2型糖尿病合并代谢功能障碍相关脂肪变性肝病患者的血糖变异性:一项病例对照研究

IF 4.3
Annals of medicine Pub Date : 2025-12-01 Epub Date: 2025-08-20 DOI:10.1080/07853890.2025.2548976
Yueqiu Wang, Jing Liu, Yaoqin Yang, Qiong Wang, Yiqiong Sun, Ruiting Shen, Mingchen Zhang
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引用次数: 0

摘要

目的:进行一项病例对照研究,以评估诊断为代谢功能障碍相关脂肪变性肝病(MASLD)和2型糖尿病(T2DM)的个体以及独立患有这两种疾病的个体的血糖变异性(GV)。方法:本研究纳入宁波市第二医院内分泌科连续住院的糖尿病患者2897例。根据年龄和性别将MASLD患者与非MASLD患者进行匹配。利用葡萄糖标准差(SD)、变异系数(CV)和血糖偏离的平均幅度(MAGE)来评估GV。HOMA- ir和HOMA-β指数评估胰岛素抵抗和胰岛β细胞功能。肝纤维化程度采用FIB-4评分分级。采用SPSS 26.0软件进行统计分析。结果:1。41.66%的T2DM住院患者诊断为MASLD。在正常体重人群中,32.45%的人患有MASLD,而在肥胖人群中,患病率显著上升至77.55%。根据FIB-4指数,47.11%的DM + MASLD患者存在发生肝纤维化的风险,7.85%的DM + MASLD患者属于晚期肝纤维化高危人群。2. 与DM+非MASLD组相比,DM+MASLD组GV明显降低,低血糖发生率降低,HOMA- ir和HOMA-β值升高(p β = 0.367, p)。结论:T2DM和MASLD患者GV降低,低血糖发生率降低,但胰岛素抵抗更严重。有效控制HbA1c对于减轻这些患者的GV至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Glycemic variability in type 2 diabetic patients with metabolic dysfunction-associated steatotic liver disease: a case-control study.

Glycemic variability in type 2 diabetic patients with metabolic dysfunction-associated steatotic liver disease: a case-control study.

Glycemic variability in type 2 diabetic patients with metabolic dysfunction-associated steatotic liver disease: a case-control study.

Glycemic variability in type 2 diabetic patients with metabolic dysfunction-associated steatotic liver disease: a case-control study.

Aims: A case-control study was conducted to assess glycemic variability (GV) in individuals diagnosed with metabolic dysfunction-associated steatotic liver disease (MASLD) and type 2 diabetes mellitus (T2DM), as well as in those with either condition independently.

Methods: This study encompassed 2897 consecutive inpatients diagnosed with diabetes at the Department of Endocrinology, Ningbo No.2 Hospital. Patients with MASLD were matched to patients without MASLD based on age and sex. GV was evaluated utilizing glucose standard deviation (SD), coefficient of variation (CV), and mean amplitude of glycemic excursions (MAGE). HOMA-IR and HOMA-β indices were used to assess insulin resistance and islet β-cell function. The degree of hepatic fibrosis was graded using the FIB-4 score. SPSS software (version 26.0) was used for the statistical analysis.

Results: 1. MASLD was diagnosed in 41.66% of T2DM inpatients. Among individuals with normal body weight, 32.45% suffered from MASLD, whereas the prevalence significantly escalated to 77.55% among those classified as obese. Based on the FIB-4 index, 47.11% of DM + MASLD patients were at risk for the development of hepatic fibrosis, with 7.85% classified as at high risk for advanced liver fibrosis. 2. In contrast to the DM+Non-MASLD cohort, the DM+MASLD group displayed markedly reduced GV, lower incidence of hypoglycemia, and elevated HOMA-IR and HOMA-β values (all p < 0.001). 3. The CV showed a direct positive correlation with HbA1c (β = 0.367, p < 0.001) in patients with coexisting T2DM and MASLD.

Conclusions: Patients with T2DM and MASLD exhibit reduced GV and a lower incidence of hypoglycemia but more serious insulin resistance. Effective control of HbA1c is essential to mitigate GV in these patients.

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