Division of Endocrinology, Hospital Universitario de Canarias, 38320 Tenerife, Spain.
Division of Gastroenterology, Hospital Universitario de Canarias,38320 Tenerife, Spain.
Int J Mol Sci. 2023 Mar 8;24(6):5194. doi: 10.3390/ijms24065194.
Disruption of the lipid profile is commonly found in patients with inflammatory bowel disease (IBD). Lipoprotein lipase (LPL) is a key molecule involved in triglyceride metabolism that plays a significant role in the progression of atherosclerosis. In this study, our aim was to study whether serum LPL levels are different in IBD patients and controls and whether IBD features are related to LPL. This was a cross-sectional study that encompassed 405 individuals; 197 IBD patients with a median disease duration of 12 years and 208 age- and sex-matched controls. LPL levels and a complete lipid profile were assessed in all individuals. A multivariable analysis was performed to determine whether LPL serum levels were altered in IBD and to study their relationship with IBD characteristics. After the fully multivariable analysis, including cardiovascular risk factors and the changes in lipid profile that the disease causes itself, patients with IBD showed significantly higher levels of circulating LPL (beta coefficient 196 (95% confidence interval from 113 to 259) ng/mL, < 0.001). LPL serum levels did not differ between Crohn's disease and ulcerative colitis. However, serum C-reactive protein levels, disease duration, and the presence of an ileocolonic Crohn's disease phenotype were found to be significantly and independently positively related to LPL. In contrast, LPL was not associated with subclinical carotid atherosclerosis. In conclusion, serum LPL levels were independently upregulated in patients with IBD. Inflammatory markers, disease duration and disease phenotype were responsible for this upregulation.
脂类谱的紊乱在炎症性肠病(IBD)患者中很常见。脂蛋白脂肪酶(LPL)是参与甘油三酯代谢的关键分子,在动脉粥样硬化的进展中起着重要作用。在这项研究中,我们旨在研究 IBD 患者和对照组的血清 LPL 水平是否不同,以及 IBD 特征是否与 LPL 有关。这是一项横断面研究,共纳入 405 人;197 名 IBD 患者,中位疾病病程为 12 年,208 名年龄和性别匹配的对照组。所有个体均评估了 LPL 水平和完整的脂质谱。进行多变量分析以确定 LPL 血清水平是否在 IBD 中发生改变,并研究其与 IBD 特征的关系。在包括心血管危险因素和疾病本身引起的脂质谱变化的完全多变量分析后,IBD 患者显示循环 LPL 水平显著升高(β系数 196(95%置信区间为 113 至 259)ng/mL,<0.001)。克罗恩病和溃疡性结肠炎之间的 LPL 血清水平没有差异。然而,血清 C 反应蛋白水平、疾病持续时间和存在回肠结肠克罗恩病表型与 LPL 呈显著且独立的正相关。相比之下,LPL 与亚临床颈动脉粥样硬化无关。总之,IBD 患者的血清 LPL 水平独立上调。炎症标志物、疾病持续时间和疾病表型是导致这种上调的原因。