Optimal vitamin D status for Chinese infants in Hong Kong: insights from the relationship between serum 25-hydroxyvitamin D and parathyroid hormone levels
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Joanna Yuet-Ling Tung
, Hung-Kwan So
, Ka-Man Yip , Sarah Wing-Yiu Poon , Gloria Shir-Wey Pang , Keith Tsz-Suen Tung , Hing-Wai Tsang , Wilfred Hing-Sang Wong and Patrick Ip
Abstract
Objectives
This study aimed to identify the 25-hydroxyvitamin D (25OHD) threshold that maximally suppressed parathyroid hormone (PTH) in a group of healthy Chinese Infants in Hong Kong.
Methods
Healthy infants detected to have low serum 25OHD less than 25 nmol/L in a population study on vitamin D status were referred to Hong Kong Children’s Hospital (HKCH) for further management. Their total 25OHD was repeated with serum calcium, phosphate, alkaline phosphatase and PTH. Three-phase segmented regression was used to identify the optimal breakpoint between 25OHD and PTH.
Results
Two hundred and twelve infants were included (59 % male). They were reassessed at a median age of 156 days (IQR: 111–247 days). Using unadjusted three-phase segmented regression, the estimated breakpoint of 25OHD on PTH suppression, after adjusting for factors including age, gender, history of vitamin D supplement and mode of feeding, was 20.0 nmol/L (95 % CI: 13.1 to 26.9).
Conclusions
The threshold of 25OHD that triggered the inflection point for PTH in our Hong Kong Chinese infants was lower than that reported in the Western literature. This might imply the cutoff for vitamin D deficiency is lower for Chinese infants. This could be explained by younger age and different ethnicity. Further study with larger sample size is needed to validate the observation.
Acknowledgments
The authors would like to thank all participants in this study.
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Research ethics: This study was performed according to the Helsinki Declaration and was approved by the Research Ethics Committee of Hong Kong Children’s Hospital (HKCH-REC-2024-024) and the Institutional Review Board of the University of Hong Kong/Hospital Authority Hong Kong West Cluster Research Ethics Committee (UW 13–055).
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Informed consent: Written informed consent was obtained from each participant.
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Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.
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Use of Large Language Models, AI and Machine Learning Tools: None declared.
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Conflict of interest: The authors state no conflict of interest.
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Research funding: This study was an extension study to the original study funded by the Health and Medical Research Fund (Vit D-HKU), Food and Health Bureau, Hong Kong SAR Government.
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Data availability: The datasets generated and/or analyzed during the current study are available from the corresponding author on reasonable request.
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© 2025 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
- Frontmatter
- Editorial
- Sunlight, supplements, and science: vitamin D as a tool for pediatric health care
- Mini Review
- Physical activity and vitamin D in children: a review of impacts on bone health and fitness
- Original Articles
- Association between overweight or obesity and vitamin D status in preschool children: an epidemiological survey in Beijing, China, 2021–2023
- Association between partial remission phase in type 1 diabetes and vitamin D receptor Fok1 rs2228570 polymorphism
- Optimal vitamin D status for Chinese infants in Hong Kong: insights from the relationship between serum 25-hydroxyvitamin D and parathyroid hormone levels
- Reviews
- The changing landscape in the evaluation of hypotonic polyuria in children and adolescents: the role of the new copeptin stimulation tests
- A systematic review and meta-analysis of the self-reported Pubertal Development Scale’s applicability to children
- Original Articles
- Assessing prediabetes and cardiometabolic risk in Danish youth with obesity
- Endocrinopathies in children with inborn errors of immunity: a single-center experience
- Relationship between blood lipids and bone mineral density in healthy preschoolers: a 12-month cohort study
- The causal role of endocrine disrupting chemicals in pubertal timing: a Mendelian randomization study
- Case Reports
- Vitamin D dependent rickets type 2A: a case series of two siblings with novel mutation in vitamin D receptor gene responded to high dose oral calcium and calcitriol
- Emergence of osteolysis as a new radiological feature in a case with a novel BMP2 gene variant
- Rare case of ACTH-independent Cushing syndrome: diagnostic challenges and management
Articles in the same Issue
- Frontmatter
- Editorial
- Sunlight, supplements, and science: vitamin D as a tool for pediatric health care
- Mini Review
- Physical activity and vitamin D in children: a review of impacts on bone health and fitness
- Original Articles
- Association between overweight or obesity and vitamin D status in preschool children: an epidemiological survey in Beijing, China, 2021–2023
- Association between partial remission phase in type 1 diabetes and vitamin D receptor Fok1 rs2228570 polymorphism
- Optimal vitamin D status for Chinese infants in Hong Kong: insights from the relationship between serum 25-hydroxyvitamin D and parathyroid hormone levels
- Reviews
- The changing landscape in the evaluation of hypotonic polyuria in children and adolescents: the role of the new copeptin stimulation tests
- A systematic review and meta-analysis of the self-reported Pubertal Development Scale’s applicability to children
- Original Articles
- Assessing prediabetes and cardiometabolic risk in Danish youth with obesity
- Endocrinopathies in children with inborn errors of immunity: a single-center experience
- Relationship between blood lipids and bone mineral density in healthy preschoolers: a 12-month cohort study
- The causal role of endocrine disrupting chemicals in pubertal timing: a Mendelian randomization study
- Case Reports
- Vitamin D dependent rickets type 2A: a case series of two siblings with novel mutation in vitamin D receptor gene responded to high dose oral calcium and calcitriol
- Emergence of osteolysis as a new radiological feature in a case with a novel BMP2 gene variant
- Rare case of ACTH-independent Cushing syndrome: diagnostic challenges and management