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Reprinted with permission from Food Science and Technology Bulletin: Functional Foods
(2009) 6 (4): 41–50; published by IFIS Publishing
The nutritional and health benefits of
almonds: a healthy food choice
David P. Richardson
DPR Nutrition Ltd, 34 Grimwade Avenue, Croydon, Surrey CR0 5DG, UK
Arne Astrup
Department of Human Nutrition, Faculty of Life Sciences, University of Copenhagen,
Roligshedsvej 30, DK-1958 Frederiksberg C, Copenhagen, Denmark
Arnaud Cocaul
L’hôpital Pitié-Salpêtrière, 103 boulevard Saint Michel, 75005 Paris, France
Peter Ellis
Biopolymers Group, Department of Biochemistry, Franklin-Wilkins Building, Kings
College London, 150 Stamford Street, London SE1 9NN, UK
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The nutritional and health benefits of almonds: a healthy
food choice
David P. Richardson
1
, Arne Astrup
2
, Arnaud Cocaul
3
and Peter Ellis
4
1
DPR Nutrition Limited, 34 Grimwade Avenue, Croydon, Surrey CR0 5DG, UK
2
Department of Human Nutrition, Faculty of Life Sciences, University of Copenhagen, Roligshedsvej 30, DK-1958
Frederiksberg C, Copenhagen, Denmark
3
L’ho
ˆpital Pitie
´-Salpe
ˆtrie
`re, 103 boulevard Saint Michel, 75005 Paris, France
4
Biopolymers Group, Department of Biochemistry, Franklin-Wilkins Building, Kings College London, 150 Stamford
Street, London SE1 9NN, UK
Abstract
Over the last decade, the research on the effects of almonds on reducing blood cholesterol levels and reduc-
tion of risk of heart disease has grown significantly. Emerging research on almonds also shows promising
health benefits linked to body weight control and diabetes. Almonds naturally contain high levels of monoun-
saturated and polyunsaturated fatty acids, protein and dietary fibre, as well as a variety of essential nutrients
including vitamin E and several trace elements. Almonds are very low in sodium and high in potassium, and
they contain a range of phytoprotective constituents. The available evidence also indicates that weight gain
may not be a concern when nuts are consumed in moderation, and that regular consumption of nuts can be
recommended in the context of a healthy balanced diet.
Keywords: almonds, nutrient density, heart health, weight control
1. Introduction
Almonds (Prunus dulcis; Gradziel 2009) are a nutrient-
dense food, and extensive research during the last decade
on the potential health benefits of almonds has linked con-
sumption patterns to reduced risk of chronic diseases such
as coronary heart disease (CHD) and type 2 diabetes, as
well as to weight maintenance and weight control. Tree
nuts such as almonds have been part of mankind’s diet
since pre-agricultural times and their popularity has con-
tinued to grow in modern times, either as snacks or as part
of a meal. Almonds can be eaten whole (fresh or roasted)
and in spreads like almond butter or they can be used in a
wide range of food products and recipes.
Almonds have complex food matrices containing
diverse nutrients and other phytoprotective substances that
favourably influence human physiology. All nuts are
energy dense and contain high levels of fat, but much of
this is unsaturated. However, there is still caution about
overt recommendations for nut consumption and a lack of
understanding and awareness of how nuts can fit into a
balanced diet.
The present article highlights that almonds are a rich
source of many essential nutrients including vitamin E and
several trace elements, that there is compelling evidence
that almonds have beneficial effects on the reduction of
plasma cholesterol levels and other heart disease risk fac-
tors, and that evidence is emerging which suggests that
almonds may have a positive role in healthy weight main-
tenance and weight loss.
2. The nutritional attributes of almonds
2.1 Almonds as a source of energy and
macronutrients
Almonds typically contain around 575 kcal per 100 g and
about 50% fat. However, the fatty acid composition of
almonds is beneficial because monounsaturated fatty acids
(MUFA) predominate and the saturated fat content (3.7 g
per 100 g almonds) is the lowest of all nuts. Table 1 shows
the nutrient composition of almonds. The total fat content
is made up of 62% MUFA and 24% of polyunsaturated
fatty acids (PUFA; Ros and Mataix 2006; Chen et al. 2006;
Food Science and Technology Bulletin: Functional Foods 6(4) 41–50
DOI: 10.1616/1476-2137.15765. Accepted 23 July 2009
ISSN 1476-2137 #IFIS Publishing 2009. All Rights Reserved
......................................................................................................................................................................
Table 1. Nutrient composition of almonds
a
Nutrient Unit Per 100 g
Per 30 g
serving
RDA for
labelling
c
Amounts to meet criteria for
nutrient content claims in EU
b
Nutrition
claim
in EU
b
‘Source’
(15% RDA
per 100 g)
‘High’
(30% RDA
per 100 g)
Macronutrients
Water g 4.70 1.41
Energy kcal 575 172
Protein g 21.22 6.37 See footnote d
Total fat g 49.42 14.83
Total sugars g 3.89 1.17 See footnote e
Dietary fibre g 12.20 3.66 See footnote f
Minerals
Calcium mg 264 79 800 120.00 240.00 HIGH
Iron mg 3.72 1.12 14 2.10 4.20 SOURCE
Magnesium mg 268 80 375 56.25 112.50 HIGH
Phosphorus mg 484 145 700 105.00 210.00 HIGH
Potassium mg 705 211 2000 300.00 600.00 HIGH
Sodium mg 1 0 See footnote g
Zinc mg 3.08 0.92 10 1.50 3.00 HIGH
Copper mg 1.00 0.30 1 0.15 0.30 HIGH
Manganese mg 2.28 0.68 2 0.30 0.60 HIGH
Selenium mg 2.50 0.75 55 8.25 16.5 —
Vitamins
Thiamin mg 0.21 0.06 1.1 0.17 0.33 SOURCE
Riboflavin mg 1.01 0.30 1.4 0.21 0.42 HIGH
Niacin mg 3.38 1.01 16 2.40 4.80 SOURCE
Pantothenic acid mg 0.47 0.14 6 0.90 1.80 —
Vitamin B
6
mg 0.14 0.04 1.4 0.21 0.42 —
Folate mg 50 15 200 30.00 60.00 SOURCE
Vitamin A (retinol equivalent) mg 0 0 800 120 240 —
Vitamin E
a-Tocopherol mg 26.22 7.87 12.00 1.80 3.60 HIGH
b-Tocopherol mg 0.29 0.09
g-Tocopherol mg 0.65 0.19
d-Tocopherol mg 0.05 0.01
Lipids
Saturated fats g 3.73 1.12
Monounsaturated fats g 30.89 9.27
18: 1 g 30.61 9.18
Polyunsaturated fats g 12.07 3.62
18: 2 g 12.06 3.62
Phytosterols mg 172 52
Stigmasterol mg 4 1
Campesterol mg 5 1
b-Sitosterol mg 132 40
Other phytosterols
h
mg 31 10
Amino acids
Lysine g 0.58 0.17
Arginine g 2.47 0.70
Other
b-Carotene mg1 0
Total phenolics mg
i
418 125
Total flavonoids
j
mg
i
23.89 7.17
a
Nutrient data obtained from the USDA National Nutrient Database for Standard Reference, Release 21 (2008)
b
Regulation (EC) No. 2006 of the European Parliament/2006 of the European Parliament and of the Council of 20th December 2006 on nutrition and health
claims made on foods. Official Journal of the European Union 18.1.2007, L 12/3
c
Commission of the European Communities. 2008/100/EC. Commission Directive amending Council Directive 90/496/EC on nutrition labelling for foodstuffs as
regards recommended daily allowances, energy conversion factors and definitions. Official Journal of the European Union L285/9. 29.10.2008
d
Whole natural almonds contain 21.22 g protein per 100 g. On an energy basis, 21.22 4 kcal = 84.88 kcal protein calories are provided by 100 g almonds contain-
ing 575 kcal. Hence, 14.7% of the energy is derived from protein. Almonds can claim ‘natural source of protein’ under the new European legislation, which requires
at least 12% of the energy value of a food to be provided by protein
e
Whole natural almonds contain 3.89 g total sugars per 100 g. Almonds can claim ‘naturally low in sugars’ because they contain no more than 5 g sugars per 100 g
f
Whole natural almonds contain 12.20 g dietary fibre per 100 g, sufficient to claim ‘naturally high in fibre’ under the new European regulation, which requires at
least 6 g fibre per 100 g
g
Whole natural, unsalted almonds contain 1 mg sodium per 100 g, which is within the claim criteria for sodium free or salt free, namely that the food should contain
no more than 0.005 g sodium, or the equivalent value for salt, per 100 g
h
Other phytosterols include d5-avenasterol, sitostanol, campestanol, and other minor phytosterols
i
Expressed as gallic acid equivalents (Wu et al. 2004)
j
Determined from Butte, Carmel, Fritz, Nonpareil, Mission, Monterey, Padre and Price varieties and adjusted for their market contribution.
Ternus et al. 2009). The fatty acids from almonds are impor-
tant contributors to the beneficial health effects of frequent
nut consumption, namely reduced risk of cardiovascular dis-
ease and sudden cardiac death, lowering of blood choles-
terol, preservation or enhancement of low density lipopro-
tein (LDL) resistance to oxidation and improvement of
endothelial function (Ros and Mataix 2006; Griel and Kris-
Etherton 2006). The total protein content of almonds is
21.2%, making them a good source of plant protein, and the
proteins in almonds are high in arginine (Ahrens et al. 2005).
Almonds also contain around 3.9 g total sugars per 100 g,
and because they contain less than 5 g sugars per 100 g they
can be described as ‘naturally low in sugars’ under the new
European regulation on nutrition 1924/2006 on nutrition and
health claims (European Parliament and Council 2007).
2.2 Almonds are naturally high in fibre
Whole natural almonds contain around 12 g dietary fibre
per 100 g (Table 1), which is sufficient to claim ‘naturally
high in fibre’ under the new European regulation. There is
a general consensus based on epidemiological and human
intervention studies that dietary fibre from the plant cell
walls of foods such as whole grain cereals, vegetables,
legumes, fruits and nuts is associated with a range of
health benefits. These benefits include reduction in the risk
of developing CHD and diabetes and positive effects on
the digestive system, e.g. prebiotic effects. Plant cell walls
are supramolecular networks of cellulose, hemicelluloses,
pectic substances and non-carbohydrate components (e.g.
phenolic compounds), and they are the major source of
dietary fibre (Ellis et al. 2004). Different types of dietary
fibre can attenuate the rise in postprandial glycaemia and
lower plasma concentrations of cholesterol. Increasing the
intake of dietary fibre can also increase satiety and reduce
body weight gain over time. The addition of nuts such as
almonds to low calorie diets for weight loss may increase
satiation and result in incomplete intestinal absorption of
fat. These latter two effects may be due largely to the high
fibre and protein contents of nuts. Plant cell walls are known
to influence the rate and extent of lipid release from plant
food tissues during digestion, and the structural characteris-
tics of almond cell walls (dietary fibre) play an important
role (Ellis et al. 2004).
A typical serving of almonds (28–30 g) provides about
14% of the daily fibre requirement.
2.3 Micronutrients
Almonds are one of the most nutrient-rich forms of food
available (Blomhoff et al. 2006). Table 1 shows the vitamin
and mineral contents naturally present in whole almonds,
along with the nutrition claims that meet the conditions laid
down in the EU Regulation 1924/2006. Almonds are natu-
rally high in vitamin E, riboflavin (vitamin B
2
) and the
minerals calcium, magnesium, phosphorus, potassium, zinc,
copper and manganese.
2.4 Sodium and potassium content
From Table 1, it can be seen that almonds are essentially
sodium free and high in potassium. On the basis of the EU
nutrition claim criteria, almonds are naturally high in potas-
sium, naturally sodium free and fit well into low sodium/
high potassium diets.
2.5 Phytosterols and antioxidants
Tree nuts, including almonds, contain no dietary choles-
terol but are rich in the chemically related phytosterols, a
class of compounds that interfere with cholesterol absorp-
tion and thus help maintain healthy blood cholesterol
levels. The most abundant phytosterols in plants are cam-
Table 2. Phytosterol content of nuts in mg/100 g edible portion*
b-Sitosterol Campesterol Stigmasterol 5-Avenasterol
Total
phytosterols
Almonds 132
a
143
b
5
a
5
b
4
a
5
b
20
b
120 199
Brazil nuts nd 66 nd 2 nd 6 14 nd 95
Cashews nd 113 nd 9 nd 1 14 158 150
Hazelnuts 89 102 6 7 1 2 3 96 121
Macadamia nuts 108 144 8 10 0 nd 13 116 187
Peanuts, dry roasted nd 77 nd 13 nd 12 18 nd 137
Pecans 89 117 5 6 3 3 15 102 157
Pine nuts nd 132 nd 20 nd 1 40 141 236
Pistachios 198 210 10 10 5 2 26 214 279
Walnuts 64 89 7 5 1 nd 7 72 113
*Sources: adapted from Segura et al. (2006)
nd, not determined
a
US Department of Agriculture National Nutrient Database for Standard Reference, Release 21
b
Phillips et al. (2005).
43The nutritional and health benefits of almonds: a healthy food choice D.P. Richardson et al.
pesterol, b-sitosterol, 5-avenasterol and stigmasterol. The
phytosterol content of nuts is shown in Table 2. The cho-
lesterol-lowering efficacy of nuts in human studies has
often been higher than predicted on the basis of fatty acid
exchange and the high content of MUFAs (Griel and Kris-
Etherton 2006). Phytosterols in nuts may be responsible in
part for this effect.
As well as the antioxidant vitamin E, several nuts are
among those dietary plants with the highest contents of
total antioxidants (Blomhoff et al. 2006). Dietary flavo-
noids are hypothesised to play a significant role as antioxi-
dants in vivo, thereby reducing risk of chronic disease.
However, their role has been challenged because of the
observations that only very low amounts of flavonoids are
achieved in plasma after consumption of flavonoid-rich
foods. In this area of emerging science, in vitro and ani-
mal studies have indicated that flavonoids from almond
skins are bioavailable and act synergistically with vitamins
C and E to enhance LDL cholesterol resistance to oxida-
tion (Chen et al. 2005). The potential effects of almond
consumption on DNA damage and oxidative stress among
cigarette smokers has also been studied (Jia et al. 2005).
Research is now focusing on the complete characterisation
and quantification of almond polyphenolics and antioxi-
dants, on the antioxidant activity of almond seed extracts,
on flavonoids from almond skins, and on the effects of
almond skin polyphenols and quercetin on human LDLs
and biomarkers of lipid peroxidation.
The unique combination of MUFAs, phytosterols and
antioxidants, together with the high nutrient density of
almonds with respect to vitamin E, folate, calcium, mag-
nesium and potassium combined with low sodium, may all
contribute to the health benefits observed in epidemiologi-
cal studies and human trials.
3. Bioaccessibility of protein, lipid and vitamin E
from almonds
Compared with other tree nuts, almonds are unusual for
the large amounts of protein and vitamin E (a-tocopherol)
they contain. The main component of almonds is fat, and
it has been observed in human volunteers that a significant
proportion of lipid seems to be slowly digested and
absorbed or remains completely undigested. The term
‘bioaccessibility’ is defined as the proportion of a nutrient
that can be released from a complex food matrix and
therefore becomes potentially available for absorption in
the gastrointestinal tract (Ellis et al. 2004). The evaluation
of the bioaccessibility of almond nutrients is an active
area of research (Berry et al. 2008; Frecka et al. 2008;
Mandalari et al. 2008a, 2008b; Cassady et al. 2009)
because it may have implications for the management of
overweight and obesity, as well as for reduced risk of car-
diovascular disease. The effects of mastication on particle
size directly affects the bioaccessibility of lipid, protein
and vitamin E (Mandalari et al. 2008a), and early studies
indicate that prolonged chewing increases the number of
fractured plant cells, thereby increasing the bioavailability
of vitamin E and lipid. This decrease in the absorption of
the fat energy from almonds could reduce their theoretical
contribution to energy intake by around 7% (Mattes
2008). Moreover, the rate and extent of lipid bioaccessibil-
ity of almonds, which is primarily regulated by the integ-
rity of the plant cell walls (dietary fibre) that encapsulate
the lipids, play an important role in determining postpran-
dial lipaemia (Berry et al. 2008). Results of in vitro stu-
dies and ileostomy digestibility studies have also demon-
strated that the dietary fibre, lipid and protein present in
almond tissue after duodenal digestion are available for
fermentation in the colon by the gut microbiota (Manda-
lari et al. 2008b). Further studies have investigated the
potential prebiotic effect of almond seeds by using a full
model of the gastrointestinal tract, which simulates in vitro
gastric and duodenal digestion. The resultant residues are
used as substrates for the colonic model to assess their
influence on the composition and metabolic activity of gut
bacteria populations. Finely ground almonds significantly
increased the populations of Bifidobacteria and Enterobac-
terium rectale, resulting in a higher prebiotic index (4.43)
than was found for the commercial prebiotic fructooligo-
saccharide (4.08) after a 24 h incubation. The increase in
numbers of E. rectale during this in vitro fermentation
correlated with increased butyrate production. These initial
results indicate that almond seeds exhibit the potential to
be used as a source of prebiotics, and that more detailed
studies should be performed on human volunteers.
Data from epidemiological studies and human trials
indicate that incorporating nuts such as almonds into the
diet does not compromise body weight owing not only to
strong satiety properties and effects on resting energy
expenditure, but also because of limited lipid bioaccessi-
bility. In human studies, a significant increase in faecal
energy loss has been demonstrated that accounts for about
5–15% of the energy content of almonds (Cassady et al.
2009). It is hypothesised that by three routes, namely sati-
ety, promotion of energy expenditure and inefficient
energy utilisation, moderate nut consumption does not
pose a threat for weight gain (Mattes 2008; see Section 5).
4. Almond consumption and reduced risk of
cardiovascular disease
4.1 Observational studies
Epidemiological studies have been remarkably consistent
in showing an association between nut consumption and a
reduced risk of CHD (Sabate
´and Ang 2009). The four
major cohort studies (Fraser et al. 1992; Kushi et al.
44 The nutritional and health benefits of almonds: a healthy food choice D.P. Richardson et al.
1996; Hu et al. 1998; Albert et al. 2002) all show a clear
dose-response gradient between nut consumption and
reduced CHD risk. Taken together, these observational
studies exhibited an average risk reduction of CHD mor-
tality of 37% (relative risk (RR) ¼0.63; 95% confidence
interval (CI): 0.51, 0.83) or an average of 8.3% reduction
in risk of CHD death for each weekly serving of nuts
(Kelly and Sabate
´2006). The beneficial effects of nut con-
sumption are similar for different clinical outcomes: non-
fatal myocardial infarction, fatal CHD, and sudden cardiac
death. Collectively, these epidemiological findings provide
strong evidence of the cardioprotective benefits of nut
consumption (Sabate
´and Ang 2009).
The low incidence of CHD in Mediterranean countries
has been partly ascribed to dietary habits, and recent find-
ings from large European cohort studies (Trichopolou
et al. 2003; Knoops et al. 2004, 2006) suggest that a high
degree of adherence to the traditional Mediterranean diet
is associated with a reduction in mortality (Trichopolou
and Lagiou 1997). Tree nuts such as almonds, hazelnuts
and walnuts, which are common in the Mediterranean diet,
have favourable fatty acid profiles and are a rich source of
nutrients and other bioactive compounds, which may
account in part for the observed beneficial effects on
reduced risk of CHD. Estruch et al. (2006) reported the
results of a randomised trial in Spain. Participants were
assigned to a low fat diet (n ¼257) or to one of two
Mediterranean diets. Those allocated to Mediterranean
diets received nutrition education and either free virgin
olive oil (1 L/week (n ¼257)), or free nuts (15 g/day wal-
nuts, 7.5 g/day hazelnuts and 7.5 g/day almonds, for
3 months (n ¼258)). The completion rate was 99.6%.
Compared with the low fat diet, the two Mediterranean
diets supplemented with olive oil or nuts produced benefi-
cial effects on cardiovascular risk factors, including blood
glucose, systolic blood pressure and total cholesterol to
high density lipoprotein (HDL) ratio (Estruch et al. 2006;
Salas-Salvado et al. 2008a, 2008b). These authors con-
cluded that a Mediterranean diet including nuts such as
almonds could be a useful tool in managing individuals
who are at high risk of cardiovascular disease. Similarly, a
Mediterranean-style diet with a relatively higher intake of
nuts and legumes and high in MUFA was found to
improve glucose metabolism more than a typical Western
diet (Due et al. 2008).
In conclusion, regular nut consumption reduces the risk
of cardiovascular disease, an effect that has been observed
in several populations and is independent of other lifestyle
factors (Kris-Etherton 2001; Kelly and Sabate
´2006). Nut
eaters typically eat less meat, have lower intakes of trans
fatty acids and higher intakes of unsaturated fatty acids
and fibre (Hu and Stampfer 1999; Ternus et al. 2009).
These authors estimated that substituting 28 g of nuts for
the equivalent energy from carbohydrate in an average diet
was associated with a 30% reduction in CHD risk. They
concluded that regular nut consumption can be recom-
mended in the context of a healthy and balanced diet.
4.2 Human intervention studies
Human studies involving mixed nuts have been conducted
in six countries: Australia, Canada, Israel, India, New
Zealand and the United States. The results showed signifi-
cant reductions in plasma total cholesterol (7–25%) and
plasma LDL cholesterol (10–33%). These studies have
been reviewed by Ternus et al. (2009). Further evidence
for the cardioprotective effects of nuts is provided by
single-nut trials, including several studies using almonds.
Spiller et al. (1992) first reported that consumption of
100 g/day of almonds decreased plasma total cholesterol
by 9% and plasma LDL cholesterol by 12% in 26 hyperch-
olesterolaemic patients. Hyson et al. (2002) extended this
observation in a trial of 22 healthy subjects by achieving
reductions in plasma total cholesterol of 4% and plasma
LDL cholesterol of 6% by replacing half their fat intake
with 35 g of almond oil and 66 g of whole almonds (con-
taining 35 g of fat). Jenkins et al. (2002) demonstrated a
dose-response relationship with the addition of 28 g and 56
g of almonds daily to an isoenergetic diet, lowering plasma
total cholesterol and plasma LDL cholesterol by 4.7 and
9.9%, respectively. These authors calculated that for each
7 g/day of almond intake, plasma LDL cholesterol is
reduced by 1%. These results on almonds are consistent
with those from mixed nut studies (Ternus et al. 2009).
Recently, Phung et al. (2009) evaluated the influence of
almonds on serum lipid profiles. On the basis of a meta-
analysis, almond consumption ranging from 25 to 168 g/
day significantly lowered plasma total cholesterol and
showed a strong trend toward reducing plasma LDL cho-
lesterol. No significant effects on plasma HDL cholesterol,
triglycerides or LDL: HDL ratios were found.
In conclusion, the consumption of around 28–30 g of
natural (or roasted) almonds a day, roughly a handful, as
part of a healthy diet low in saturated fat lowers plasma
total cholesterol, thereby promoting heart health. This
cholesterol-lowering effect is similar to that of other heart-
healthy foods such as oats and soya. Furthermore, the
combination of almonds with other cholesterol-lowering
foods has been incorporated into the ‘Portfolio Eating
Plan’ (Jenkins et al. 2003, 2005, 2006), with plasma LDL
cholesterol reduction of 25–30%. In more recent research,
a study was designed to answer the question of what hap-
pens when people follow the Portfolio Eating Plan in a
real-world setting for 1 year (Jenkins et al. 2006). The diet
included almonds, plant sterols, soy protein and viscous
fibre along with lean meats and fish. After 1 year, male
and female participants with elevated cholesterol levels
experienced a statin-like effect, lowering their cholesterol
45The nutritional and health benefits of almonds: a healthy food choice D.P. Richardson et al.
by 20% or more. For those participants who followed the
plan less strictly, their plasma LDL cholesterol level
decreased by 15%. Berry et al. (2008) investigated the
effects of lipid bioaccessibility on postprandial lipaemia.
An elevated and prolonged postprandial lipaemic response
is associated with an increased risk of CHD. In a rando-
mised, crossover trial (n ¼20 men), the researchers
manipulated lipid bioaccessibility using test meals contain-
ing structurally intact almond seed or extracted almond oil
plus defatted almond seed flour, thus producing meals
with a predicted low- and high-lipid bioaccessibility,
respectively. As predicted, the low-lipid bioaccessibility
meal resulted in a significantly attenuated lipaemic
response compared with the high-lipid bioaccessibility
meals. The author concluded that manipulation of lipid
bioaccessibility of almond seeds significantly reduced the
postprandial increase in plasma triacylglycerol.
5. Almonds, satiety, weight maintenance and
type 2 diabetes
Epidemiological studies suggest that those who eat nuts
frequently (five times a week) tend to have lower body
mass indices (Garcia-Lorda et al. 2003; Bes-Rastrollo
et al. 2007; Ternus et al. 2009). These observations led to
research on almonds to understand potential mechanisms
of weight loss and weight maintenance. Almonds are high
in fibre and protein and have a low glycaemic index, all
of which are dietary factors shown to increase satiety and
suppress appetite (Holt et al. 1995).
In 2008, the energetics of nut consumption was
reviewed by Mattes, and three potential mechanisms were
proposed. The first focuses on the satiety value of nuts,
and it is hypothesised that inclusion of nuts in the diet
results in a spontaneous reduction of energy intake at
other times of the day to offset a high proportion of the
energy provided by the nuts. Second, it is postulated that
nut consumption may increase energy expenditure and
thereby dissipate a portion of the energy they provide.
Third, it is suggested that the absorption of the energy
from nuts is attenuated, thereby reducing their theoretical
contribution to energy intake (as described in Section 3).
Using almonds as a model, Hollis and Mattes (2007)
attempted to quantify the energetics of nut consumption in
a randomised crossover trial that included 20 healthy adult
female subjects with a mean body mass index (BMI) of
25.9 3.1 kg/m
2
. Two 10 week test periods were sepa-
rated by a three week washout period. During one arm of
the study, 1440 kJ/day of almonds were provided with no
dietary advice except that the day’s allotment of almonds
had to be consumed. A second arm differed only in that
nuts were disallowed.
The results revealed the strong satiating effects of
almonds, with 74% of the energy from almonds offset by
reduced energy intake from other sources. There was a
significant increase in faecal energy loss, accounting for
about 7% of the energy of almonds and a non-significant
increase in daily energy expenditure that would account
from about 14% of the energy of almonds. Accordingly,
the findings showed minimal impact of almond consump-
tion on body weight. These mechanisms help explain the
results of epidemiological and clinical studies which sug-
gest that moderate nut consumption does not pose a threat
for weight gain. For example, a southern Californian study
showed that adding a modest quantity of almonds (65 g)
to the diet for six months resulted in no significant
changes in body weight and an increase in the proportion
of unsaturated fat in the diet for 81 subjects (Fraser et al.
2002). The authors reported that food displacement
occurred after almond supplementation, and over 54–78%
of extra calories from almonds were displaced by a
decrease in intake of other less healthy foods in the habi-
tual diet (Jaceldo-Siegl et al. 2004). In another almond
study, which followed 65 overweight and obese indivi-
duals, Wien et al. (2003) showed that a moderate fat diet
with almonds resulted in more weight loss than a low fat
diet, even though the total number of calories in the six-
month study period was the same for both groups. In addi-
tion, the almond group had a 50% greater reduction in
waist circumference and a 62% greater reduction in fat
mass than the low fat diet group.
Substituting almonds for other foods in the diet that are
not as satiating is a potential strategy for weight loss
and for weight maintenance. Almonds can replace less
nutrient-dense foods in the diet, and eating more nutrient-
dense foods involves fewer calories to achieve nutrient
requirements. Data concerning the long-term association
between nut consumption and weight changes in a free-
living population are sparse. Bes-Rastrollo et al. (2009)
carried out a prospective study of nut consumption, long-
term weight change and obesity risk in women. Higher
nut consumption was not associated with greater body
weight gain during 8 years of follow-up in healthy middle
aged women. Instead, it was associated with a slightly
lower risk of weight gain and obesity. The authors con-
cluded that the incorporation of nuts into habitual diets
does not lead to greater weight gain and may contribute to
weight control. With the steady increase in the incidence
of obesity, it is becoming more important for scientists
and health professionals to understand the role of nuts in
body weight regulation and the related chronic diseases.
Review of the available data suggests that adding nuts to
habitual diets of free-living individuals does not cause
weight gain. In fact, the evidence so far indicates that nuts
have a tendency to lower body weight and fat mass
(Rajaram and Sabate
´2006).
Evidence from epidemiological and human intervention
studies is pointing towards a protective role for nuts, and
46 The nutritional and health benefits of almonds: a healthy food choice D.P. Richardson et al.
almonds in particular, in improvements in glycaemic con-
trol, insulin sensitivity and reducing risk factors for dia-
betes (Rajaram and Sabate
´2006; Ternus et al. 2009).
Although there is some evidence to suggest that almonds,
and perhaps other nuts, may have a favourable effect on
insulin sensitivity, more studies are needed to understand
the possible mechanisms. Several studies have shown that
risk of type 2 diabetes is lowered with higher intakes of
dietary fibre and lower glycaemic loads. Jenkins and col-
leagues recently evaluated the ability of either mixed nuts
or almonds to modulate glucose spikes that occur after
consuming carbohydrate-rich foods that commonly raise
blood sugar levels (Jenkins et al. 2006). The results
showed that in healthy men and women, eating nuts with
a carbohydrate-rich meal blunted the glycaemic and insu-
lin response of the body to a significant degree (Jenkins
et al. 2006, 2007; Ternus et al. 2009). In conclusion, the
research findings look sufficiently promising to be able to
continue to promote the inclusion of nuts and almonds as
part of a healthy diet.
6. Food allergy: potential risks of nuts and
tree nuts
Consumption of nuts and tree nuts including almonds has
been proven to be a healthy dietary habit. However, they
can also induce IgE-mediated adverse allergic reactions in
susceptible individuals (Chen et al. 2006). Food allergy is
estimated to affect around 1–2% of individuals over the
first decade of life, and nuts can cause anaphylactic reac-
tions and fatalities. Allergy to almonds resembles that for
other tree nuts. Methods have been developed for the
identification and detection of amandin, the major almond
storage protein (Sathe et al. 2002). The IgE-binding activ-
ity of almond proteins is reduced with typical heat proces-
sing treatments applied to almonds, such as blanching and
roasting (Venkatachalam et al. 2002).
Clear allergen labelling of food products containing nuts
and other potentially allergenic foods is required under
European food labelling legislation, and increasing efforts
are being made to help educate people living with these
allergies and their families on how to recognise early
symptoms of an allergic reaction and how to treat anaphy-
laxis promptly.
7. Almonds in the diet
Owing to the increasing evidence of beneficial health
effects, nuts such as almonds are now intrinsic to dietary
guidelines in several countries. However, there are very
few data on their intake profiles and the qualitative and
quantitative differences in their consumption patterns
within and between populations and geographic regions.
The data from European Prospective Investigation into
Cancer and Nutrition (EPIC), a cohort study of 520 000
subjects from 23 centres in ten countries of western
Europe, provides information on consumption patterns and
typical portion sizes (Jenab et al. 2006; Frecka et al.
2008). The most commonly consumed nuts were walnuts,
almonds and hazelnuts and there was a clear northern to
southern gradient of intake. In Sweden, mean intake was
0.15 g/day, with an average portion size of 15.1 g/day,
whereas in Spain mean intake was 2.99 g/day, with an
average portion size of 34.7 g/day. Average daily portion
size for almonds was typically around 20 g. Clearly, cul-
tural trends in southern Europe resemble the Mediterra-
nean-style diet, and the intake patterns are only a 24 h
snapshot of nut intake. Interestingly, in the United King-
dom there was a health-conscious sub-section of the popula-
tion that had higher intakes of nuts. The average portion size
of almonds in this health-conscious cohort was 26.1 g/day
compared with 10.2 g/day in the general population.
There are many social, demographic, economic and
lifestyle changes that determine our nutritional status, and
for a variety of reasons many people are not achieving
the recommended daily amount (RDA) or even the lower
reference nutrient intake (LNRI) for specific, essential
micronutrients (SACN 2008). As such, there is a gap
between the ideal balanced diet and the reality of what
people actually eat on a daily basis. For individuals at all
stages of life where food selections may compromise
optimal nutrition, encouragement to eat a healthier diet
could easily incorporate the greater use of nuts like
almonds. For example, in the United Kingdom, popula-
tions at risk include women of childbearing age, children
aged 18 and under, the elderly, people trying to lose
weight, those on restricted diets, socio-economically
underprivileged groups, alcoholics and smokers (SACN
2008). Health professionals and policy makers currently
focus on the fat, sugar and sodium contents of the diet.
Much more attention needs to be paid to the nutrient den-
sity of the whole diet and to the special needs of vulnerable
groups in society.
8. Conclusions and recommendations
Almonds provide a nutrient-dense source of vitamin E,
riboflavin, manganese, magnesium, calcium, phosphorus,
potassium, copper, iron and zinc as well as protein, dietary
fibre and MUFA. Almonds also provide an excellent
source of bioavailable a-tocopherol (vitamin E), and increas-
ing their intake enhances the resistance of LDL cholesterol
to oxidation (Chen et al. 2006). In addition, the polypheno-
lic constituents of whole almonds have been characterised
and found to possess antioxidant action (Amarowicz et al.
2005; Chen et al. 2005, 2007; Chen and Blumberg 2008).
Nuts such as almonds are considered to be an important
component of a healthy diet, and increased consumption
47The nutritional and health benefits of almonds: a healthy food choice D.P. Richardson et al.
has the potential to improve public health, especially if
they replace foods that are high in saturated fatty acids,
sugars and salt, or those lacking in vitamins, minerals and
phytoprotective constituents.
It is clear from this review that almonds bring signifi-
cant benefits regarding the lowering of blood cholesterol
and the health of the cardiovascular system, particularly
when eaten as part of a diet low in saturated fat.
Researchers have found an increasing effect on cholesterol
levels as almond consumption increases (Sabate
´et al.
2003), and it has been shown that almonds can be part of
an effective cholesterol-lowering diet (Jenkins et al.
2006). The strong body of evidence on the benefits of con-
suming almonds was a factor in the approval of the nut
qualified health claim by the US Food and Drug Adminis-
tration (2003), which states, ‘‘Scientific evidence suggests
but does not prove that eating 1.5 ounces per day of most
nuts, such as almonds, as part of a diet low in saturated
fat may reduce the risk of heart disease’’.
As interest in incorporating almonds into the habitual
diet grows, it is important that consumers understand how
to include them in a healthy diet without promoting
weight gain. Nuts, as a food category, are high-fat,
energy-dense foods and can therefore contribute to posi-
tive energy balance. However, evidence is accumulating
from epidemiological studies, which indicates that nut
consumption is not associated with higher body weight
and that habitual nut consumers have a lower body mass
index than non-consumers. Similarly, human intervention
trials indicate that the inclusion of nuts in the diet leads to
little or no weight gain (Mattes et al. 2007).
A key area of research is the identification of foods
and food constituents that can help contribute to healthy
weight maintenance or weight loss using foods such as
almonds that have a low glycaemic index, high-protein and
high-fibre contents and that require mastication. Almonds
appear to possess three properties that could be exploited
to facilitate weight control and weight loss, namely
enhancement of satiety, decreased efficiency of energy
absorption and augmentation of energy expenditure (Mattes
2009). Chewing of almonds may also play a more complex
role in the digestion process, impacting on nutrient absorp-
tion and endocrine responses influencing satiety. Further
research is also required to gain better understanding of the
role that bioavailability and bioaccessibility of almond con-
stituents, and the synergy between them, play in their asso-
ciated health outcomes. The importance of mastication in
the context of weight management and suppression of hun-
ger also needs further investigation.
Very few data exist on profiles of nut intake and the
qualitative and quantitative differences in their consump-
tion patterns within and between populations and geo-
graphic regions. More research is needed into the intake
of nuts and disease risk to underpin development of food
policies and intake recommendations for this important
food group.
From a public health point of view, this review has
shown that nuts such as almonds, in the context of a
healthy, balanced diet can help reduce the risk of CHD,
help to mitigate weight gain and help avoid the risk of
overweight and development of obesity. It is important to
stress that nutrition messages aimed at the general popula-
tion should clearly indicate that nuts should replace the
consumption of other foods and snacks that are energy-
dense, high in saturated fats, sugars and salt, and low in
essential nutrients. Consumers should also be made aware
of the need to maintain overall energy balance.
In a nutshell, almonds offer a nutritious contribution to
the habitual diet, with potentially beneficial effects on car-
diovascular health without weight gain, making them a
natural healthy food choice.
9. Acknowledgements
This article was supported by the Almond Board of Cali-
fornia. The authors would like to express their thanks to
Gary Foster (Professor of Medicine and Public Health,
Director of the Centre for Obesity Research and Educa-
tion, Temple University, 3223 N. Broad Street, Suite 175,
Philadelphia, PA 19140, USA), Susan Jebb (Medical
Research Council Human Nutrition Research, Elsie Wid-
dowson Laboratory, 120 Fulbourn Road, Cambridge CB1
9NL, UK) and Richard D. Mattes (Purdue University,
Department of Foods and Nutrition, 700 W. State Street,
West Lafayette, IN 47907-2059, USA) for their helpful
comments and suggestions.
10. References
Ahrens, S., Venkatachalam, M., Mistry, A. M., Lapsley, K. and
Sathe, S. K. 2005. Almond (Prunus dulcis L.) protein quality.
Plant Foods in Human Nutrition 60: 123-128.
Albert, C. M., Gaziano, J., Willett, W. C. and Manson, J. E.
2002. Nut consumption and decreased risk of sudden cardiac
death in the Physicians’ Health Study. Archives of Internal
Medicine 162: 1382-1387.
Amarowicz, R., Agnieszka, T., Troszynska, F. and Shahidi, F.
2005. Antioxidant activity of almond seed extract and its frac-
tions. Journal of Food Lipids 12: 344-358.
Berry, S. E. E., Tydeman, E. A., Lewis, H. B., Phalora, R.,
Rosborough, J., Picout, D. R. and Ellis, P. R. 2008. Manipula-
tion of lipid bioaccessibility of almond seeds influences post-
prandial lipemia in healthy human subjects. American Journal
of Clinical Nutrition 88: 922-929.
Bes-Rastrollo, M., Sabate
´, J., Go
´mez-Gracia, E., Alonso, A.,
Martı
´nez, J. A. and Martı
´nez-Gonza
´lez, M. A. 2007. Nut con-
sumption and weight gain in a Mediterranean cohort: the SUN
study. Obesity 15: 107-116.
Bes-Rastrollo, M., Wedik, N. M., Martinez-Gonzalez, M. A., Li,
T. Y., Sampson, L. and Hu, F. B. 2009. Prospective study of
nut consumption, long-term weight change, and obesity risk in
48 The nutritional and health benefits of almonds: a healthy food choice D.P. Richardson et al.
women. American Journal of Clinical Nutrition 89: 1-7.
Blomhoff, R., Carlsen, M. H., Andersen, L. F. and Jacobs, D. R.
Jr. 2006. Health benefits of nuts: potential role of antioxidants.
British Journal of Nutrition 96: S52-S60.
Cassady, B. A., Hollis, J. H., Fulford, A. D., Considine, R. V.
and Mattes, R. D. 2009. Mastication of almonds: effects of
lipid bioaccessibility, appetite and hormone response. Ameri-
can Journal of Clinical Nutrition 62: 1231-1238.
Chen, C.-Y., Lapsley, K. and Blumberg, J. 2006. A nutrition and
health perspective on almonds. Journal of the Science of Food
and Agriculture 86: 2245-2250.
Chen, C.-Y., Milbury, P. E., Lapsley, K. and Blumberg, J. B.
2005. Flavonoids from almond skins are bioavailable and act
synergistically with vitamins C and E to enhance hamster and
human LDL metabolism to oxidation. Journal of Nutrition
135: 1366-1373.
Chen, C.-Y. O. and Blumberg, J. B. 2008. In vitro activity of
almond skin polyphenols for scavenging free radicals and
inducing quinine reductase. Journal of Agricultural and Food
Chemistry 56: 4427-4434.
Chen, C.-Y. O., Milbury, P. E., Chung, S.-K. and Blumbert, J.
2007. Effect of almond skin polyphenols and quercetin on
human LDL and apolipoprotein B-100 oxidation and confor-
mation. Journal of Nutritional Biochemistry 18: 785-794.
Due, A., Larsen, T. M., Hermansen, K., Stender, S., Holst, J. J.,
Toubro, S., Martinussen, T. and Astrup, A. 2008. Comparison
of the effects on insulin resistance and glucose tolerance of
6-mo high-monounsaturated-fat, low-fat and control diets.
American Journal of Clinical Nutrition 87: 855-862.
Ellis, P. R., Kendall, C. W. C., Ron, Y., Parker, C., Pacy, J. F.,
Waldron, K. W. and Jenkins, D. J. 2004. Role of cell walls in
the bioaccessibility of lipids in almond seeds. American Jour-
nal of Clinical Nutrition 80: 604-613.
Estruch, R., Martinez-Gonzalez, A. M., Corella, D., Salas-
Salvado, J. et al. 2006. Effects of a Mediterranean-style diet on car-
diovascular risk factors. Annals of Internal Medicine 145:1-11.
European Parliament and Council. 2007. Corrigendum to Regula-
tion (EC) No. 1924/2006 of the European Parliament and of
the Council of 20th December 2006 on nutrition and health
claims made on foods. Official Journal of the European
Union: L404 30 December 2006, published 18 January 2007.
Fraser, G. E., Bennett, H. W., Jaceldo, K. B. and Sabate
´,J.
2002. Effect on bodyweight of a free 76 kilojoule (320 calorie)
daily supplement of almonds for six months. Journal of the
American College of Nutrition 21: 275-283.
Fraser, G. E., Sabate
´, J., Beeson, W. L. and Strachan, M. A. 1992. A
possible protective effect of nut consumption on risk of coronary
heart disease. Archives of Internal Medicine 152: 1416-1424.
Frecka, J. M., Hollis, J. H. and Mattes, R. D. 2008. Effects of
appetite, BMI, food form and flavour on mastication: almonds
as a test food. European Journal of Clinical Nutrition 62:
1231-1238.
Garcı
´a-Lorda, P., Megius Rangil, I. and Salas-Salvado
´, J. 2003.
Nut consumption, bodyweight and insulin resistance. European
Journal of Clinical Nutrition 57: 8S-11S.
Gradziel, T.M. 2009. Almond (Prunus dulcis) breeding. In: Jain,
S.M. and Priyadarshan, P.M., editors. Breeding plantation tree
crops: temperate species: 1-31. Springer Science + Business
Media, LLC.
Griel, A. E. and Kris-Etherton, P. M. 2006. Nuts: source of
energy and macronutrients. British Journal of Nutrition 96:
S29-S35.
Hollis, J. and Mattes, R. 2007. Effect of chronic consumption of
almonds on bodyweight in healthy humans. British Journal of
Nutrition 98: 651-656.
Holt, S. H., Miller, J. C., Petocz, P. and Farmakalidis, E. 1995.
A satiety index of common foods. European Journal of Clini-
cal Nutrition 49: 675-690.
Hu, F. B. and Stamfer, M. J. 1999. Nut consumption and risk of
coronary heart disease: a review of epidemiological evidence.
Current Atherosclerosis Reports 1: 204-209.
Hu, F. B., Stampfer, M. J., Manson, J. E. et al. 1998. Frequent nut
consumption and risk of coronary heart disease in women: pro-
spective cohort study. British Medical Journal 317: 1341-1315.
Hyson, D. A., Schneeman, B. O. and Davis, P. A. 2002. Almonds
and almond oil have similar effects on plasma lipids and LDL
oxidation in healthy men and women. Journal of Nutrition 132:
703-707.
Jaceldo-Siegl, K., Sabate
´, J., Rajaram, S. and Fraser, G. E. 2004.
Long term almond supplementation without advice on food
replacement induces favourable nutrient modification to the
habitual diets of free-living individuals. British Journal of
Nutrition 92: 533-540.
Jenab, M., Sabate
´, J., Slimani, N., Ferrari, P., Mazuir, M.,
Casagrande, C. et al. 2006. Consumption and portion sizes of
tree nuts, peanuts and seeds in the European Prospective
Investigation into Cancer and Nutrition (EPIC) cohorts from
10 European countries. British Journal of Nutrition 96 (Suppl.
2): S12-S23. Erratum in British Journal of Nutrition 2008, 99:
447-448.
Jenkins, D. J., Kendall, C. W., Josse, A. R., Salvatore, S.,
Brighenti, F., Augustin, L. S., Ellis, P. R., Vidgen, E. and
Rao, A. V. 2006. Almonds decrease postprandial glycemia,
insulinemia and oxidative damage in healthy individuals.
Journal of Nutrition 136: 2987-2992.
Jenkins, D. J., Kendall, C. W., Marchie, A., Parker, T. L.,
Connelly, P. W. et al. 2002. Dose response of almonds on cor-
onary heart disease risk factors: blood lipids, oxidised low
density lipoproteins, lipoprotein (a), homocysteine and pul-
monary nitric oxide: a randomised, controlled, cross-over trial.
Circulation 106: 1327-1332.
Jenkins, D. J., Kendall, C. W., Marchie, A., Faulkner, D. A.,
Vidgen, E., Lapsley, K. G. et al. 2003. The effect of combin-
ing plant sterols, soy protein, viscous fibres and almonds in
treating hypercholesterolemia. Metabolism 52: 1478-1483.
Jenkins, D. J., Kendall, C. W., Marchie, A., Faulkner, D. A.,
Wong, J. M., de Souza, R. et al. 2005. Direct comparison of a
dietary portfolio of cholesterol-lowering foods with a statin in
hypercholesterolemic participants. American Journal of Clini-
cal Nutrition 81:380-387.
Jia, X., Li, N., Zhang, W., Zhang, X., Lapsley, K., Huang, G.,
Blumberg, J., Ma, G. and Chen, J. 2006. A pilot study on the
effects of almond consumption on DNA damage and oxidative
stress in smokers. Nutrition and Cancer 54: 179-183.
Kelly, J. H. and Sabate
´, J. 2006. Nuts and coronary heart disease:
an epidemiological perspective. British Medical Journal 96:
S61-S67.
Knoops, K. T., de Groot, L. C., Krombout, D., Perrin, A. E.
et al. 2004. Mediterranean diet, lifestyle factors and 10-year
mortality in elderly European men and women: the HALE pro-
ject. Journal of the American Medical Association 292: 1433-
1439.
Knoops, K. T., Groot, L. C., Fidanza, F., Alberti-Fidanza, A.,
Kromhout, D. and van Staveren, W. A. 2006. Comparison of
three different dietary scores in relation to 10-year mortality in
elderly European subjects: the HALE project. European Jour-
nal of Clinical Nutrition 60: 746-755.
Kris-Etherton, P. M., Zhao, G., Binkoski, A. E., Coval, S. M.
and Etherton, T. D. 2001. The effects of nuts on coronary
heart disease risk. Nutrition Reviews 59: 103-111.
49The nutritional and health benefits of almonds: a healthy food choice D.P. Richardson et al.
Kushi, L. H., Folsom, A. R., Prineas, R. J., Mink, P. J., Wu, Y.
and Bostick, R. M. 1996. Dietary antioxidant vitamins and
death from coronary heart disease in post-menopausal women.
New England Journal of Medicine 334: 1156-1162.
Mandalari, G., Faulks, R. M., Rich, G. T., Turco, V. L., Picout,
D. R., Curto, R. B. L. et al. 2008a. Release of protein, lipid
and vitamin E from almond seeds during digestion. Journal of
Agricultural and Food Chemistry 56: 3409-3416.
Mandalari, G., Nueno-Palop, C., Bisignano, G., Wickham, M. S. J.
and Narbad, A. 2008b. Potential prebiotic properties of almond
(Amygdalus communis L.) seeds. Applied and Environmental
Microbiology 74: 4264-4270.
Mattes, R. D. 2008. The energetics of nut consumption. Asia
Pacific Journal of Clinical Nutrition 17: 337-339.
Mattes, R. D., Kris-Etherton, P. M. and Foster, G. D. 2007.
Impact of peanuts and tree-nuts on bodyweight and healthy
weight loss in adults. Journal of Nutrition 138: 1741S-1745S.
Phillips, K. M., Ruggio, D. M. and Ashraf-Khorassani, M. 2005.
Phytosterol composition of nuts and seeds commonly con-
sumed in the United States. Journal of Agricultural and Food
Chemistry 53: 9436-9445.
Phung, O. J., Makanji, S. S., White, M. and Coleman, C. I.
2009. Almonds have a neutral effect on serum lipid profiles: a
meta-analysis of randomised trials. Journal of the American
Dietetic Association 109: 865-873.
Rajaram, S. and Sabate
´, J. 2006. Nuts bodyweight and insulin
resistance. British Journal of Nutrition 96: 79S-86S.
Ros, E. and Mataix, J. 2006. Fatty acid composition of nuts—
implications for cardiovascular health. British Journal of
Nutrition 96 (Suppl. 2): S29-S35.
Sabate
´, J. and Ang, Y. 2009. Nuts and health outcomes: new epi-
demiological evidence. American Journal of Clinical Nutrition
89 (Suppl. 1): 1643S-1648S.
Sabate
´, J., Haddad, E., Tanzman, J. S., Jambazian, P. and
Rajaram, S. 2003. Serum lipid response to the graduated
enrichment of a Step 1 diet with almonds: a randomized feed-
ing trial. American Journal of Clinical Nutrition 77: 1379-
1384.
Salas-Salvado
´, J., Bullo
´, M., Pe
´rez-Heras, A. and Ros, E. 2006.
Dietary fibre, nuts and cardiovascular diseases. British Journal
of Nutrition 96: S45-S51.
Salas-Salvado, J., Fernandez-Ballart, J., Ros, E., Martinez-Gonzalez,
M.-G. et al. 2008a. Effects of a Mediterranean-style diet supple-
mented with nuts on metabolic syndrome status. Archives of
Internal Medicine 168: 2449-2458.
Salas-Salvado, J., Garcia-Arellano, A., Estruch, R., Marquez-
Sandoval, F. et al. for the PREDIMED investigators. 2008b.
Components of the Mediterranean-type food pattern and serum
inflammatory markers among patients at high risk for cardio-
vascular disease. European Journal of Clinical Nutrition 62:
651-659.
Sathe, S. K., Wolf, W. J., Roux, K. H., Teuber, S. S., Venhata-
chalan, M. and Sze-Tao, K. W. C. 2002. Biochemical charac-
terisation of amandin, the major storage protein in almond
(Prunus dulcis L.). Journal of Agricultural and Food Chemis-
try 50: 4333-4341.
Scientific Advisory Committee on Nutrition. 2008. Nutrition
well-being of the British population. TSO, London, UK.
Segura, R., Javierre, C., Lizarraga, M. A. and Ros, E. 2006.
Other relevant components of nuts: phytosterols, folate and
minerals. British Journal of Nutrition 96: S36-S44.
Spiller, G. A., Jenkins, D. J., Cragen, L. N., Gates, J. E., Bosello,
O., Berra, K., Rudd, C., Stevenson, M. and Superko, R. 1992.
Effect of a diet high in monounsaturated fat from almonds on
plasma cholesterol and lipoprotieins. Journal of the American
College of Nutrition 11: 126-130.
Ternus, M. E., Lapsley, K. and Geiger, C. J. 2009. Health bene-
fits of tree nuts. In: Alasalver, C. and Shahidi, F., editors. Tree
nuts: composition, phytochemicals and health effects: 37-64.
CRC Press, Taylor and Francis Group, Boca Raton.
Trichopolou, A. and Lagiou, P. 1997. Healthy traditional Medi-
terranean diet: an expression of culture, history and lifestyle.
Nutrition Reviews 55: 383-389.
Trichopolou, A., Costacou, T., Bamia, C. and Trichopolou, D.
2003. Adherence to a Mediteranean diet and survival in a
Greek population. New England Journal of Medicine 348:
2599-2608.
U.S. Department of Agriculture, Agricultural Research Service.
2008. USDA National Nutrient Database for Standard Refer-
ence, Release 21. Nutrient Data Laboratory Home Page. Avail-
able at: www.ars.usda.gov/ba/bhnrc/ndl.
U.S. Food and Drug Administration Centre for Food Safety and
Applied Nutrition. 2003. Qualified health claims subject to
enforcement discretion. Nuts & heart disease. Docket No. 02P-
0505. Available at: www.fda.gov.
Venkatachalam, M., Teuber, S. S., Roux, K. H. and Sathe, S. K.
2002. Effects of roasting, blanching, autoclaving and microwave
heating on antigenicity of almond (Prunus dulcis L.) proteins.
Journal of Agricultural and Food Chemistry 50: 3544-3548.
Wien, M. A., Sabate
´, J. M., Ikle
´, D. N., Cole, S. E. and Kandeel,
F. R. 2003. Almonds vs complex carbohydrates in a weight
reduction program. International Journal of Obesity and
Related Metabolic Disorders 27: 1365-1372.
Wu et al. 2004. Lipophilic and hydrophilic antioxidant capacities
of common foods in the U.S. Journal of Agricultural and
Food Chemistry 52: 4026-4037.
50 The nutritional and health benefits of almonds: a healthy food choice D.P. Richardson et al.