Effect of Vitamin D Supplementation on Bone Mass in Infants With 25-Hydroxyvitamin D Concentrations Less Than 50 nmol/L

Author:

Gharibeh Nathalie1,Razaghi Maryam1,Vanstone Catherine A.1,Sotunde Olusola F.1,Glenn Laura1,Mullahoo Kristina1,Farahnak Zahra12,Khamessan Ali3,Wei Shu Qin4,McNally Dayre5,Rauch Frank6,Jones Glenville7,Kaufmann Martin7,Weiler Hope A.18

Affiliation:

1. School of Human Nutrition, McGill University, Sainte-Anne-de-Bellevue, Quebec, Canada

2. Department of Biochemistry, Memorial University of Newfoundland, St John’s, Newfoundland and Labrador, Canada

3. Europharm International Canada Inc, Montreal, Quebec, Canada

4. Institut National de Santé Publique du Québec, Montreal, Quebec, Canada

5. Department of Pediatrics, Children’s Hospital of Eastern Ontario, University of Ottawa, Ottawa, Ontario, Canada

6. Shriners Hospital for Children, Montreal, Quebec, Canada

7. Department of Biomedical and Molecular Sciences, Queen’s University, Kingston, Ontario, Canada

8. Nutrition Research Division, Bureau of Nutritional Sciences, Health Products and Food Branch, Health Canada, Ottawa, Ontario, Canada

Abstract

ImportanceThe dose of supplemental vitamin D needed in infants born with serum 25-hydroxyvitamin D (25[OH]D) concentrations less than 50 nmol/L (ie, 20 ng/mL) is unclear.ObjectiveTo determine whether a higher dose (1000 IU vs 400 IU per day) is required in infants born with 25(OH)D concentrations less than 50 nmol/L for bone mineral accretion across infancy.Design, Setting, and ParticipantsIn this prespecified secondary analysis of a double-blinded randomized clinical trial, conducted from March 2016 to March 2019 in a single center in Greater Montreal, Quebec, Canada, a consecutive sample of 139 healthy term singletons were recruited from 866 infants screened for vitamin D status at birth. Data were analyzed from June 2021 to November 2022.InterventionsCapillary blood was collected 24 to 36 hours after birth to measure serum total 25(OH)D concentrations. Infants with 25(OH)D concentrations less than 50 nmol/L were randomized to receive either 1000 IU or 400 IU per day of oral vitamin D3 supplementation from age 1 to 12 months. Infants with 25(OH)D concentrations of 50 nmol/L or greater formed a reference group.Main Outcomes and MeasuresMeasures at age 1, 3, 6, and 12 months were preplanned and included whole-body bone mineral content, lumbar spine bone mineral content, and bone mineral density using dual-energy x-ray absorptiometry, and serum 25(OH)D3 using liquid chromatography tandem mass spectrometry.ResultsOf 139 included infants, 81 (58.3%) were male, and the median (IQR) gestational age at birth was 39.6 (38.9-40.6) weeks. A total of 49 infants were included in the 1000 IU per day group, 49 infants in the 400 IU per day group, and 41 in the reference group. Mean (SD) whole-body bone mineral content was not different between trial groups over time (1000 IU per day, 173.09 [2.36] g; 400 IU per day, 165.94 [66.08] g). Similarly, no differences were observed in lumbar spine bone mineral content or density. Mean (SD) serum 25(OH)D3 concentrations were significantly higher in the 1000 IU per day group from age 3 to 12 months (3 months, 115.2 [35.3] nmol/L; 6 months, 121.6 [34.4] nmol/L; 12 months, 99.6 [28.8] nmol/L) compared with the 400 IU per day trial group (3 months, 77.4 [23.3] nmol/L; 6 months, 85.1 [18.6] nmol/L; 12 months, 82.3 [14.3] nmol/L).Conclusions and RelevanceIn this study, a higher dose of vitamin D supplementation in infants born with 25(OH)D concentrations less than 50 nmol/L did not present advantages to bone mass in infancy. This study supports a standard dose of 400 IU per day of vitamin D supplementation for breastfed infants in Montreal.Trial RegistrationClinicalTrials.gov Identifier: NCT02563015

Publisher

American Medical Association (AMA)

Subject

Pediatrics, Perinatology and Child Health

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