Clinical, genetic and microbiological findings in a Brazilian family with aggressive periodontitis

被引:34
作者
Trevilatto, PC
Tramontina, VA
Machado, MAN
Gonçalves, RB
Sallum, AW
Line, SRP
机构
[1] Univ Estadual Campinas, Fac Odontol Piracicaba, Dept Morphol, Dent Sch Piracicaba, BR-13414018 Piracicaba, SP, Brazil
[2] Univ Estadual Campinas, Dent Sch Piracicaba, Dept Periodontol, Piracicaba, SP, Brazil
[3] Univ Estadual Campinas, Dent Sch Piracicaba, Dept Oral Diag, Piracicaba, SP, Brazil
关键词
aggressive periodontitis; cytokine; risk factors; gene polymorphism; periopathogens;
D O I
10.1034/j.1600-051x.2002.290309.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background, aim: Aggressive periodontitis comprises a group of rapidly progressive forms of periodontitis. Besides bacteria, a high level of subject susceptibility must be involved in the expression of disease. In the present study, we report the clinical, microbiological and genetic profile of a 14-individual family with aggressive periodontitis. Method: PCR was utilized to detect pathogenic bacteria of affected sites. DNA was obtained from epithelial cells through a mouthwash with 3% glucose and scrapping of the oral mucosa. RFLP-PCR was used to analyze cytokine genetic polymorphisms. Results: Localized aggressive periodontitis was diagnosed for an 18-year-old systemically healthy non-smoking proband, with siblings displaying aggressive periodontitis. Bacteroides forsythus and Treponema denticola were the most frequent pathogens. The proband presented Actinobacillus actinomycetemcomitans and detectable levels of Porphyromonas gingivalis, Bacteroides forsythus and Treponema denticola. Allele 2 of IL-1alpha (-889) polymorphism was found in all individuals as well as allele 1 of the IL-1beta (+3953) gene. Alleles 1 and 2 (50 each) of IL-1beta (-511), allele 1 of TNF-alpha (-308) and allele 2 (in homo or heterozygosity) of IL-RN (intron 2) gene were present. Conclusion: The results show that the present microbiological and genetic parameters were not relevant for the prediction of periodontitis susceptibility in this family.
引用
收藏
页码:233 / 239
页数:7
相关论文
共 39 条
[11]  
Galbraith GMP, 1999, J CLIN PERIODONTOL, V26, P705
[12]   HOST RESPONSES IN PERIODONTAL-DISEASES - CURRENT CONCEPTS [J].
GENCO, RJ .
JOURNAL OF PERIODONTOLOGY, 1992, 63 (04) :338-355
[13]   Interleukin-1β+3953 allele 2:: association with disease status in adult periodontitis [J].
Gore, EA ;
Sanders, JJ ;
Pandey, JP ;
Palesch, Y ;
Galbraith, GMP .
JOURNAL OF CLINICAL PERIODONTOLOGY, 1998, 25 (10) :781-785
[14]   PCR-DNA probe assays for identification and detection of Prevotella intermedia sensu stricto and Prevotella nigrescens [J].
Guillot, E ;
Mouton, C .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (07) :1876-1882
[15]   REINTERPRETATION OF THE EVIDENCE FOR X-LINKED DOMINANT INHERITANCE OF JUVENILE PERIODONTITIS [J].
HART, TC ;
MARAZITA, ML ;
SCHENKEIN, HA ;
DIEHL, SR .
JOURNAL OF PERIODONTOLOGY, 1992, 63 (03) :169-173
[16]   Clinical and genetic analysis of a large north European Caucasian family affected by early-onset periodontitis [J].
Hodge, PJ ;
Teague, PW ;
Wright, AF ;
Kinane, DF .
JOURNAL OF DENTAL RESEARCH, 2000, 79 (03) :857-863
[17]   The interleukin-1 genotype as a severity factor in adult periodontal disease [J].
Kornman, KS ;
Crane, A ;
Wang, HY ;
diGiovine, FS ;
Newman, MG ;
Pirk, FW ;
Wilson, TG ;
Higginbottom, FL ;
Duff, GW .
JOURNAL OF CLINICAL PERIODONTOLOGY, 1997, 24 (01) :72-77
[18]  
LENCH N, 1988, LANCET, V1, P1356
[19]   GINGIVAL INDEX PLAQUE INDEX AND RETENTION INDEX SYSTEMS [J].
LOE, H .
JOURNAL OF PERIODONTOLOGY, 1967, 38 (6P2) :610-&
[20]   NOVEL GENETIC ASSOCIATION BETWEEN ULCERATIVE-COLITIS AND THE ANTIINFLAMMATORY CYTOKINE INTERLEUKIN-1 RECEPTOR ANTAGONIST [J].
MANSFIELD, JC ;
HOLDEN, H ;
TARLOW, JK ;
DIGIOVINE, FS ;
MCDOWELL, TL ;
WILSON, AG ;
HOLDSWORTH, CD ;
DUFF, GW .
GASTROENTEROLOGY, 1994, 106 (03) :637-642