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Similar hepatic outcome by SGLT2i vs. DPP4i for at-risk cohort with CHB & T2DM: A nationwide target trial emulation study

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dc.contributor.authorYun, Byungyoon-
dc.contributor.authorOh, Juyeon-
dc.contributor.authorPark, Heejoo-
dc.contributor.authorLee, Jian-
dc.contributor.authorKim, Beom Kyung-
dc.contributor.authorYoon, Jin-Ha-
dc.date.accessioned2026-03-18T06:27:07Z-
dc.date.available2026-03-18T06:27:07Z-
dc.date.created2026-03-06-
dc.date.issued2026-01-
dc.identifier.issn1665-2681-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/211420-
dc.description.abstractIntroduction and Objectives: The prevalence of diabetes is rising among patients with chronic hepatitis B (CHB). However, the comparative efficacy of sodium-glucose cotransporter-2 inhibitors (SGLT2i) versus dipeptidyl peptidase-4 inhibitors (DPP4i) in this high-risk population remains unclear. We aimed to determine if SGLT2i significantly reduces the risk of liver-related events (LREs) compared with DPP4i, using a target trial emulation approach. Materials and Methods: We used a nationwide database to identify CHB patients with diabetes (age >= 40 years) receiving SGLT2i or DPP4i alongside metformin for >= 60 consecutive days between January 2015 and December 2020. The primary outcome was LRE, defined as hepatocellular carcinoma (HCC), liver cirrhosis (LC), transplantation, or liver-related mortality. Multivariable Cox-regression models with per-protocol analysis and propensity score matching (PSM) were performed to estimate LRE risk. Results: Among 16,070 patients (median age, 57 years; 66.9% male), 695 developed LREs (4.7% in SGLT2i group vs. 4.3% in DPP4i group; p=0.413). In the entire cohort, the LRE risk in the SGLT2i group was comparable to that in the DPP4i group: adjusted hazard ratio (aHR) of 0.89 (95% confidence interval [CI] 0.71-1.11). The risk of secondary outcomes in the SGLT2i group was similar to that of the DPP4i group: aHRs of 0.89 (95% CI 0.58-1.37) for HCC, 0.92 (95% CI 0.72-1.17) for LC, and 0.82 (95% CI 0.29-2.35) for all-cause mortality. These trends were consistent in the PSM cohort. Conclusions: The overall hepatic prognosis was comparable between the SGLT2i and the DPP4i groups. Further prospective studies are required to reach robust conclusions. (c) 2025 Fundaci & oacute;n Cl & iacute;nica M & eacute;dica Sur, A.C. Published by Elsevier Espa & ntilde;a, S.L.U. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)-
dc.languageEnglish-
dc.publisherEdiciones Medicina y Cultura-
dc.relation.isPartOfANNALS OF HEPATOLOGY(Annals of Hepatology)-
dc.titleSimilar hepatic outcome by SGLT2i vs. DPP4i for at-risk cohort with CHB & T2DM: A nationwide target trial emulation study-
dc.typeArticle-
dc.contributor.googleauthorYun, Byungyoon-
dc.contributor.googleauthorOh, Juyeon-
dc.contributor.googleauthorPark, Heejoo-
dc.contributor.googleauthorLee, Jian-
dc.contributor.googleauthorKim, Beom Kyung-
dc.contributor.googleauthorYoon, Jin-Ha-
dc.identifier.doi10.1016/j.aohep.2025.102175-
dc.relation.journalcodeJ04718-
dc.identifier.pmid41443474-
dc.subject.keywordTarget trial emulation-
dc.subject.keywordOral antidiabetic drugs-
dc.subject.keywordLiver-related events-
dc.subject.keywordPropensity score matching-
dc.subject.keywordPer protocol analysis-
dc.contributor.affiliatedAuthorYun, Byungyoon-
dc.contributor.affiliatedAuthorOh, Juyeon-
dc.contributor.affiliatedAuthorPark, Heejoo-
dc.contributor.affiliatedAuthorLee, Jian-
dc.contributor.affiliatedAuthorKim, Beom Kyung-
dc.contributor.affiliatedAuthorYoon, Jin-Ha-
dc.identifier.scopusid2-s2.0-105027696347-
dc.identifier.wosid001674334600001-
dc.citation.volume31-
dc.citation.number1-
dc.identifier.bibliographicCitationANNALS OF HEPATOLOGY(Annals of Hepatology), Vol.31(1), 2026-01-
dc.identifier.rimsid91649-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorTarget trial emulation-
dc.subject.keywordAuthorOral antidiabetic drugs-
dc.subject.keywordAuthorLiver-related events-
dc.subject.keywordAuthorPropensity score matching-
dc.subject.keywordAuthorPer protocol analysis-
dc.subject.keywordPlusHEPATOCELLULAR-CARCINOMA-
dc.subject.keywordPlusINHIBITOR-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryGastroenterology & Hepatology-
dc.relation.journalResearchAreaGastroenterology & Hepatology-
dc.identifier.articleno102175-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Preventive Medicine (예방의학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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