Association Between VDR FokI Polymorphism and Intervertebral Disk Degeneration
Intervertebral disk degeneration (IDD) is strongly associated with genetic predisposition and environmental susceptibility. Several studies been conducted to investigate the potential association between IDD and FokI polymorphism located in the gene encoding the vitamin D receptor (VDR), and inconsi...
Main Authors: | , , , , |
---|---|
Format: | Online |
Language: | English |
Published: |
Elsevier
2015
|
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4747649/ |
id |
pubmed-4747649 |
---|---|
recordtype |
oai_dc |
spelling |
pubmed-47476492016-03-01 Association Between VDR FokI Polymorphism and Intervertebral Disk Degeneration Zhao, Jian Yang, Mingyuan Shao, Jie Bai, Yushu Li, Ming Letter Intervertebral disk degeneration (IDD) is strongly associated with genetic predisposition and environmental susceptibility. Several studies been conducted to investigate the potential association between IDD and FokI polymorphism located in the gene encoding the vitamin D receptor (VDR), and inconsistent conclusions had been reached among different ethnic populations. In order to assess the association between the FokI polymorphism and the risk of IDD, we performed a comprehensive and systematic meta-analysis. Candidate articles were retrieved from PubMed, EMBASE, China National Knowledge Infrastructure (CNKI), and China Biology Medical (CBM) with strict inclusion criteria in January 2015. Among the 54 articles that were retrieved, only eight studies met the inclusion criteria. The pooled data analysis based on allele contrast, homozygote, heterozygote, dominant, and recessive models revealed no significant correlation between the FokI polymorphism and the risk of IDD. However, when stratified by ethnicity, significant associations were detected for Hispanics based on allele contrast (OR = 1.395, 95% CI = 1.059–1.836, P = 0.018), homozygote (OR = 1.849, 95% CI = 1.001–3.416, P = 0.049), heterozygote (OR = 1.254, 95% CI = 1.049–1.498, P = 0.013), and dominant (OR = 1.742, 95% CI = 1.174–2.583, P = 0.006) models, and for Asians using the dominant model (OR = 1.293, 95% CI = 1.025–1.632, P = 0.030), whereas there is no significant association detected for Caucasians. In conclusion, FokI polymorphism is not generally associated with IDD, but there is increased risk for IDD in Hispanics and Asians carrying FokI allele T. Elsevier 2015-12 2016-01-06 /pmc/articles/PMC4747649/ /pubmed/26772150 http://dx.doi.org/10.1016/j.gpb.2015.11.003 Text en © 2016 The Authors. Production and hosting by Elsevier B.V. on behalf of Beijing Institute of Genomics, Chinese Academy of Sciences and Genetics Society of China. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
repository_type |
Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
building |
NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Zhao, Jian Yang, Mingyuan Shao, Jie Bai, Yushu Li, Ming |
spellingShingle |
Zhao, Jian Yang, Mingyuan Shao, Jie Bai, Yushu Li, Ming Association Between VDR FokI Polymorphism and Intervertebral Disk Degeneration |
author_facet |
Zhao, Jian Yang, Mingyuan Shao, Jie Bai, Yushu Li, Ming |
author_sort |
Zhao, Jian |
title |
Association Between VDR FokI Polymorphism and Intervertebral Disk Degeneration |
title_short |
Association Between VDR FokI Polymorphism and Intervertebral Disk Degeneration |
title_full |
Association Between VDR FokI Polymorphism and Intervertebral Disk Degeneration |
title_fullStr |
Association Between VDR FokI Polymorphism and Intervertebral Disk Degeneration |
title_full_unstemmed |
Association Between VDR FokI Polymorphism and Intervertebral Disk Degeneration |
title_sort |
association between vdr foki polymorphism and intervertebral disk degeneration |
description |
Intervertebral disk degeneration (IDD) is strongly associated with genetic predisposition and environmental susceptibility. Several studies been conducted to investigate the potential association between IDD and FokI polymorphism located in the gene encoding the vitamin D receptor (VDR), and inconsistent conclusions had been reached among different ethnic populations. In order to assess the association between the FokI polymorphism and the risk of IDD, we performed a comprehensive and systematic meta-analysis. Candidate articles were retrieved from PubMed, EMBASE, China National Knowledge Infrastructure (CNKI), and China Biology Medical (CBM) with strict inclusion criteria in January 2015. Among the 54 articles that were retrieved, only eight studies met the inclusion criteria. The pooled data analysis based on allele contrast, homozygote, heterozygote, dominant, and recessive models revealed no significant correlation between the FokI polymorphism and the risk of IDD. However, when stratified by ethnicity, significant associations were detected for Hispanics based on allele contrast (OR = 1.395, 95% CI = 1.059–1.836, P = 0.018), homozygote (OR = 1.849, 95% CI = 1.001–3.416, P = 0.049), heterozygote (OR = 1.254, 95% CI = 1.049–1.498, P = 0.013), and dominant (OR = 1.742, 95% CI = 1.174–2.583, P = 0.006) models, and for Asians using the dominant model (OR = 1.293, 95% CI = 1.025–1.632, P = 0.030), whereas there is no significant association detected for Caucasians. In conclusion, FokI polymorphism is not generally associated with IDD, but there is increased risk for IDD in Hispanics and Asians carrying FokI allele T. |
publisher |
Elsevier |
publishDate |
2015 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4747649/ |
_version_ |
1613536336830005248 |