Literature DB >> 29541461

Association analysis of FAS-670A/G and FASL-844C/T polymorphisms with risk of generalized aggressive periodontitis disease.

Rezvan Asgari1, Kheirollah Yari1,2, Kamran Mansouri1, Mitra Bakhtiari3.   

Abstract

The interaction of FAS/FAS ligand (FASL) serves an important role in the upregulation of apoptotic processes through different mechanisms in cells. Previous studies have established that the polymorphisms FAS-670A/G and FASL-844C/T are associated with risk of generalized aggressive periodontitis (GAP) in different ethnic populations. Therefore, in the present study, it was investigated for the first time whether FAS-670A/G and FASL-844C/T polymorphisms were associated with risk of GAP in Iran. This case-control study performed the polymerase chain reaction-restriction fragment length polymorphism method in 25 patients with GAP and 110 normal subjects as controls. The results indicated that there was no significant difference in FAS-670A/G genotype frequency between the GAP and control groups. A higher frequency of the combined genotype (AG+GG) was observed in the GAP patients (96.0%) compared with the control subjects (90.9%), though this was not significant [χ2=0.705, degrees of freedom (df)=1, P=0.401]. Similarly, the prevalence of the G allele was non-significantly higher in the GAP group (62.0%) compared with that in the controls (60.0%; χ2=0.012, df=1, P=0.913). For FASL-844C/T polymorphism, the frequency of the combined genotype (CT+TT) was higher in the GAP group (96.0%) when compared with the control subjects (91.8%); however its association was not statistically significant (χ2=0.519, df=1, P=0.471). The frequency of the T allele only marginally differed between the groups, being 60.0% in the GAP group and 50.9% in the controls (χ2=3.627, df=1, P=0.057). These results indicated that there were no significant associations between the FAS-670A/G and FASL-844C/T polymorphisms and the risk of disease in GAP patients when compared with normal individuals.

Entities:  

Keywords:  FAS-670A/G; FASL-844C/T; Iranian population; aggressive periodontitis; polymorphism

Year:  2018        PMID: 29541461      PMCID: PMC5838290          DOI: 10.3892/br.2018.1060

Source DB:  PubMed          Journal:  Biomed Rep        ISSN: 2049-9434


  31 in total

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Authors:  Q R Huang; D Morris; N Manolios
Journal:  Mol Immunol       Date:  1997-06       Impact factor: 4.407

5.  Apoptosis is increased in a model of diabetes-impaired wound healing in genetically diabetic mice.

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Journal:  J Immunol       Date:  2003-01-01       Impact factor: 5.422

9.  Association between FAS polymorphism and prostate cancer development.

Authors:  L Lima; A Morais; F Lobo; F M Calais-da-Silva; F E Calais-da-Silva; R Medeiros
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10.  Posttranslational regulation of Fas ligand function.

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