Journal of Jilin University(Medicine Edition) ›› 2026, Vol. 52 ›› Issue (1): 219-227.doi: 10.13481/j.1671-587X.20260123

• Research in clinical medicine • Previous Articles     Next Articles

Mendelian randomization analysis on causal association between plasma lipids with nonalcoholic fatty liver disease and liver enzymes

Zhifei LIU1,Yaru BI2,Chenglin SUN2,3,Suyan TIAN1()   

  1. 1.Department of Clinical Research,First Hospital,Jilin University,Changchun 130021,China
    2.Department of Endocrinology and Metabolism,First Hospital,Jilin University,Changchun 130021,China
    3.Department of Clinical Nutrition,First Hospital,Jilin University,Changchun 130021,China
  • Received:2025-01-04 Accepted:2025-04-25 Online:2026-01-28 Published:2026-02-24
  • Contact: Suyan TIAN E-mail:wmxt@jlu.edu.cn

Abstract:

Objective To investigate the potential causal associations of specific plasma lipids with nonalcoholic fatty liver disease (NAFLD) and liver enzymes, and elucidate the potential impact of specific plasma lipid on liver health. Methods Two-sample Mendelian randomization (MR) analyses were conducted to investigate potential causal relationships between 179 plasma lipids and both NAFLD and 4 liver enzymes: alanine aminotransferase (ALT), aspartate aminotransferase (AST), gamma-glutamyl transferase (GGT), and alkaline phosphatase (ALP). The inverse-variance weighted method served as the primary analysis approach, supplemented by MR-Egger, weighted median, weighted mode, and simple mode. Sensitivity analyses including MR-Egger intercept test and MR-PRESSO Global test were conducted to ensure the reliability of the results. Multivariable MR analysis was conducted to adjust for the potential effect of body mass index (BMI) on the association between plasma lipids and NAFLD. Results The analyses revealed that phosphatidylcholine (18:0/20:5) [odd ratio(OR)=0.988, 95% confidence interval(CI) (0.977, 0.999), P=0.028] exhibited a protective effect on NAFLD, while phosphatidylinositol (16:0/18:2) [OR=1.016, 95%CI(1.000, 1.032), P=0.046] and phosphatidylinositol (18:0/18:2) [OR=1.012, 95%CI (1.002, 1.022), P=0.021] increased NAFLD risk. After adjustment for BMI, the association between phosphatidylinositol (18:0/18:2) [OR=1.019, 95%CI (1.007, 1.035), P=0.008] and NAFLD remained significant. Elevated levels of phosphatidylcholine (16:0/20:5) [β=0.026, 95%CI(0.015, 0.036), P=9.93×10-7], phosphatidylcholine (O-16:0/22:5) [β=0.057, 95%CI(0.035, 0.078), P=1.79×10-7], triacylglycerol (56:7) [β=0.057, 95%CI (0.035,0.079), P=2.53×10-7] and triacylglycerol (56:8) [β=0.067, 95%CI (0.047,0.087), P=1.19×10-10] were significantly associated with increased ALT levels. Triacylglycerol (53:2) [β=0.160, 95% CI (0.123, 0.197), P=1.55×10-17] showed a significant positive causal association with AST levels. Conclusion Specific plasma lipids were causally associated with NAFLD risk and liver enzyme levels, with some associations independent of BMI.

Key words: Plasma lipidome, Liver enzymes, Nonalcoholic fatty liver disease, Mendelian randomization, Causal association

CLC Number: 

  • R575.5