Unit of Clinical Nutrition, Careggi University Hospital, Florence, Italy.
Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Phytother Res. 2024 Sep;38(9):4614-4627. doi: 10.1002/ptr.8288. Epub 2024 Jul 30.
Licorice (Glycyrrhiza spp.) has been a cornerstone of traditional Chinese and Japanese medicine. This systematic review and meta-analysis aimed to evaluate the efficacy of licorice formulations, alone or in combination with other herbs, on liver function enzymes in patients with primary liver disease. We systematically searched MEDLINE, Embase, Scopus, Web of Science, and Cochrane Library up to April 2024. Randomized controlled trials (RCTs) comparing the effects of Glycyrrhiza spp. preparations versus placebo or standard of care controls were included. Standard Cochrane methods were used to extract data and appraise eligible studies. A total of 15 RCTs, involving 1367 participants, were included in the analysis. The studies varied widely in geographical location, duration, and licorice preparations used. Licorice significantly reduced alanine aminotransferase (ALT) by 15.63 U/L (95% CI: -25.08, -6.18; p = 0.001) and aspartate aminotransferase (AST) by 7.37 U/L (95% CI: -13.13, -1.61; p = 0.01) compared to control groups. Subgroup analyses revealed that purified glycyrrhizic acid compounds were particularly effective, showing greater reductions in ALT and AST without significant heterogeneity. Although licorice treatment did not significantly impact gamma-glutamyl transferase and total bilirubin (TBIL) levels overall, specific licorice-herb preparations did show a notable reduction in TBIL. The safety profile of licorice was consistent with known side effects, predominantly mild and related to its mineralocorticoid effects. Despite heterogeneity and potential language bias, the findings suggest that licorice can enhance liver function. Further studies should standardize licorice preparations and explore its role in multifaceted herbal formulations to better understand its hepatoprotective mechanisms.
甘草(Glycyrrhiza spp.)一直是中医和日本传统医学的基石。本系统评价和荟萃分析旨在评估甘草制剂单独或与其他草药联合使用对原发性肝病患者肝功能酶的疗效。我们系统地检索了 MEDLINE、Embase、Scopus、Web of Science 和 Cochrane Library,检索时间截至 2024 年 4 月。纳入比较甘草属植物制剂与安慰剂或标准对照治疗效果的随机对照试验(RCT)。使用标准 Cochrane 方法提取数据并评价合格研究。共有 15 项 RCT 纳入分析,涉及 1367 名参与者。这些研究在地理位置、持续时间和使用的甘草制剂方面差异很大。与对照组相比,甘草显著降低丙氨酸氨基转移酶(ALT)15.63 U/L(95%CI:-25.08,-6.18;p=0.001)和天冬氨酸氨基转移酶(AST)7.37 U/L(95%CI:-13.13,-1.61;p=0.01)。亚组分析显示,纯化甘草酸化合物特别有效,ALT 和 AST 降低幅度更大,且无显著异质性。虽然甘草治疗总体上对γ-谷氨酰转移酶和总胆红素(TBIL)水平没有显著影响,但特定的甘草-草药制剂确实显示 TBIL 有显著降低。甘草的安全性与已知的副作用一致,主要是轻微的,与它的盐皮质激素作用有关。尽管存在异质性和潜在的语言偏倚,但这些发现表明甘草可以增强肝功能。进一步的研究应标准化甘草制剂,并探索其在多方面草药配方中的作用,以更好地了解其肝保护机制。