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The Correlation Between Bronchopulmonary Dysplasia and Platelet Metabolism in Preterm Infants
Longli Yan1, Zhuxiao Ren1, Jianlan Wang1
1Department of Neonatology, Guangdong Women and Children Hospital, Guangzhou Medical University, Guangzhou, China.
Insights
Platelet metabolism is linked to bronchopulmonary dysplasia (BPD) in premature infants. Infants with BPD showed lower platelet counts but higher platelet activation and thrombopoietin (TPO) levels, suggesting a role in disease development.
Area of Science:
- Neonatology
- Hematology
- Pulmonology
Background:
- Platelets are crucial for pulmonary vascular development.
- Thrombocytopenia is prevalent in pulmonary diseases.
- Limited research exists on platelet involvement in bronchopulmonary dysplasia (BPD).
Purpose of the Study:
- To investigate the association between platelet metabolism and BPD in preterm infants.
- To explore platelet counts, megakaryocyte counts, activation markers, and thrombopoietin (TPO) levels in relation to BPD.
Main Methods:
- A prospective case-control study included preterm infants (<32 weeks gestation, <1,500 g birth weight).
- Infants were grouped into BPD and control cohorts.
- Platelet count, circulating megakaryocyte (MK) count, CD62P, CD63, and TPO were measured at 28 days post-birth.
Main Results:
- Infants with BPD exhibited significantly lower platelet counts (180.3 vs. 345.6 × 10^9/L) compared to controls.
- Higher circulating MK counts (30.7 vs. 13.3/ml) and elevated CD62P, CD63, and TPO levels were observed in the BPD group.
- TPO concentration negatively correlated with platelet count in BPD infants with thrombocytopenia.
Conclusions:
- Platelet metabolism appears to play a role in the pathogenesis of BPD in preterm infants.
- Mechanisms may involve increased platelet activation and feedback-driven TPO production.
Abstract:
Background: Platelets play an important role in the formation of pulmonary blood vessels, and thrombocytopenia is common in patients with pulmonary diseases. However, a few studies have reported on the role of platelets in bronchopulmonary dysplasia. Objective: The objective of the study was to explore the relationship between platelet metabolism and bronchopulmonary dysplasia in premature infants. Methods: A prospective case-control study was performed in a cohort of premature infants (born with a gestational age <32 weeks and a birth weight <1,500 g) from June 1, 2017 to June 1, 2018. Subjects were stratified into two groups according to the diagnostic of bronchopulmonary dysplasia: with bronchopulmonary dysplasia (BPD group) and without bronchopulmonary dysplasia (control group). Platelet count, circulating megakaryocyte count (MK), platelet-activating markers (CD62P and CD63), and thrombopoietin (TPO) were recorded and compared in two groups 28 days after birth; then serial thrombopoietin levels and concomitant platelet counts were measured in infants with BPD. Results: A total of 252 premature infants were included in this study. Forty-eight premature infants developed BPD, 48 premature infants without BPD in the control group who were matched against the study infants for gestational age, birth weight, and admission diagnosis at the age of postnatal day 28. Compared with the controls, infants with BPD had significantly lower peripheral platelet count [BPD vs. controls: 180.3 (24.2) × 109/L vs. 345.6 (28.5) × 109/L, p = 0.001]. Circulating MK count in the BPD group was significantly more abundant than that in the control group [BPD vs. controls: 30.7 (4.5)/ml vs. 13.3 (2.6)/ml, p = 0.025]. The level of CD62p, CD63, and TPO in BPD group was significantly higher than the control group [29.7 (3.1%) vs. 14.5 (2.5%), 15.4 (2.0%) vs. 5.8 (1.7%), 301.4 (25.9) pg/ml vs. 120.4 (14.2) pg/ml, all p < 0.05]. Furthermore, the concentration of TPO was negatively correlated with platelet count in BPD group with thrombocytopenia. Conclusions: Our findings suggest that platelet metabolism is involved in the development of BPD in preterm infants. The possible mechanism might be through increased platelet activation and promoted TPO production by feedback.
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