Chronic heart failure (CHF) is a complex syndrome involving activation of m
ultiple cellular, metabolic, and neurohumoral pathways following the initia
l myocardial insult. Recently, there have been considerable advances in the
pharmacologic management of CHF. The current approach to treatment recogni
zes the need to target neurohormonal activation, and the use of angiotensin
-converting enzyme (ACE) inhibitors and beta blockers should now be regarde
d as part of standard therapy in many patients with CHF. However, because o
f the complexity of the disease, blockade of additional pathways is Likely
to be required to maximize the therapeutic benefit of intervention. To this
end, there are several agents under active late-phase clinical evaluation.
The most advanced of these new strategies (beyond renin-angiotensin-aldost
erone blockade) is inhibition of the endothelin system. There is a substant
ial body of evidence that this system is intimately involved in CHF disease
progression. Early-phase clinical data are very encouraging and support th
e potential utility of long-term endothelin inhibition. Other novel approac
hes involve the use of cytokine antagonists: (e.g., agents that block tumor
necrosis factor-alpha activity) and the augmentation of natriuretic peptid
es. If all these potential agents prove to be of benefit in CHF, the questi
on of which agent or combination of agents to use in which patients will ar
ise. There is therefore a need to develop scientific approaches in order to
be able to identify more accurately patients who will obtain benefit from
specific classes or combinations of drugs.