Gingival overgrowth is a well-documented unwanted effect, associated w
ith phenytoin, cyclosporin, and the calcium channel blockers. The path
ogenesis of drug-induced gingival overgrowth is uncertain, and there a
ppears 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-induce
d inflammatory and immunological changes and activation of growth fact
ors. Of these, genetic factors which give rise to fibroblast heterogen
eity, gingival inflammation, and pharmacokinetic variables appear to b
e significant in the expression of gingival overgrowth. A more thoroug
h understanding of the pathogenesis of this unwanted effect will hopef
ully elucidate appropriate mechanisms for its control. (C) Munksgaard,
1996.