Associations of vitamin D binding protein variants with the vitamin D-induced increase in serum 25-hydroxyvitamin D.
Clin Nutr ESPEN. 2019 Feb;29:59-64. doi: 10.1016/j.clnesp.2018.12.005. Epub 2018 Dec 28.
Mehramiz M1, Khayyatzadeh SS2, Esmaily H3, Ghasemi F4, Sadeghi-Ardekani K4, Tayefi M4, Mirmousavi SJ5, Hanachi P6, Bahrami-Taghanaki H7, Eslami S8, Vatanparast H9, Ferns GA10, Ghayour-Mobarhan M11, Avan A12.
178 items in Vitamin D Binding Protein category
See also Vitamin D Receptor. Genetics
- Obesity might be related to Vitamin D genes – July 2018
- Response to Vitamin D varies with Vitamin D Binding Protein gene – RCT May 2018
- 10 reasons for poor response to Vitamin D (race, binding protein, etc.) – Nov 2017
Note: A poor VDBP is not detectable by Vitamin D Tests
Download the PDF from Sci-Hub via VitaminDWiki
BACKGROUND:
Vitamin D deficiency is a global problem that may be improved by vitamin D supplementation; however, the individual's response to the intervention varies. We aimed to investigate possible genetic factors that may modify the impact of environmental exposure on vitamin D status. The candidate gene variant we investigated was the Gc gene-rs4588 polymorphism at the vitamin D receptor (DBP) locus.
METHODS:
A total of 619 healthy adolescent Iranian girls received 50000 IU of vitamin D3 weekly for 9 weeks. Serum 25(OH) D concentrations, metabolic profiles and dietary intake were measured at baseline and after 9 weeks of supplementation. The genotypes of the DBP variant (rs4588) were analyzed using the TaqMan genotyping assay.
RESULTS:
Our results revealed that the rs4588 polymorphism might be associated with serum 25-hydroxy vitamin D both at baseline (p value = 0.03) and after intervention (p value = 0.008). It seemed that the outcome of the intervention was gene-related so that the subjects with common AA genotype were a better responder to vitamin D supplementation (Changes (%) 469.5 (427.1) in AA carriers vs. 335.8 (530) in GG holders), and carriers of the less common GG genotype experienced a rise in fasting blood glucose after 9 weeks (Changes (%) 0 (1.5)). Our findings also showed that the statistical interaction between this variant and supplementation was statistically significant (intervention effect p-value<0.001 and p-value SNP effect = 0.03). The regression model also revealed that after adjusted for potential confounders, likelihood of affecting serum 25(OH)D in individuals who were homozygous for the uncommon allele G was less than those homozygous for the more common AA genotype (OR = 4.407 (1.82-8.89); p = 0.001).
CONCLUSION:
Serum vitamin 25(OH) D following vitamin 25(OH) D3 supplementation appears to be modified by genetic background. The Gc genetic variant, rs4588 encoding the vitamin D receptor seems to influence the response to vitamin D supplementation.
Poor Vitamin D binding had 30 percent less response to Vitamin D (50,000 IU weekly) – Feb 2019
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See also Vitamin D Receptor. Genetics
- Obesity might be related to Vitamin D genes – July 2018
- Response to Vitamin D varies with Vitamin D Binding Protein gene – RCT May 2018
- 10 reasons for poor response to Vitamin D (race, binding protein, etc.) – Nov 2017
Note: A poor VDBP is not detectable by Vitamin D Tests
Download the PDF from Sci-Hub via VitaminDWiki
BACKGROUND:
Vitamin D deficiency is a global problem that may be improved by vitamin D supplementation; however, the individual's response to the intervention varies. We aimed to investigate possible genetic factors that may modify the impact of environmental exposure on vitamin D status. The candidate gene variant we investigated was the Gc gene-rs4588 polymorphism at the vitamin D receptor (DBP) locus.
METHODS:
A total of 619 healthy adolescent Iranian girls received 50000 IU of vitamin D3 weekly for 9 weeks. Serum 25(OH) D concentrations, metabolic profiles and dietary intake were measured at baseline and after 9 weeks of supplementation. The genotypes of the DBP variant (rs4588) were analyzed using the TaqMan genotyping assay.
RESULTS:
Our results revealed that the rs4588 polymorphism might be associated with serum 25-hydroxy vitamin D both at baseline (p value = 0.03) and after intervention (p value = 0.008). It seemed that the outcome of the intervention was gene-related so that the subjects with common AA genotype were a better responder to vitamin D supplementation (Changes (%) 469.5 (427.1) in AA carriers vs. 335.8 (530) in GG holders), and carriers of the less common GG genotype experienced a rise in fasting blood glucose after 9 weeks (Changes (%) 0 (1.5)). Our findings also showed that the statistical interaction between this variant and supplementation was statistically significant (intervention effect p-value<0.001 and p-value SNP effect = 0.03). The regression model also revealed that after adjusted for potential confounders, likelihood of affecting serum 25(OH)D in individuals who were homozygous for the uncommon allele G was less than those homozygous for the more common AA genotype (OR = 4.407 (1.82-8.89); p = 0.001).
CONCLUSION:
Serum vitamin 25(OH) D following vitamin 25(OH) D3 supplementation appears to be modified by genetic background. The Gc genetic variant, rs4588 encoding the vitamin D receptor seems to influence the response to vitamin D supplementation.
| 5340 visitors, last modified 04 Feb, 2019, |