Literature DB >> 2005225

Clinical risk indicators for periodontal attachment loss.

A D Haffajee1, S S Socransky, J Lindhe, R L Kent, H Okamoto, T Yoneyama.   

Abstract

The purpose of the present investigation was to evaluate the association of baseline clinical parameters of periodontal disease with disease progression in the following year. 271 randomly selected subjects from Ushiku Japan were monitored for overt gingivitis and plaque accumulation at 4 sites per tooth and probing pocket depth, probing attachment level and bleeding on probing at 6 sites per tooth for all teeth at baseline and 1 year. A subject was considered to exhibit additional attachment loss if one or more sites increased 3 mm or more in a probing attachment level measurement in one year. The clinical variables included age, sex, number of missing teeth, mean pocket depth and attachment level. In addition, the % of sites which exhibited overt gingivitis, visible plaque, pocket depths, attachment levels or gingival recession over certain mm thresholds or bled on probing were determined. Chi 2 analysis was used to seek significant associations between the baseline clinical variables and subsequent attachment loss in a subject. Only 74 of the 271 subjects (27.3%) exhibited additional attachment loss of 3 mm or more at 1 or more sites after 1 year. Older subjects had a greater risk of disease progression than younger subjects. There were no significant differences in % of individuals exhibiting additional attachment loss when divided on the basis of sex, number of missing teeth or % of sites with overt gingivitis. However, the greater the % of sites with visible plaque or which bled on probing, the greater was the likelihood of subsequent attachment loss. Increasing mean levels of pocket depth or attachment level or increasing %s of sites exhibiting prior attachment loss were strongly related to the proportion of individuals with subsequent attachment loss. Gingival recession exhibited similar but weaker relationships. Log-linear analysis suggested that the association between bleeding on probing, age, or plaque levels with additional attachment loss may be explained by the association of these variables with baseline attachment loss. The analyses were repeated with a positive subject defined as having only 1 active site or 2 or more active sites. 37 subjects fit the 1st criterion and the remaining 37 the 2nd criterion. The associations observed were almost identical to those found when subjects were considered positive on the basis of 1 or more changing sites. Discriminant analysis was used to classify subjects as active or inactive using up to 11 predictor variables.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1991        PMID: 2005225     DOI: 10.1111/j.1600-051x.1991.tb01700.x

Source DB:  PubMed          Journal:  J Clin Periodontol        ISSN: 0303-6979            Impact factor:   8.728


  19 in total

1.  Relationship between C-telopeptide pyridinoline cross-links (ICTP) and putative periodontal pathogens in periodontitis.

Authors:  M D Palys; A D Haffajee; S S Socransky; W V Giannobile
Journal:  J Clin Periodontol       Date:  1998-11       Impact factor: 8.728

2.  Inflammation and genetic risk indicators for early periodontitis in adults.

Authors:  Philip Stashenko; Thomas Van Dyke; Patrice Tully; Ralph Kent; Stephen Sonis; Anne C R Tanner
Journal:  J Periodontol       Date:  2010-11-08       Impact factor: 6.993

3.  C-telopeptide pyridinoline cross-links (ICTP) and periodontal pathogens associated with endosseous oral implants.

Authors:  R J Oringer; M D Palys; A Iranmanesh; J P Fiorellini; A D Haffajee; S S Socransky; W V Giannobile
Journal:  Clin Oral Implants Res       Date:  1998-12       Impact factor: 5.977

Review 4.  Oral fluid-based biomarkers of alveolar bone loss in periodontitis.

Authors:  Janet S Kinney; Christoph A Ramseier; William V Giannobile
Journal:  Ann N Y Acad Sci       Date:  2007-03       Impact factor: 5.691

5.  Clinical and other risk indicators for early periodontitis in adults.

Authors:  Anne C R Tanner; Ralph Kent; Thomas Van Dyke; Steven T Sonis; Lora A Murray
Journal:  J Periodontol       Date:  2005-04       Impact factor: 6.993

6.  Regulation of Nur77 gene expression by prostanoids in cementoblastic cells.

Authors:  Sanda M Moldovan; Jeanne M Nervina; Sotirios Tetradis; Paulo M Camargo
Journal:  Arch Oral Biol       Date:  2009-02-23       Impact factor: 2.633

7.  Evaluation of bleeding on probing and gingival crevicular fluid enzyme activity for detection of periodontally active sites during supportive periodontal therapy.

Authors:  Hiroshi Ito; Yukihiro Numabe; Satoshi Sekino; Etsuko Murakashi; Hitomi Iguchi; Shuichi Hashimoto; Daisuke Sasaki; Takashi Yaegashi; Kazushi Kunimatsu; Hideki Takai; Masaru Mezawa; Yorimasa Ogata; Hisashi Watanabe; Satsuki Hagiwara; Yuichi Izumi; Yuka Hiroshima; Jun-Ichi Kido; Toshihiko Nagata
Journal:  Odontology       Date:  2012-11-22       Impact factor: 2.634

8.  Crevicular fluid biomarkers and periodontal disease progression.

Authors:  Janet S Kinney; Thiago Morelli; Min Oh; Thomas M Braun; Christoph A Ramseier; Jim V Sugai; William V Giannobile
Journal:  J Clin Periodontol       Date:  2013-12-12       Impact factor: 8.728

9.  There is a paucity of economic evaluations of prediction methods of caries and periodontitis-A systematic review.

Authors:  Helena Fransson; Thomas Davidson; Madeleine Rohlin; Helena Christell
Journal:  Clin Exp Dent Res       Date:  2021-02-16

10.  Periodontal disease: a covert source of inflammation in chronic kidney disease patients.

Authors:  Gener Ismail; Horia Traian Dumitriu; Anca Silvia Dumitriu; Fidan Bahtiar Ismail
Journal:  Int J Nephrol       Date:  2013-06-06
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