HOMA-IR is an effective biomarker of non-alcoholic fatty liver disease in non-diabetic population

Author:

Zeng Pei1ORCID,Cai Xiangsheng2,Yu Xiaozhou3,Huang Lu4,Chen Xi4

Affiliation:

1. Outpatient Department, Guangzhou Cadre Health Management Center, Guangzhou, China

2. Clinical Laboratory, Guangzhou Cadre Health Management Center, Guangzhou, China

3. Department of Medical Statistics, School of Public Health, Sun Yat-Sen University, Guangzhou, China

4. Department of Health Assessment Intervention, Guangzhou Cadre Health Management Center, Guangzhou, China

Abstract

Objectives This study aimed to investigate the correlation between homeostasis model assessment of insulin resistance (HOMA-IR) and non-alcoholic fatty liver disease (NAFLD) in the non-diabetic population and establish its diagnostic efficacy. Methods This observational study involved participants divided into NAFLD and non-NAFLD groups, and baseline data were analyzed. Univariate and multivariate logistic regression analyses were used to correlate HOMA-IR with the risk of NAFLD. Receiver operating characteristic (ROC) curves were used to evaluate the diagnostic efficacy of HOMA-IR for NAFLD. Subgroup analyses of non-obese individuals were performed. Results Overall, 2234 non-diabetic participants were included. The HOMA-IR was significantly higher in the NAFLD group than in the non-NAFLD group. Multivariate logistic regression analysis showed that HOMA-IR was a strong and independent risk factor for NAFLD after correcting for confounding factors. The area under the ROC curve (AUC) value of HOMA-IR for predicting NAFLD was 0.792. In the non-obese non-diabetic population, HOMA-IR was an independent risk factor for increased risk of lean NAFLD after correcting for confounding factors. The AUC value of HOMA-IR for predicting lean NAFLD was 0.770. Conclusions HOMA-IR is independently associated with the risk of NAFLD in the non-diabetic and non-obese non-diabetic populations and has good diagnostic value.

Funder

Guangzhou Municipal Science and Technology Project

Publisher

SAGE Publications

Subject

Biochemistry (medical),Cell Biology,Biochemistry,General Medicine

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