Kitsunai Hiroya, Shinozaki Yuka, Furusawa Sho, Kitao Naoyuki, Ito Miki, Kurihara Hiroyoshi, Oba-Yamamoto Chiho, Takeuchi Jun, Nakamura Akinobu, Takiyama Yumi, Nomoto Hiroshi
Division of Endocrinology, Metabolism, and Rheumatology, Department of Internal Medicine, Asahikawa Medical University, Asahikawa 078-8510, Hokkaido, Japan.
Department of Rheumatology, Endocrinology and Nephrology, Faculty of Medicine, Graduate School of Medicine, Hokkaido University, Sapporo 060-8638, Hokkaido, Japan.
Pharmaceuticals (Basel). 2025 Jan 19;18(1):129. doi: 10.3390/ph18010129.
BACKGROUND/OBJECTIVES: Metabolic dysfunction-associated steatotic liver disease (MASLD) is an important common comorbidity in subjects with type 2 diabetes, and liver fibrosis is a factor directly related to its prognosis. Glucagon-like peptide-1 receptor agonists are useful treatment options for MASLD; however, the efficacy of oral semaglutide in treating liver steatosis/fibrosis has not been fully elucidated.
A secondary analysis of a multicenter, retrospective, observational study investigating the efficacy and safety of oral semaglutide in Japanese subjects with type 2 diabetes in a real-world clinical setting (the Sapporo-Oral SEMA study) was conducted. Subjects in the original cohort were divided into groups as follows: subjects with suspected MASLD (alanine aminotransferase > 30 U/L) were placed in an overall group; a subpopulation from an overall group at high risk for hepatic fibrosis (fibrosis-4 (FIB-4) index ≥ 1.3 or platelet count < 200,000/µL) was placed in a high-risk group; and the remaining subjects were placed in a low-risk group. Changes in the hepatic steatosis index and FIB-4 index after oral semaglutide induction were explored using a paired -test or the Wilcoxon signed-rank test.
Overall, 169 subjects (including 131 that switched from other medications) were analyzed, and 67 and 102 subjects were selected for the high-risk and low-risk groups, respectively. Oral semaglutide significantly improved the hepatic steatosis index (from 46.1 to 44.6, < 0.001) and FIB-4 index (from 1.04 to 0.96, < 0.001) as well as several metabolic parameters in all cohorts. The efficacy of semaglutide in treating liver fibrosis was confirmed by the addition of, and switching from, existing agent groups. Furthermore, improvement in the FIB-4 index was significantly negatively correlated with the baseline FIB-4 index.
The induction of oral semaglutide might be a useful treatment option for subjects with type 2 diabetes at high risk for liver fibrosis, even when switching from conventional medications for diabetes.
背景/目的:代谢功能障碍相关脂肪性肝病(MASLD)是2型糖尿病患者重要的常见合并症,肝纤维化是与其预后直接相关的一个因素。胰高血糖素样肽-1受体激动剂是治疗MASLD的有效选择;然而,口服司美格鲁肽治疗肝脂肪变性/纤维化的疗效尚未完全阐明。
对一项多中心、回顾性、观察性研究进行二次分析,该研究在真实临床环境中调查口服司美格鲁肽对日本2型糖尿病患者的疗效和安全性(札幌口服司美格鲁肽研究)。原始队列中的受试者分为以下几组:疑似MASLD(丙氨酸氨基转移酶>30 U/L)的受试者归入总体组;总体组中肝纤维化高危亚组(纤维化-4(FIB-4)指数≥1.3或血小板计数<200,000/µL)归入高危组;其余受试者归入低危组。采用配对t检验或Wilcoxon符号秩检验探讨口服司美格鲁肽诱导后肝脂肪变性指数和FIB-4指数的变化。
总体上,分析了169名受试者(包括131名从其他药物转换而来的受试者),分别为高危组和低危组选择了67名和102名受试者。口服司美格鲁肽显著改善了所有队列的肝脂肪变性指数(从46.1降至44.6,P<0.001)和FIB-4指数(从1.04降至0.96,P<0.001)以及几个代谢参数。通过现有药物组的加用和转换,证实了司美格鲁肽治疗肝纤维化的疗效。此外,FIB-4指数的改善与基线FIB-4指数显著负相关。
即使从传统糖尿病药物转换而来,口服司美格鲁肽诱导治疗可能是肝纤维化高危2型糖尿病患者的一种有效治疗选择。