{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["EMPA-KIDNEY Collaborative Group"],"funding":["Kidney Research UK","Boehringer Ingelheim","Medical Research Council","National Institute for Health Research (NIHR)","Eli Lilly and Company"],"pagination":["51-60"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC7618536"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["12(1)"],"pubmed_abstract":["<h4>Background</h4>The EMPA-KIDNEY trial showed that empagliflozin reduced the risk of the primary composite outcome of kidney disease progression or cardiovascular death in patients with chronic kidney disease mainly through slowing progression. We aimed to assess how effects of empagliflozin might differ by primary kidney disease across its broad population.<h4>Methods</h4>EMPA-KIDNEY, a randomised, controlled, phase 3 trial, was conducted at 241 centres in eight countries (Canada, China, Germany, Italy, Japan, Malaysia, the UK, and the USA). Patients were eligible if their estimated glomerular filtration rate (eGFR) was 20 to less than 45 mL/min per 1·73 m<sup>2</sup>, or 45 to less than 90 mL/min per 1·73 m<sup>2</sup> with a urinary albumin-to-creatinine ratio (uACR) of 200 mg/g or hi"],"journal":["The lancet. Diabetes & endocrinology"],"pubmed_title":["Impact of primary kidney disease on the effects of empagliflozin in patients with chronic kidney disease: secondary analyses of the EMPA-KIDNEY trial."],"pmcid":["PMC7618536"],"funding_grant_id":["17/140/02","MR/R007764/1"],"pubmed_authors":["Hooi L","Ghanem A","Chavagnon T","Iwasa M","Sumi M","Wanner C","Schulz E","Kaneko K","Watanabe M","Whelton P","Burnette S","Watanabe K","Uchida T","Budoff M","Ryder M","Fletcher L","Uchida H","Kupper A","Bagwell B","Busch M","Yamanouchi Y","McLaughlin S","Yarlagadda S","Rahbari-Oskoui F","White K","Cao H","Hutchinson C","Eldon H","Kuwabara N","Wei W","Sato Y","Yu H","Yamasaki N","Macleod P","Marx K","Massey D","Miyaji M","Totaro F","Yu Y","Barot C","Sato D","Hosein D","Sato A","Valletta C","Zhu D","Latif F","Sato T","Tonks L","Zhu L","Yamasaki Y","Lustig R","Ramsey T","Sato J","Sato H","Zhu S","Kajio H","Murray S","Richmond L","Vettoretti S","Cipressa L","Vourvou M","Hagan S","Laundy E","Liberti L","Chen 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P"],"additional_accession":[]},"is_claimable":false,"name":"Impact of primary kidney disease on the effects of empagliflozin in patients with chronic kidney disease: secondary analyses of the EMPA-KIDNEY trial.","description":"<h4>Background</h4>The EMPA-KIDNEY trial showed that empagliflozin reduced the risk of the primary composite outcome of kidney disease progression or cardiovascular death in patients with chronic kidney disease mainly through slowing progression. We aimed to assess how effects of empagliflozin might differ by primary kidney disease across its broad population.<h4>Methods</h4>EMPA-KIDNEY, a randomised, controlled, phase 3 trial, was conducted at 241 centres in eight countries (Canada, China, Germany, Italy, Japan, Malaysia, the UK, and the USA). Patients were eligible if their estimated glomerular filtration rate (eGFR) was 20 to less than 45 mL/min per 1·73 m<sup>2</sup>, or 45 to less than 90 mL/min per 1·73 m<sup>2</sup> with a urinary albumin-to-creatinine ratio (uACR) of 200 mg/g or hi","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Jan","modification":"2026-06-06T04:24:53.098Z","creation":"2026-05-25T03:12:17.632Z"},"accession":"S-EPMC7618536","cross_references":{"pubmed":["38061372"],"doi":["10.1016/S2213-8587(23)00322-4"]}}