Copyright: ©Author(s) 2026.
World J Clin Pediatr. Jun 9, 2026; 15(2): 117843
Published online Jun 9, 2026. doi: 10.5409/wjcp.v15.i2.117843
Published online Jun 9, 2026. doi: 10.5409/wjcp.v15.i2.117843
Table 2 Strengths and limitations of animal models
| Strengths | Limitations |
| Allow direct control of diet, microbes, and inflammatory triggers | Rodent neurodevelopmental timelines differ from humans |
| Enable mechanistic dissection of the gut-immune-brain axis | Necrotizing enterocolitis and colitis models do not perfectly replicate human disease complexity |
| Permit invasive measurements: Cytokine profiling, neural imaging, electrophysiology | Microbiome composition differs significantly between species |
| Facilitate genetic manipulation (e.g., knockout mice) | Behavioral tests may not fully translate to human cognition or socio-emotional behavior |
| Allow testing of causal relationships via fecal microbiota transplantation, antibiotics, germ-free models | Artificial induction of inflammation may exaggerate severity relative to human infants |
- Citation: Al-Beltagi M, Saeed NK, El-Sawaf Y, Bediwy AS, Elbeltagi R. Early-life gastrointestinal inflammation and the developing brain: Unravelling the pathways to long-term cognitive dysfunction. World J Clin Pediatr 2026; 15(2): 117843
- URL: https://www.wjgnet.com/2219-2808/full/v15/i2/117843.htm
- DOI: https://dx.doi.org/10.5409/wjcp.v15.i2.117843