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October 3, 2025BMC Endocrine Disorders2 citationsOpen Access

Association between AIP and incident T2DM in patients with NAFLD: a retrospective study

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YCYan ChenQBQiufang BaiHHHua Hao

Key Points

  • Elevated atherogenic index of plasma increases the risk of incident type 2 diabetes mellitus in NAFLD patients.
  • The highest tertile of AIP showed a 1.99-fold increased risk of T2DM compared to the lowest tertile.
  • Multivariable logistic regression confirmed AIP as an independent predictor for incident T2DM in various subgroups.
  • AIP outperformed traditional markers in predicting T2DM risk, indicating its clinical utility as a predictive biomarker.

Abstract

This study aimed to investigate the relationship between atherogenic index of plasma (AIP) and incident type 2 diabetes mellitus (T2DM) in non-alcoholic fatty liver disease (NAFLD) patients. In this retrospective study, 2,370 NAFLD patients were stratified into tertiles based on AIP levels. Baseline demographic, anthropometric, and biochemical characteristics were compared across tertiles. Multivariable logistic regression models were employed to assess the association between AIP and incident T2DM, adjusting for potential confounders, including age, sex, body mass index (BMI), hemoglobin A1c (HbA1c), smoking status, high blood pressure (HBP), and liver enzymes. Restricted cubic splines (RCS) evaluated dose-response relationships, and receiver operating characteristic (ROC) curves compared the predictive performance of AIP against individual parameters. In the fully adjusted model (Model 3), the highest tertile (Q3) demonstrated a 1.99-fold increased T2DM risk (OR = 1.99, 95% CI: 1.29–3.08, P = 0.002) versus Q1. A linear dose-response relationship was observed (P for non-linearity = 0.663), with each 1-unit AiP increase corresponding to a 2.76-fold higher T2DM risk (OR = 2.76, 95% CI: 1.54–4.93, P 0.05). Elevated AIP is independently associated with an increased risk of incident T2DM in NAFLD patients, highlighting its potential as a predictive biomarker for diabetes in this high-risk population.

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Cite This Study

Chen et al. (2025) studied this question.

synapsesocial.com/papers/68dfe935daa1363beb049cd4https://doi.org/10.1186/s12902-025-02046-4
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