Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Meta-Analysis
. 2024 Mar 14;16(6):832.
doi: 10.3390/nu16060832.

Plant-Derived Substances for Prevention of Necrotising Enterocolitis: A Systematic Review of Animal Studies

Affiliations
Meta-Analysis

Plant-Derived Substances for Prevention of Necrotising Enterocolitis: A Systematic Review of Animal Studies

Cheryl Anne Mackay et al. Nutrients. .

Abstract

Inflammation, oxidative injury, and gut dysbiosis play an important role in the pathogenesis of necrotising enterocolitis (NEC). Plant-derived substances have historically been used as therapeutic agents due to their anti-inflammatory, antioxidant, and antimicrobial properties. We aimed to review pre-clinical evidence for plant-derived substances in the prevention and treatment of NEC. A systematic review was conducted using the following databases: PubMed, EMBASE, EMCARE, MEDLINE and Cochrane Library (PROSPERO CRD42022365477). Randomized controlled trials (RCTs) and quasi-RCTs that evaluated a plant-derived substance as an intervention for NEC in an animal model of the illness and compared pre-stated outcomes (e.g., clinical severity, severity of intestinal injury, mortality, laboratory markers of inflammation and oxidative injury) were included. Sixteen studies (n = 610) were included in the systematic review. Ten of the sixteen included RCTs (Preterm rat pups: 15, Mice: 1) reported mortality and all reported NEC-related histology. Meta-analysis showed decreased mortality [12/134 vs. 27/135; RR: 0.48 (95% CI: 0.26 to 0.87); p = 0.02, 10 RCTs] and decreased NEC in the experimental group [24/126 vs. 55/79; RR: 0.34 (95% CI: 0.22 to 0.52); p < 0.001, 6 RCTs]. Markers of inflammation (n = 11) and oxidative stress (n = 13) improved in all the studies that have reported this outcome. There was no significant publication bias for the outcome of mortality. Plant-derived substances have the potential to reduce the incidence and severity of histologically diagnosed NEC and mortality in rodent models. These findings are helpful in guiding further pre-clinical studies towards developing a food supplement for the prevention of NEC in preterm infants.

Keywords: animal; necrotizing enterocolitis; newborn; plant-derived substance.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
PRISMA flow chart for study selection.
Figure 2
Figure 2
Forrest plot for the outcome of mortality in the included studies [25,27,33,35,36,37,39,43,44,45].
Figure 3
Figure 3
Forrest plot for the outcome of NEC histology in the included studies [35,36,37,41,42,44].
Figure 4
Figure 4
Funnel plot for the outcome of mortality.

Similar articles

Cited by

References

    1. Andrews R.E., Coe K.L. Clinical Presentation and Multifactorial Pathogenesis of Necrotizing Enterocolitis in the Preterm Infant. Adv. Neonatal Care. 2021;21:349–355. doi: 10.1097/ANC.0000000000000880. - DOI - PubMed
    1. Gupta A., Paria A. Etiology and medical management of NEC. Early Hum. Dev. 2016;97:17–23. doi: 10.1016/j.earlhumdev.2016.03.008. - DOI - PubMed
    1. Matei A., Montalva L., Goodbaum A., Lauriti G., Zani A. Neurodevelopmental impairment in necrotising enterocolitis survivors: Systematic review and meta-analysis. Arch. Dis. Child. Fetal Neonatal Ed. 2019;105:432–439. doi: 10.1136/archdischild-2019-317830. - DOI - PubMed
    1. Neu J. Necrotizing Enterocolitis: The Future. Neonatology. 2020;117:240–244. doi: 10.1159/000506866. - DOI - PubMed
    1. Obladen M. Necrotizing enterocolitis—150 years of fruitless search for the cause. Neonatology. 2009;96:203–210. doi: 10.1159/000215590. - DOI - PubMed