Association of vitamin D‐binding protein polymorphisms and serum 25(OH)D concentration varies among Chinese healthy infants of different VDR‐FokI genotypes: A multi‐centre cross‐sectional study
Article Swipe
Hing Wai Tsang
,
Keith T. S. Tung
,
Rosa S. Wong
,
Siew Yan Wong
,
Joanna Yuet‐ling Tung
,
Gilbert T. Chua
,
M. Ho
,
Chi Pui Pang
,
Wilfred Hing Sang Wong
,
Gcf Chan
,
Ian Chi Kei Wong
,
Patrick Ip
·
YOU?
·
· 2023
· Open Access
·
· DOI: https://doi.org/10.1111/nbu.12656
YOU?
·
· 2023
· Open Access
·
· DOI: https://doi.org/10.1111/nbu.12656
Hypovitaminosis D during infancy is associated with the development of chronic diseases and poor health later in life. While the effect of environmental factors on vitamin D concentration has been extensively explored, this study aimed to explore the effect of genetic factors on vitamin D concentration among Chinese infants. We conducted a multi‐centre cross‐sectional study in Hong Kong from July 2019 to May 2021. A candidate genetic approach was adopted to study four selected genetic variants of the vitamin D‐binding protein (DBP) and vitamin D receptor (VDR) (rs4588, rs7041, rs2282679 and rs2228570) to examine their associations with measured serum 25(OH)D concentration. A total of 378 Chinese infants aged 2–12 months were recruited in this study. Peripheral blood samples were collected from the infants to measure serum 25(OH)D concentration and extract DNA. Results showed that rs7041T and rs2282679C were significantly associated with lower serum 25(OH)D concentration. Further analysis of the DBP variants revealed that the GC1F allele was significantly associated with lower 25(OH)D concentration and identified as the risk DBP isoform in infants. While our results revealed that there is no direct association between VDR‐FokI genotype and serum 25(OH)D concentration, a VDR‐FokI genotype‐specific pattern was observed in the association between DBP isoforms and serum 25(OH)D concentration. Specifically, significant associations were observed in the DBP genotypes GC1F/F , GC1F/2 and GC1S/2 among VDR‐FokI TT/TC carriers, but not in VDR‐FokI CC carriers. Our findings lay down the basis for the potential of genetic screening to identify high risk of hypovitaminosis D in Chinese infants.
Related Topics
Concepts
FokI
Calcitriol receptor
Vitamin D and neurology
Genotype
Vitamin D-binding protein
Internal medicine
Allele
Medicine
Endocrinology
vitamin D deficiency
Polymorphism (computer science)
Biology
Genetics
Gene
Metadata
- Type
- article
- Language
- en
- Landing Page
- https://doi.org/10.1111/nbu.12656
- https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/nbu.12656
- OA Status
- hybrid
- Cited By
- 6
- References
- 57
- Related Works
- 10
- OpenAlex ID
- https://openalex.org/W4390232029
All OpenAlex metadata
Raw OpenAlex JSON
- OpenAlex ID
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https://openalex.org/W4390232029Canonical identifier for this work in OpenAlex
- DOI
-
https://doi.org/10.1111/nbu.12656Digital Object Identifier
- Title
-
Association of vitamin D‐binding protein polymorphisms and serum 25(OH)D concentration varies among Chinese healthy infants of different
VDR‐FokI genotypes: A multi‐centre cross‐sectional studyWork title - Type
-
articleOpenAlex work type
- Language
-
enPrimary language
- Publication year
-
2023Year of publication
- Publication date
-
2023-12-26Full publication date if available
- Authors
-
Hing Wai Tsang, Keith T. S. Tung, Rosa S. Wong, Siew Yan Wong, Joanna Yuet‐ling Tung, Gilbert T. Chua, M. Ho, Chi Pui Pang, Wilfred Hing Sang Wong, Gcf Chan, Ian Chi Kei Wong, Patrick IpList of authors in order
- Landing page
-
https://doi.org/10.1111/nbu.12656Publisher landing page
- PDF URL
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https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/nbu.12656Direct link to full text PDF
- Open access
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YesWhether a free full text is available
- OA status
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hybridOpen access status per OpenAlex
- OA URL
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https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/nbu.12656Direct OA link when available
- Concepts
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FokI, Calcitriol receptor, Vitamin D and neurology, Genotype, Vitamin D-binding protein, Internal medicine, Allele, Medicine, Endocrinology, vitamin D deficiency, Polymorphism (computer science), Biology, Genetics, GeneTop concepts (fields/topics) attached by OpenAlex
- Cited by
-
6Total citation count in OpenAlex
- Citations by year (recent)
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2025: 5, 2024: 1Per-year citation counts (last 5 years)
- References (count)
-
57Number of works referenced by this work
- Related works (count)
-
10Other works algorithmically related by OpenAlex
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