Docosahexaenoic acid and bronchopulmonary dysplasia in preterm infants: a systematic review and meta-analysis
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Kosuke Tanaka1, Shiori Tanaka2, Nidhi Shah3
1Department of Pediatrics, Saitama Medical Center, Saitama Medical University, Kawagoe, Japan.
Insights
Docosahexaenoic acid (DHA) supplementation did not reduce the risk of bronchopulmonary dysplasia (BPD) in preterm infants. This systematic review found no significant clinical benefits for DHA in treating BPD or other neonatal complications.
Area of Science:
- Neonatal Medicine
- Nutritional Science
- Respiratory Medicine
Background:
- Bronchopulmonary dysplasia (BPD) is a significant complication in extremely preterm infants.
- Docosahexaenoic acid (DHA), known for anti-inflammatory properties, is explored for BPD management.
- This study systematically reviews DHA's impact on BPD.
Purpose of the Study:
- To evaluate the efficacy of docosahexaenoic acid (DHA) supplementation in preventing or treating bronchopulmonary dysplasia (BPD).
- To assess the effects of DHA on other neonatal morbidities in preterm infants.
Main Methods:
- A systematic literature search was performed across multiple databases up to June 2017.
- Included studies were randomized controlled trials (RCTs) involving preterm infants (<33 weeks gestational age).
- Meta-analysis was conducted on data from four RCTs involving 1,966 neonates.
Main Results:
- DHA supplementation did not decrease the risk of BPD at 36 weeks postmenstrual age (low certainty of evidence).
- No significant reduction in other neonatal morbidities was observed, including death, BPD at 28 days, necrotizing enterocolitis, intraventricular hemorrhage, severe retinopathy of prematurity, or sepsis.
- Evidence certainty varied from low to moderate for different outcomes.
Conclusions:
- Docosahexaenoic acid (DHA) supplementation may not provide significant clinical benefits for treating BPD in preterm infants.
- DHA supplementation does not appear to significantly reduce the risk of other common neonatal morbidities.
- Further research may be needed to clarify the role of DHA in neonatal care.
Background:
Bronchopulmonary dysplasia (BPD) is a common and serious complication of extremely preterm birth. Given the anti-inflammatory properties, docosahexaenoic acid (DHA) supplementation has been proposed as a strategy for the management of BPD. This study aimed to investigate the effects of DHA supplementation on BPD based on a systematic review.
Methods:
A comprehensive literature search was conducted using ClinicalTrials.Gov, CINAHL, Cochrane Library, EMBASE, MEDLINE, PubMed, and the WHO ICTRP from their respective dates of inception to June 2017. The studies included were randomized controlled trials (RCTs) that enrolled preterm infants <33 weeks of gestational age. Trials were included if DHA supplementation was compared with a control.
Results:
Four RCTs from five reports (1,966 neonates) met our inclusion criteria. The meta-analysis of these studies showed that DHA supplementation did not decrease the risk of BPD at 36 weeks of postmenstrual age among preterm infants (low certainty of evidence). DHA supplementation did not significantly reduce the risk of other neonatal morbidities including death (low certainty of evidence), BPD at 28 days of life (moderate certainty of evidence), necrotizing enterocolitis (low certainty of evidence), intraventricular hemorrhage, severe retinopathy of prematurity, or sepsis.
Conclusion:
DHA supplementation may not exert significant clinical benefits in the treatment of BPD and other neonatal morbidities.
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