Questioning the adequacy of standardized vitamin D supplementation protocol in very low birth weight infants: a prospective cohort study
Abstract
Objectives
Preterm infants are at increased risk for vitamin D deficiency (VDD). We aimed to assess the adequacy of standardized vitamin D supplementation protocol in very low birth weight (VLBW) infants. Additionally, vitamin D status of mother/infant couples and the associations between vitamin D status at birth and morbidities of the infants were investigated.
Methods
In this single-center, prospective cohort study blood samples were collected from 55 mothers just before delivery and from their infants at birth and on the 30th day of life (DOL) for 25 hydroxy vitamin D (25OHD) measurements. Vitamin D was initiated in dose of 160 IU/kg by parenteral nutrition on the first DOL and oral vitamin D supplementation (400 IU/day) was administered when enteral feedings reached 50% of total intake or on the 15th DOL.
Results
The median 25OHD levels of the infants were 16.12 (9.14–20.50) in cord blood and 36.32 (31.10–44.44) in venous blood on the 30th DOL (p<0.01). In 98% of the VLBW infants 25OHD reached sufficient levels on the 30th DOL. None of the mothers had sufficient vitamin D levels (25OHD >30 ng/mL). Maternal 25OHD levels were correlated with the 25OHD levels of the infants in cord blood (r=0.665, p<0.001). There was a significant difference in mean cord 25OHD levels between winter (13.65 ± 5.69 ng/mL) and summer seasons (19.58 ± 11.67 ng/mL) (p=0.021). No association was found between neonatal morbidity and vitamin D status.
Conclusions
The results clearly show that by utilizing the current supplementation protocol, the majority of VLBW infants with deficient/insufficient serum 25OHD levels reached sufficient levels on the 30th DOL. Furthermore, vitamin D levels in mother/infant couples were found to be highly correlated.
Acknowledgements
This study was Hatice Sarıdemir’s Thesis in Pediatrics, and Ayse Neslihan Tekin served as the Thesis advisor.
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Research funding: None declared.
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Author contributions: H.S. and A.N.T. equally contributed to the conception and design of the research, acquisition and analysis of the data; O.S.O. contributed to design, acquisition, analysis, interpretation of data and drafted manuscript. O.A. contributed to the acquisition, analysis and interpretation of the data. All authors critically revised the manuscript, agree to be fully accountable for ensuring the integrity and accuracy of the work, and read and approved the final manuscript.
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Competing interests: Authors state no conflict of interest.
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Informed consent: An informed consent was obtained after the participants had received a detailed introduction to the study.
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Ethical approval: The Institutional Ethics Committee approved the study (No. 10-28.06.2018).
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© 2021 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
- Frontmatter
- Review Article
- Calcitonin and complementary biomarkers in the diagnosis of hereditary medullary thyroid carcinoma in children and adolescents
- Original Articles
- Genotype and phenotypic spectrum of vitamin D dependent rickets type 1A: our experience and systematic review
- Questioning the adequacy of standardized vitamin D supplementation protocol in very low birth weight infants: a prospective cohort study
- Growth hormone replacement therapy: is it safe to use in children with asymptomatic pituitary lesions?
- Comparing adolescent self staging of pubertal development with hormone biomarkers
- Reverse circadian glucocorticoid treatment in prepubertal children with congenital adrenal hyperplasia
- The concordance between ultrasonographic stage of breast and Tanner stage of breast for overweight and obese girls: a school population-based study
- Cross-sectional analysis: clinical presentation of children with persistently low ALP levels
- The utility of continuous glucose monitoring systems in the management of children with persistent hypoglycaemia
- Long-term effect of conventional phosphate and calcitriol treatment on metabolic recovery and catch-up growth in children with PHEX mutation
- Role of magnetic resonance diffusion weighted imaging in diagnosis of diabetic nephropathy in children living with type 1 diabetes mellitus
- Investigation of quality of life in obese adolescents: the effect of psychiatric symptoms of obese adolescent and/or mother on quality of life
- Predictive value of WHO vs. IAP BMI charts for identification of metabolic risk in Indian children and adolescents
- Case Reports
- COVID-19 triggered encephalopathic crisis in a patient with glutaric aciduria type 1
- Aromatase deficiency in an Ontario Old Order Mennonite family
- A case of monogenic diabetes mellitus caused by a novel heterozygous RFX6 nonsense mutation in a 14-year-old girl
Articles in the same Issue
- Frontmatter
- Review Article
- Calcitonin and complementary biomarkers in the diagnosis of hereditary medullary thyroid carcinoma in children and adolescents
- Original Articles
- Genotype and phenotypic spectrum of vitamin D dependent rickets type 1A: our experience and systematic review
- Questioning the adequacy of standardized vitamin D supplementation protocol in very low birth weight infants: a prospective cohort study
- Growth hormone replacement therapy: is it safe to use in children with asymptomatic pituitary lesions?
- Comparing adolescent self staging of pubertal development with hormone biomarkers
- Reverse circadian glucocorticoid treatment in prepubertal children with congenital adrenal hyperplasia
- The concordance between ultrasonographic stage of breast and Tanner stage of breast for overweight and obese girls: a school population-based study
- Cross-sectional analysis: clinical presentation of children with persistently low ALP levels
- The utility of continuous glucose monitoring systems in the management of children with persistent hypoglycaemia
- Long-term effect of conventional phosphate and calcitriol treatment on metabolic recovery and catch-up growth in children with PHEX mutation
- Role of magnetic resonance diffusion weighted imaging in diagnosis of diabetic nephropathy in children living with type 1 diabetes mellitus
- Investigation of quality of life in obese adolescents: the effect of psychiatric symptoms of obese adolescent and/or mother on quality of life
- Predictive value of WHO vs. IAP BMI charts for identification of metabolic risk in Indian children and adolescents
- Case Reports
- COVID-19 triggered encephalopathic crisis in a patient with glutaric aciduria type 1
- Aromatase deficiency in an Ontario Old Order Mennonite family
- A case of monogenic diabetes mellitus caused by a novel heterozygous RFX6 nonsense mutation in a 14-year-old girl