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Purpose <p>This study aims to examine the relationship between early fetal hemoglobin (HbF) decline, as a marker of oxidative stress, and the risk of bronchopulmonary dysplasia (BPD) in very low birth weight (VLBW) infants, with a focus on identifying critical risk thresholds.</p> Methods <p>A prospective cohort study was conducted on VLBW infants admitted to the First Hospital of Jilin University. HbF decline was assessed by measuring absolute reduction and rate of decline within the first 7 days of life. The primary outcomes were mortality and/or development of BPD.</p> Results <p>A total of 294 infants were included in the study, of whom 5 (1.70%) died, and 142 (48.3%) developed BPD. A nonlinear relationship between HbF decline in the first 7 days and the primary outcomes was observed. Thresholds of 3&#xa0;g/L for absolute HbF decline and 0.05 for the rate of decline were identified using a two-piecewise linear regression model. Infants were classified into low and high HbF decline groups based on these thresholds. Multivariate logistic regression showed a significantly higher risk of BPD in the high HbF decline group (OR = 2.77, 95% CI 1.52–5.02, <i>P</i> &lt; 0.001) Subgroup analyses largely confirmed these findings.</p> Conclusions <p>A nonlinear correlation was identified between HbF decline in the first 7 days and the risk of mortality and/or BPD in VLBW infants. An absolute HbF decline &gt; 3&#xa0;g/L or a rate &gt; 0.05 was significantly associated with increased risk, offering a basis for BPD risk prediction.</p>

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Association of early postnatal decline in fetal hemoglobin with bronchopulmonary dysplasia in very low birth weight infants: a cohort study

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年8月19日

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  • Chunying Niu,
  • Hui Wu,
  • Zhang Lin,
  • Xiangpan Li,
  • Dan Dang,
  • Xin Mu

摘要

Purpose

This study aims to examine the relationship between early fetal hemoglobin (HbF) decline, as a marker of oxidative stress, and the risk of bronchopulmonary dysplasia (BPD) in very low birth weight (VLBW) infants, with a focus on identifying critical risk thresholds.

Methods

A prospective cohort study was conducted on VLBW infants admitted to the First Hospital of Jilin University. HbF decline was assessed by measuring absolute reduction and rate of decline within the first 7 days of life. The primary outcomes were mortality and/or development of BPD.

Results

A total of 294 infants were included in the study, of whom 5 (1.70%) died, and 142 (48.3%) developed BPD. A nonlinear relationship between HbF decline in the first 7 days and the primary outcomes was observed. Thresholds of 3 g/L for absolute HbF decline and 0.05 for the rate of decline were identified using a two-piecewise linear regression model. Infants were classified into low and high HbF decline groups based on these thresholds. Multivariate logistic regression showed a significantly higher risk of BPD in the high HbF decline group (OR = 2.77, 95% CI 1.52–5.02, P < 0.001) Subgroup analyses largely confirmed these findings.

Conclusions

A nonlinear correlation was identified between HbF decline in the first 7 days and the risk of mortality and/or BPD in VLBW infants. An absolute HbF decline > 3 g/L or a rate > 0.05 was significantly associated with increased risk, offering a basis for BPD risk prediction.