<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>19(4)</volume><submitter>Lavu V</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>The objectives of this study were to determine the association between single nucleotide polymorphisms (SNPs) in IL1B (-511, +3954), IL1A (-889, +4845), and the variable number of tandem repeats (VNTRs) polymorphism in the IL-1RN gene with chronic periodontitis susceptibility and to analyze gene-gene interactions in a hospital-based sample population from South India.&lt;h4>Subjects and methods&lt;/h4>A total of 400 individuals were recruited for this study; 200 individuals with healthy gingiva and 200 chronic periodontitis patients. Genomic DNA was isolated from peripheral blood samples and genotyping was performed for the above-mentioned single nucleotide and VNTR polymorphisms by polymerase chain reaction, DNA sequencing, and agarose gel electrophoresis.&lt;h4>Results&lt;/h4>A higher proportion of the variant alleles were observed in the chronic periodontitis group for all the SNPs examined. The SNP at +3954 (C>T) in the IL1B gene was found to be significantly associated with chronic periodontitis (p=0.007). VNTR genotypes (χ(2) value: 5.163, df=1, p=0.023) and alleles (χ(2) value: 6.818, df=1, p=0.009) were found to have a significant association with chronic periodontitis susceptibility.&lt;h4>Conclusion&lt;/h4>In the study population examined, the SNP in the IL1B gene (+3954) and VNTR polymorphisms in the IL1RN gene were found to have a significant association with chronic periodontitis susceptibility.</pubmed_abstract><journal>Genetic testing and molecular biomarkers</journal><pagination>175-81</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4394157</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Polymorphic regions in the interleukin-1 gene and susceptibility to chronic periodontitis: a genetic association study.</pubmed_title><pmcid>PMC4394157</pmcid><pubmed_authors>Venkata Kameswara Subrahmanya Lakkakula B</pubmed_authors><pubmed_authors>Venkatesan V</pubmed_authors><pubmed_authors>Paul SF</pubmed_authors><pubmed_authors>Lavu V</pubmed_authors><pubmed_authors>Rao SR</pubmed_authors><pubmed_authors>Venugopal P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Polymorphic regions in the interleukin-1 gene and susceptibility to chronic periodontitis: a genetic association study.</name><description>&lt;h4>Objective&lt;/h4>The objectives of this study were to determine the association between single nucleotide polymorphisms (SNPs) in IL1B (-511, +3954), IL1A (-889, +4845), and the variable number of tandem repeats (VNTRs) polymorphism in the IL-1RN gene with chronic periodontitis susceptibility and to analyze gene-gene interactions in a hospital-based sample population from South India.&lt;h4>Subjects and methods&lt;/h4>A total of 400 individuals were recruited for this study; 200 individuals with healthy gingiva and 200 chronic periodontitis patients. Genomic DNA was isolated from peripheral blood samples and genotyping was performed for the above-mentioned single nucleotide and VNTR polymorphisms by polymerase chain reaction, DNA sequencing, and agarose gel electrophoresis.&lt;h4>Results&lt;/h4>A higher proportion of the variant alleles were observed in the chronic periodontitis group for all the SNPs examined. The SNP at +3954 (C>T) in the IL1B gene was found to be significantly associated with chronic periodontitis (p=0.007). VNTR genotypes (χ(2) value: 5.163, df=1, p=0.023) and alleles (χ(2) value: 6.818, df=1, p=0.009) were found to have a significant association with chronic periodontitis susceptibility.&lt;h4>Conclusion&lt;/h4>In the study population examined, the SNP in the IL1B gene (+3954) and VNTR polymorphisms in the IL1RN gene were found to have a significant association with chronic periodontitis susceptibility.</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Apr</publication><modification>2024-11-13T18:21:09.462Z</modification><creation>2019-03-27T01:49:48Z</creation></dates><accession>S-EPMC4394157</accession><cross_references><pubmed>25710474</pubmed><doi>10.1089/gtmb.2014.0275</doi></cross_references></HashMap>