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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 30, No 4, July/August 2019

236

AFRICA

esters to be inversely associated with abdominal obesity in a recent

cross-sectional study of 60-year-old men and women.

57

Alpha-

linolenic acid (C18:3n-3) is an essential FA and a precursor from

which n-3 LC-PUFAs are synthesised. Increased consumption

of C18:3n-3-rich foods elevates its tissue levels as well as levels

of C22:6n-3 and C20:5n-3 in the liver lipids.

58

Alpha-linolenic

acid can be beneficial to health. Firstly, C18:3n-3 intake was

associated with a moderately lower risk of cardiovascular disease

in randomised, controlled studies as outlined in reviews.

59,60

Secondly, as explained above, C18:3n-3 competes for the same

metabolic enzymes, as does C18:2n-6, and increased dietary

intake may be a worthy approach to decrease elongation of n-6

FAs leading to reduced plasma C20:4n-6 levels and increased

plasma levels of C22:6n-3 and C20:5n-3.

58

As C18:3n-3 is an

essential FA, this pattern, identified in our study participants,

is probably related to food intake and therefore indicative of a

higher intake of vegetable oils, legumes, nuts and seeds.

61

Strengths and limitations

A rigorous methodological approach of sequential regression

modelling enabled us to investigate the associations between

dietary FA and plasma phospholipid FA patterns, respectively,

and measures of adiposity and the MetS. Another strength of

our study is the use of both dietary FA and plasma phospholipid

FA patterns,

27

which is a preferred method to investigate the

association between diet and diseases.

27

Our work is not free of limitations. Firstly, inaccuracies

associated with collecting dietary intake data may have

influenced the dietary FA results; however, in our population,

fieldworkers collecting dietary data were intensively trained and

supervised, and both under- and over-reporters of dietary intake

were excluded.

50

In addition, repeatability of the QFFQ was

also demonstrated.

10

Secondly, the cross-sectional design does

not account for possible reverse causation between measures

of adiposity and dietary FA intake or plasma phospholipid

FA concentration, nor can causality be inferred. Thirdly, a

possible limitation of the study is incomplete information on FA

composition in the food composition databases. This limitation

was compensated for by our study design that also considered

plasma phospholipid FAs. Fourthly, we assessed the associations

with indirect measurements of adiposity, including BMI, WHtR

and WC, as secondary markers of total and central adiposity,

whereas imaging methods would better differentiate between

lean and fat mass.

Conclusion

To our knowledge, this is the first study to investigate and

document novel data on dietary FA and plasma phospholipid

FA patterns and their association with measures of adiposity

and the MetS in a selected group of black South African adults.

This study presents evidence that although marginal association

was found with dietary FA patterns, some circulating plasma

phospholipid FA patterns were more strongly and significantly

associated with BMI, WC, WHtR and the MetS. The high-

Satfat and n-3 VLC-PUFA patterns were positively associated

with adiposity and the MetS, whereas the n-9 LC-MUFA and

n-3 EFA patterns were inversely associated with adiposity. These

patterns may suggest possible differences in FA metabolism

between lean and overweight/obese individuals. It should also

be considered that, in a study population with low-fat intakes,

such as the PURE participants, plasma FA levels may reflect

endogenous FA generation rather than dietary intakes, which

could result in different findings than those reported in other

studies from affluent communities.

Our results are not sufficiently conclusive to make

recommendations on dietary FA intakes in this population.

Further prospective cohort studies that explain possible

differences in characteristics of FA metabolism among black

South African men and women are needed. More studies that

apply the use of dietary FA and plasma or tissue FA patterns are

required to determine whether the results from the current study

can be generalised to the black population of African descent.

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