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Effect of Docosahexaenoic Acid Supplementation vs Placebo on Developmental Outcomes of Toddlers Born Preterm: A Randomized Clinical Trial.
Keim, Sarah A; Boone, Kelly M; Klebanoff, Mark A; Turner, Abigail Norris; Rausch, Joseph; Nelin, Mary Ann; Rogers, Lynette K; Yeates, Keith Owen; Nelin, Leif; Sheppard, Kelly W.
Affiliation
  • Keim SA; Center for Biobehavioral Health, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
  • Boone KM; Department of Pediatrics, College of Medicine, The Ohio State University, Columbus.
  • Klebanoff MA; Division of Epidemiology, College of Public Health, The Ohio State University, Columbus.
  • Turner AN; Center for Biobehavioral Health, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
  • Rausch J; Crane Center for Early Childhood Research and Policy, The Ohio State University, Columbus.
  • Nelin MA; Department of Pediatrics, College of Medicine, The Ohio State University, Columbus.
  • Rogers LK; Division of Epidemiology, College of Public Health, The Ohio State University, Columbus.
  • Yeates KO; Center for Perinatal Research, The Research Institute at Nationwide Children's Hospital, Columbus.
  • Nelin L; Department of Obstetrics and Gynecology, College of Medicine, The Ohio State University, Columbus.
  • Sheppard KW; Division of Epidemiology, College of Public Health, The Ohio State University, Columbus.
JAMA Pediatr ; 172(12): 1126-1134, 2018 12 01.
Article in En | MEDLINE | ID: mdl-30357263
Importance: Intake of dietary docosahexaenoic acid (DHA) among toddlers is low. Supplementation may benefit developmental outcomes of toddlers who were born preterm. Objective: To determine whether 6 months of daily DHA supplementation improves developmental outcomes of toddlers who were born preterm. Design, Setting, and Participants: A randomized, fully masked, placebo-controlled trial was conducted from April 26, 2012, to March 24, 2017, at a large US pediatric academic center with 9 neonatal intensive care units. Children born at less than 35 weeks' gestation who were 10 to 16 months corrected age underwent 6 months of intervention. Of 2363 children assessed, 982 were eligible, 605 declined, and 377 enrolled and were randomized. Analyses were according to intent to treat. Interventions: One-to-one allocation to receive daily microencapsulated DHA, 200 mg, and arachidonic acid (AA), 200 mg (DHA+AA), or microencapsulated corn oil (placebo). Main Outcomes and Measures: The primary outcome specified a priori was Bayley Scales of Infant and Toddler Development, third edition (Bayley-III), cognitive composite score at 16 to 22 months corrected age. Secondary outcomes were Bayley-III language and motor composite scores and Infant Behavior Questionnaire-Revised and Early Childhood Behavior Questionnaire effortful control and activity level scores. Subgroup analyses defined a priori were by income, sex, and birth weight. Results: Among 377 children randomized and included in the analysis (182 girls and 195 boys; median corrected age, 15.7 months), 338 children (89.7%) had complete data on the primary outcome. Bayley-III cognitive scores did not differ between the DHA+AA and placebo groups (difference in change, 0.5 [95% CI, -1.8 to 2.8]; effect size, 0.05; P = .66). Assignment to the DHA+AA group had a small to medium negative effect on Bayley-III language scores among children with lower birth weights (eg, a child with a birth weight of 1000 g assigned to receive DHA+AA experienced a 4.1-point relative decrease, while a child assigned to placebo did not; P = .03 for interaction). Supplementation had a similar negative effect on effortful control scores among children with annual household incomes greater than $35 000 (difference in change, -0.3 [95% CI, -0.4 to -0.1]; effect size, -0.37; P = .01). Bayley-III motor scores and activity level scores were unaffected. Conclusions and Relevance: Daily supplementation with 200 mg of DHA and 200 mg of AA for 6 months resulted in no improvement in cognitive development and early measures of executive function vs placebo, and may have resulted in negative effects on language development and effortful control in certain subgroups of children. These findings do not support DHA supplementation in the second year of life for children who are born preterm. Trial Registration: ClinicalTrials.gov Identifier: NCT01576783.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Child Development / Docosahexaenoic Acids / Cognition Type of study: Clinical_trials / Prognostic_studies Limits: Female / Humans / Infant / Male / Newborn Language: En Journal: JAMA Pediatr Year: 2018 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Child Development / Docosahexaenoic Acids / Cognition Type of study: Clinical_trials / Prognostic_studies Limits: Female / Humans / Infant / Male / Newborn Language: En Journal: JAMA Pediatr Year: 2018 Document type: Article Country of publication: