Yarmohammadi Samira, Hosseini-Ghatar Reza, Foshati Sahar, Moradi Mojgan, Hemati Niloofar, Moradi Sajjad, Kermani Mohammad Ali Hojjati, Farzaei Mohammad Hosein, Khan Haroon
Internal Medicine Department, Kermanshah University of Medical Sciences, Kermanshah 67158-47141, Iran.
Department of Immunology, School of Medicine, Isfahan University of Medical Sciences, Isfahan 81746-73461, Iran.
Clin Nutr Res. 2021 Jan 29;10(1):83-94. doi: 10.7762/cnr.2021.10.1.83. eCollection 2021 Jan.
This study presents a comprehensive systematic review and meta-analysis of randomized controlled trials (RCTs) on () supplementation and liver function biomarkers. Pertinent studies were identified using Scopus, ISI Web of Science, PubMed, and Cochrane library databases up to August 2020. Mean differences were pooled using a random-effects model. Pooling 7 RCTs together showed that supplementation led to a significant reduction of serum aspartate aminotransferase (AST) levels (weighted mean difference [WMD], -9.15 U/L; 95% confidence interval [CI], -16.09, -2.21), but not alanine aminotransferase (ALT) or alkaline phosphatase (ALP) levels compared to the placebo consumption. Subgroup-analysis indicated that supplementation had more effect on AST decreasing among non-alcoholic fatty liver disease patients (WMD, -16.42 U/L; 95% CI, -29.75, -3.09) than others. Furthermore, subgroup analysis based on kind of compression showed that supplementation significantly decreased ALT levels (WMD, -4.65 U/L; 95% CI, -8.88, -0.42) compared with the placebo, but not metformin consumption. It seems that supplementation mainly affects AST levels rather than ALT and ALP levels, however, as mentioned the effect of on those enzymes might be context-dependent. Therefore, further investigations with a large number of patients as well as on different disorders are necessary and can provide more definitive evidence.
本研究对关于()补充剂与肝功能生物标志物的随机对照试验(RCT)进行了全面的系统评价和荟萃分析。截至2020年8月,使用Scopus、ISI科学网、PubMed和Cochrane图书馆数据库检索相关研究。采用随机效应模型汇总平均差异。汇总7项随机对照试验结果显示,与服用安慰剂相比,补充()可显著降低血清天冬氨酸氨基转移酶(AST)水平(加权平均差[WMD],-9.15 U/L;95%置信区间[CI],-16.09,-2.21),但对丙氨酸氨基转移酶(ALT)或碱性磷酸酶(ALP)水平无影响。亚组分析表明,与其他患者相比,补充()对非酒精性脂肪性肝病患者的AST降低作用更大(WMD,-16.42 U/L;95%CI,-29.75,-3.09)。此外,基于补充剂类型的亚组分析显示,与安慰剂相比,补充()可显著降低ALT水平(WMD,-4.65 U/L;95%CI,-8.88,-0.42),但与二甲双胍相比无此作用。补充()似乎主要影响AST水平,而非ALT和ALP水平,然而,如前所述,()对这些酶的影响可能取决于具体情况。因此,有必要对大量患者以及不同疾病进行进一步研究,以提供更确凿的证据。