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Faecal calprotectin concentrations in neonates with CHD: pilot study
Graeme O'Connor1,2, Katherine L Brown1,2, Andrew M Taylor1,2,3
1Heart and Lung Department, Cardiothoracic Intensive Care Unit, Great Ormond Street Children's Hospital, London, UK.
Insights
Faecal calprotectin may indicate gut inflammation in neonates with congenital heart disease (CHD). Elevated levels correlate with necrotising enterocolitis (NEC), aiding early detection and management in at-risk infants.
Area of Science:
- Neonatalogy
- Pediatric Surgery
- Gastroenterology
Background:
- Neonates with congenital heart disease (CHD) face increased risk of necrotising enterocolitis (NEC) due to mesenteric hypoperfusion.
- NEC leads to feeding interruptions, poor growth, and increased mortality risk in neonates with CHD.
- Abdominal radiography has limitations in early NEC detection, particularly when pneumatosis intestinalis is absent.
Purpose of the Study:
- To investigate the correlation between fecal calprotectin concentration and gut inflammation in neonates with CHD.
- To assess the utility of fecal calprotectin as a biomarker for NEC in this vulnerable population.
Main Methods:
- Prospective single-center study of term neonates with duct-dependent CHD (March 2018-March 2019).
- Measurement of fecal calprotectin concentrations using enzyme-linked immunosorbent assay (ELISA) in post-surgical patients.
- Analysis included 30 patients, comparing calprotectin levels across NEC, suspected NEC, and no NEC groups.
Main Results:
- Significantly higher fecal calprotectin concentrations in neonates with NEC (3528 µg/g) and suspected NEC (1339 µg/g) compared to those without (390 µg/g) (p=0.0001).
- Patients with suspected NEC experienced a longer hospital stay (average 18 days longer) (p=0.03).
- Elevated calprotectin levels may reflect the severity of gut inflammation.
Conclusions:
- Fecal calprotectin shows promise as a non-invasive biomarker for detecting and assessing gut inflammation in neonates with CHD.
- Higher calprotectin levels are associated with NEC and suspected NEC, potentially indicating increased disease severity.
- Early identification of NEC through biomarkers like calprotectin could lead to timely interventions, reducing prolonged nil-by-mouth periods and hospital stays.
Abstract:
Neonates with CHD are at increased risk of developing necrotising enterocolitis due to mesenteric hypoperfusion. Necrotising enterocolitis results in repeated feed interruptions contributing to poor growth during the early post-operative phase. Poor weight gain and longer hospital stay are risk factors for death in neonates with CHD. Abdominal radiography is used as a diagnostic tool for necrotising enterocolitis; however, its utility is limited in the early stages of necrotising enterocolitis when pneumatosis intestinalis is absent. Calprotectin is a neutrophil activation biomarker, and elevated levels are evident in inflammatory diseases such as necrotising enterocolitis. The aim of this study was to determine whether there is a correlation between faecal calprotectin concentration and gut inflammation in neonates with CHD. This prospective single-centre study recruited newly diagnosed term patients with duct-dependent CHD between March 2018 and March 2019. Faecal calprotectin concentrations were measured in post-surgical patients using enzyme-linked immunosorbent assay methods. A total of 30 patients were included in the analysis. Calprotectin concentration for patients who developed necrotising enterocolitis was 3528 µg/g compared with 390 µg/g without, compared with 1339 µg/g in patients with suspected necrotising enterocolitis (p = 0.0001). Patients with suspected necrotising enterocolitis had a significantly longer length of hospital stay, on average 18 days longer compared to patients without necrotising enterocolitis (p = 0.03). Faecal calprotectin concentrations may reflect severity of gut inflammation in neonates with CHD. Suspected necrotising enterocolitis contributes to longer days nil by mouth and an increase in length of hospital stay.
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