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The effect of leucocytosis on retinopathy of prematurity
Zhihong Sun1, Lu He1, Congcong Zhao1
1Department of Neonatology, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital, Zhengzhou Children's Hospital, 33 Longhuwaihuan Road, Zhengzhou, 450018, Henan, China.
Insights
Postnatal leukocytosis, a sign of inflammation, is linked to severe retinopathy of prematurity (ROP) in preterm infants. Early detection using white blood cell count may improve outcomes for high-risk newborns.
Area of Science:
- Neonatal Medicine
- Ophthalmology
- Pediatric Critical Care
Background:
- Postnatal leukocytosis indicates inflammation and is associated with various infant health issues.
- Inflammatory processes are known risk factors for retinopathy of prematurity (ROP) and other visual impairments.
Purpose of the Study:
- To investigate the association between postnatal leukocytosis and the incidence and severity of ROP in preterm infants.
- To determine if white blood cell (WBC) count can predict severe ROP in extremely premature neonates.
Main Methods:
- A cohort study included preterm infants (<28 weeks gestation) admitted between September 2015 and March 2021.
- Infants were categorized into a leukocytosis group (WBC ≥ 30 × 10^9/L) and a matched control group.
- Incidence and prognosis of ROP were compared; ROC curves analyzed WBC count correlation with severe ROP.
Main Results:
- The leukocytosis group exhibited higher incidences of intracranial hemorrhage, leukomalacia, sepsis, and bronchopulmonary dysplasia.
- Severe ROP incidence and need for ranibizumab injections were significantly higher in infants with leukocytosis.
- A WBC count cutoff of 19.1 × 10^9/L demonstrated high sensitivity (88.6%) and specificity (77.3%) for detecting severe ROP.
Conclusions:
- Postnatal leukocytosis is associated with an increased risk of severe ROP in preterm infants.
- Elevated white blood cell counts may serve as a predictive marker for severe ROP in this vulnerable population.
Abstract:
Postnatal leukocytosis reflects the general condition of inflammatory. Infection and inflammatory reaction have been proven to affect the occurrence of ROP and other visual dysfunction. Infants with a gestational age of < 28 weeks who were less than three days of age and admitted to the hospital between September 2015 and March 2021 were included in the study. Infants with a white blood cell (WBC) count ≥ 30 × 109/L were assigned to the leucocytosis group (n = 82). Gestational age- and weight-matched infants without leucocytosis were included as a control group (n = 85). The incidence and prognosis of ROP in preterm infants were compared between the groups. Receiver operating characteristic (ROC) curves were used to analyse the correlation between the WBC count and severe ROP. Compared to the infants in the control group, those in the leucocytosis group had lower 1-min Apgar scores (p < 0.001); higher C-reactive protein (p < 0.001) and procalcitonin (p < 0.001); and higher incidences of intracranial haemorrhage (p = 0.007), leukomalacia (p = 0.045), sepsis (p = 0.006), bronchopulmonary dysplasia (p = 0.017). The maternal age was higher in the leucocytosis group (p < 0.001). After adjusting for gestational age at 45 weeks, the incidence of severe ROP (p = 0.001) and the requirement for ranibizumab injections (p = 0.004) were higher in the leucocytosis group. The cut-off WBC count was determined to be 19.1 × 109/L, with a sensitivity of 88.6%, a specificity of 77.3%, and an area under the curve of 0.941 (95% confidence interval: 0.904-0.978) for the detection of severe ROP. Leucocytosis may be associated with severe ROP in premature infants.
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