IL-1 gene polymorphism and smoking as risk factors for peri-implant bone loss in a well-maintained population

: The aim of the present study was (i) to investigate the relation between specific interleukin‐1 (IL‐1) gene polymorphisms and peri‐implant bone loss at osseointegrated ITI® dental implants and (ii) to explore the association between these allelic variants of the IL‐1 gene complex and peri‐implant...

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Veröffentlicht in:Clinical oral implants research 2003-02, Vol.14 (1), p.10-17
Hauptverfasser: Feloutzis, Andreas, Lang, Niklaus P., Tonetti, Maurizio S., Bürgin, Walter, Brägger, Urs, Buser, Daniel, Duff, Gordon W., Kornman, Kenneth S.
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Sprache:eng
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Zusammenfassung:: The aim of the present study was (i) to investigate the relation between specific interleukin‐1 (IL‐1) gene polymorphisms and peri‐implant bone loss at osseointegrated ITI® dental implants and (ii) to explore the association between these allelic variants of the IL‐1 gene complex and peri‐implant mucosal inflammation, in both smoking and non‐smoking individuals. A sample of 90 consecutive Caucasian patients (aged 33–88 years), treated with at least one ITI‐implant participated in this retrospective investigation. Standardized periapical radiographs were taken after prosthetic rehabilitation (133.6 days, SD 136.9 days) and at the time of the re‐examination, on average 5.6 years (SD 2.5 years) thereafter. The radiographs were analyzed by a calibrated examiner for changes in peri‐implant bone levels. The examiner was blind with respect to clinical parameters and IL‐1 status. The distance between the implant shoulder and the first visible bone‐implant contact (DIB) at the respective time points were measured using a computerized method. The absolute bone level difference during the years of service (ABL) and the annual bone loss (ΔBL/year) were calculated for all the implants. Percentages of full mouth bleeding on probing (BOP), as well as of BOP calculated separately for teeth and implants, were determined for all visits and averaged for the entire observation period. Out of the total patient sample, there were 14 heavy smokers (= 20 cigarettes/day), 14 moderate smokers (5–19 cigarettes/day), 23 previous smokers (smoking cessation > 5 years) and 39 non‐smokers. Twenty‐eight (31.11%) patients were IL‐1 genotype positive. Upon stratification for smoking status, significant differences were found for the variables ABL (P 
ISSN:0905-7161
1600-0501
DOI:10.1034/j.1600-0501.2003.140102.x