Visceral Fat and Diabetes: Associations With Liver Fibrosis in Metabolic Dysfunction–Associated Steatotic Liver Disease

IF 3.3 Q2 GASTROENTEROLOGY & HEPATOLOGY Journal of Clinical and Experimental Hepatology Pub Date : 2024-07-19 DOI:10.1016/j.jceh.2024.102378
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Abstract

Background

The prevalence of metabolic dysfunction–associated steatotic liver disease (MASLD), previously known as non-alcoholic fatty liver disease, is increasing globally. Noninvasive methods, such as bioelectrical impedance analysis (BIA), which measures body composition, including visceral fat, are gaining interest in evaluating MASLD patients. Our study aimed to identify factors associated with significant liver fibrosis, compare noninvasive scores, and highlight the importance of visceral fat measurement using BIA.

Methods

MASLD patients seen in our out-patient department underwent comprehensive evaluations, including liver stiffness using transient elastography, body composition analysis using BIA, and metabolic measurements. Significant fibrosis was defined as a liver stiffness measurement of ≥8.2 kPa. Using multivariate analysis, we identified factors associated with significant liver fibrosis and compared four noninvasive scores with a novel diabetes-visceral fat 15 (DVF15) score.

Results

We analyzed data from 609 MASLD patients seen between February 2022 and March 2023. The median age was 43 years (81% male). Among these, 78 (13%) had significant fibrosis. Patients with significant fibrosis had higher rates of type 2 diabetes (41% vs 21%, P < 0.001) and elevated levels of aspartate aminotransferase, alanine aminotransferase, hemoglobin A1c, Fibosis-4, aspartate-aminotransferase-to platelet-ratio index, and NAFLD fibrosis scores. They also exhibited higher visceral and subcutaneous fat. Binary logistic regression revealed type 2 diabetes and a visceral fat level of >15% as associated with significant liver fibrosis. Additionally, the DVF15 score, combining these factors, showed a modest area under the receiver operating characteristic curve of 0.664 (P < 0.001).

Conclusion

Our study identified diabetes and high visceral fat as factors associated with significant liver fibrosis in MASLD patients. We recommend that visceral fat measurement using BIA be an essential part of MASLD evaluation. The presence of either diabetes or a visceral fat level of >15% should prompt clinicians to check for significant fibrosis in MASLD patients. Further research is warranted to validate our findings and evaluate the utility of the DVF15 score in larger cohorts and diverse populations.

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内脏脂肪和糖尿病:代谢功能障碍相关性脂肪肝(MASLD)与肝纤维化的关系
背景代谢功能障碍相关性脂肪性肝病(MASLD)以前被称为非酒精性脂肪肝,其发病率在全球范围内呈上升趋势。生物电阻抗分析(BIA)等无创方法可以测量身体成分,包括内脏脂肪,在评估代谢功能障碍相关性脂肪肝患者方面越来越受到关注。我们的研究旨在确定与明显肝纤维化相关的因素,比较无创评分,并强调使用生物电阻抗分析测量内脏脂肪的重要性。方法在我们门诊部就诊的MASLD患者接受了全面评估,包括使用瞬态弹性成像进行肝脏硬度评估、使用生物电阻抗分析进行身体成分分析以及代谢测量。肝脏硬度测量值≥8.2 kPa即为明显纤维化。通过多变量分析,我们确定了与明显肝纤维化相关的因素,并将四种无创评分与新型糖尿病-内脏脂肪 15 (DVF15) 评分进行了比较。结果我们分析了 2022 年 2 月至 2023 年 3 月期间就诊的 609 名 MASLD 患者的数据。中位年龄为 43 岁(81% 为男性)。其中 78 人(13%)有明显纤维化。有明显纤维化的患者患2型糖尿病的比例较高(41% vs 21%,P < 0.001),天门冬氨酸氨基转移酶、丙氨酸氨基转移酶、血红蛋白A1c、纤维化-4、天门冬氨酸氨基转移酶与血小板比值指数和非酒精性脂肪肝纤维化评分水平升高。他们的内脏和皮下脂肪也较高。二元逻辑回归显示,2型糖尿病和内脏脂肪水平达到15%与肝纤维化显著相关。此外,结合这些因素的 DVF15 评分显示接收器操作特征曲线下的适度面积为 0.664(P <0.001)。我们建议将使用 BIA 测量内脏脂肪作为 MASLD 评估的重要组成部分。出现糖尿病或内脏脂肪水平达到15%,都应促使临床医生检查MASLD患者是否有明显的肝纤维化。我们有必要开展进一步的研究,以验证我们的发现,并评估 DVF15 评分在更大的群体和不同人群中的实用性。
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来源期刊
Journal of Clinical and Experimental Hepatology
Journal of Clinical and Experimental Hepatology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
4.90
自引率
16.70%
发文量
537
审稿时长
64 days
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