Effects of <i>VDBP</i> rs4588 and rs7041 gene polymorphism on vitamin D status in obese individuals

Vitamin D plays a major role in bone metabolism regulating body phosphorus and calcium metabolism. Vitamin D binding protein (VDBP) binds to vitamin D metabolites and transports them to target tissues. It is hypothesized that polymorphisms in VDBP affect the absorption of vitamin D in the body. However, the relationship between VDBP polymorphisms and vitamin D levels in individuals with obesity has yet to be sufficiently investigated. This work aimed to identify the relationship between vitamin D [25(OH)D3] blood levels in obese and non-obese individuals and the rs4588 and rs7041 polymorphisms in VDBP. The study included a total of 80 participants from the Kaliningrad region. The sample was stratified based on vitamin D status (normal, insufficiency, deficiency, and acute deficiency) and body mass index (BMI). Vitamin D blood levels were determined using enzyme immunoassay. Genomic DNA was extracted from whole blood samples. VDBP polymorphisms were identified using HaeIII and ErhI restriction endonucleases. No significant differences in vitamin D blood levels between obese and non-obese individuals were revealed. The rs4588 C A genotypes were associated with no significant differences in vitamin D levels between individuals with different body mass index (CC, p=0.147; CA, p=0.646; AA, insufficient data). However, for the VDBP rs4588 polymorphism, a significant difference was demonstrated in allele frequency between the groups with different vitamin D levels, i.e., normal vitamin D level group vs. insufficiency group (p=0.009) and normal vitamin D level group vs. acute deficiency group (p 0.0001). The analysis of the individuals with the VDBP rs7041 T G polymorphism demonstrated that there were no significant differences in the vitamin D levels between the BMI groups with specific genotypes (TG, p=0.502; GG, p=0.283; TT, insufficient data). However, the control and acute deficiency groups differed significantly (p 0.0001) in allele frequencies of individuals with the rs7041 polymorphism. Vitamin D blood levels in obese patients were comparable to those of non-obese individuals. VDBP rs7041 and rs4588 polymorphisms do not correlate with variations in vitamin D blood levels among individuals with different BMI. However, the VDBP rs4588 A polymorphism is associated with low vitamin D levels, while the VDBP rs4588 G polymorphism is more common among individuals with normal vitamin D blood levels.

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Journal
Cytokines and inflammation
Published
2024-11-19
DOI
https://doi.org/10.17816/ci634869
Citations
1
Primary Topic
Vitamin D Research Studies
Type
article
Field-Weighted Citation Impact
0.42
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article

Effects of VDBP rs4588 and rs7041 gene polymorphism on vitamin D status in obese individuals

Maria Vulf, Н. Д. Газатова, Л. С. Литвинова, Maria Bograya et al.
1 citations
Cytokines and inflammation
Vitamin D Research Studies
0.42
article

Effects of VDBP rs4588 and rs7041 gene polymorphism on vitamin D status in obese individuals

Maria Vulf, Н. Д. Газатова, Л. С. Литвинова, Maria Bograya, Л. В. Михайлова, Dimitri Vladimirovich Paskidov, Varvara Alekseevna Shnar
article en
1 citations

Abstract

Vitamin D plays a major role in bone metabolism regulating body phosphorus and calcium metabolism. Vitamin D binding protein (VDBP) binds to vitamin D metabolites and transports them to target tissues. It is hypothesized that polymorphisms in VDBP affect the absorption of vitamin D in the body. However, the relationship between VDBP polymorphisms and vitamin D levels in individuals with obesity has yet to be sufficiently investigated. This work aimed to identify the relationship between vitamin D [25(OH)D3] blood levels in obese and non-obese individuals and the rs4588 and rs7041 polymorphisms in VDBP. The study included a total of 80 participants from the Kaliningrad region. The sample was stratified based on vitamin D status (normal, insufficiency, deficiency, and acute deficiency) and body mass index (BMI). Vitamin D blood levels were determined using enzyme immunoassay. Genomic DNA was extracted from whole blood samples. VDBP polymorphisms were identified using HaeIII and ErhI restriction endonucleases. No significant differences in vitamin D blood levels between obese and non-obese individuals were revealed. The rs4588 C A genotypes were associated with no significant differences in vitamin D levels between individuals with different body mass index (CC, p=0.147; CA, p=0.646; AA, insufficient data). However, for the VDBP rs4588 polymorphism, a significant difference was demonstrated in allele frequency between the groups with different vitamin D levels, i.e., normal vitamin D level group vs. insufficiency group (p=0.009) and normal vitamin D level group vs. acute deficiency group (p 0.0001). The analysis of the individuals with the VDBP rs7041 T G polymorphism demonstrated that there were no significant differences in the vitamin D levels between the BMI groups with specific genotypes (TG, p=0.502; GG, p=0.283; TT, insufficient data). However, the control and acute deficiency groups differed significantly (p 0.0001) in allele frequencies of individuals with the rs7041 polymorphism. Vitamin D blood levels in obese patients were comparable to those of non-obese individuals. VDBP rs7041 and rs4588 polymorphisms do not correlate with variations in vitamin D blood levels among individuals with different BMI. However, the VDBP rs4588 A polymorphism is associated with low vitamin D levels, while the VDBP rs4588 G polymorphism is more common among individuals with normal vitamin D blood levels.

Cytokines and inflammationVol. 21(1)
Immanuel Kant Baltic Federal University (RU)
Openalex Percentile: Top 33%
Vitamin D Research Studies
0.42
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