SAT-021 Efficacy of Vitamin D Supplementation According to Vitamin D Binding Protein Polymorphisms

The study aimed to determine the influence of DBP gene polymorphisms in vitamin D metabolites before and after vitamin D supplementation. Out of 234 participants (126 females and 108 males), 146 had vitamin D deficiency (25(OH)D

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Veröffentlicht in:Journal of the Endocrine Society 2019-04, Vol.3 (Supplement_1)
Hauptverfasser: Al-Daghri, Nasser, Bukhari, Ihtisham, Rikli, Maryam, Abdi, Saba, Ansari, Mohammed, Abdulkhader, Mohammed, Sabico, Shaun, Hussain, Syed Danish, Alenad, Amal, Al-Saleh, Yousef, Alokail, Majed
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container_issue Supplement_1
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container_title Journal of the Endocrine Society
container_volume 3
creator Al-Daghri, Nasser
Bukhari, Ihtisham
Rikli, Maryam
Abdi, Saba
Ansari, Mohammed
Abdulkhader, Mohammed
Sabico, Shaun
Hussain, Syed Danish
Alenad, Amal
Al-Saleh, Yousef
Alokail, Majed
description The study aimed to determine the influence of DBP gene polymorphisms in vitamin D metabolites before and after vitamin D supplementation. Out of 234 participants (126 females and 108 males), 146 had vitamin D deficiency (25(OH)D
doi_str_mv 10.1210/js.2019-SAT-021
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Out of 234 participants (126 females and 108 males), 146 had vitamin D deficiency (25(OH)D &lt;50nmol/l) and were given 2000IU daily dose of vitamin D for 12 months. Two common single nucleotide polymorphisms (SNPs), (rs4588 and rs7041) of the DBP gene were assessed. Post supplementation median 25(OH)D was significantly higher [61.2 (46.3-76.8) and 66.6 (53.2-83.7)] in participants with CC genotype of rs4588 and GG genotype of rs7041 than other genotypes (p&lt;0.001). Participants with T allele are 2.9 (1.9-4.5) times more likely to be a non-responder (unable to achieve serum 25(OH)D post-supplementation) than those with G allele (p&lt;0.001). Participants with A allele are 3.7 (2.1-6.6) times more likely to be a non-responder than those with C allele (p&lt;0.001). Furthermore, participants with TT and TG are 6.2 and 4.2 times more likely to be a non-responder than those with the GG genotype (p-values &lt;0.001) even after adjustments for age, gender, BMI, baseline 25(OH)D concentration and other alleles. Participants with AA and CA genotypes are 12.4 (1.4-110) and 4.1 (2.1-8.0) times more likely to be non-responders as compared to those with CC genotype but lost significance after adjustment. The SNPs, rs7041 and rs4588 variants of the DBP gene are associated with baseline 25(OH)D levels and modifies 25(OH)D response after vitamin D supplementation in Saudi adults.</description><identifier>ISSN: 2472-1972</identifier><identifier>EISSN: 2472-1972</identifier><identifier>DOI: 10.1210/js.2019-SAT-021</identifier><language>eng</language><publisher>Washington, DC: Endocrine Society</publisher><subject>Steroid Hormones and Receptors</subject><ispartof>Journal of the Endocrine Society, 2019-04, Vol.3 (Supplement_1)</ispartof><rights>Copyright © 2019 Endocrine Society 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1821-55c2ccfaa5afe3089b151b961b8a6ec263a72e85a1b727585209b768e6c5a3153</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6552145/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6552145/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,53791,53793</link.rule.ids></links><search><creatorcontrib>Al-Daghri, Nasser</creatorcontrib><creatorcontrib>Bukhari, Ihtisham</creatorcontrib><creatorcontrib>Rikli, Maryam</creatorcontrib><creatorcontrib>Abdi, Saba</creatorcontrib><creatorcontrib>Ansari, Mohammed</creatorcontrib><creatorcontrib>Abdulkhader, Mohammed</creatorcontrib><creatorcontrib>Sabico, Shaun</creatorcontrib><creatorcontrib>Hussain, Syed Danish</creatorcontrib><creatorcontrib>Alenad, Amal</creatorcontrib><creatorcontrib>Al-Saleh, Yousef</creatorcontrib><creatorcontrib>Alokail, Majed</creatorcontrib><title>SAT-021 Efficacy of Vitamin D Supplementation According to Vitamin D Binding Protein Polymorphisms</title><title>Journal of the Endocrine Society</title><description>The study aimed to determine the influence of DBP gene polymorphisms in vitamin D metabolites before and after vitamin D supplementation. Out of 234 participants (126 females and 108 males), 146 had vitamin D deficiency (25(OH)D &lt;50nmol/l) and were given 2000IU daily dose of vitamin D for 12 months. Two common single nucleotide polymorphisms (SNPs), (rs4588 and rs7041) of the DBP gene were assessed. Post supplementation median 25(OH)D was significantly higher [61.2 (46.3-76.8) and 66.6 (53.2-83.7)] in participants with CC genotype of rs4588 and GG genotype of rs7041 than other genotypes (p&lt;0.001). Participants with T allele are 2.9 (1.9-4.5) times more likely to be a non-responder (unable to achieve serum 25(OH)D post-supplementation) than those with G allele (p&lt;0.001). Participants with A allele are 3.7 (2.1-6.6) times more likely to be a non-responder than those with C allele (p&lt;0.001). Furthermore, participants with TT and TG are 6.2 and 4.2 times more likely to be a non-responder than those with the GG genotype (p-values &lt;0.001) even after adjustments for age, gender, BMI, baseline 25(OH)D concentration and other alleles. Participants with AA and CA genotypes are 12.4 (1.4-110) and 4.1 (2.1-8.0) times more likely to be non-responders as compared to those with CC genotype but lost significance after adjustment. 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Out of 234 participants (126 females and 108 males), 146 had vitamin D deficiency (25(OH)D &lt;50nmol/l) and were given 2000IU daily dose of vitamin D for 12 months. Two common single nucleotide polymorphisms (SNPs), (rs4588 and rs7041) of the DBP gene were assessed. Post supplementation median 25(OH)D was significantly higher [61.2 (46.3-76.8) and 66.6 (53.2-83.7)] in participants with CC genotype of rs4588 and GG genotype of rs7041 than other genotypes (p&lt;0.001). Participants with T allele are 2.9 (1.9-4.5) times more likely to be a non-responder (unable to achieve serum 25(OH)D post-supplementation) than those with G allele (p&lt;0.001). Participants with A allele are 3.7 (2.1-6.6) times more likely to be a non-responder than those with C allele (p&lt;0.001). Furthermore, participants with TT and TG are 6.2 and 4.2 times more likely to be a non-responder than those with the GG genotype (p-values &lt;0.001) even after adjustments for age, gender, BMI, baseline 25(OH)D concentration and other alleles. Participants with AA and CA genotypes are 12.4 (1.4-110) and 4.1 (2.1-8.0) times more likely to be non-responders as compared to those with CC genotype but lost significance after adjustment. The SNPs, rs7041 and rs4588 variants of the DBP gene are associated with baseline 25(OH)D levels and modifies 25(OH)D response after vitamin D supplementation in Saudi adults.</abstract><cop>Washington, DC</cop><pub>Endocrine Society</pub><doi>10.1210/js.2019-SAT-021</doi><oa>free_for_read</oa></addata></record>
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subjects Steroid Hormones and Receptors
title SAT-021 Efficacy of Vitamin D Supplementation According to Vitamin D Binding Protein Polymorphisms
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