TY - JOUR
T1 - Non-laboratory-based simple screening model for nonalcoholic fatty liver disease in patients with type 2 diabetes developed using multi-center cohorts
AU - Kim, Jiwon
AU - Lee, Minyoung
AU - Kim, Soo Yeon
AU - Kim, Ji Hye
AU - Nam, Ji Sun
AU - Chun, Sung Wan
AU - Park, Se Eun
AU - Kim, Kwang Joon
AU - Lee, Yong Ho
AU - Nam, Joo Young
AU - Kang, Eun Seok
N1 - Publisher Copyright:
© 2021 Korean Endocrine Society. All rights reserved.
PY - 2021/8
Y1 - 2021/8
N2 - 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.
AB - 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.
KW - Diabetes mellitus, type 2
KW - Non-alcoholic fatty liver disease
KW - Screening
KW - Transient elastography
UR - https://www.scopus.com/pages/publications/85115119249
U2 - 10.3803/ENM.2021.1074
DO - 10.3803/ENM.2021.1074
M3 - Article
C2 - 34474517
AN - SCOPUS:85115119249
SN - 2093-596X
VL - 36
SP - 823
EP - 834
JO - Endocrinology and Metabolism
JF - Endocrinology and Metabolism
IS - 4
ER -