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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
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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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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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
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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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
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
Journal Article

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

2025
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Overview
Background The 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. Methods In 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. Results Combination 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). Conclusions Combination 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 registration The trial was registered at ClinicalTrials.gov (registration number: NCT03646292).
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
Subject

Abdomen

/ Adiponectin

/ Aged

/ Alcohol

/ Antidiabetics

/ Benzhydryl Compounds - administration & dosage

/ Benzhydryl Compounds - therapeutic use

/ Bile ducts

/ Biomedicine

/ Blood pressure

/ Blood vessels

/ Body composition

/ Body mass index

/ Care and treatment

/ Cholesterol

/ Complications and side effects

/ Dextrose

/ Diabetes

/ Diabetes mellitus (non-insulin dependent)

/ Diabetes Mellitus, Type 2 - complications

/ Diabetes Mellitus, Type 2 - drug therapy

/ Diabetes therapy

/ Diagnosis

/ Dosage and administration

/ Drug dosages

/ Drug Synergism

/ Drug therapy

/ Drug Therapy, Combination

/ Drugs

/ Fatty liver

/ Fatty Liver - complications

/ Fatty Liver - drug therapy

/ Female

/ Glucose

/ Glucosides - administration & dosage

/ Glucosides - therapeutic use

/ Humans

/ Hypoglycemic agents

/ Hypoglycemic Agents - administration & dosage

/ Hypoglycemic Agents - therapeutic use

/ Insulin resistance

/ Labels

/ Liver

/ Liver - diagnostic imaging

/ Liver diseases

/ Magnetic resonance imaging

/ Male

/ Medical colleges

/ Medical history

/ Medical imaging

/ Medicine

/ Medicine & Public Health

/ Metabolic dysfunction-associated steatotic liver disease

/ Metabolism

/ Middle Aged

/ Pioglitazone

/ Pioglitazone - administration & dosage

/ Pioglitazone - therapeutic use

/ Proton density (concentration)

/ Risk factors

/ Side effects

/ Sodium-glucose cotransporter

/ Sodium-glucose cotransporter 2 inhibitor

/ Sodium-Glucose Transporter 2 Inhibitors - therapeutic use

/ Stiffness

/ Therapy

/ Thiazolidinedione

/ Thiazolidinediones

/ Thiazolidinediones - administration & dosage

/ Thiazolidinediones - therapeutic use

/ Treatment Outcome

/ Type 2 diabetes