Wang Xiaobing, Ni Yu, Wang Ziwen, Li Changhui, Hui Xinyu, Xu Hongyu
Department of Gastroenterology, The First Affiliated hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Medicine (Baltimore). 2024 Nov 22;103(47):e40507. doi: 10.1097/MD.0000000000040507.
Liver cirrhosis is a chronic disease caused by long-term inflammation and fibrosis of the liver. Early identification and intervention in liver cirrhosis have become an important goal for researchers to explore the influence of some metabolic factors on the risk of liver cirrhosis in terms of genetic susceptibility. Data from genome-wide association studies (GWASs) of fourteen metabolic factors and liver cirrhosis were obtained from publicly available databases. To make the results more credible, we selected 2 GWASs for liver cirrhosis to be validated separately. The causal effect of metabolic factors on liver cirrhosis was assessed separately using 2-sample Mendelian Randomization (MR). The inverse variance weighted (IVW) method was used as the main analysis method. The present MR analysis confirmed that fasting insulin level (IVW-OR = 2.89, 95% CI: 1.36-6.15, P = .006) and ALT (IVW-OR = 1.42, 95% CI: 1.11-1.80, P = .004) were positively causally associated with the risk of liver cirrhosis, and there was a negative causal relationship between hypertension and the risk of liver cirrhosis (IVW-OR = 0.40, 95% CI: 0.23-0.72, P = .002) in 1 liver cirrhosis GWAS. In replication analysis, our MR proved the positive causal effect between ALT (IVW-OR = 2.09, 95% CI: 1.61-2.72, P < .001) and BMI (IVW-OR = 1.44, 95% CI: 1.17-1.77, P < .001) and the risk of liver cirrhosis. A causal relationship between other metabolic factors and the risk of liver cirrhosis could not be established in the current selection of data. Our MR study revealed a causal and positive association between ALT and the risk of liver cirrhosis, suggesting an important role of effective control of ALT in liver cirrhosis prevention. The causal relationship between thirteen other metabolic factors and the risk of liver cirrhosis remains to be further verified.
肝硬化是一种由肝脏长期炎症和纤维化引起的慢性疾病。早期识别和干预肝硬化已成为研究人员从遗传易感性角度探索某些代谢因素对肝硬化风险影响的重要目标。从公开可用数据库中获取了关于14种代谢因素和肝硬化的全基因组关联研究(GWAS)数据。为使结果更可信,我们选择了2项关于肝硬化的GWAS进行单独验证。使用两样本孟德尔随机化(MR)分别评估代谢因素对肝硬化的因果效应。采用逆方差加权(IVW)方法作为主要分析方法。当前的MR分析证实,空腹胰岛素水平(IVW-OR = 2.89,95%CI:1.36 - 6.15,P = 0.006)和谷丙转氨酶(ALT)(IVW-OR = 1.42,95%CI:1.11 - 1.80,P = 0.004)与肝硬化风险呈正因果关联,在一项肝硬化GWAS中,高血压与肝硬化风险呈负因果关系(IVW-OR = 0.40,95%CI:0.23 - 0.72,P = 0.002)。在重复分析中,我们的MR证实了ALT(IVW-OR = 2.09,95%CI:1.61 - 2.72,P < 0.001)和体重指数(BMI)(IVW-OR = 1.44,95%CI:1.17 - 1.77,P < 0.001)与肝硬化风险之间的正因果效应。在当前所选数据中,无法确定其他代谢因素与肝硬化风险之间的因果关系。我们的MR研究揭示了ALT与肝硬化风险之间的因果正相关,表明有效控制ALT在预防肝硬化中具有重要作用。其他13种代谢因素与肝硬化风险之间的因果关系仍有待进一步验证。