a1 Department of Nutritional Sciences, Faculty of Medicine, University of Toronto, Toronto, ON, Canada M5S 3E2
a2 Clinical Nutrition and Risk Factor Modification Center, St Michael's Hospital, Toronto, ON, Canada
a3 Division of Nutrition and Dietetics, College of Pharmacy and Nutrition, University of Saskatchewan, Saskatoon, SK, Canada
a4 The Almond Board of California, Modesto, CA, USA
a5 Department of Pathology and Molecular Medicine, Faculty of Health Sciences, McMaster University, Hamilton, ON, Canada
a6 Division of Endocrinology and Metabolism, St Michael's Hospital, Toronto, ON, Canada
a7 Li Ka Shing Knowledge Institute, St Michael's Hospital, Toronto, ON, Canada
a8 Department of Medicine, Faculty of Medicine, University of Toronto, Toronto, ON, Canada
Consumption of almonds has been shown to be associated with a decreased risk of CHD, which may be related to their fatty acid (FA) composition. However, the effect of almond consumption on the serum FA composition is not known. Therefore, in the present study, we investigated whether almond consumption would alter the serum FA profile and risk of CHD, as calculated using Framingham's 10-year risk score, in a dose-dependent manner in hyperlipidaemic individuals when compared with a higher-carbohydrate control group using dietary interventions incorporating almonds. A total of twenty-seven hyperlipidaemic individuals consumed three isoenergetic (mean 1770 kJ/d) supplements during three 1-month dietary phases: (1) full-dose almonds (50–100 g/d); (2) half-dose almonds with half-dose muffins; (3) full-dose muffins. Fasting blood samples were obtained at weeks 0 and 4 for the determination of FA concentrations. Almond intake (g/d) was found to be inversely associated with the estimated Framingham 10-year CHD risk score (P= 0·026). In both the half-dose and full-dose almond groups, the proportions of oleic acid (OA) and MUFA in the TAG fraction (half-almond: OA P= 0·003; MUFA P= 0·004; full-almond: OA P< 0·001; MUFA P< 0·001) and in the NEFA fraction (half-almond: OA P= 0·01; MUFA P= 0·04; full-almond: OA P= 0·12; MUFA P= 0·06) increased. The estimated Framingham 10-year CHD risk score was inversely associated with the percentage change of OA (P= 0·011) and MUFA (P= 0·016) content in the TAG fraction. The proportions of MUFA in the TAG and NEFA fractions were positively associated with changes in HDL-cholesterol concentrations. Similarly, the estimated Framingham 10-year CHD risk score was inversely associated with the percentage change of OA (P= 0·069) and MUFA content in the NEFA fraction (P= 0·009). In conclusion, the results of the present study indicate that almond consumption increases OA and MUFA content in serum TAG and NEFA fractions, which are inversely associated with CHD lipid risk factors and overall estimated 10-year CHD risk.
(Received September 15 2013)
(Revised January 16 2014)
(Accepted February 11 2014)
Abbreviations: FA, fatty acids; HDL-C, HDL-cholesterol; LDL-C, LDL-cholesterol; OA, oleic acid; PREDIMED, Prevención con Dieta Mediterránea
List of Figures and Tables
Fig. 1 Effect of almond dose on the change in oleic acid (18 : 1n-9) (A) and MUFA (B) proportions in the serum NEFA () and TAG () fractions of hyperlipidaemic subjects. Values are means, with standard errors represented by vertical bars. * Mean value was significantly different from that in the NEFA fraction (P< 0·05). a,bMean values with unlike letters were significantly different (P< 0·05).
Fig. 2 Regression analysis on the association between almond consumption and percentage change of the estimated 10-year CHD risk score using the Framingham equation (R − 0·247, n 81, P= 0·026).
Table 1 Fatty acid composition of supplements used in the study (Mean values with their standard errors)
Table 2 Effect of dietary treatments on the proportion of fatty acids in the serum phospholipid fraction (Mean values with their standard errors)
Table 3 Effect of dietary treatments on the proportions of fatty acids in the serum TAG fraction (Mean values with their standard errors)
Table 4 Effect of dietary treatments on the proportions of fatty acids in the serum NEFA fraction (Mean values with their standard errors)
Epidemiological( 1 – 4 ) and clinical studies( 5 , 6 ) have shown that nut consumption decreases the risk of developing CHD and improves blood lipid risk factors. Almond consumption has been shown to reduce LDL-cholesterol (LDL-C) concentrations and increase HDL-cholesterol (HDL-C) concentrations in hyperlipidaemic individuals( 7 , 8 ). Although almonds contain a variety of constituents that may exert cardioprotective effects through various mechanisms( 9 ), their ability to improve blood lipid profiles and reduce CHD risk may primarily be related to their healthy fatty acid (FA) profile, which is low in saturated fats (SFA) and high in monounsaturated fats (MUFA)( 10 , 11 ), particularly oleic acid (OA)( 12 , 13 ). Epidemiological studies suggest that diets with a high proportion of MUFA in the form of OA, such as the Mediterranean diet, reduce CHD risk( 14 , 15 ). However, the effect of almond consumption on the serum FA profile and its association with CHD risk have not been investigated.
Therefore, in the present study, we investigated whether almond consumption would alter the serum FA profile and risk of CHD, as calculated using Framingham's 10-year risk score, in a dose-dependent manner in hyperlipidaemic individuals compared with a higher-carbohydrate control group using dietary interventions incorporating almonds( 7 ). This is a secondary analysis of a trial that primarily aimed to assess the effect of almond consumption on blood lipid risk factors for CHD( 7 ).
The study methods have been described in detail previously( 7 ).
A total of twenty-seven subjects completed three 1-month dietary phases in a randomised cross-over manner, with each phase being separated by a washout period of minimum 2 weeks. The three dietary phases comprised a muffin phase (control) and two almond phases: full-dose almond phase and half-dose almond plus half-dose muffin phase. During all the dietary phases, the subjects followed their own self-selected, low-fat therapeutic diets into which they incorporated the supplements. The subjects were counselled on strategies to facilitate weight maintenance.
After an overnight fast (12–14 h), body weight measurements, blood samples and blood pressure measurements were obtained at the start of the study and at weeks 2 and 4 of each 4-week dietary phase. Before baseline and at week 4 of each dietary phase, 7 d diet records were obtained from the subjects. The subjects were instructed to weigh all the food consumed with the self-rating electronic food scales provided during the weeks when dietary intake was recorded.
The present study was conducted according to the guidelines laid down in the Declaration of Helsinki, and all procedures involving human subjects were approved by the Ethics Committee of the University of Toronto and St Michael's Hospital. Written informed consent was obtained from all subjects. The present trial was registered at ClinicalTrials.gov (no. NCT00507520).
Healthy hyperlipidaemic men and postmenopausal women were recruited through newspaper advertisement and from among patients visiting the Risk Factor Modification Centre of St Michael's Hospital, a University of Toronto teaching hospital. As has been reported previously( 7 ), sixteen of the forty-three subjects who were initially recruited withdrew during or after completing one or two dietary phases: three discontinued for reasons directly related to the study (food allergies, n 2; abdominal discomfort, n 1) and thirteen withdrew for unrelated reasons. The characteristics of these sixteen subjects were similar to those of the subjects who completed the study. The remaining twenty-seven subjects completed all the three dietary phases: fifteen men and twelve postmenopausal women (mean age 64 (sd 9) years (range: 48–86 years; four subjects aged ≥ 75 years); mean BMI 25·7 (sd 3·0) kg/m2 (range: 20·5–31·5 kg/m2) and mean baseline LDL-C concentrations 4·32 (sd 0·63) mmol/l (range 2·77–5·32 mmol/l)). All subjects had elevated LDL-C concentrations during initial assessment at recruitment (>4·1 mmol/l), despite lower values being detected in some subjects at baseline, and TAG concentrations < 4·0 mmol/l. None of the subjects used tobacco and had clinical or biochemical evidence of diabetes, liver disease or renal disease. Among the twenty-seven subjects, three men and five women were taking the following medications: a hypolipidaemic agent (statin) (n 2); β-blocking agents (n 3); angiotensin-converting enzyme inhibitors (n 3); angiotensin II receptor blockers (n 1); thiazide diuretics (n 2); levothyroxine (n 2); hormone replacement therapy (n 2). Medication use was stable for at least 2 weeks before the study. Medication dosages were kept constant throughout the study. The subjects were asked to maintain their habitual levels of physical activity throughout the study.
Before the start of the study, all subjects had been instructed to follow a therapeutic National Cholesterol Education Program Step 2 diet ( < 7 % energy from saturated fats and < 200 mg/d dietary cholesterol). All subjects took all the three supplements: whole raw unblanched almonds (73 (sd 3) g/d); muffins (147 (sd 6) g/d); and half portions of almonds (37 (sd 2) g/d) plus muffins (75 (sd 3) g/d), as described previously( 6 ). The amount of supplements ingested was based on the estimated daily energy requirement of the subjects( 16 ). For subjects requiring < 6694 kJ/d ( < 1600 kcal/d), the full portions of almonds and muffins were 50 g (one package) and 100 g (two muffins), respectively (1201 kJ/d (287 kcal/d) supplement). The respective values for those requiring 6694–10 042 kJ/d (1600–2400 kcal/d) were 75 g of almonds and 150 g of muffins (three muffins; 1799 kJ/d (430 kcal/d) supplement) and for those requiring >10 042 kJ/d (>2400 kcal/d) were 100 g of almonds and 200 g of muffins (four muffins; 2402 kJ/d (574 kcal/d) supplement). During the half-almond plus half-muffin phase, the subjects consumed each supplement at half the full amount for each of the energy requirements described above. The muffins were made from whole-wheat flour with an amount of maize oil sufficient to provide the same amounts of SFA, PUFA and fibre provided by almonds. Skimmed milk powder and egg-whites were used to maintain the level of protein between the supplements, although the protein in the muffins was 46 % animal origin. MUFA (kJ) in almonds balanced the starch in muffins. The macronutrient composition of the muffins as a percentage of energy was as follows: 14·7 % protein; 53·3 % available carbohydrate; 32·1 % fat; 4·3 % SFA; 7·6 % MUFA; 18·9 % PUFA with 4·3 g/1000 kJ (18 g/1000 kcal) cholesterol. Non-hydrogenated maize oil was the only fat used in muffin preparation to prevent the addition of trans-FA to the supplements. Muffin supplements were provided to the subjects at biweekly intervals and were stored in a freezer until the day before use. The subjects were instructed to reduce their total food intake, especially starchy foods (breads, bagels, non-study muffins and breakfast cereals), to allow supplements to be incorporated in their diet without increasing total energy intake and to keep the background diet constant across all the three dietary phases. To minimise changes in body weight and diet composition, the subjects were given detailed dietary counselling before and at weeks 1 and 2 of each dietary phase. During the study, the subjects were asked to not consume any additional nuts or nut products or alter their intake of dietary fibre or vegetable protein foods. Compliance was assessed from 7 d diet records, a supplement checklist in which the subjects recorded the supplements consumed, and return of uneaten supplements, which were weighed and recorded.
Serum was analysed according to the Lipid Research Clinics protocol( 17 , 18 ) for total cholesterol, TAG and HDL-C after dextran sulphate–magnesium chloride precipitation, and LDL-C concentrations were calculated( 19 ) as described previously( 7 ). The present study focused on serum FA concentrations and estimated 10-year CHD risk based on the Framingham equation( 16 ). The following variables were used in the Framingham equation to determine the 10-year CHD risk at baseline and end of each intervention period: age; sex; systolic blood pressure; total cholesterol; HDL-C; total cholesterol:HDL-C ratio; smoking status; diabetes diagnosis. Values obtained for the 10-year CHD risk were then compared with those of the ideal risk, where total cholesterol:HDL-C ratio was set at 4·44, systolic blood pressure at 120 mmHg, and smoking status as non-smoker, to obtain relative risk values.
To assess FA fractions, total lipids were extracted from the serum according to the Folch method( 20 ). TLC plates were activated by heating at 100°C for 1 h. Total lipids were then loaded onto the plates and placed in a tank with solvents. FA fractions were separated along with authentic standards in heptane–diethyl ether–glacial acetic acid (60:40:2, v/v). Bands corresponding to total phospholipid, NEFA, TAG and cholesterol esters were visualised under UV light, after staining with 8-anilino-1-naphthalene sulphonic acid (0·1 %, w/v). Known amounts of an unesterified heptadecanoic acid standard were added to test-tubes containing hexane and each scraped band. These were converted to FA methyl esters with 14 % boron trifluoride–methanol at 100°C for 1 h. FA methyl esters were quantified on a Varian-430 gas chromatograph (Varian, Inc.) equipped with a Varian Factor Four capillary column (VF-23ms, 30 m × 0·25 mm inner diameter × 0·25 μm film thickness; Agilent Technologies) and a flame ionisation detector. Samples were injected in splitless mode. The temperature of the injector and detector ports was set at 250°C. FA methyl esters were eluted using a temperature programme set initially at 50°C for 2 min, increased at 20°C/min and held at 170°C for 1 min and then at 3°C/min and held at 212°C for 5 min to complete the run in 28 min. The carrier gas used was helium, set to a constant flow rate of 0·7 ml/min. Peaks were identified by the retention times of FA methyl ester standards (Nu-Chek-Prep, Inc.). FA concentrations (nmol/ml serum) were calculated by proportional comparison of GC peak areas with that of the heptadecanoic acid internal standard. Plasma SFA, MUFA and PUFA concentrations were calculated by adding the concentrations of all the respective FA with twelve to twenty-four carbon atoms within the treatment groups for each FA fraction, excluding 20 : 0 or 18 : 3n-3, as these FA did not get separated in the column.
Results are expressed as means with their standard errors. The primary outcomes of the original study were total cholesterol, LDL-C, HDL-C, TAG, apoB and apoA1( 7 ). The present study focused on FA fractions in the serum of subjects who completed the study (n 27) and estimated CHD risk using the Framingham equation( 16 ).
Treatment effects were tested using Student's t test for within-group analysis and one-way repeated-measures ANOVA for between-group analysis (Microsoft Excel, 2007). Pearson's correlation analyses were conducted to test the associations between FA concentrations and CHD risk (SAS Institute Inc., version 9.3). Statistical significance was set at P< 0·05 for all analyses.
The baseline characteristics of the subjects, as well as data obtained at baseline and after the dietary interventions, have been reported previously( 7 ). There were no differences in the effects of dietary treatments on the anthropometric or lipid profiles analysed between those who completed the study and those who did not (see Supplementary table, available online).
Serum lipid data have been published previously( 7 ). In brief, serum total cholesterol concentrations were significantly lower in both the half-dose and full-dose almond groups than in the control group. Serum LDL-C concentrations were significantly lower and serum HDL-C concentrations were significantly higher in the full-dose almond group than in the control group. Serum TAG concentrations were not affected by the dietary treatments( 7 ). There were no significant differences in body weight among the dietary treatment groups( 7 ).
FA analysis of the almond and muffin supplements revealed that almonds had significantly higher amounts of OA (18 : 1n-9) and total FA than muffins when compared on an equal amount by weight basis (Table 1). Similar findings were recorded when the supplements were analysed on a per energy basis. As has been mentioned previously, the MUFA in almonds balanced the carbohydrate in muffins.
Fatty acid composition of supplements used in the study (Mean values with their standard errors)
*Mean values were significantly different from that of the muffin-supplemented group (P< 0·05).
Changes in plasma FA concentrations after the dietary treatments reflected the FA profile of the supplements, confirming subjects' compliance with the dietary protocol. These changes were in agreement with subjects' reported compliance with the dietary protocol, which was good, ranging from 97·8 (sem 0·7) to 99·5 (sem 0·6) % for all the three dietary treatments.
There was a significant increase in the concentrations of serum OA in the full-dose and half-dose almond groups (weeks 0–4) (P= 0·001 and P= 0·024, respectively), while there was no significant difference in the concentrations from baseline in the control group (Table 2).
Effect of dietary treatments on the proportion of fatty acids in the serum phospholipid fraction (Mean values with their standard errors)
AA, arachidonic acid.
*Mean value was significantly different from that at week 0 (P< 0·05).
†Mean values were significantly different between the dietary treatment groups (P< 0·05).
The proportions of SFA in the phospholipid fraction were positively associated with the 10-year CHD risk (R 0·270, n 80, P= 0·015), while those of PUFA in the fraction were inversely associated with it (R − 0·294, n 80, P= 0·008).
There was a significant increase in the proportions of OA and MUFA in the serum TAG fraction in the half-dose (P= 0·003 and P= 0·004, respectively) and full-dose (P< 0·001 and P< 0·001, respectively) almond groups, while there was no change in the control group (Table 3; Fig. 1). The proportions of OA and MUFA in the almond groups increased significantly in a dose-dependent manner when compared with those in the control group (P< 0·05).
Effect of dietary treatments on the proportions of fatty acids in the serum TAG fraction (Mean values with their standard errors)
AA, arachidonic acid.
*Mean value was significantly different from that at week 0 (P< 0·05).
†Mean values were significantly different between the dietary treatment groups (P< 0·05).
Effect of almond dose on the change in oleic acid (18 : 1n-9) (A) and MUFA (B) proportions in the serum NEFA () and TAG () fractions of hyperlipidaemic subjects. Values are means, with standard errors represented by vertical bars. * Mean value was significantly different from that in the NEFA fraction (P< 0·05). a,bMean values with unlike letters were significantly different (P< 0·05).
There was a significant decrease in the proportion of palmitic acid (16 : 0) in the half-dose and full-dose almond groups when compared with that in the control group (P< 0·05). The proportion of palmitic acid was positively associated with serum TAG concentrations (R 0·475, n 80, P< 0·001) and the total cholesterol:HDL-C ratio (R 0·325, n 80, P= 0·003) and inversely associated with HDL-C concentrations (R 0·444, n 80, P< 0·001).
The 10-year CHD risk was inversely associated with the proportions of OA (R − 0·283, n 80, P= 0·011) and MUFA (R − 0·269, n 80, P= 0·016) in the TAG fraction; this association was no longer significant when all the MUFA, except OA, were assessed (data not shown). The proportions of SFA were negatively associated with HDL-C concentrations (R − 0·428, n 80, P≤ 0·001) and positively associated with the 10-year CHD risk (R 0·300, n 80, P= 0·007).
No significant associations were observed between PUFA proportions and 10-year CHD risk.
There were no significant differences in the proportions of serum OA or MUFA from baseline within or between the dietary treatment groups or any significant associations between FA concentrations and blood lipid profiles or CHD risk (data not shown).
The proportions of individual FA in the serum NEFA fraction are given in Table 4. There was no change in the proportion of OA (18 : 1n-9) in the control group, but an increase was observed in the almond groups (Fig. 1). However, this increase was only significant in the half-dose almond group (P= 0·01), and the lack of a significant increase in the full-dose almond group is possibly due to high variability. Similarly, there was an increase in the proportions of serum MUFA in the half-dose and full-dose almond groups, but it was significant only in the half-dose almond group (P= 0·04 and P= 0·06, respectively; Fig. 2).
Effect of dietary treatments on the proportions of fatty acids in the serum NEFA fraction (Mean values with their standard errors)
AA, arachidonic acid.
*Mean value was significantly different from that at week 0 (P< 0·05).
The proportions of MUFA in the NEFA fraction were positively associated with HDL-C concentrations (R 0·329, n 80, P= 0·003) and inversely associated with the 10-year CHD risk (R − 0·290, n 80, P= 0·009); however, this association was significant when all the MUFA, except OA, were assessed together (data not shown). In contrast, the proportions of SFA and palmitic acid (16 : 0) were inversely associated with HDL-C concentrations (R − 0·319, n 80, P= 0·004; R − 0·297, n 80, P= 0·007, respectively), possibly related to the reduction in the proportions of palmitic acid and total SFA and increase in those of MUFA after almond supplementation. The proportions of SFA and palmitic acid were also positively associated with the 10-year CHD risk (R 0·273, n 80, P= 0·014; R 0·331, n 80, P= 0·003, respectively).
No significant associations were observed between the proportions of OA or PUFA in the NEFA fraction and the risk of CHD.
Almond intake was found to be associated with a decrease in the percentage change of the estimated Framingham 10-year CHD risk score during the study (R − 0·247, n 81, P= 0·026), where for every 30 g increase in almond intake, a 3·5 % decrease in the 10-year CHD risk was observed (Fig. 2).
The results of the present study indicate that an isoenergetic incorporation of almonds (approximately 10 and 20 % of energy from half-dose and full-dose almonds, respectively) into a National Cholesterol Education Program Step 2 diet improves the FA profile of hyperlipidaemic adults by increasing the OA and MUFA content of serum TAG and NEFA fractions, which are inversely associated with CHD lipid risk factors and overall 10-year CHD risk.
Much of the interest in the role of MUFA in the prevention of CHD arises from the observed beneficial effects of a Mediterranean dietary pattern( 21 ), which is high in olive oil, providing 14–40 % of energy( 22 – 25 ), and consequently high in MUFA (16–29 % of energy( 23 , 26 – 29 )) and OA. The European Prospective Investigation into Cancer and Nutrition (EPIC)-Spain cohort study not only showed an association between decreased morbidity and MUFA and olive oil intake, but also showed a gradual decrease in the risk of CVD mortality with an increase in olive oil intake, where an increase of 10 g/8368 kJ per d (10 g/2000 kcal per d) was found to be associated with a 13 % decreased risk( 30 ). Similar to olive oil, almonds contain significantly high amounts of MUFA in the form of OA. The beneficial effects of almonds, particularly the MUFA component, on CHD risk observed in the present study are consistent with previous findings, including those of the Prevención con Dieta Mediterránea (PREDIMED) study( 31 ). The results of a PREDIMED-based cross-over trial indicated that almonds are as effective as virgin olive oil at improving risk factors for CVD( 31 ). In a 3-month substudy of PREDIMED, total cholesterol and TAG concentrations were found to decrease in only the Mediterranean diet with nuts (i.e. almonds, walnuts and hazelnuts) group but not in the virgin olive oil group when compared with the control group( 32 ). Additional trials within PREDIMED have supported the beneficial effects of nut consumption on CHD risk. A 1-year randomised clinical trial showed that a Mediterranean dietary pattern supplemented with nuts had an anti-inflammatory effect with significant reductions in the plasma concentrations of TNF receptor, IL-6 and intercellular adhesion molecule 1, which are circulating inflammatory biomarkers associated with CHD risk( 33 ). This dietary pattern was further shown to be protective against the primary endpoints of CHD. The resulting multivariate analysis value obtained in a long-term (median 4·8 years) PREDIMED randomised multicentre trial of a Mediterranean diet with nuts v. a control diet was 0·72 (95 % CI 0·54, 0·96; P= 0·03) with respect to the primary endpoint, which was a composite of myocardial infarction, stroke and death from cardiovascular causes( 6 ).
Although the mechanism by which almonds modify CHD risk is unclear, it has been proposed that almonds may exert an effect exogenously and endogenously. It has been proposed that dietary incorporation of almonds exogenously reduces serum cholesterol concentrations by replacing saturated fats with monounsaturated fats in the diet. In a randomised, controlled, parallel study, the SFA concentrations of thirty-eight hypercholesterolaemic adults who consumed 100 g of raw almonds daily over a 4-week period were found to be lower( 34 ). Furthermore, increasing MUFA intake has been reported to be associated with an increase in HDL-C concentrations, as demonstrated by a randomised, controlled trial of twenty-four hypercholesterolaemic adults( 35 ). The improvement in blood lipid profiles has generally been associated with a reduced risk of CHD. However, this may not apply to the present study as we focused on a MUFA–carbohydrate substitution. It has also been proposed that almonds may act endogenously to exert a cardioprotective effect. Dietary FA are rapidly incorporated into lipoprotein lipids. Enrichment of lipoprotein particles with MUFA at the expense of PUFA may enhance their resistance to oxidative stress as there are few double bonds to react with, thus potentiating the anti-atherogenic effect( 36 – 38 ). Plasma phospholipid, cholesterol ester, TAG and NEFA compositions are responsive to total dietary fat content, though NEFA and TAG are the major forms of lipids found in circulation( 39 ).
There are several limitations to the present study. α-Linolenic acid (18 : 3n-3) did not get separated from arachidic acid (20 : 0) during chromatographic analysis. Almonds are low in α-linolenic acid( 10 ) and would not be expected to significantly alter serum concentrations; however, neither this nor any associations between changes in serum α-linolenic acid concentrations and CHD risk could be verified from the findings of the present study. Moreover, in the present study, almond consumption was found to increase faecal MUFA excretion (RP Bazinet and CWC Kendal, unpublished results), indicating an attenuated effect due to the inaccessibility of some of the nutrients and energy from almonds for absorption( 40 ). This is further supported by findings from previous studies, which suggest that nuts contain less metabolisable energy than expected based on Atwater general factors and that the lipid from nuts is more poorly absorbed than that from other food sources( 41 ).
Despite these limitations, the findings of the present study suggest that the FA profile of almonds has the potential to contribute to the total reduction of CHD risk. The cholesterol-lowering effect of almond consumption is explained, in part, by the FA profile of almonds, especially MUFA; however, there may be other bioactive components in almonds that further reduce CHD risk. In addition to unsaturated FA, almonds are a good source of vitamin E, fibre and phytochemicals (phenols, flavonoids, proanthocyanidins and phytosterols), arginine, Cu and Mg, which may beneficially influence CHD risk( 42 – 44 ). Many of these nutrients may act synergistically to produce the observed favourable outcomes, although further studies are required to prove this postulation( 42 ). Further analysis of LDL particle size may provide a better understanding of potential mechanisms by which almonds and other foods rich in MUFA influence TAG concentrations.
In conclusion, the results of the present study indicate that almond consumption favourably alters the serum FA profile by increasing the proportions of OA and total MUFA and decreasing those of SFA. These changes in the FA profile are correlated with improvements in blood lipoproteins and with a decreased 10-year CHD risk.
To view supplementary material for this article, please visit http://dx.doi.org/10.1017/S0007114514001640
The authors thank Tzu Han Chuck Chen and Byung Jun Song for their exceptional technical assistance.
Aspects of the present study have been presented at Experimental Biology, San Diego, CA, 21–25 April 2012.
The present study was supported by the Canada Research Chair Endowment of the Federal Government of Canada and the Almond Board of California, Modesto, CA, USA. None of the funding organisations or sponsors played any role in the design and conduct of the study; in the collection, management, analysis and interpretation of the data; or in the preparation, review or approval of the manuscript.
C. W. C. K., R. P. B. and D. J. A. J. had full access to all the data in the study and were responsible for the integrity of the data and the accuracy of the data analysis. C. W. C. K. and D. J. A. J. obtained funding. C. W. C. K., R. P. B., K. G. L. and D. J. A. J. were responsible for study concept and design. S. N., C. W. C. K., R. P. B., B. B., A.-M. G. and D. J. A. J. were responsible for the acquisition and analysis of data. S. N., C. W. C. K., A.-M. G., R. P. B., K. G. L., L. S. A. A., J. L. S. and D. J. A. J. were responsible for the interpretation of data. S. N., C. W. C. K. and R. P. B. drafted the manuscript. S. N., C. W. C. K., A.-M. G., R. P. B., B. B., K. G. L., L. S. A. A. and J. L. S. provided administrative, technical and material support. C. W. C. K., R. P. B., B. B. and D. J. A. J. supervised the study. All authors critically revised the manuscript for important intellectual content and approved the manuscript submitted for publication.
D. J. A. J. has served on the Scientific Advisory Board of Unilever, Sanitarium Company, California Strawberry Commission, Loblaw Supermarket, Herbal Life International, Nutritional Fundamental for Health, Pacific Health Laboratories, Metagenics, Bayer Consumer Care, Orafti, Dean Foods, Kellogg's, Quaker Oats, Procter & Gamble, Coca-Cola, NuVal Griffin Hospital, Abbott, Pulse Canada, Saskatchewan Pulse Growers and Canola Council of Canada; is receiving honoraria for scientific advice from the Almond Board of California, International Tree Nut Council Nutrition Research and Education Foundation, Barilla, Unilever Canada, Solae, Oldways, Kellogg's, Quaker Oats, Procter & Gamble, Coca-Cola, NuVal Griffin Hospital, Abbott, Canola Council of Canada, Dean Foods, California Strawberry Commission, Hain Celestial and Alpro Foundation; is on the speakers panel of the Almond Board of California; is receiving research grants from Loblaw Brands Limited, Unilever, Barilla, Almond Board of California, Solae, Hain Celestial, Sanitarium Company, Orafti, International Tree Nut Council Nutrition Research & Education Foundation, and Peanut Institute and receiving travel support to meetings from the Almond Board of California, Unilever, Alpro Foundation, and International Tree Nut Council, Canadian Institutes for Health Research, Canada Foundation for Innovation, Ontario Research Fund. D. J. A. J. is receiving salary support as a Canada Research Chair from the federal government of Canada. His wife is a director of Glycemic Index Laboratories, Toronto, Ontario, Canada. C. W. C. K. has received research grants, travel funding, consultant fees and honoraria from and has served on the Scientific Advisory Board of Abbott Laboratories, Advanced Food Materials Network, Agrifoods and Agriculture Canada, Almond Board of California, American Peanut Council, American Pistachio Growers, Barilla, California Strawberry Commission, Energy Control Council, Canadian Institutes of Health Research (CIHR), Canola Council of Canada, The Coca-Cola Company (investigator initiated, unrestricted), Danone, General Mills, Hain Celestial, International Tree Nut Council, Kellogg's, Kraft, Loblaw Brands Limited, Nutrition Foundation of Italy, Oldways, Orafti, Paramount Farms, Peanut Institute, Pepsi-Co, Pulse Canada, Saskatchewan Pulse Growers, Solae, Sun-Maid, Tate & Lyle, and Unilever. J. L. S. has received research support from the CIHR, Energy Control Council, The Coca-Cola Company (investigator initiated, unrestricted grant), Pulse Canada, and International Tree Nut Council Nutrition Research & Education Foundation. He has received travel funding, speaker fees and/or honoraria from the American Heart Association, American College of Physicians, American Society for Nutrition (ASN), National Institute of Diabetes and Digestive and Kidney Diseases of the National Institutes of Health, Canadian Diabetes Association (CDA), Canadian Nutrition Society, Calorie Control Council, Diabetes and Nutrition Study Group of the European Association for the Study of Diabetes (EASD), International Life Sciences Institute (ILSI) North America, ILSI Brazil, Abbott Laboratories, Pulse Canada, University of South Carolina, University of Alabama at Birmingham, Oldways Preservation Trust, Nutrition Foundation of Italy (NFI), Corn Refiners Association, World Sugar Research Association, Dr Pepper Snapple Group and The Coca-Cola Company. He has consulting arrangements with Winston & Strawn LLP and Tate and Lyle. He is on the Clinical Practice Guidelines Expert Committee for Nutrition Therapy of both the CDA and EASD, as well as on the ASN writing panel for a scientific statement on the metabolic and nutritional effects of fructose, sucrose and high-fructose corn syrup. He is an unpaid scientific advisor for the ILSI North America, Food, Nutrition, and Safety Program. His wife is an employee of Unilever Canada. K. G. L. is an employee of the Almond Board of California. No other potential conflicts of interest relevant to the study exist.