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Similar hepatic outcome by SGLT2i vs. DPP4i for at-risk cohort with CHB & T2DM: A nationwide target trial emulation study
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Yun, Byungyoon | - |
| dc.contributor.author | Oh, Juyeon | - |
| dc.contributor.author | Park, Heejoo | - |
| dc.contributor.author | Lee, Jian | - |
| dc.contributor.author | Kim, Beom Kyung | - |
| dc.contributor.author | Yoon, Jin-Ha | - |
| dc.date.accessioned | 2026-03-18T06:27:07Z | - |
| dc.date.available | 2026-03-18T06:27:07Z | - |
| dc.date.created | 2026-03-06 | - |
| dc.date.issued | 2026-01 | - |
| dc.identifier.issn | 1665-2681 | - |
| dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/211420 | - |
| dc.description.abstract | Introduction 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.language | English | - |
| dc.publisher | Ediciones Medicina y Cultura | - |
| dc.relation.isPartOf | ANNALS OF HEPATOLOGY(Annals of Hepatology) | - |
| dc.title | Similar hepatic outcome by SGLT2i vs. DPP4i for at-risk cohort with CHB & T2DM: A nationwide target trial emulation study | - |
| dc.type | Article | - |
| dc.contributor.googleauthor | Yun, Byungyoon | - |
| dc.contributor.googleauthor | Oh, Juyeon | - |
| dc.contributor.googleauthor | Park, Heejoo | - |
| dc.contributor.googleauthor | Lee, Jian | - |
| dc.contributor.googleauthor | Kim, Beom Kyung | - |
| dc.contributor.googleauthor | Yoon, Jin-Ha | - |
| dc.identifier.doi | 10.1016/j.aohep.2025.102175 | - |
| dc.relation.journalcode | J04718 | - |
| dc.identifier.pmid | 41443474 | - |
| dc.subject.keyword | Target trial emulation | - |
| dc.subject.keyword | Oral antidiabetic drugs | - |
| dc.subject.keyword | Liver-related events | - |
| dc.subject.keyword | Propensity score matching | - |
| dc.subject.keyword | Per protocol analysis | - |
| dc.contributor.affiliatedAuthor | Yun, Byungyoon | - |
| dc.contributor.affiliatedAuthor | Oh, Juyeon | - |
| dc.contributor.affiliatedAuthor | Park, Heejoo | - |
| dc.contributor.affiliatedAuthor | Lee, Jian | - |
| dc.contributor.affiliatedAuthor | Kim, Beom Kyung | - |
| dc.contributor.affiliatedAuthor | Yoon, Jin-Ha | - |
| dc.identifier.scopusid | 2-s2.0-105027696347 | - |
| dc.identifier.wosid | 001674334600001 | - |
| dc.citation.volume | 31 | - |
| dc.citation.number | 1 | - |
| dc.identifier.bibliographicCitation | ANNALS OF HEPATOLOGY(Annals of Hepatology), Vol.31(1), 2026-01 | - |
| dc.identifier.rimsid | 91649 | - |
| dc.type.rims | ART | - |
| dc.description.journalClass | 1 | - |
| dc.description.journalClass | 1 | - |
| dc.subject.keywordAuthor | Target trial emulation | - |
| dc.subject.keywordAuthor | Oral antidiabetic drugs | - |
| dc.subject.keywordAuthor | Liver-related events | - |
| dc.subject.keywordAuthor | Propensity score matching | - |
| dc.subject.keywordAuthor | Per protocol analysis | - |
| dc.subject.keywordPlus | HEPATOCELLULAR-CARCINOMA | - |
| dc.subject.keywordPlus | INHIBITOR | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalWebOfScienceCategory | Gastroenterology & Hepatology | - |
| dc.relation.journalResearchArea | Gastroenterology & Hepatology | - |
| dc.identifier.articleno | 102175 | - |
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