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Synergistic benefit of thiazolidinedione and sodium-glucose cotransporter 2 inhibitor for metabolic dysfunction-associated steatotic liver disease in type 2 diabetes: a 24-week, open-label, randomized controlled trial

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dc.contributor.authorLee, Minyoung-
dc.contributor.authorHong, Sukchul-
dc.contributor.authorCho, Yongin-
dc.contributor.authorRhee, Hyungjin-
dc.contributor.authorYu, Min Heui-
dc.contributor.authorBae, Jaehyun-
dc.contributor.authorLee, Yong-ho-
dc.contributor.authorLee, Byung-Wan-
dc.contributor.authorKang, Eun Seok-
dc.contributor.authorCha, Bong-Soo-
dc.date.accessioned2025-11-10T01:55:17Z-
dc.date.available2025-11-10T01:55:17Z-
dc.date.created2025-08-22-
dc.date.issued2025-05-
dc.identifier.issn1741-7015-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/208521-
dc.description.abstractBackgroundThe close interplay between metabolic dysfunction-associated steatotic liver disease (MASLD) and type 2 diabetes supports the need to identify beneficial combination therapies of antidiabetic medications targeted for the treatment of MASLD. This study aimed to investigate the complementary effects of combination therapy with pioglitazone (PIO) and empagliflozin (EMPA) on MASLD in individuals with type 2 diabetes.MethodsIn a randomized, open-label trial, 50 participants with type 2 diabetes and MASLD were assigned 1:1:1 to receive PIO 15 mg, EMPA 10 mg, or a combination (PIO 15 mg plus EMPA 10 mg) daily for 24 weeks. Liver fat fraction and stiffness were evaluated using magnetic resonance imaging-proton density fat fraction (MRI-PDFF) and magnetic resonance elastography (MRE), respectively.ResultsCombination therapy resulted in the largest reduction in liver fat and stiffness among treatment groups. Participants experiencing a relative reduction >= 30% or an absolute reduction >= 5% in liver fat were the most prevalent in the combination group (100.0% vs. 57.1% in PIO and 87.5% in EMPA, p = 0.010). In addition, the combination group showed the highest proportion of individuals with a relative reduction >= 30% in liver fat and >= 20% in liver stiffness than the monotherapy groups (50.0% vs. 21.4% in PIO and 6.3% in EMPA, p = 0.029). Combination therapy did not induce the changes in subcutaneous fat deposition observed in the monotherapy groups, but it did show the most substantial reduction in visceral fat, concurrently showing the largest increase in adiponectin level across the three groups (p = 0.036).ConclusionsCombination therapy of PIO with EMPA showed synergistic benefits for MASLD in individuals with type 2 diabetes, compensating for the inadequate or unfavorable effects of monotherapies; ClincialTrials.gov number, NCT03646292.Trial registrationThe trial was registered at ClinicalTrials.gov (registration number: NCT03646292).-
dc.languageEnglish-
dc.publisherBioMed Central-
dc.relation.isPartOfBMC MEDICINE-
dc.relation.isPartOfBMC MEDICINE-
dc.subject.MESHAged-
dc.subject.MESHBenzhydryl Compounds* / administration & dosage-
dc.subject.MESHBenzhydryl Compounds* / therapeutic use-
dc.subject.MESHDiabetes Mellitus, Type 2* / complications-
dc.subject.MESHDiabetes Mellitus, Type 2* / drug therapy-
dc.subject.MESHDrug Synergism-
dc.subject.MESHDrug Therapy, Combination-
dc.subject.MESHFatty Liver* / complications-
dc.subject.MESHFatty Liver* / drug therapy-
dc.subject.MESHFemale-
dc.subject.MESHGlucosides* / administration & dosage-
dc.subject.MESHGlucosides* / therapeutic use-
dc.subject.MESHHumans-
dc.subject.MESHHypoglycemic Agents* / administration & dosage-
dc.subject.MESHHypoglycemic Agents* / therapeutic use-
dc.subject.MESHLiver / diagnostic imaging-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPioglitazone* / administration & dosage-
dc.subject.MESHPioglitazone* / therapeutic use-
dc.subject.MESHSodium-Glucose Transporter 2 Inhibitors* / therapeutic use-
dc.subject.MESHThiazolidinediones* / administration & dosage-
dc.subject.MESHThiazolidinediones* / therapeutic use-
dc.subject.MESHTreatment Outcome-
dc.titleSynergistic benefit of thiazolidinedione and sodium-glucose cotransporter 2 inhibitor for metabolic dysfunction-associated steatotic liver disease in type 2 diabetes: a 24-week, open-label, randomized controlled trial-
dc.typeArticle-
dc.contributor.googleauthorLee, Minyoung-
dc.contributor.googleauthorHong, Sukchul-
dc.contributor.googleauthorCho, Yongin-
dc.contributor.googleauthorRhee, Hyungjin-
dc.contributor.googleauthorYu, Min Heui-
dc.contributor.googleauthorBae, Jaehyun-
dc.contributor.googleauthorLee, Yong-ho-
dc.contributor.googleauthorLee, Byung-Wan-
dc.contributor.googleauthorKang, Eun Seok-
dc.contributor.googleauthorCha, Bong-Soo-
dc.identifier.doi10.1186/s12916-025-04017-x-
dc.relation.journalcodeJ00364-
dc.identifier.eissn1741-7015-
dc.identifier.pmid40336058-
dc.subject.keywordMetabolic dysfunction-associated steatotic liver disease-
dc.subject.keywordType 2 diabetes-
dc.subject.keywordThiazolidinedione-
dc.subject.keywordSodium-glucose cotransporter 2 inhibitor-
dc.contributor.affiliatedAuthorLee, Minyoung-
dc.contributor.affiliatedAuthorHong, Sukchul-
dc.contributor.affiliatedAuthorRhee, Hyungjin-
dc.contributor.affiliatedAuthorYu, Min Heui-
dc.contributor.affiliatedAuthorLee, Yong-ho-
dc.contributor.affiliatedAuthorLee, Byung-Wan-
dc.contributor.affiliatedAuthorKang, Eun Seok-
dc.contributor.affiliatedAuthorCha, Bong-Soo-
dc.identifier.scopusid2-s2.0-105004436795-
dc.identifier.wosid001484303800003-
dc.citation.volume23-
dc.citation.number1-
dc.identifier.bibliographicCitationBMC MEDICINE, Vol.23(1), 2025-05-
dc.identifier.rimsid88781-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorMetabolic dysfunction-associated steatotic liver disease-
dc.subject.keywordAuthorType 2 diabetes-
dc.subject.keywordAuthorThiazolidinedione-
dc.subject.keywordAuthorSodium-glucose cotransporter 2 inhibitor-
dc.subject.keywordPlusPIOGLITAZONE-
dc.subject.keywordPlusMETAANALYSIS-
dc.subject.keywordPlusSTATEMENT-
dc.subject.keywordPlusEFFICACY-
dc.subject.keywordPlusFIBROSIS-
dc.subject.keywordPlusPLACEBO-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryMedicine, General & Internal-
dc.relation.journalResearchAreaGeneral & Internal Medicine-
dc.identifier.articleno266-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Radiology (영상의학교실) > 1. Journal Papers

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