CI, −2.43 to 6.73]; P=0.57). Empagliflozin caused a nonsignificant increase in fractional excretion of sodium at day 3, which was absent at week 6 (mean difference day 3, 0.30% [95% CI, −0.03 to 0.63]; P=0.09; week 6, 0.11% [95% CI, −0.22 to 0.44]; P>0.99), and a significant increase in electrolyte-free water clearance at week 6 (mean difference, 312 mL [95% CI, 26–598]; P=0.026) compared with placebo. Empagliflozin also caused significant reductions in body weight and serum urate at week 6.
CONCLUSIONS:Empagliflozin caused a significant increase in 24-hour urine volume without an increase in urinary sodium when used in combination with loop diuretic.
REGISTRATION:URLhttps://www.clinicaltrials.gov; Unique IdentifierNCT03226457.</abstract><cop>United States</cop><pub>by the American College of Cardiology Foundation and the American Heart Association, Inc</pub><pmid>32865004</pmid><doi>10.1161/CIRCULATIONAHA.120.048739</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-7358-9712</orcidid><orcidid>https://orcid.org/0000-0002-4530-3078</orcidid><orcidid>https://orcid.org/0000-0002-3957-1981</orcidid><oa>free_for_read</oa></addata></record> |
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title | Renal and Cardiovascular Effects of SGLT2 Inhibition in Combination With Loop Diuretics in Patients With Type 2 Diabetes and Chronic Heart Failure: The RECEDE-CHF Trial |
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