Mozaffarian and his
colleagues published a paper recently in the
Annals of Internal Medicine analyzed data from 2692 U.S. adults aged 74
years (±5 years) without prevalent cardiovascular diseases at baseline, who participated
in the National Heart, Lung, and Blood
Institute (NHLBI)-funded cohort, The Cardiovascular Health Study (CHS).
The investigators measured the blood circulating levels of 3 types of long-chain
omega-3 polyunsaturated fatty acids (omega-3 PUFAs); eicosapentaenoic acid
(EPA), docosapentaenoic acid (DPA), and docosahexaenoic acid (DHA). These were
measured from the blood that was collected from the participants in 1992. They
then followed them longitudinally for 16 years (1992 through 2008) to evaluate
the relationship with total and cause-specific mortality and incident fatal or
nonfatal CHD and stroke.
The authors found that the individual levels of EPA, DPA, and DHA, and
their total levels (omega-3 PUFA) were associated with lower total mortality across
three robust models of adjusted Cox proportional hazards models (age, gender,
various demographic and co-morbid conditions, and dietary factors):
The participants in the higher
quintile of the total omega-3 PUFAs had 27% lower risk
The participants in the higher
quintile of EPA had 17% lower risk
The participants in the higher
quintile of DPA had 23% lower risk
The participants in the higher
quintile of DHA had 20% lower risk
All results were statistically significant with narrow 95% confidence
internals.
For cause-specific mortality, and using the same adjustment models of
the total mortality risk data, total omega-3 PUFAs, and most of the individual levels
of the three subtypes, were associated with cause-specific mortality. Total omega-3
PUFAs was associated with:
35% lower risk from cardiovascular
mortality
40% lower risk from
coronary heart disease mortality
45% lower risk from arrhythmic
coronary heart disease (CHD) mortality
28% lower risk from non-arrhythmic
CHD mortality
40% lower risk from stroke mortality
28% lower risk from total fatal
and nonfatal CHD mortality
17% lower risk from nonfatal
myocardial infarction mortality
25% lower risk from total fatal
and nonfatal stroke mortality
37% lower risk from Ischemic
stroke mortality
This data strongly suggests that fish consumption or fish oil
supplementation would reduce both total mortality and cause-specific mortality
in older adults. The steepest dose-response relationship between the
circulating blood levels of omega-3 PUFAs and the decreased risk came from as
low as 400 mg per day dietary intake, or two servings of fatty fish per week.
This will lead to an average increase of about 2 more years of life in those
with higher levels compared to those with lower levels.
My opinion:
This conclusion is supported by the robust statistical analyses with adjustment
to many confounders, as well as a quantification of the omega-3 PUFAs rather
than the amount of fish intake from Food Frequency Questionnaires (FFQ) or
similar tool. Despite some limitations in this paper, it is a landmark paper in
supporting increased fish intake to decrease the risk of mortality in older
adults.