Cargando…

Lack of association between the risk of prostate cancer and vitamin D receptor Bsm I polymorphism: a meta-analysis of 27 published studies

BACKGROUND: The association between vitamin D receptor gene Bsm I (rs1544410) polymorphism and prostate cancer (PCa) risk has been investigated by numerous previous studies, which yielded inconsistent results. We conducted this meta-analysis to derive a relatively precise description of this associa...

Descripción completa

Detalles Bibliográficos
Autores principales: Kang, Shaosan, Zhao, Yansheng, Wang, Lei, Liu, Jian, Chen, Xi, Liu, Xiaofeng, Shi, Zhijie, Gao, Weixing, Cao, Fenghong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078094/
https://www.ncbi.nlm.nih.gov/pubmed/30122987
http://dx.doi.org/10.2147/CMAR.S171305
_version_ 1783345035699290112
author Kang, Shaosan
Zhao, Yansheng
Wang, Lei
Liu, Jian
Chen, Xi
Liu, Xiaofeng
Shi, Zhijie
Gao, Weixing
Cao, Fenghong
author_facet Kang, Shaosan
Zhao, Yansheng
Wang, Lei
Liu, Jian
Chen, Xi
Liu, Xiaofeng
Shi, Zhijie
Gao, Weixing
Cao, Fenghong
author_sort Kang, Shaosan
collection PubMed
description BACKGROUND: The association between vitamin D receptor gene Bsm I (rs1544410) polymorphism and prostate cancer (PCa) risk has been investigated by numerous previous studies, which yielded inconsistent results. We conducted this meta-analysis to derive a relatively precise description of this association. METHODS: All studies published up to December 2017 were identified via a systematic search of PubMed, Embase, and China National Knowledge Infrastructure databases. Pooled odds ratios (ORs) with their 95% confidence intervals (CIs) were estimated to describe the strength of the relationship between Bsm I and PCa risk. RESULTS: In this meta-analysis, 27 studies with 9,993 cases and 9,345 controls were included. The pooled results revealed that Bsm I polymorphism was not associated with PCa risk in the overall analysis. Moreover, no significant relationship was found in the subgroup analyses by ethnicities, genotyping methods, Hardy–Weinberg equilibrium status, and Gleason score. In the stratified analysis by the source of controls and clinical stages, controls of benign prostatic hyperplasia (BPH) seemed to be in the particular groups in which the association of PCa risk with Bsm I polymorphism was significant (Bb vs. bb: OR=0.643, 95% CI=0.436–0.949, p=0.026; BB/Bb vs. bb: OR=0.627, 95% CI=0.411–0.954, p=0.029; B vs. b: OR=0.715, 95% CI=0.530–0.965, p=0.029). CONCLUSION: Our results suggest that Bsm I polymorphism is weakly associated with PCa risk, and hence, it cannot be considered as a predictor of the occurrence and development of PCa in clinical practice. Future studies with a larger number of samples are needed to verify our results.
format Online
Article
Text
id pubmed-6078094
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Dove Medical Press
record_format MEDLINE/PubMed
spelling pubmed-60780942018-08-17 Lack of association between the risk of prostate cancer and vitamin D receptor Bsm I polymorphism: a meta-analysis of 27 published studies Kang, Shaosan Zhao, Yansheng Wang, Lei Liu, Jian Chen, Xi Liu, Xiaofeng Shi, Zhijie Gao, Weixing Cao, Fenghong Cancer Manag Res Original Research BACKGROUND: The association between vitamin D receptor gene Bsm I (rs1544410) polymorphism and prostate cancer (PCa) risk has been investigated by numerous previous studies, which yielded inconsistent results. We conducted this meta-analysis to derive a relatively precise description of this association. METHODS: All studies published up to December 2017 were identified via a systematic search of PubMed, Embase, and China National Knowledge Infrastructure databases. Pooled odds ratios (ORs) with their 95% confidence intervals (CIs) were estimated to describe the strength of the relationship between Bsm I and PCa risk. RESULTS: In this meta-analysis, 27 studies with 9,993 cases and 9,345 controls were included. The pooled results revealed that Bsm I polymorphism was not associated with PCa risk in the overall analysis. Moreover, no significant relationship was found in the subgroup analyses by ethnicities, genotyping methods, Hardy–Weinberg equilibrium status, and Gleason score. In the stratified analysis by the source of controls and clinical stages, controls of benign prostatic hyperplasia (BPH) seemed to be in the particular groups in which the association of PCa risk with Bsm I polymorphism was significant (Bb vs. bb: OR=0.643, 95% CI=0.436–0.949, p=0.026; BB/Bb vs. bb: OR=0.627, 95% CI=0.411–0.954, p=0.029; B vs. b: OR=0.715, 95% CI=0.530–0.965, p=0.029). CONCLUSION: Our results suggest that Bsm I polymorphism is weakly associated with PCa risk, and hence, it cannot be considered as a predictor of the occurrence and development of PCa in clinical practice. Future studies with a larger number of samples are needed to verify our results. Dove Medical Press 2018-08-01 /pmc/articles/PMC6078094/ /pubmed/30122987 http://dx.doi.org/10.2147/CMAR.S171305 Text en © 2018 Kang 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
Kang, Shaosan
Zhao, Yansheng
Wang, Lei
Liu, Jian
Chen, Xi
Liu, Xiaofeng
Shi, Zhijie
Gao, Weixing
Cao, Fenghong
Lack of association between the risk of prostate cancer and vitamin D receptor Bsm I polymorphism: a meta-analysis of 27 published studies
title Lack of association between the risk of prostate cancer and vitamin D receptor Bsm I polymorphism: a meta-analysis of 27 published studies
title_full Lack of association between the risk of prostate cancer and vitamin D receptor Bsm I polymorphism: a meta-analysis of 27 published studies
title_fullStr Lack of association between the risk of prostate cancer and vitamin D receptor Bsm I polymorphism: a meta-analysis of 27 published studies
title_full_unstemmed Lack of association between the risk of prostate cancer and vitamin D receptor Bsm I polymorphism: a meta-analysis of 27 published studies
title_short Lack of association between the risk of prostate cancer and vitamin D receptor Bsm I polymorphism: a meta-analysis of 27 published studies
title_sort lack of association between the risk of prostate cancer and vitamin d receptor bsm i polymorphism: a meta-analysis of 27 published studies
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078094/
https://www.ncbi.nlm.nih.gov/pubmed/30122987
http://dx.doi.org/10.2147/CMAR.S171305
work_keys_str_mv AT kangshaosan lackofassociationbetweentheriskofprostatecancerandvitamindreceptorbsmipolymorphismametaanalysisof27publishedstudies
AT zhaoyansheng lackofassociationbetweentheriskofprostatecancerandvitamindreceptorbsmipolymorphismametaanalysisof27publishedstudies
AT wanglei lackofassociationbetweentheriskofprostatecancerandvitamindreceptorbsmipolymorphismametaanalysisof27publishedstudies
AT liujian lackofassociationbetweentheriskofprostatecancerandvitamindreceptorbsmipolymorphismametaanalysisof27publishedstudies
AT chenxi lackofassociationbetweentheriskofprostatecancerandvitamindreceptorbsmipolymorphismametaanalysisof27publishedstudies
AT liuxiaofeng lackofassociationbetweentheriskofprostatecancerandvitamindreceptorbsmipolymorphismametaanalysisof27publishedstudies
AT shizhijie lackofassociationbetweentheriskofprostatecancerandvitamindreceptorbsmipolymorphismametaanalysisof27publishedstudies
AT gaoweixing lackofassociationbetweentheriskofprostatecancerandvitamindreceptorbsmipolymorphismametaanalysisof27publishedstudies
AT caofenghong lackofassociationbetweentheriskofprostatecancerandvitamindreceptorbsmipolymorphismametaanalysisof27publishedstudies