Liu Yutong, Sequeira-Bisson Ivana R, Ko Juyeon, Shamaitijiang Xiatiguli, Skudder-Hill Loren, Petrov Maxim S
School of Medicine, University of Auckland, Auckland, New Zealand.
Human Nutrition Unit, School of Biological Sciences, University of Auckland, Auckland, New Zealand.
Diabetes Obes Metab. 2025 Nov;27(11):6674-6681. doi: 10.1111/dom.70077. Epub 2025 Sep 1.
To investigate the associations of intra-pancreatic fat deposition (IPFD) with low-density lipoprotein (LDL) subfractions and hepatic lipase.
IPFD was quantified using a single 3.0 Tesla magnetic resonance imaging scanner. LDL subfractions were assessed with a commercially available system employing non-denaturing polyacrylamide gel electrophoresis. The LDL profile included six subfractions, grouped into two subclasses: large LDL (LDL-1 and LDL-2) and small LDL (LDL-3 to LDL-6). Univariate and multivariate linear regression analyses were conducted to examine associations, with adjustments made for age, sex, ethnicity, obesity, insulin resistance and triglyceride levels.
A total of 174 individuals were included in the analysis. IPFD was not significantly associated with any LDL subfraction or subclass in any of the statistical models. Similarly, hepatic lipase showed no significant association with IPFD. However, hepatic lipase was significantly and inversely associated with the LDL-1 and LDL-2 subfractions, as well as the LDL-large subclass, across all three statistical models. In the most adjusted model, each unit increase in hepatic lipase was associated with a 0.24-unit decrease in LDL-1 (p = 0.002), a 0.22-unit decrease in LDL-2 (p = 0.003) and a 0.27-unit decrease in the LDL-large subclass (p < 0.001).
The lack of a significant association between IPFD and LDL subfractions suggests that the link between IPFD and cardiovascular disease is likely mediated through mechanisms other than alterations in LDL particle distribution.
探讨胰腺内脂肪沉积(IPFD)与低密度脂蛋白(LDL)亚组分及肝脂酶之间的关联。
使用一台3.0特斯拉磁共振成像扫描仪对IPFD进行定量。采用非变性聚丙烯酰胺凝胶电泳的市售系统评估LDL亚组分。LDL谱包括六个亚组分,分为两个亚类:大LDL(LDL-1和LDL-2)和小LDL(LDL-3至LDL-6)。进行单因素和多因素线性回归分析以检验关联,并对年龄、性别、种族、肥胖、胰岛素抵抗和甘油三酯水平进行校正。
共有174名个体纳入分析。在任何统计模型中,IPFD与任何LDL亚组分或亚类均无显著关联。同样,肝脂酶与IPFD也无显著关联。然而,在所有三个统计模型中,肝脂酶与LDL-1和LDL-2亚组分以及大LDL亚类均呈显著负相关。在调整最充分的模型中,肝脂酶每增加一个单位,LDL-1降低0.24个单位(p = 0.002),LDL-2降低0.22个单位(p = 0.003),大LDL亚类降低0.27个单位(p < 0.001)。
IPFD与LDL亚组分之间缺乏显著关联表明,IPFD与心血管疾病之间的联系可能是通过LDL颗粒分布改变以外的机制介导的。