2009
DOI: 10.1902/jop.2009.080465
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Association Between Vitamin D Receptor Gene Polymorphisms and Severe Chronic Periodontitis in a Chinese Population

Abstract: TaqI SNP of VDR gene might be associated with severe CP in Chinese patients.

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Cited by 46 publications
(45 citation statements)
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References 36 publications
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“…In particular, the TT genotype and the presence of T allele are associated with chronic periodontal disease in Japanese, Chinese and Caucasian subjects (23)(24)(25)(26)(27). This data is also in accordance with our previous study which showed a strong correlation between TT genotype of Italian subjects and chronic periodontitis (OR 3.59) but also with aggressive periodontal disease (28).…”
Section: Taqisupporting
confidence: 92%
“…In particular, the TT genotype and the presence of T allele are associated with chronic periodontal disease in Japanese, Chinese and Caucasian subjects (23)(24)(25)(26)(27). This data is also in accordance with our previous study which showed a strong correlation between TT genotype of Italian subjects and chronic periodontitis (OR 3.59) but also with aggressive periodontal disease (28).…”
Section: Taqisupporting
confidence: 92%
“…Hennig et al (1999) concluded that carriage of the less frequent t allele in VDR was associated with an increased risk for localized, but not generalized, disease. Sun et al (2002) and Tachi et al (2001) found that the VDR TaqI Tt genotype and the t allele may be a risk factor for aggressive periodontitis in Chinese patients, while the opposite genotype and allele were found to be associated with severe CP (Wang et al, 2009a). These evidences were consistent with our findings, which indicated that the association between VDR TaqI variants and periodontitis might be due to not only the ethnic background, regions, and sample size, but also the difference in mechanisms between CP and AP.…”
Section: Discussionsupporting
confidence: 88%
“…After screening the titles and abstracts, 48 articles were excluded according to the exclusion criteria outlined earlier. Of the 15 potentially relevant articles (Tachi et al, 2001;Ma, 2002;Sun et al, 2002;Li et al, 2008;Wang, 2009;Yang et al, 2009;Zhang et al, 2005Zhang et al, , 2010Zhang et al, , 2011Shao, 2013;Wang et al, 2009aWang et al, ,b, 2013Cao et al, 2015;Wu et al, 2015) identified for full study retrieval, five studies (Tachi et al, 2001;Ma, 2002;Wang, 2009;Wang et al, 2009b;Yang et al, 2009) were excluded due to duplication; two studies were excluded due to lack of controls or genotype data (Wang et al, 2013;Cao et al, 2015). Finally, eight articles (including 9 case-control studies) (Sun et al, 2002;Li et al, 2008;Wang et al, 2009a;Zhang et al, 2005Zhang et al, , 2010Zhang et al, , 2011Shao, 2013;Wu et al, 2015) met the inclusion criteria.…”
Section: Discussionmentioning
confidence: 99%
“…An Abf haplotype containing rs2228570 has been reported to confer an elevated risk of severe CP in Japanese men (Naito et al, 2007), while several other studies found no significant association between rs2228570 and CP susceptibility (Tachi et al, 2003;Wang et al, 2009;Chen et al, 2012;Tanaka et al, 2013). No significant association was found in a previous meta-analysis of 15 studies including 1338 cases and 1302 controls between rs2228570 and CP (Chen et al, 2012).…”
Section: Discussionmentioning
confidence: 91%