Correlation between hs-CRP-triglyceride glucose index and NAFLD and liver fibrosis

BMC Gastroenterol. 2025 Apr 12;25(1):252. doi: 10.1186/s12876-025-03870-7.

Abstract

Background: The novel serum high-sensitivity C-reactive protein-triglyceride glucose index (CTI) has been recognized as an optimal parameter encompassing both insulin resistance (IR) and inflammation, which are potential mechanisms contributing to non-alcoholic fatty liver disease (NAFLD). This study aims to examine the correlation between CTI and NAFLD/liver fibrosis in American adults.

Methods: This is a cross-sectional study utilizing data from NHANES during the period from 2017 to 2020. The composite CTI was calculated through the formula: 0.412×Ln [(high-sensitivity C-reactive protein(hs-CRP)] + Ln(triglycerides × fasting plasma glucose/2). To explore the correlation between CTI and NAFLD/liver fibrosis, multivariate logistic regression analyses, subgroup analyses, restricted cubic spline (RCS) regression, and receiver operating characteristic (ROC) analysis were employed.

Results: Among 3,488 participants, 42.7% (n = 1,488) were diagnosed as NAFLD, while 9.4% (n = 329) exhibited liver fibrosis. Logistic regression and RCS regression analyses demonstrated a significant positive linear correlation between CTI and the prevalence of NAFLD (OR = 1.94, 95% CI: 1.70, 2.22) as well as liver fibrosis (OR = 1.38, 95% CI: 1.14, 1.67), even after being adjusted for potential confounding variables. Furthermore, a significant correlation between CTI and the prevalence of NAFLD/liver fibrosis was observed across various subgroups. ROC analysis revealed that CTI can serve as a more robust identify for the prevalence of NAFLD (AUC = 0.756) and liver fibrosis (AUC = 0.702) compared to triglyceride glucose index (TyG) and hs-CRP alone.

Conclusion: Elevated levels of CTI are directly associated with significant liver fibrosis and the presence of NAFLD, indicating its potential utility as a biomarker for liver fibrosis and NAFLD.

Keywords: Chronic inflammation; Diabetes; Insulin resistance; NAFLD; TyG.

MeSH terms

  • Adult
  • Biomarkers / blood
  • Blood Glucose* / analysis
  • Blood Glucose* / metabolism
  • C-Reactive Protein* / analysis
  • C-Reactive Protein* / metabolism
  • Cross-Sectional Studies
  • Female
  • Humans
  • Insulin Resistance
  • Liver Cirrhosis* / blood
  • Liver Cirrhosis* / epidemiology
  • Logistic Models
  • Male
  • Middle Aged
  • Non-alcoholic Fatty Liver Disease* / blood
  • Non-alcoholic Fatty Liver Disease* / epidemiology
  • Nutrition Surveys
  • Prevalence
  • ROC Curve
  • Triglycerides* / blood
  • United States / epidemiology

Substances

  • C-Reactive Protein
  • Blood Glucose
  • Triglycerides
  • Biomarkers