Browse by author
Lookup NU author(s): Emeritus Professor Robin Seymour
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
Gingival overgrowth is a well-documented unwanted effect, associated with phenytoin, cyclosporin, and the calcium channel blockers. The pathogenesis of drug-induced gingival overgrowth is uncertain, and there appears to be no unifying hypothesis that links together the 3 commonly implicated drugs. In this review, we consider a multifactorial model which expands on the interaction between drug and/or metabolite, with the gingival fibroblasts. Factors which impact upon this model include age, genetic predisposition, pharmacokinetic variables, plaque-induced inflammatory and immunological changes and acti vation of growth factors. Of these, genetic factors which give rise to fibroblast heterogeneity, gingival inflammation, and pharmacokinetic variables appear to be significant in the expression of gingival overgrowth. A more thorough understanding of the pathogenesis of this unwanted effect will hopefully elucidate appropriate mechanisms for its control. © Munksgaard, 1996.
Author(s): Seymour RA
Publication type: Article
Publication status: Published
Journal: Journal of Clinical Periodontology
Year: 1996
Volume: 23
Issue: 3
Pages: 165-175
Print publication date: 01/01/1996
ISSN (print): 0303-6979
ISSN (electronic): 1600-051X
Publisher: Wiley-Blackwell Publishing
URL: http://dx.doi.org/10.1111/j.1600-051X.1996.tb02072.x
DOI: 10.1111/j.1600-051X.1996.tb02072.x
PubMed id: 8707974
Altmetrics provided by Altmetric