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肥胖是新定义的代谢功能障碍相关脂肪性肝病严重程度的一个重要决定因素。

Obesity is an important determinant of severity in newly defined metabolic dysfunction-associated fatty liver disease.

机构信息

Division of Endocrinology and Metabolism, Department of Internal Medicine, Hallym University Sacred Heart Hospital, Anyang 14068, Korea.

Division of Geriatrics, Department of Internal Medicine, Yonsei University College of Medicine, Seoul 03722, Korea; Division of Endocrinology and Metabolism, Department of Internal Medicine, Yonsei University College of Medicine, Seoul 03722, Korea.

出版信息

Hepatobiliary Pancreat Dis Int. 2022 Jun;21(3):241-247. doi: 10.1016/j.hbpd.2022.03.009. Epub 2022 Mar 22.

Abstract

BACKGROUND

The recently proposed definition of metabolic dysfunction-associated fatty liver disease (MAFLD) is based on the co-existence of hepatic steatosis with other metabolic disorders, including obesity and metabolic risk abnormalities such as hyperglycemia, high blood pressure and dyslipidemia. This study aimed to assess MAFLD severity according to the presence of metabolic abnormalities and obesity.

METHODS

Using transient elastography, hepatic steatosis and fibrosis severity were assessed by measuring the controlled attenuation parameter and liver stiffness measurement. A total of 1163 patients with MAFLD were categorized into the following four groups according to metabolic risk abnormalities and obesity presence: non-obese without metabolic risk abnormality group (Group 1; reference group); non-obese with metabolic risk abnormality group (Group 2); obese without metabolic risk abnormality group (Group 3); and obese with metabolic risk abnormality group (Group 4). A multiple logistic regression analysis was performed to determine severe hepatic steatosis and fibrosis risk in each group in both unadjusted and adjusted models.

RESULTS

In the adjusted model, the odds ratios (ORs) [95% confidence interval (CI)] for severe hepatic steatosis in Groups 2, 3, and 4 were 1.07 (0.61-1.88), 2.43 (1.44-4.08), and 4.07 (2.56-6.48), respectively (P < 0.001). For liver fibrosis, compared with Group 1, Group 2 showed no significant increases in OR, whereas Groups 3 and 4 (obese groups) showed significant increases (OR = 4.70, 95% CI: 1.24-17.82 and OR = 6.43, 95% CI: 1.88-22.02, respectively).

CONCLUSIONS

Obesity, rather than metabolic abnormality, is the principal determinant of severe hepatic steatosis and fibrosis in patients with MAFLD.

摘要

背景

最近提出的代谢相关脂肪性肝病(MAFLD)的定义基于肝脂肪变性与其他代谢紊乱的共存,包括肥胖和代谢风险异常,如高血糖、高血压和血脂异常。本研究旨在根据代谢异常和肥胖情况评估 MAFLD 的严重程度。

方法

使用瞬时弹性成像技术,通过测量受控衰减参数和肝硬度测量值来评估肝脂肪变性和纤维化的严重程度。根据代谢风险异常和肥胖的存在情况,将 1163 例 MAFLD 患者分为以下四组:无代谢风险异常的非肥胖组(第 1 组;参考组);无代谢风险异常的非肥胖组(第 2 组);无代谢风险异常的肥胖组(第 3 组);有代谢风险异常的肥胖组(第 4 组)。采用多因素逻辑回归分析在未调整和调整模型中确定每组发生严重肝脂肪变性和纤维化的风险。

结果

在调整模型中,第 2、3 和 4 组发生严重肝脂肪变性的比值比(OR)[95%置信区间(CI)]分别为 1.07(0.61-1.88)、2.43(1.44-4.08)和 4.07(2.56-6.48)(P<0.001)。对于肝纤维化,与第 1 组相比,第 2 组的 OR 无显著增加,而第 3 和 4 组(肥胖组)的 OR 显著增加(OR=4.70,95%CI:1.24-17.82 和 OR=6.43,95%CI:1.88-22.02)。

结论

肥胖而非代谢异常是 MAFLD 患者严重肝脂肪变性和纤维化的主要决定因素。

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