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Non-Laboratory-Based Simple Screening Model for Nonalcoholic Fatty Liver Disease in Patients with Type 2 Diabetes Developed Using Multi-Center Cohortsopen access

Authors
Kim, JiwonLee, MinyoungKim, Soo YeonKim, Ji-HyeNam, Ji SunChun, Sung WanPark, Se EunKim, Kwang JoonLee, Yong-hoNam, Joo YoungKang, Eun Seok
Issue Date
1-Aug-2021
Publisher
대한내분비학회
Keywords
Non-alcoholic fatty liver disease; Diabetes mellitus; type 2; Transient elastography; Screening
Citation
Endocrinology and Metabolism, v.36, no.4, pp 823 - 834
Pages
12
Journal Title
Endocrinology and Metabolism
Volume
36
Number
4
Start Page
823
End Page
834
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/19865
DOI
10.3803/EnM.2021.1074
ISSN
2093-596X
2093-5978
Abstract
Background: Nonalcoholic fatty liver disease (NAFLD) is the most prevalent cause of chronic liver disease worldwide. Type 2 diabetes mellitus (T2DM) is a risk factor that accelerates NAFLD progression, leading to fibrosis and cirrhosis. Thus, here we aimed to develop a simple model to predict the presence of NAFLD based on clinical parameters of patients with T2DM. Methods: A total of 698 patients with T2DM who visited five medical centers were included. NAFLD was evaluated using transient elastography. Univariate logistic regression analyses were performed to identify potential contributors to NAFLD, followed by multivariable logistic regression analyses to create the final prediction model for NAFLD. Results: Two NAFLD prediction models were developed, with and without serum biomarker use. The non-laboratory model comprised six variables: age, sex, waist circumference, body mass index (BMI), dyslipidemia, and smoking status. For a cutoff value of >= 60, the prediction accuracy was 0.780 (95% confidence interval [CI], 0.743 to 0.817). The second comprehensive model showed an improved discrimination ability of up to 0.815 (95% CI, 0.782 to 0.847) and comprised seven variables: age, sex, waist circumference, BMI, glycated hemoglobin, triglyceride, and alanine aminotransferase to aspartate aminotransferase ratio. Our non-laboratory model showed non-inferiority in the prediction of NAFLD versus previously established models, including serum parameters. Conclusion: The new models are simple and user-friendly screening methods that can identify individuals with T2DM who are at high-risk for NAFLD. Additional studies are warranted to validate these new models as useful predictive tools for NAFLD in clinical practice.
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