A longitudinal study of interleukin-1 gene polymorphisms and periodontal disease in a general adult population
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作者:
Cullinan, MP
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Univ Queensland, Sch Dent, Oral Care Res Programme, Brisbane, Qld 4072, AustraliaUniv Queensland, Sch Dent, Oral Care Res Programme, Brisbane, Qld 4072, Australia
Cullinan, MP
[1
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Westerman, B
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机构:Univ Queensland, Sch Dent, Oral Care Res Programme, Brisbane, Qld 4072, Australia
Westerman, B
Hamlet, SM
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机构:Univ Queensland, Sch Dent, Oral Care Res Programme, Brisbane, Qld 4072, Australia
Hamlet, SM
Palmer, JE
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机构:Univ Queensland, Sch Dent, Oral Care Res Programme, Brisbane, Qld 4072, Australia
Palmer, JE
Faddy, MJ
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机构:Univ Queensland, Sch Dent, Oral Care Res Programme, Brisbane, Qld 4072, Australia
Faddy, MJ
Lang, NP
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机构:Univ Queensland, Sch Dent, Oral Care Res Programme, Brisbane, Qld 4072, Australia
Lang, NP
Seymour, GJ
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机构:Univ Queensland, Sch Dent, Oral Care Res Programme, Brisbane, Qld 4072, Australia
Seymour, GJ
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[1] Univ Queensland, Sch Dent, Oral Care Res Programme, Brisbane, Qld 4072, Australia
Background: Cross-sectional studies have demonstrated that a specific polymorphism (allele 2 of both IL-1A +4845 and IL-1B +3954) in the IL-1 gene cluster has been associated with an increased susceptibility to severe periodontal disease and to an increased bleeding tendency during periodontal maintenance. The aim of the present study was to investigate the relationship between IL-1 genotype and periodontitis in a prospective longitudinal study in an adult population of essentially European heritage. Methods: From an ongoing study of the Oral Care Research Programme of The University of Queensland, 295 subjects consented to genotyping for IL-1 allele 2 polymorphisms. Probing depths and relative attachment levels were recorded at baseline, 6, 12, 24, 36, 48 and 60 months using the Florida probe. Periodontitis progression at a given site was defined as attachment loss greater than or equal to2 mm at any observation period during the 5 years of the study and the extent of disease progression determined by the number of sites showing attachment loss. Porphyromonas gingivalis, Actinobacillus actinomycetemcomitans and Prevotella intermedia were detected using ELISA. Results: 38.9% of the subjects were positive for the composite IL-1 genotype. A relationship between the IL-1 positive genotype and increased mean probing pocket depth in non-smokers greater than 50 years of age was found. Further, IL-1 genotype positive smokers and genotype positive subjects with P. gingivalis in their plaque had an increase in the number of probing depths greater than or equal to3.5 mm, There was a consistent trend for IL-1 genotype positive subjects to experience attachment loss when compared with IL-1 genotype negative subjects. Conclusion: The results of this study have shown an interaction of the IL-1 positive genotype with age, smoking and P. gingivalis which suggests that IL-1 genotype is a contributory but non-essential risk factor for periodontal disease progression in this population.
机构:
Univ Tehran Med Sci, Mol Immunol & Immunogenet Res Ctr, Tehran, Iran
Univ Tehran Med Sci, Vali Asr Hosp, EMRC, Tehran, Iran
Univ Tehran Med Sci, Sch Med, Dept Immunol, Immunogenet Lab, Tehran, IranUniv Tehran Med Sci, Mol Immunol & Immunogenet Res Ctr, Tehran, Iran
Khalilzadeh, O.
Anvari, M.
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Univ Tehran Med Sci, Mol Immunol & Immunogenet Res Ctr, Tehran, Iran
Univ Tehran Med Sci, Vali Asr Hosp, EMRC, Tehran, IranUniv Tehran Med Sci, Mol Immunol & Immunogenet Res Ctr, Tehran, Iran
Anvari, M.
Esteghamati, A.
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Univ Tehran Med Sci, Vali Asr Hosp, EMRC, Tehran, IranUniv Tehran Med Sci, Mol Immunol & Immunogenet Res Ctr, Tehran, Iran
Esteghamati, A.
Momen-Heravi, F.
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Univ Tehran Med Sci, Mol Immunol & Immunogenet Res Ctr, Tehran, Iran
Univ Tehran Med Sci, Sch Med, Dept Immunol, Immunogenet Lab, Tehran, IranUniv Tehran Med Sci, Mol Immunol & Immunogenet Res Ctr, Tehran, Iran
Momen-Heravi, F.
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Mahmoudi, M.
Rashidi, A.
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Univ Tehran Med Sci, Vali Asr Hosp, EMRC, Tehran, IranUniv Tehran Med Sci, Mol Immunol & Immunogenet Res Ctr, Tehran, Iran
Rashidi, A.
Amiri, H. M.
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Univ Tehran Med Sci, Mol Immunol & Immunogenet Res Ctr, Tehran, IranUniv Tehran Med Sci, Mol Immunol & Immunogenet Res Ctr, Tehran, Iran
Amiri, H. M.
Ranjbar, M.
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Univ Tehran Med Sci, Mol Immunol & Immunogenet Res Ctr, Tehran, Iran
Univ Tehran Med Sci, Sch Med, Dept Immunol, Immunogenet Lab, Tehran, IranUniv Tehran Med Sci, Mol Immunol & Immunogenet Res Ctr, Tehran, Iran
Ranjbar, M.
Tabataba-Vakili, S.
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Univ Tehran Med Sci, Mol Immunol & Immunogenet Res Ctr, Tehran, IranUniv Tehran Med Sci, Mol Immunol & Immunogenet Res Ctr, Tehran, Iran
Tabataba-Vakili, S.
Amirzargar, A.
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Univ Tehran Med Sci, Mol Immunol & Immunogenet Res Ctr, Tehran, Iran
Univ Tehran Med Sci, Sch Med, Dept Immunol, Immunogenet Lab, Tehran, IranUniv Tehran Med Sci, Mol Immunol & Immunogenet Res Ctr, Tehran, Iran