Why the study?
Non-alcoholic fatty liver disease (NAFLD) has become an increasing public health concern, prompting examination of the association between the serum hs-CRP to HDL-C ratio (HCHR) and NAFLD prevalence, hepatic steatosis, and fibrosis.
Is the serum high-sensitivity C-reactive protein to high-density lipoprotein cholesterol ratio associated with the prevalence of NAFLD and liver fibrosis in US adults?
Is the serum high-sensitivity C-reactive protein to high-density lipoprotein cholesterol ratio associated with the prevalence of NAFLD and liver fibrosis in US adults?
Increased HCHR is independently associated with a higher risk of NAFLD, liver fibrosis, and severity of hepatic steatosis in US adults, suggesting its potential as a biomarker.
HCHR may support NAFLD risk stratification in US adults; leaves open its added value beyond standard markers in prospective cohorts.
Non-alcoholic fatty liver disease (NAFLD) has become an increasing public health concern. We examined the association between serum high-sensitivity C-reactive protein(hs-CRP)to high-density lipoprotein cholesterol (HDL-C) ratio (HCHR) and the prevalence of NAFLD, extent of hepatic steatosis and fibrosis in the general US population. This cross-sectional analysis included 4039 adult participants from the 2017 to 2018 National Health and Nutrition Examination Survey. Multivariable logistic regression and multivariable linear regression analyses were used to assess the association between HCHR levels and NAFLD, fatty liver degree, and liver fibrosis. Generalized additive models examined the nonlinear relationship between the HCHR and NAFLD. In the three models, HCHR was positively associated with NAFLD, model 1 (OR 1.315, 95% CI 1.273, 1.359), model 2 (OR 1.364, 95% CI 1.317, 1.412) and model 3 (OR 1.120, 95% CI 1.074, 1.168). Stratified analyses showed that the association was more prominent in women, those younger than 40 years, Mexican-Americans, and those with a 25–30 kg/m 2 BMI. Nonlinear association analysis revealed a threshold effect between HCHR and NAFLD, with a threshold inflection point of 2.598. We also found a significant link between HCHR and liver steatosis and the risk of liver fibrosis. In the US adult population, the increased risk of NAFLD, liver fibrosis, and severity of hepatic steatosis are independently associated with increased HCHR, and the HCHR may serve as a potential marker for NAFLD and liver fibrosis.
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Xuan et al. (2025) studied this question.
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