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Association between galectin-3 and hepatosteatosis in a community-based cross-sectional study

医学 内科学 优势比 混淆 置信区间 体质指数 横断面研究 胃肠病学 丙氨酸转氨酶 天冬氨酸转氨酶 转氨酶 脂肪肝 病理 疾病 生物化学 化学 碱性磷酸酶
作者
Ming‐Shyan Lin,Ya-Chi Tu,Yu-Sheng Lin,Meng‐Hung Lin,Chun‐Liang Lin,Ming-Horng Tsai,Yung‐Yu Hsieh,Tien‐Hsing Chen,Mei‐Yen Chen,Chung‐Sheng Shi
出处
期刊:Therapeutic Advances in Chronic Disease [SAGE]
卷期号:15
标识
DOI:10.1177/20406223241302719
摘要

Background: Hepatosteatosis is a common condition that can lead to cirrhosis and liver cancer. Galectin-3 (GAL-3) has been implicated in liver fibrosis and inflammation. Objectives: The purpose of this study was to investigate the association between GAL-3 and hepatosteatosis. Design: This study is a retrospective secondary analysis of data from a community health screening program. Methods: A total of 766 participants were included in the final analysis. Hepatosteatosis was diagnosed using ultrasonography, and GAL-3 levels were measured using enzyme-linked immunosorbent assay. Logistic regression analysis was used to examine the association between GAL-3 levels and the presence of hepatosteatosis, adjusting for age, sex, and other potential confounding factors. Results: The prevalence of moderate-to-severe hepatosteatosis in the study population was 31.5%. The participants with hepatosteatosis had a significantly higher mean level of GAL-3 compared to those without hepatosteatosis (16.6 ± 7.3 vs 13.5 ± 7.3 ng/ml; p < 0.001). After adjusting for age, sex, body mass index, and other potential confounding factors, a higher level of GAL-3 was significantly associated with an increased risk of moderate-to-severe hepatosteatosis (adjusted odds ratio (aOR) 1.24, 95% confidence interval (CI) 1.05–1.46, p = 0.010). The coexistence of alanine transaminase/aspartate transaminase ratio >1 and GAL-3 >14.4 ng/ml was associated with a significantly increased risk (aOR 3.37, 95% CI: 1.90–5.99, p < 0.001). Conclusion: Our findings suggest that GAL-3 level is significantly associated with the presence of moderate-to-severe hepatosteatosis, independent of other known cardiometabolic risk factors.

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