High-Dose Docosahexaenoic Acid in Newborns Born at Less Than 29 Weeks’ Gestation and Behavior at Age 5 Years

Author:

Gould Jacqueline F.123,Roberts Rachel M.3,Anderson Peter J.4,Makrides Maria12,Sullivan Thomas R.15,Gibson Robert A.16,McPhee Andrew J.7,Doyle Lex W.8,Bednarz Jana M.1,Best Karen P.12,Opie Gillian9,Travadi Javeed1011,Cheong Jeanie L. Y.12,Davis Peter G.12,Sharp Mary13,Simmer Karen14,Tan Kenneth15,Morris Scott16,Lui Kei17,Bolisetty Srinivas18,Liley Helen19,Stack Jacqueline20,Collins Carmel T.12

Affiliation:

1. SAHMRI Women and Kids, South Australian Health and Medical Research Institute, North Adelaide, South Australia, Australia

2. Discipline of Paediatrics, Faculty of Health and Medical Sciences, The University of Adelaide, North Terrace Adelaide, South Australia, Australia

3. School of Psychology, Faculty of Health and Medical Sciences, The University of Adelaide, North Terrace Adelaide, Adelaide, South Australia, Australia

4. Turner Institute for Brain and Mental Health, School of Psychological Sciences, Monash University, Melbourne, Victoria, Australia

5. School of Public Health, Faculty of Health and Medical Sciences, The University of Adelaide, North Terrace Adelaide, South Australia, Australia

6. School of Agriculture, Food and Wine, The University of Adelaide, Waite Campus, Glen Osmond, South Australia, Australia

7. Neonatal Medicine, Women’s and Children’s Hospital, North Adelaide, South Australia, Australia

8. Department of Obstetrics and Gynaecology, The Royal Women’s Hospital, Parkville, Melbourne, Victoria, Australia

9. Neonatal Services, Mercy Hospital for Women, Heidelberg, Melbourne, Victoria, Australia

10. Newborn Services, John Hunter Children’s Hospital, New Lambton Heights, New South Wales, Australia

11. Neonatal Intensive Care Unit, Department of Paediatrics, Te Whatu Ora Waikato, Waikato Hospital, Hamilton, New Zealand

12. Neonatal Medicine, The Royal Women’s Hospital, Parkville, Melbourne, Victoria, Australia

13. King Edward Memorial Hospital, Perth, Western Australia, Australia

14. The University of Western Australia, Perth, Western Australia, Australia

15. Department of Paediatrics, Monash University, Monash Children’s Hospital, Clayton, Victoria, Australia

16. Neonatal-Perinatal Medicine, Flinders Medical Centre, Flinders Drive, Bedford Park, South Australia, Australia

17. School of Clinical Medicine, Discipline of Paediatrics and Child Health, University of New South Wales, Sydney, New South Wales, Australia

18. Royal Hospital for Women, Randwick, New South Wales, Australia

19. Mater Research – The Faculty of Medicine, The University of Queensland, South Brisbane, Queensland, Australia

20. Neonatal Intensive Care Unit, Liverpool Hospital, Elizabeth, Liverpool, New South Wales, Australia

Abstract

ImportanceChildren born at less than 29 weeks’ gestation are at risk of behavioral difficulties. This may be due in part to the lack of transplacental supply of docosahexaenoic acid (DHA), a key fatty acid with structural and functional roles in the brain.ObjectiveTo determine whether meeting the neonatal DHA requirement through supplementation is associated with improved behavioral functioning of children born at less than 29 weeks’ gestation.Design, Setting and ParticipantsThis was a follow-up of children from 10 Australian participating centers in a multi-center, blinded, parallel group randomized clinical trial of infants born at less than 29 weeks’ gestation conducted from June 2012 and September 2015, excluding those with additional fatty acid supplementation or major congenital or chromosomal abnormalities. Follow-up took place from August 2018 to May 2021. Parents of surviving children who had not withdrawn from the original trial were invited to complete questionnaires when the child turned 5 years’ corrected age.InterventionsInfants were randomized to receive daily enteral emulsions providing 60 mg/kg/d of DHA or a soy-oil emulsion (with no DHA) from within the first 3 days of enteral feeding until 36 weeks’ postmenstrual age or discharge home, whichever occurred first.Main Outcomes and MeasuresThe primary outcome of this follow-up was parent-rated behavior and emotional functioning as indicated by the Total Difficulties score of the Strengths and Difficulties Questionnaire. Parents also completed questionnaires about their child’s behavioral manifestations of executive functioning, as well as a range of health outcomes to assess potential longer-term side effects of DHA intervention.ResultsPrimary outcome data were available for 731 children (76% of 958 surviving eligible children; 361 in the intervention group and 370 in the control group). Of these 731, 452 (47%) were female, and the mean (SD) corrected age at follow-up was 5.4 (0.5) years. Following imputation for missing data, the mean Total Difficulties score was the same in both groups (intervention group, n = 465; mean [SD], 11.8 [6.3]; control group, n = 493; mean [SD], 11.8 [6.0]; mean difference adjusted for sex, gestational age stratum, and hospital, 0.01; 95% CI, −0.87 to 0.89; P = .98). There was no evidence for differences between the groups in any secondary outcomes of behavior, executive functioning, or health.Conclusions and RelevanceIn this follow-up of a randomized clinical trial, enteral DHA supplementation at the equivalent of the estimated in utero dose for infants born at less than 29 weeks’ gestation did not improve behavioral functioning at age 5 years. There were no indications of adverse effects with DHA supplementation.Trial RegistrationAustralian New Zealand Clinical Trial Registry: ACTRN12612000503820

Publisher

American Medical Association (AMA)

Subject

Pediatrics, Perinatology and Child Health

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