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Cardiovascular and renal outcomes by baseline albuminuria status and renal function: Results from the LEADER randomized trial
Diabetes, Obesity and Metabolism, Volume: 22, Issue: 11, Pages: 2077 - 2088
Swansea University Author: Steve Bain
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DOI (Published version): 10.1111/dom.14126
Abstract
AimTo assess cardiorenal outcomes by baseline urinary albumin-to-creatinine ratio (UACR) and estimated glomerular filtration rate (eGFR) in the contemporary LEADER cohort.Materials and methodsLEADER was a multinational, double-blind trial. Patients with type 2 diabetes and high cardiovascular (CV) r...
Published in: | Diabetes, Obesity and Metabolism |
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ISSN: | 1462-8902 1463-1326 |
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Wiley
2020
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URI: | https://cronfa.swan.ac.uk/Record/cronfa54750 |
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<?xml version="1.0"?><rfc1807><datestamp>2022-12-02T19:16:51.8929353</datestamp><bib-version>v2</bib-version><id>54750</id><entry>2020-07-15</entry><title>Cardiovascular and renal outcomes by baseline albuminuria status and renal function: Results from the LEADER randomized trial</title><swanseaauthors><author><sid>5399f4c6e6a70f3608a084ddb938511a</sid><ORCID>0000-0001-8519-4964</ORCID><firstname>Steve</firstname><surname>Bain</surname><name>Steve Bain</name><active>true</active><ethesisStudent>false</ethesisStudent></author></swanseaauthors><date>2020-07-15</date><deptcode>MEDS</deptcode><abstract>AimTo assess cardiorenal outcomes by baseline urinary albumin-to-creatinine ratio (UACR) and estimated glomerular filtration rate (eGFR) in the contemporary LEADER cohort.Materials and methodsLEADER was a multinational, double-blind trial. Patients with type 2 diabetes and high cardiovascular (CV) risk were randomized 1:1 to the glucagon-like peptide-1 analogue liraglutide (≤1.8 mg daily; n = 4668) or placebo (n = 4672) plus standard care and followed for 3.5 to 5 years. Primary composite outcomes were time to first non-fatal myocardial infarction, non-fatal stroke or CV death. Post hoc Cox regression analyses of outcomes by baseline UACR and eGFR subgroups were conducted with adjustment for baseline variables.ResultsIn the LEADER population, 1598 (17.5%), 2917 (31.9%), 1200 (13.1%), 1611 (17.6%), 845 (9.2%) and 966 (10.6%) had UACR = 0, >0 to <15, 15 to <30, 30 to <100, 100 to <300 and ≥300 mg/g, respectively. Increasing UACR and decreasing eGFR were linked with higher risks of the primary outcome, heart failure hospitalization, a composite renal outcome and death (P-values for the Cochran-Armitage test for trends were all <.0001). Across UACR and eGFR subgroups, risks of cardiorenal events and death were generally lower or similar with liraglutide versus placebo.ConclusionsIn a contemporary type 2 diabetes population, increasing baseline UACR and declining eGFR were linked with higher risks of cardiorenal events and death.</abstract><type>Journal Article</type><journal>Diabetes, Obesity and Metabolism</journal><volume>22</volume><journalNumber>11</journalNumber><paginationStart>2077</paginationStart><paginationEnd>2088</paginationEnd><publisher>Wiley</publisher><placeOfPublication/><isbnPrint/><isbnElectronic/><issnPrint>1462-8902</issnPrint><issnElectronic>1463-1326</issnElectronic><keywords>Albuminuria; glomerular filtration rate; liraglutide; cardiovascular outcomes; mortality; renal outcomes</keywords><publishedDay>1</publishedDay><publishedMonth>11</publishedMonth><publishedYear>2020</publishedYear><publishedDate>2020-11-01</publishedDate><doi>10.1111/dom.14126</doi><url/><notes/><college>COLLEGE NANME</college><department>Medical School</department><CollegeCode>COLLEGE CODE</CollegeCode><DepartmentCode>MEDS</DepartmentCode><institution>Swansea University</institution><apcterm/><funders>This work was supported by Novo Nordisk.</funders><projectreference/><lastEdited>2022-12-02T19:16:51.8929353</lastEdited><Created>2020-07-15T11:53:57.1945412</Created><path><level id="1">Faculty of Medicine, Health and Life Sciences</level><level id="2">Swansea University Medical School - Medicine</level></path><authors><author><firstname>Ofri</firstname><surname>Mosenzon</surname><orcid>0000-0002-5702-7584</orcid><order>1</order></author><author><firstname>Steve</firstname><surname>Bain</surname><orcid>0000-0001-8519-4964</orcid><order>2</order></author><author><firstname>Hiddo J. 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2022-12-02T19:16:51.8929353 v2 54750 2020-07-15 Cardiovascular and renal outcomes by baseline albuminuria status and renal function: Results from the LEADER randomized trial 5399f4c6e6a70f3608a084ddb938511a 0000-0001-8519-4964 Steve Bain Steve Bain true false 2020-07-15 MEDS AimTo assess cardiorenal outcomes by baseline urinary albumin-to-creatinine ratio (UACR) and estimated glomerular filtration rate (eGFR) in the contemporary LEADER cohort.Materials and methodsLEADER was a multinational, double-blind trial. Patients with type 2 diabetes and high cardiovascular (CV) risk were randomized 1:1 to the glucagon-like peptide-1 analogue liraglutide (≤1.8 mg daily; n = 4668) or placebo (n = 4672) plus standard care and followed for 3.5 to 5 years. Primary composite outcomes were time to first non-fatal myocardial infarction, non-fatal stroke or CV death. Post hoc Cox regression analyses of outcomes by baseline UACR and eGFR subgroups were conducted with adjustment for baseline variables.ResultsIn the LEADER population, 1598 (17.5%), 2917 (31.9%), 1200 (13.1%), 1611 (17.6%), 845 (9.2%) and 966 (10.6%) had UACR = 0, >0 to <15, 15 to <30, 30 to <100, 100 to <300 and ≥300 mg/g, respectively. Increasing UACR and decreasing eGFR were linked with higher risks of the primary outcome, heart failure hospitalization, a composite renal outcome and death (P-values for the Cochran-Armitage test for trends were all <.0001). Across UACR and eGFR subgroups, risks of cardiorenal events and death were generally lower or similar with liraglutide versus placebo.ConclusionsIn a contemporary type 2 diabetes population, increasing baseline UACR and declining eGFR were linked with higher risks of cardiorenal events and death. Journal Article Diabetes, Obesity and Metabolism 22 11 2077 2088 Wiley 1462-8902 1463-1326 Albuminuria; glomerular filtration rate; liraglutide; cardiovascular outcomes; mortality; renal outcomes 1 11 2020 2020-11-01 10.1111/dom.14126 COLLEGE NANME Medical School COLLEGE CODE MEDS Swansea University This work was supported by Novo Nordisk. 2022-12-02T19:16:51.8929353 2020-07-15T11:53:57.1945412 Faculty of Medicine, Health and Life Sciences Swansea University Medical School - Medicine Ofri Mosenzon 0000-0002-5702-7584 1 Steve Bain 0000-0001-8519-4964 2 Hiddo J. L. Heerspink 0000-0002-3126-3730 3 Thomas Idorn 4 Johannes F. E. Mann 5 Frederik Persson 0000-0001-6242-6638 6 Richard E. Pratley 7 Søren Rasmussen 8 Peter Rossing 9 Bernt Johan von Scholten 10 Itamar Raz 0000-0003-0209-4453 11 (LEADER Trial Investigators) 12 54750__18497__d7232bc0b3014ad690e531fc3cb149f2.pdf 54750.pdf 2020-10-26T15:41:32.5964555 Output 1189189 application/pdf Version of Record true This is an open access article under the terms of the Creative Commons Attribution-Non Commercial License true eng https://creativecommons.org/licenses/by-nc/4.0/ |
title |
Cardiovascular and renal outcomes by baseline albuminuria status and renal function: Results from the LEADER randomized trial |
spellingShingle |
Cardiovascular and renal outcomes by baseline albuminuria status and renal function: Results from the LEADER randomized trial Steve Bain |
title_short |
Cardiovascular and renal outcomes by baseline albuminuria status and renal function: Results from the LEADER randomized trial |
title_full |
Cardiovascular and renal outcomes by baseline albuminuria status and renal function: Results from the LEADER randomized trial |
title_fullStr |
Cardiovascular and renal outcomes by baseline albuminuria status and renal function: Results from the LEADER randomized trial |
title_full_unstemmed |
Cardiovascular and renal outcomes by baseline albuminuria status and renal function: Results from the LEADER randomized trial |
title_sort |
Cardiovascular and renal outcomes by baseline albuminuria status and renal function: Results from the LEADER randomized trial |
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author_id_fullname_str_mv |
5399f4c6e6a70f3608a084ddb938511a_***_Steve Bain |
author |
Steve Bain |
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Ofri Mosenzon Steve Bain Hiddo J. L. Heerspink Thomas Idorn Johannes F. E. Mann Frederik Persson Richard E. Pratley Søren Rasmussen Peter Rossing Bernt Johan von Scholten Itamar Raz (LEADER Trial Investigators) |
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Diabetes, Obesity and Metabolism |
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10.1111/dom.14126 |
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Wiley |
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AimTo assess cardiorenal outcomes by baseline urinary albumin-to-creatinine ratio (UACR) and estimated glomerular filtration rate (eGFR) in the contemporary LEADER cohort.Materials and methodsLEADER was a multinational, double-blind trial. Patients with type 2 diabetes and high cardiovascular (CV) risk were randomized 1:1 to the glucagon-like peptide-1 analogue liraglutide (≤1.8 mg daily; n = 4668) or placebo (n = 4672) plus standard care and followed for 3.5 to 5 years. Primary composite outcomes were time to first non-fatal myocardial infarction, non-fatal stroke or CV death. Post hoc Cox regression analyses of outcomes by baseline UACR and eGFR subgroups were conducted with adjustment for baseline variables.ResultsIn the LEADER population, 1598 (17.5%), 2917 (31.9%), 1200 (13.1%), 1611 (17.6%), 845 (9.2%) and 966 (10.6%) had UACR = 0, >0 to <15, 15 to <30, 30 to <100, 100 to <300 and ≥300 mg/g, respectively. Increasing UACR and decreasing eGFR were linked with higher risks of the primary outcome, heart failure hospitalization, a composite renal outcome and death (P-values for the Cochran-Armitage test for trends were all <.0001). Across UACR and eGFR subgroups, risks of cardiorenal events and death were generally lower or similar with liraglutide versus placebo.ConclusionsIn a contemporary type 2 diabetes population, increasing baseline UACR and declining eGFR were linked with higher risks of cardiorenal events and death. |
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2020-11-01T19:55:28Z |
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