Department of Pharmacology and Therapeutics, College of Medicine and Medical Sciences, Arabian Gulf University, Manama, Bahrain
School of Oral Health, College of Medicine, Nursing and Health Sciences, Fiji National University, Suva, Fiji.
Postgrad Med J. 2018 Oct;94(1116):556-565. doi: 10.1136/postgradmedj-2018-135967. Epub 2018 Oct 19.
Several drugs have been used for treating non-alcoholic fatty liver disease (NAFLD). The present study is a network meta-analysis of such drugs.
DESIGN, SETTING AND PATIENTS: Randomised clinical trials comparing drug interventions in patients with NAFLD were analysed. OR and weighted mean difference (95 % CI) were the effect estimates for categorical and numerical outcomes, respectively. Random-effects model was used to generate pooled estimates. Surface under the cumulative ranking curve was used to rank the treatments.
Proportion of responders was the primary outcome measure and non-alcoholic steatohepatitis scores, liver enzymes, lipid profile, body mass index, homeostatic model assessment of insulin resistance, intrahepatic fat and adverse events were the key secondary outcomes.
116 studies were included in the systematic review and 106 in the meta-analysis. Elafibranor, gemfibrozil, metadoxine, obeticholic acid, pentoxifylline, pioglitazone, probiotics, telmisartan, vildagliptin and vitamin E significantly increased the response rate than standard of care. Various other drugs were observed to modify the secondary outcomes favourably. Probiotics was found with a better response in children; and elafibranor, obeticholic acid, pentoxifylline and pioglitazone in patients with type 2 diabetes mellitus. The quality of evidence observed was either low or very low.
In patients with NAFLD, several drugs have been shown to have variable therapeutic benefit. However, the estimates and the inferences should be considered with extreme caution as it might change with the advent of future head-to-head clinical trials.
有多种药物被用于治疗非酒精性脂肪性肝病(NAFLD)。本研究对这些药物进行了网状荟萃分析。
设计、设置和患者:分析了比较 NAFLD 患者药物干预的随机临床试验。OR 和加权均数差值(95%CI)分别为分类和数值结局的效应估计值。使用随机效应模型生成汇总估计值。累积排序曲线下面积(SUCRA)用于对治疗方法进行排序。
应答者比例是主要观察指标,非酒精性脂肪性肝炎评分、肝酶、血脂谱、体重指数、稳态模型评估的胰岛素抵抗、肝内脂肪和不良事件是关键次要观察指标。
系统评价纳入了 116 项研究,荟萃分析纳入了 106 项研究。Elafibranor、吉非贝齐、美他多辛、奥贝胆酸、己酮可可碱、吡格列酮、益生菌、替米沙坦、维格列汀和维生素 E 与标准治疗相比显著提高了应答率。其他各种药物也被观察到对次要结局有有利的影响。益生菌在儿童中表现出更好的应答;Elafibranor、奥贝胆酸、己酮可可碱和吡格列酮在 2 型糖尿病患者中表现出更好的应答。观察到的证据质量要么低,要么非常低。
在 NAFLD 患者中,几种药物已显示出不同的治疗益处。然而,由于未来可能会出现头对头临床试验,因此应该极其谨慎地考虑这些估计值和推论,因为它们可能会发生变化。