Department of Gastroenterology and Hepatology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Gastroenterology Division, National Hospital Organization Yokohama Medical Center, Yokohama, Japan.
Hepatol Commun. 2022 Sep;6(9):2273-2285. doi: 10.1002/hep4.1993. Epub 2022 May 16.
The incidence of nonalcoholic fatty liver disease (NAFLD) has recently increased and is related to obesity and the associated surge in type 2 diabetes mellitus (T2DM) and metabolic syndromes. This trial follows up on our previous work and forms part of the ToPiND study. We aimed to combine tofogliflozin and pioglitazone treatment for hepatic steatosis in patients with NAFLD and T2DM. In this open-label, prospective, single-center, randomized clinical trial, patients with NAFLD with T2DM and a hepatic fat fraction of ≥10% were assessed based on magnetic resonance imaging proton density fat fraction. Eligible patients received either 20 mg tofogliflozin or 15-30 mg pioglitazone orally, once daily for 24 weeks, followed by combination therapy with both medicines for an additional 24 weeks. The effects on diabetes mellitus and hepatic steatosis were examined at baseline and after the completion of monotherapy and combination therapy. Thirty-two eligible patients received the combination therapy of tofogliflozin and pioglitazone. The combination therapy showed additional improvement in glycated hemoglobin compared with each monotherapy group and showed improvement in steatosis, hepatic stiffness, and alanine aminotransferase levels compared with the tofogliflozin monotherapy group. Pioglitazone monotherapy-mediated increase in body weight decreased following concomitant use of tofogliflozin. The combination therapy resulted in lower triglyceride, higher high-density lipoprotein cholesterol, higher adiponectin, and higher ketone body levels. Conclusion: In addition to the additive effects of tofogliflozin and pioglitazone in patients with T2DM and NAFLD, combination therapy was suggested to reduce weight gain and induce cardioprotective effect. Further studies with more patients are needed to investigate the combination therapy of various drugs.
非酒精性脂肪性肝病(NAFLD)的发病率最近有所增加,与肥胖以及随之而来的 2 型糖尿病(T2DM)和代谢综合征有关。本试验是在我们之前的工作基础上进行的,是 ToPiND 研究的一部分。我们旨在将托格列净和吡格列酮联合用于治疗非酒精性脂肪性肝病合并 2 型糖尿病患者的肝脂肪变性。在这项开放标签、前瞻性、单中心、随机临床试验中,根据磁共振成像质子密度脂肪分数,对患有 T2DM 和肝脂肪分数≥10%的非酒精性脂肪性肝病患者进行评估。符合条件的患者接受托格列净 20mg 或吡格列酮 15-30mg 口服,每日一次,持续 24 周,然后联合两种药物治疗 24 周。在单药治疗和联合治疗结束时,检查对糖尿病和肝脂肪变性的影响。32 名符合条件的患者接受了托格列净和吡格列酮的联合治疗。与每种单药治疗组相比,联合治疗组的糖化血红蛋白进一步改善,与托格列净单药治疗组相比,肝脂肪变性、肝硬度和丙氨酸氨基转移酶水平也有所改善。吡格列酮单药治疗引起的体重增加在联合使用托格列净后减少。联合治疗可降低甘油三酯,升高高密度脂蛋白胆固醇,升高脂联素和酮体水平。结论:除了托格列净和吡格列酮在 T2DM 和 NAFLD 患者中的相加作用外,联合治疗还可减少体重增加并诱导心脏保护作用。需要更多患者的进一步研究来探讨各种药物的联合治疗。