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Impact of vitamin D binding protein (GC) and vitamin D receptor (VDR) gene polymorphism on the risk of developing preeclampsia

OBJECTIVE: Preeclampsia is a multifactorial disease characterized by high blood pressure and protein in the urine. In this study, we investigated the association of vitamin D binding protein (GC) and vitamin D receptor (VDR) gene polymorphism with the risk of developing preeclampsia. METHODS: 25-hyd...

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Autores principales: Rahman, Md Mostafijur, Nawfal, Tamima, Khabir, Fabliha Afiea, Hosen, Md Bayejid, Washif, Mubasshir, Kabir, Yearul, Howlader, M Zakir Hossain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406621/
https://www.ncbi.nlm.nih.gov/pubmed/37560440
http://dx.doi.org/10.1016/j.bbrep.2023.101526
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author Rahman, Md Mostafijur
Nawfal, Tamima
Khabir, Fabliha Afiea
Hosen, Md Bayejid
Washif, Mubasshir
Kabir, Yearul
Howlader, M Zakir Hossain
author_facet Rahman, Md Mostafijur
Nawfal, Tamima
Khabir, Fabliha Afiea
Hosen, Md Bayejid
Washif, Mubasshir
Kabir, Yearul
Howlader, M Zakir Hossain
author_sort Rahman, Md Mostafijur
collection PubMed
description OBJECTIVE: Preeclampsia is a multifactorial disease characterized by high blood pressure and protein in the urine. In this study, we investigated the association of vitamin D binding protein (GC) and vitamin D receptor (VDR) gene polymorphism with the risk of developing preeclampsia. METHODS: 25-hydroxyvitamin D was measured using High-performance Liquid Chromatography. Vitamin D binding protein and vitamin D receptor gene polymorphisms were determined by polymerase chain reaction-restriction fragment length polymorphism. RESULTS: The control subjects have significant higher level of 25-hydroxyvitamin D (33.5 ± 1.194 ng/mL) relative to patients (23.97 ± 1.604 ng/mL) (p < 0.05). Vitamin D receptor rs1544410 and rs2228570 dominant model (GA + AA; TC + CC) showed significant higher risk of developing Preeclampsia (OR = 4.11, 95% CI = 0.62–27.09, p < 0.01; OR = 3.58, 95%CI = 0.78–16.38, p < 0.001 respectively). Similarly, vitamin D binding protein rs7041 and rs4588, dominant model (TG + GG; CA + AA) showed higher risk of preeclampsia development compared to control people (OR = 1.69, 95%CI = 0.35–8.19, p < 0.05; OR = 1.06, 95%CI = 0.25–4.44, p < 0.05 respectively). AA genotype of rs4588 of GC gene was significantly associated with 25-hydroxyvitamin D level in serum relative to CC and CA (p < 0.05). CONCLUSION: From our study, we can conclude that a low level of 25-hydroxyvitamin D, GC (rs1544410 and rs2228570), and VDR (rs4588 and rs7041) gene polymorphism is linked with an increased risk of developing preeclampsia.
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spelling pubmed-104066212023-08-09 Impact of vitamin D binding protein (GC) and vitamin D receptor (VDR) gene polymorphism on the risk of developing preeclampsia Rahman, Md Mostafijur Nawfal, Tamima Khabir, Fabliha Afiea Hosen, Md Bayejid Washif, Mubasshir Kabir, Yearul Howlader, M Zakir Hossain Biochem Biophys Rep Research Article OBJECTIVE: Preeclampsia is a multifactorial disease characterized by high blood pressure and protein in the urine. In this study, we investigated the association of vitamin D binding protein (GC) and vitamin D receptor (VDR) gene polymorphism with the risk of developing preeclampsia. METHODS: 25-hydroxyvitamin D was measured using High-performance Liquid Chromatography. Vitamin D binding protein and vitamin D receptor gene polymorphisms were determined by polymerase chain reaction-restriction fragment length polymorphism. RESULTS: The control subjects have significant higher level of 25-hydroxyvitamin D (33.5 ± 1.194 ng/mL) relative to patients (23.97 ± 1.604 ng/mL) (p < 0.05). Vitamin D receptor rs1544410 and rs2228570 dominant model (GA + AA; TC + CC) showed significant higher risk of developing Preeclampsia (OR = 4.11, 95% CI = 0.62–27.09, p < 0.01; OR = 3.58, 95%CI = 0.78–16.38, p < 0.001 respectively). Similarly, vitamin D binding protein rs7041 and rs4588, dominant model (TG + GG; CA + AA) showed higher risk of preeclampsia development compared to control people (OR = 1.69, 95%CI = 0.35–8.19, p < 0.05; OR = 1.06, 95%CI = 0.25–4.44, p < 0.05 respectively). AA genotype of rs4588 of GC gene was significantly associated with 25-hydroxyvitamin D level in serum relative to CC and CA (p < 0.05). CONCLUSION: From our study, we can conclude that a low level of 25-hydroxyvitamin D, GC (rs1544410 and rs2228570), and VDR (rs4588 and rs7041) gene polymorphism is linked with an increased risk of developing preeclampsia. Elsevier 2023-08-04 /pmc/articles/PMC10406621/ /pubmed/37560440 http://dx.doi.org/10.1016/j.bbrep.2023.101526 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Rahman, Md Mostafijur
Nawfal, Tamima
Khabir, Fabliha Afiea
Hosen, Md Bayejid
Washif, Mubasshir
Kabir, Yearul
Howlader, M Zakir Hossain
Impact of vitamin D binding protein (GC) and vitamin D receptor (VDR) gene polymorphism on the risk of developing preeclampsia
title Impact of vitamin D binding protein (GC) and vitamin D receptor (VDR) gene polymorphism on the risk of developing preeclampsia
title_full Impact of vitamin D binding protein (GC) and vitamin D receptor (VDR) gene polymorphism on the risk of developing preeclampsia
title_fullStr Impact of vitamin D binding protein (GC) and vitamin D receptor (VDR) gene polymorphism on the risk of developing preeclampsia
title_full_unstemmed Impact of vitamin D binding protein (GC) and vitamin D receptor (VDR) gene polymorphism on the risk of developing preeclampsia
title_short Impact of vitamin D binding protein (GC) and vitamin D receptor (VDR) gene polymorphism on the risk of developing preeclampsia
title_sort impact of vitamin d binding protein (gc) and vitamin d receptor (vdr) gene polymorphism on the risk of developing preeclampsia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406621/
https://www.ncbi.nlm.nih.gov/pubmed/37560440
http://dx.doi.org/10.1016/j.bbrep.2023.101526
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