We are just beginning to uncover the genetic determinants of coronary
heart disease. The genotype phenotype associations are complex as a co
nsequence of pleiotropy, variation with age, selection owing to the hi
gh lethality of the disease, and interaction between genes and with en
vironmental factors. Nevertheless, identification of the gene variants
involved in the chronic and acute processes of coronary heart disease
appears possible; this could considerably improve our understanding o
f the aetiology and mechanisms of this disease. Simultaneous analysis
of several predisposing alleles should provide the means to identify h
igh-risk individuals and to adapt therapeutic approaches to the geneti
c make-up of patients.