Shehab Mohammad, Al-Fajri Sharifa, Alanqar Ahmed, Alborom Mohammad, Alrashed Fatema, Alshammaa Fatemah, Alfadhli Ahmad, Devarajan Sriraman, Alkhairi Irina, Cherian Preethi, Abubaker Jehad, Abu-Farha Mohamed, Al-Mulla Fahd
Division of Gastroenterology, Department of Internal Medicine, Mubarak Alkabeer, University Hospital, Kuwait University, Jabriya 47060, Kuwait.
Department of Translational Research, Dasman Diabetes Institute, Dasman, Kuwait City 15462, Kuwait.
J Clin Med. 2025 Jul 15;14(14):5006. doi: 10.3390/jcm14145006.
Crohn's disease (CD) is a chronic disease perpetuated through key pro-inflammatory molecules, including tumor necrosis factor-alpha (TNFα). Angiopoietin-like protein 8 (ANGPTL8) may contribute to inflammation cascades. This study aimed to investigate how ANGPTL8 levels are influenced in patients with CD prior to and following anti-TNF therapy. Patients were divided into 3 groups. Patients with CD in clinical remission receiving IFX for at least 24 weeks (IFX-experienced group), patients scheduled to start IFX (IFX-naïve group), and healthy controls (control group). In the IFX-experienced group, ANGPTL8 levels were measured 24 h before the next maintenance IFX dose. In the IFX-naïve group, levels were measured at week 0 and week 24, and in the control group, they were measured randomly. The total number of participants was 166. The numbers of IFX-experienced, IFX-naïve patients, and healthy controls were 82, 13, and 71, respectively. Mean age ranged from 27 to 33 years of age across the three groups. Eighty-four (51%) participants were female. ANGPTL8 levels were significantly higher in patients with CD (138.26 ± 8.47 pmol) compared to the healthy control group (102.52 ± 5.99 pmol, = 0.001). Among IFX-naïve patients receiving anti-TNFα treatment, ANGPTL8 levels decreased significantly from 145.06 ± 17.93 pmol pre-treatment (week 0) to 81.78 ± 10.61 pmol post-treatment (week 24), = 0.007. Our findings suggest that ANGPTL8 levels are elevated in CD and may be involved in the inflammatory process. The marked reduction in ANGPTL8 levels following anti-TNFα treatment indicates its potential as a biomarker for treatment response. Further research should focus on the exact mechanisms through which ANGPTL8 influences CD progression and its utility in clinical practice.
克罗恩病(CD)是一种通过关键促炎分子(包括肿瘤坏死因子-α (TNFα))持续存在的慢性疾病。血管生成素样蛋白8(ANGPTL8)可能参与炎症级联反应。本研究旨在调查抗TNF治疗前后CD患者中ANGPTL8水平是如何受到影响的。患者被分为3组。临床缓解且接受英夫利昔单抗(IFX)治疗至少24周的CD患者(IFX经验组)、计划开始IFX治疗的患者(IFX初治组)和健康对照者(对照组)。在IFX经验组中,在下一次维持性IFX给药前24小时测量ANGPTL8水平。在IFX初治组中,在第0周和第24周测量水平,在对照组中,随机测量。参与者总数为166人。IFX经验组、IFX初治患者和健康对照者的人数分别为82人、13人和71人。三组的平均年龄在27至33岁之间。84名(51%)参与者为女性。与健康对照组(102.52±5.99 pmol,P = 0.001)相比,CD患者的ANGPTL8水平显著更高(138.26±8.47 pmol)。在接受抗TNFα治疗的IFX初治患者中,ANGPTL8水平从治疗前(第0周)的145.06±17.93 pmol显著降至治疗后(第24周)的81.