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Polymorphisms of vitamin D receptor gene TaqI susceptibility of prostate cancer: a meta-analysis

OBJECTIVE: Many studies have investigated the association of the vitamin D receptor gene TaqI polymorphism with prostate cancer (PCa) risk. However, the evidence is inadequate to draw robust conclusions. To shed light on these inconclusive findings, we conducted a meta-analysis. MATERIALS AND METHOD...

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Autores principales: Fei, Xiawei, Liu, Nannan, Li, Huifeng, Shen, Yanting, Guo, Jianming, Wu, Zhenqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4780196/
https://www.ncbi.nlm.nih.gov/pubmed/27042096
http://dx.doi.org/10.2147/OTT.S99428
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author Fei, Xiawei
Liu, Nannan
Li, Huifeng
Shen, Yanting
Guo, Jianming
Wu, Zhenqi
author_facet Fei, Xiawei
Liu, Nannan
Li, Huifeng
Shen, Yanting
Guo, Jianming
Wu, Zhenqi
author_sort Fei, Xiawei
collection PubMed
description OBJECTIVE: Many studies have investigated the association of the vitamin D receptor gene TaqI polymorphism with prostate cancer (PCa) risk. However, the evidence is inadequate to draw robust conclusions. To shed light on these inconclusive findings, we conducted a meta-analysis. MATERIALS AND METHODS: We searched PubMed for eligible articles. The relevant data were abstracted by two independent reviewers with the Stata 11.0 software. RESULTS: A total of 27 studies were included. The pooled outcomes indicated that the TaqI genetic polymorphisms were significantly associated with the risk of PCa (T vs t allele: odds ratio [OR] =1.11, 95% confidence interval [CI] =1.03–1.21, P=0.008; TT vs tt: OR =1.19, 95% CI =1.01–1.42, P=0.040; TT + Tt vs tt: OR =1.18, 95% CI =1.02–1.38, P=0.031), especially in the Asian population (T vs t allele: OR =1.11, 95% CI =1.03–1.21, P=0.008; TT/Tt vs tt: OR =1.93, 95% CI =1.02–3.66, P=0.043). In the tumor stage stratified analyses, the pooled results showed no significant difference in genetic polymorphisms between the local tumor group and the control group or between the local tumor group and the advanced tumor group. However, the genotypes TT and TT/Tt were significantly higher in the advanced PCa group compared to the control group (T vs t allele: OR =1.20, 95% CI =1.01–1.42, P=0.040; TT vs tt: OR =1.34, 95% CI =1.08–1.67, P=0.009; TT/Tt vs tt: OR =1.28, 95% CI =1.05–1.56, P=0.015). CONCLUSION: The vitamin D receptor gene TaqI allele polymorphism might be associated with a PCa risk, especially in Asians, which might provide new clues for the pathogenesis research and clinical diagnosis of PCa in the future.
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spelling pubmed-47801962016-04-01 Polymorphisms of vitamin D receptor gene TaqI susceptibility of prostate cancer: a meta-analysis Fei, Xiawei Liu, Nannan Li, Huifeng Shen, Yanting Guo, Jianming Wu, Zhenqi Onco Targets Ther Original Research OBJECTIVE: Many studies have investigated the association of the vitamin D receptor gene TaqI polymorphism with prostate cancer (PCa) risk. However, the evidence is inadequate to draw robust conclusions. To shed light on these inconclusive findings, we conducted a meta-analysis. MATERIALS AND METHODS: We searched PubMed for eligible articles. The relevant data were abstracted by two independent reviewers with the Stata 11.0 software. RESULTS: A total of 27 studies were included. The pooled outcomes indicated that the TaqI genetic polymorphisms were significantly associated with the risk of PCa (T vs t allele: odds ratio [OR] =1.11, 95% confidence interval [CI] =1.03–1.21, P=0.008; TT vs tt: OR =1.19, 95% CI =1.01–1.42, P=0.040; TT + Tt vs tt: OR =1.18, 95% CI =1.02–1.38, P=0.031), especially in the Asian population (T vs t allele: OR =1.11, 95% CI =1.03–1.21, P=0.008; TT/Tt vs tt: OR =1.93, 95% CI =1.02–3.66, P=0.043). In the tumor stage stratified analyses, the pooled results showed no significant difference in genetic polymorphisms between the local tumor group and the control group or between the local tumor group and the advanced tumor group. However, the genotypes TT and TT/Tt were significantly higher in the advanced PCa group compared to the control group (T vs t allele: OR =1.20, 95% CI =1.01–1.42, P=0.040; TT vs tt: OR =1.34, 95% CI =1.08–1.67, P=0.009; TT/Tt vs tt: OR =1.28, 95% CI =1.05–1.56, P=0.015). CONCLUSION: The vitamin D receptor gene TaqI allele polymorphism might be associated with a PCa risk, especially in Asians, which might provide new clues for the pathogenesis research and clinical diagnosis of PCa in the future. Dove Medical Press 2016-03-01 /pmc/articles/PMC4780196/ /pubmed/27042096 http://dx.doi.org/10.2147/OTT.S99428 Text en © 2016 Fei et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Fei, Xiawei
Liu, Nannan
Li, Huifeng
Shen, Yanting
Guo, Jianming
Wu, Zhenqi
Polymorphisms of vitamin D receptor gene TaqI susceptibility of prostate cancer: a meta-analysis
title Polymorphisms of vitamin D receptor gene TaqI susceptibility of prostate cancer: a meta-analysis
title_full Polymorphisms of vitamin D receptor gene TaqI susceptibility of prostate cancer: a meta-analysis
title_fullStr Polymorphisms of vitamin D receptor gene TaqI susceptibility of prostate cancer: a meta-analysis
title_full_unstemmed Polymorphisms of vitamin D receptor gene TaqI susceptibility of prostate cancer: a meta-analysis
title_short Polymorphisms of vitamin D receptor gene TaqI susceptibility of prostate cancer: a meta-analysis
title_sort polymorphisms of vitamin d receptor gene taqi susceptibility of prostate cancer: a meta-analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4780196/
https://www.ncbi.nlm.nih.gov/pubmed/27042096
http://dx.doi.org/10.2147/OTT.S99428
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