Journal of Diabetes Investigation (May 2024)

Elevated small dense low‐density lipoprotein cholesterol to high‐density lipoprotein cholesterol ratio is associated with an increased risk of metabolic dysfunction associated fatty liver disease in Chinese patients with type 2 diabetes mellitus

  • Shouxing Yang,
  • Jing Xu

DOI
https://doi.org/10.1111/jdi.14148
Journal volume & issue
Vol. 15, no. 5
pp. 634 – 642

Abstract

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ABSTRACT Introduction It is demonstrated that elevated small dense low‐density lipoprotein cholesterol (sdLDL‐C), and reduced high‐density lipoprotein cholesterol (HDL‐C) is associated with Metabolic dysfunction‐associated fatty liver disease (MAFLD). This study aims to explore the relationship between sdLDL‐C to HDL‐C ratio (SHR) and MAFLD in Chinese patients with type 2 diabetes mellitus (T2DM). Materials and Methods A cross‐sectional study was performed among 1904 patients with T2DM. Weighted multivariable logistic regression analysis was conducted to explore the relationship between the SHR and the risk of MAFLD. In addition, this study used a two‐part linear regression model to identify threshold effects. Subgroup analysis, interaction tests and receiver operating characteristic (ROC) curve analysis were also carried out. Results The overall MAFLD prevalence reached 48.1%. Multiple logistic regression analysis showed that SHR was positively correlated with the risk of MAFLD (OR = 2.37, 95% CI = 1.80–3.12). Subgroup analysis stratified by age, gender, hypertension and BMI showed that there was a consistent positive correlation. A non‐linear relationship and saturation effect between SHR and MAFLD risk were identified, with an inverted L shaped curve and an inflection point at 1.02. The area under the curve (AUC) for SHR in the ROC analysis was significantly greater than sdLDL‐C and HDL‐C, with a sensitivity of 71.2% and a specificity of 62.1%. Conclusions Elevated levels of SHR is independently associated with an increased risk of MAFLD in patients with T2DM. SHR may be taken as practical indicators to assess the risk of MAFLD in T2DM patients.

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