Why the study?
ANGPTL8 may contribute to inflammation cascades, but how its levels are influenced in patients with Crohn's disease before and after anti-TNF therapy was unclear.
Does anti-TNF-alpha therapy (infliximab) reduce circulating angiopoietin-like protein 8 (ANGPTL8) levels in adult patients with moderate-to-severe Crohn's disease?
Does anti-TNF-alpha therapy (infliximab) reduce circulating angiopoietin-like protein 8 (ANGPTL8) levels in adult patients with moderate-to-severe Crohn's disease?
Circulating ANGPTL8 levels are significantly elevated in patients with Crohn's disease compared to healthy controls and decrease substantially after 24 weeks of infliximab therapy, indicating potential utility as a biomarker for inflammatory activity and treatment response.
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ANGPTL8 reduction with anti-TNF may signal response in CD; leaves open its value as biomarker or target pending validation.
Background: 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. Methods: 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. Results: 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, p = 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), p = 0.007. Conclusions: 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.
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Shehab et al. (2025) studied this question.
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