Institute of Digestive Diseases, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200032, China.
Clinical Research Academy, Peking University Shenzhen Hospital, Shenzhen, 518032, China.
Front Med. 2022 Oct;16(5):745-759. doi: 10.1007/s11684-021-0880-3. Epub 2022 Apr 26.
Lingguizhugan Decoction (LGZG) has been investigated in basic studies, with satisfactory effects on insulin resistance in non-alcoholic fatty liver disease (NAFLD). This translational approach aimed to explore the effect and underlying mechanism of LGZG in clinical setting. A randomized, double-blinded, placebo-controlled trial was performed. A total of 243 eligible participants with NAFLD were equally allocated to receive LGZG (two groups: standard dose and low dose) or placebo for 12 weeks on the basis of lifestyle modifications. The primary efficacy variable was homeostasis model assessment of insulin resistance (HOMA-IR). Analyses were performed in two populations in accordance with body mass index (BMI; overweight/obese, BMI ⩾ 24 kg/m; lean, BMI < 24 kg/m). For overweight/obese participants, low-dose LGZG significantly decreased their HOMA-IR level compared with placebo (-0.19 (1.47) versus 0.08 (1.99), P = 0.038). For lean subjects, neither dose of LGZG showed a superior effect compared with placebo. Methylated DNA immunoprecipitation sequencing and real-time qPCR found that the DNA N6-methyladenine modification levels of protein phosphatase 1 regulatory subunit 3A (PPP1R3A) and autophagy related 3 (ATG3) significantly increased after LGZG intervention in overweight/obese population. Low-dose LGZG effectively improved insulin resistance in overweight/obese subjects with NAFLD. The underlying mechanism may be related to the regulation of DNA N6-methyladenine modification of PPP1R3A and ATG3. Lean subjects may not be a targeted population for LGZG.
灵龟护肝汤(LGZG)在基础研究中已被证实对非酒精性脂肪性肝病(NAFLD)的胰岛素抵抗具有满意的疗效。本转化研究旨在临床实践中探索 LGZG 的疗效及其作用机制。一项随机、双盲、安慰剂对照试验进行。共有 243 名符合条件的 NAFLD 患者,根据生活方式的改变,被平均分为 LGZG(高、低剂量)组和安慰剂组,分别接受为期 12 周的治疗。主要疗效变量是稳态模型评估的胰岛素抵抗指数(HOMA-IR)。根据体重指数(BMI;超重/肥胖,BMI ⩾ 24 kg/m;非超重,BMI < 24 kg/m),对两组人群进行了分析。对于超重/肥胖患者,与安慰剂相比,低剂量 LGZG 可显著降低其 HOMA-IR 水平(-0.19(1.47)比 0.08(1.99),P = 0.038)。而非超重患者中,LGZG 两种剂量均未显示优于安慰剂的效果。甲基化 DNA 免疫沉淀测序和实时 qPCR 发现,在超重/肥胖人群中,LGZG 干预后蛋白磷酸酶 1 调节亚基 3A(PPP1R3A)和自噬相关蛋白 3(ATG3)的 DNA N6-甲基腺嘌呤修饰水平显著增加。低剂量 LGZG 可有效改善超重/肥胖的 NAFLD 患者的胰岛素抵抗。其作用机制可能与 PPP1R3A 和 ATG3 的 DNA N6-甲基腺嘌呤修饰的调节有关。非超重患者可能不是 LGZG 的目标人群。