Renal, Cardiovascular, and Safety Outcomes of Canagliflozin by Baseline Kidney Function: A Secondary Analysis of the CREDENCE Randomized Trial

dc.contributor.authorJardine, Meg J.
dc.contributor.authorZhou, Zien
dc.contributor.authorMahaffey, Kenneth W.
dc.contributor.authorOshima, Megumi
dc.contributor.authorAgarwal, Rajiv
dc.contributor.authorBakris, George
dc.contributor.authorBajaj, Harpreet S.
dc.contributor.authorBull, Scott
dc.contributor.authorCannon, Christopher P.
dc.contributor.authorCharytan, David M.
dc.contributor.authorde Zeeuw, Dick
dc.contributor.authorDi Tanna, Gian Luca
dc.contributor.authorGreene, Tom
dc.contributor.authorHeerspink, Hiddo J.L.
dc.contributor.authorLevin, Adeera
dc.contributor.authorNeal, Bruce
dc.contributor.authorPollock, Carol
dc.contributor.authorQiu, Rose
dc.contributor.authorSun, Tao
dc.contributor.authorWheeler, David C.
dc.contributor.authorZhang, Hong
dc.contributor.authorZinman, Bernard
dc.contributor.authorRosenthal, Norman
dc.contributor.authorPerkovic, Vlado
dc.contributor.departmentMedicine, School of Medicineen_US
dc.date.accessioned2022-11-04T12:57:21Z
dc.date.available2022-11-04T12:57:21Z
dc.date.issued2020-05
dc.description.abstractBackground: Canagliflozin reduced renal and cardiovascular events in people with type 2 diabetes in the CREDENCE trial. We assessed efficacy and safety of canagliflozin by initial estimated glomerular filtration rate (eGFR). Methods: CREDENCE randomly assigned 4401 participants with an eGFR of 30 to <90 ml/min per 1.73 m2 and substantial albuminuria to canagliflozin 100 mg or placebo. We used Cox proportional hazards regression to analyze effects on renal and cardiovascular efficacy and safety outcomes within screening eGFR subgroups (30 to <45, 45 to <60, and 60 to <90 ml/min per 1.73 m2) and linear mixed effects models to analyze the effects on eGFR slope. Results: At screening, 1313 (30%), 1279 (29%), and 1809 (41%) participants had an eGFR of 30 to <45, 45 to <60, and 60 to <90 ml/min per 1.73 m2, respectively. The relative benefits of canagliflozin for renal and cardiovascular outcomes appeared consistent among eGFR subgroups (all P interaction >0.11). Subgroups with lower eGFRs, who were at greater risk, exhibited larger absolute benefits for renal outcomes. Canagliflozin's lack of effect on serious adverse events, amputations, and fractures appeared consistent among eGFR subgroups. In all subgroups, canagliflozin use led to an acute eGFR drop followed by relative stabilization of eGFR loss. Among those with an eGFR of 30 to <45 ml/min per 1.73 m2, canagliflozin led to an initial drop of 2.03 ml/min per 1.73 m2. Thereafter, decline in eGFR was slower in the canagliflozin versus placebo group (-1.72 versus -4.33 ml/min per 1.73 m2; between-group difference 2.61 ml/min per 1.73 m2). Conclusions: Canagliflozin safely reduced the risk of renal and cardiovascular events, with consistent results across eGFR subgroups, including the subgroup initiating treatment with an eGFR of 30 to <45 ml/min per 1.73 m2. Absolute benefits for renal outcomes were greatest in subgroups with lower eGFR.en_US
dc.identifier.citationJardine MJ, Zhou Z, Mahaffey KW, et al. Renal, Cardiovascular, and Safety Outcomes of Canagliflozin by Baseline Kidney Function: A Secondary Analysis of the CREDENCE Randomized Trial. J Am Soc Nephrol. 2020;31(5):1128-1139. doi:10.1681/ASN.2019111168en_US
dc.identifier.urihttps://hdl.handle.net/1805/30467
dc.language.isoen_USen_US
dc.publisherAmerican Society of Nephrologyen_US
dc.relation.isversionof10.1681/ASN.2019111168en_US
dc.relation.journalJournal of the American Society of Nephrologyen_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectSGLT2 inhibitoren_US
dc.subjectCanagliflozinen_US
dc.subjectChronic kidney diseaseen_US
dc.subjectDiabetesen_US
dc.subjectEnd-stage kidney diseaseen_US
dc.titleRenal, Cardiovascular, and Safety Outcomes of Canagliflozin by Baseline Kidney Function: A Secondary Analysis of the CREDENCE Randomized Trialen_US
dc.typeArticleen_US
ul.alternative.fulltexthttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217416/en_US
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