Ingestion of dietary supplements of n-3 fatty acids has been consistently s
hown to reduce both the number of tender joints on physical examination and
the amount of morning stiffness in patients with rheumatoid arthritis. In
these cases, supplements were consumed daily in addition to background medi
cations and the clinical benefits of the n-3 fatty acids were not apparent
until they were consumed for greater than or equal to 12 wk. It appears tha
t a minimum daily dose of 3 g eicosapentaenoic and docosahexaenoic acids is
necessary to derive the expected benefits. These doses of n-3 fatty acids
are associated with significant reductions in the release of leukotriene B-
4 from stimulated neutrophils and of interleukin 1 from monocytes. Both of
these mediators of inflammation are thought to contribute to the inflammato
ry events that occur in the rheumatoid arthritis disease process. Several i
nvestigators have reported that rheumatoid arthritis patients consuming n-3
dietary supplements were able to lower or discontinue their background dos
es of nonsteroidal antiinflammatory drugs or disease-modifying antirheumati
c drugs. Because the methods used to determine whether patients taking n-3
supplements can discontinue taking these agents are variable, confirmatory
and definitive studies are needed to settle this issue. n-3 Fatty acids hav
e virtually no reported serious toxicity in the dose range used in rheumato
id arthritis and are generally very well tolerated.