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Lower cardiorenal risk with sodium-glucose cotransporter-2 inhibitors versus dipeptidyl peptidase-4 inhibitors in patients with type 2 diabetes without cardiovascular and renal diseases: A large multinational observational study

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dc.contributor.authorBirkeland, KI-
dc.contributor.authorBodegard, J-
dc.contributor.authorBanerjee, A-
dc.contributor.authorKim, DJ-
dc.contributor.authorNorhammar, A-
dc.contributor.authorEriksson, JW-
dc.contributor.authorThuresson, M-
dc.contributor.authorOkami, S-
dc.contributor.authorHa, KH-
dc.contributor.authorKossack, N-
dc.contributor.authorMamza, JB-
dc.contributor.authorZhang, R-
dc.contributor.authorYajima, T-
dc.contributor.authorKomuro, I-
dc.contributor.authorKadowaki, T-
dc.date.accessioned2022-11-29T01:43:36Z-
dc.date.available2022-11-29T01:43:36Z-
dc.date.issued2021-
dc.identifier.issn1462-8902-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/23031-
dc.description.abstractAIMS: We compared the new use of sodium-glucose cotransporter-2 inhibitor (SGLT2i) versus dipeptidyl peptidase-4 inhibitor (DPP4i) and the risk of cardiorenal disease, heart failure (HF) or chronic kidney disease (CKD), in patients with type 2 diabetes without a history of prevalent cardiovascular and renal disease, defined as cardiovascular and renal disease (CVRD) free, managed in routine clinical practice.

MATERIALS AND METHODS: In this observational cohort study, patients were identified from electronic health records from England, Germany, Japan, Norway, South Korea and Sweden, during 2012-2018. In total, 1 006 577 CVRD-free new users of SGLT2i or DPP4i were propensity score matched 1:1. Unadjusted Cox regression was used to estimate hazard ratios (HRs) for outcomes: cardiorenal disease, HF, CKD, stroke, myocardial infarction (MI), cardiovascular and all-cause mortality.

RESULTS: Baseline characteristics were well balanced between the treatment groups (n = 105 130 in each group) with total follow-up of 187 955 patient years. Patients had a mean age of 56 years, 43% were women and they were indexed between 2013 and 2018. The most commonly used agents were dapagliflozin (91.7% of exposure time) and sitagliptin/linagliptin (55.0%), in the SGLT2i and DPP4i, groups, respectively. SGLT2i was associated with lower risk of cardiorenal disease, HF, CKD, all-cause and cardiovascular mortality; HR (95% confidence interval), 0.56 (0.42-0.74), 0.71 (0.59-0.86), 0.44 (0.28-0.69), 0.67 (0.59-0.77), and 0.61 (0.44-0.85), respectively. No differences were observed for stroke [0.87 (0.69-1.09)] and MI [0.94 (0.80-1.11)].

CONCLUSION: In this multinational observational study, SGLT2i was associated with a lower risk of HF and CKD versus DPP4i in patients with type 2 diabetes otherwise free from both cardiovascular and renal disease.
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dc.language.isoen-
dc.subject.MESHCardiovascular Diseases-
dc.subject.MESHDiabetes Mellitus, Type 2-
dc.subject.MESHDipeptidyl-Peptidase IV Inhibitors-
dc.subject.MESHEngland-
dc.subject.MESHFemale-
dc.subject.MESHGermany-
dc.subject.MESHGlucose-
dc.subject.MESHHumans-
dc.subject.MESHJapan-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNorway-
dc.subject.MESHRepublic of Korea-
dc.subject.MESHSodium-
dc.subject.MESHSodium-Glucose Transporter 2 Inhibitors-
dc.subject.MESHSweden-
dc.titleLower cardiorenal risk with sodium-glucose cotransporter-2 inhibitors versus dipeptidyl peptidase-4 inhibitors in patients with type 2 diabetes without cardiovascular and renal diseases: A large multinational observational study-
dc.typeArticle-
dc.identifier.pmid32893440-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756303-
dc.subject.keyworddapagliflozin-
dc.subject.keyworddiabetic nephropathy-
dc.subject.keywordDPP‐IV inhibitor-
dc.subject.keywordheart failure-
dc.subject.keywordobservational study-
dc.subject.keywordSGLT2 inhibitor-
dc.contributor.affiliatedAuthorKim, DJ-
dc.contributor.affiliatedAuthorHa, KH-
dc.type.localJournal Papers-
dc.identifier.doi10.1111/dom.14189-
dc.citation.titleDiabetes, obesity & metabolism-
dc.citation.volume23-
dc.citation.number1-
dc.citation.date2021-
dc.citation.startPage75-
dc.citation.endPage85-
dc.identifier.bibliographicCitationDiabetes, obesity & metabolism, 23(1). : 75-85, 2021-
dc.identifier.eissn1463-1326-
dc.relation.journalidJ014628902-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Endocrinology & Metabolism
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