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RESEARCH ARTICLE

SA JOURNAL OF DIABETES & VASCULAR DISEASE

68

VOLUME 16 NUMBER 2 • NOVEMBER 2019

Among dietary FAs, the first extracted pattern presented with

high positive loadings of saturated FAs, MUFAs,

α

-linolenic acid

(C18:3

n-

3) and

n-

6 FAs, and therefore was named the ‘no

n-

marine’ FA pattern. The second pattern was named the ‘marine’ FA

pattern because it was characterised by high positive loadings of

eicosapentaenoic acid (C20:5

n-

3) and C22:6

n-

3.

The six plasma phospholipid FA patterns are discussed in the

order in which they were derived. The first pattern presented with

positive loadings of LC-SFAs, C18:0, C20:0, C22:0 and C24:0 and

very high negative loadings of C16:1

n-

7, C18:1

n-

7 and C18:1

n-

9; we named it the ‘high-Satfat’ pattern. The second pattern was

named ‘

n-

3 VLC-PUFA’ and presented with high positive loadings

of docosapentaenoic acid (C22:5

n-

3), C22:6

n-

3 and C20:5

n-

3, as

well as C20:4

n-

6. The third pattern presented the highest positive

loadings of C18:2

n-

6 and eicosadienoic acid (C20:2

n-

6) and was

named accordingly as the ‘high-LA’ pattern. The fourth pattern was

named ‘

n-

6 VLC-PUFA’ since it was characterised with high positive

loadings of adrenic acid (C22:4

n-

6), C22:2-

n

6 and C20:3

n-

6. The

fifth pattern extracted was named the ‘

n-

9 LC-MUFA’ pattern and

presented with positive loadings of C24:1

n-

9 and gondoic acid

(C20:1

n-

9). The sixth and last pattern had a positive loading of one

FA, i.e. C18:3

n-

3, and we named it ‘

n-

3 EFA’ pattern.

Dietary FA patterns were weakly associated with measured

outcomes (Table 4). The no

n-

marine FA pattern showed marginal

positive associations with WC in the crude model and the

association remained marginal after adjusting for age and gender

(

β

= 0.06, 95% CI = –0.01–0.13,

p

= 0.09). The association was

lost after adjustment for lifestyle variables and energy intake. On

the other hand, we did not find any associations with the marine

FA pattern (Table 4). Neither pattern revealed any association with

BMI, WHtR or the MetS. Further adjustment to the regressions for

total fat, fibre, carbohydrates and added sugar did not result in

any significant associations. The variables in the adjusted models

explained 0.02 to 27% of the variation in measures of adiposity

and 0.4 to 20% of the variation in the MetS.

Plasma phospholipid FA patterns resulted in stronger associations

with measures of adiposity and the MetS (Table 5). The high-Satfat

and

n-

3 VLC-PUFA patterns were positively associated with all

measures of adiposity and the MetS. The associations remained

significant in the fully adjusted model. The omega-6 VLC-PUFA

pattern showed marginal and positive associations with WC and

WHtR in the crude model, but associations were lost after further

adjustments. This pattern also showed higher odds for having the

MetS and remained significantly associated in the fully adjusted

model (odds ratio, OR = 1.25, 95% CI = 1.02–1.54,

p

= 0.03).

The

n-

9 LC-MUFA pattern was inversely associated with WC and

WHtR in the crude model as well as after adjustment for age and

gender. The associations were, however, lost after adjustments for

lifestyle variables and energy intake. This pattern also showed lower

odds for having the MetS and remained significantly associated in

the fully adjusted model (OR = 0.61, 95% CI = 0.50–0.75,

p

0.0001).

The omega-3 EFA pattern showed an inverse association with

BMI, WC and WHtR, but in the fully adjusted model marginal

significance remained for BMI only. This pattern also showed lower

odds for having the MetS and remained significantly associated in

the fully adjusted model (OR = 0.81, 95% CI = 0.66–0.99,

p

=

0.04). The variables in all the adjusted models explained 14 to 34%

of the variation in measures of adiposity, and 18 to 31% of the

variation in the MetS.

We further adjusted all regression models for use of

contraceptives and intakes of total fat, fibre, carbohydrates, and

energy from added sugar in association with plasma phospholipid

FAs. Additional adjustment for these variables did not result in

different associations with anthropometric indices. The association

between high-LA pattern and the MetS remained marginally

significant after adjusting for additional variables, whereas the

associations with the

n-

6 VLC-PUFA and

n-

3 EFA patterns were lost.

Discussion

The results of this study add new information about identified FA

patterns both in diet and plasma phospholipids among a selected

group of black South Africans from the North West Province. We

identified for the first time two dietary FA patterns and six plasma

phospholipid FA patterns (Table 3) by means of factor analysis

in this group of black adults. The dietary no

n-

marine FA pattern

showed a weak positive association with WC, whereas the marine

pattern did not show any associations with outcomes measured.

On the other hand, two plasma phospholipid FA patterns

(high-Satfat and

n-

3 VLC-PUFA) were positively associated with

all measures of adiposity and the MetS. The omega-6 VLC-PUFA

pattern showed a positive association with the MetS, but not

with measures of adiposity. The

n-

9 LC-MUFA and the

n-

3 EFA

patterns showed an inverse association with the MetS in fully

adjusted models and tended to be negatively associated with some

measures of adiposity. The high-LA pattern was neither associated

with measures of adiposity nor the MetS. Our findings indicate

that dietary FA patterns were weakly associated, whereas plasma

phospholipid FA patterns were more strongly associated with

measures of adiposity and the MetS.

Previous studies have reported FA patterns, derived fromdifferent

components of blood and tissue in association with obesity

29

and

the MetS,

22,30

but not with dietary patterns. These patterns were

generated by varying numbers of FAs ranging from nine to 34

FAs,

22,29,30

and some included estimated desaturase activities,

30

by

means of use of factor

29,30

and cluster

22

analysis. Consequently,

these derived patterns differed from that obtained in our study.

A dietary pattern, consisting of SFAs, PUFAs, MUFAs and

other nutrients, was not associated with obesity among Iranian

adults.

45

On the contrary, a multiracial study in the USA reported

a positive association of intakes of total fat, total saturated fat,

LC-SFAs, myristic acid (C14:0), C16:0 and C18:0, and MUFAs with

BMI.

46

Furthermore, a study investigating the association of dietary

patterns with the MetS concluded that a pattern high in meat

products was associated with a higher prevalence of the MetS.

47

In our study, the dietary no

n-

marine FA pattern showed marginal

and positive associations with WC, but not with other measures

of adiposity or the MetS. The no

n-

marine FA pattern had positive

loadings of FAs from SFAs, MUFAs and PUFAs, specifically from

two SFAs (C16:0 and C18:0), two MUFAs (C16:1

n-

7, C18:1

n-

9)

and two PUFAs (C18:2

n-

6 and C18:3

n-

3). The dietary marine FA

pattern showed no association with outcomes measured.

Our results are in agreement with a study in the USA that also

found no associations of

n-

3 LC-PUFAs with BMI due to low intakes

of these FAs in their participants.46 In our study and the study in

the USA, lower intakes of

n-

3 PUFA compared to the FAO/WHO

recommendation of 0.25–2 g/day were found.

48

Under-reporting

of dietary intake may significantly influence nutrient pattern

investigation and association with disease,

49

however, in the PURE