Rong Lim, Ch'ng Daniel, Jia Pingping, Tsoi Kelvin K F, Wong Sunny H, Sung Joseph J Y
Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore.
The Jockey Club School of Public Health and Primary Care, The Chinese University of Hong Kong, Shatin, Hong Kong SAR.
J Gastroenterol Hepatol. 2023 Oct;38(10):1682-1694. doi: 10.1111/jgh.16256. Epub 2023 Jul 6.
Patients with non-alcoholic fatty liver disease (NAFLD) exhibit compositional changes in their gut microbiome, which represents a potential therapeutic target. Probiotics, prebiotics, and synbiotics are microbiome-targeted therapies that have been proposed as treatment for NAFLD. We aim to systematically review the effects of these therapies in liver-related outcomes of NAFLD patients.
We conducted a systematic search in Embase (Ovid), Medline (Ovid), Scopus, Cochrane, and EBSCOhost from inception to August 19, 2022. We included randomized controlled trials (RCTs) that treated NAFLD patients with prebiotics and/or probiotics. We meta-analyzed the outcomes using standardized mean difference (SMD) and assessed study heterogeneity using Cochran's Q test and I statistics. Risk of bias was assessed using the Cochrane Risk-of-Bias 2 tool.
A total of 41 (18 probiotics, 17 synbiotics, and 6 prebiotics) RCTs were included. Pooled data demonstrated that the intervention had significantly improved liver steatosis (measured by ultrasound grading) (SMD: 4.87; 95% confidence interval [CI]: 3.27, 7.25), fibrosis (SMD: -0.61 kPa; 95% CI: -1.12, -0.09 kPa), and liver enzymes including alanine transaminase (SMD: -0.86 U/L; 95% CI: -1.16, -0.56 U/L), aspartate transaminase (SMD: -0.87 U/L; 95% CI: -1.22, -0.52 U/L), and gamma-glutamyl transferase (SMD: -0.77 U/L; 95% CI: -1.26, -0.29 U/L).
Microbiome-targeted therapies were associated with significant improvements in liver-related outcomes in NAFLD patients. Nevertheless, limitations in existing literature like heterogeneity in probiotic strains, dosage, and formulation undermine our findings. This study was registered with PROSPERO (CRD42022354562) and supported by the Nanyang Technological University Start-up Grant and Wang Lee Wah Memorial Fund.
非酒精性脂肪性肝病(NAFLD)患者的肠道微生物群组成发生变化,这是一个潜在的治疗靶点。益生菌、益生元及合生元是以微生物群为靶点的治疗方法,已被提议用于治疗NAFLD。我们旨在系统评价这些治疗方法对NAFLD患者肝脏相关结局的影响。
我们在Embase(Ovid)、Medline(Ovid)、Scopus、Cochrane和EBSCOhost数据库中进行了从建库至2022年8月19日的系统检索。我们纳入了用益生元或益生菌治疗NAFLD患者的随机对照试验(RCT)。我们使用标准化均数差(SMD)对结局进行荟萃分析,并使用Cochran Q检验和I统计量评估研究的异质性。使用Cochrane偏倚风险2工具评估偏倚风险。
共纳入41项RCT(18项关于益生菌,17项关于合生元,6项关于益生元)。汇总数据表明,干预措施显著改善了肝脏脂肪变性(通过超声分级测量)(SMD:4.87;95%置信区间[CI]:3.27,7.25)、纤维化(SMD:-0.61kPa;95%CI:-1.12,-0.09kPa)以及包括丙氨酸转氨酶(SMD:-0.86U/L;95%CI:-1.16,-0.56U/L)、天冬氨酸转氨酶(SMD:-0.87U/L;95%CI:-1.22,-0.52U/L)和γ-谷氨酰转移酶(SMD:-0.77U/L;95%CI:-1.26,-0.29U/L)在内的肝脏酶指标。
以微生物群为靶点的治疗方法与NAFLD患者肝脏相关结局的显著改善相关。然而,现有文献存在局限性,如益生菌菌株、剂量和制剂的异质性,这影响了我们的研究结果。本研究已在国际前瞻性系统评价注册库(PROSPERO)注册(CRD42022354562),并得到南洋理工大学启动基金和王李华纪念基金的支持。