Misra 2010
Misra 2010
Misra 2010
To cite this article: Anoop Misra MD, Neha Singhal MSc & Lokesh Khurana MBBS (2010) Obesity, the Metabolic Syndrome,
and Type 2 Diabetes in Developing Countries: Role of Dietary Fats and Oils, Journal of the American College of Nutrition,
29:sup3, 289S-301S, DOI: 10.1080/07315724.2010.10719844
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Review
Developing countries are undergoing rapid nutrition transition concurrent with increases in obesity, the
metabolic syndrome, and type 2 diabetes mellitus (T2DM). From a healthy traditional high-fiber, low-fat, low-
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calorie diet, a shift is occurring toward increasing consumption of calorie-dense foods containing refined
carbohydrates, fats, red meats, and low fiber. Data show an increase in the supply of animal fats and increased
intake of saturated fatty acid (SFAs) (obtained from coconut oil, palm oil, and ghee [clarified butter]) in many
developing countries, particularly in South Asia and South-East Asia. In some South Asian populations,
particularly among vegetarians, intake of n-3 polyunsaturated fatty acids (PUFAs) (obtained from flaxseed,
mustard, and canola oils) and long-chain (LC) n-3 PUFAs (obtained from fish and fish oils) is low. Further, the
effect of supplementation of n-3 PUFAs on metabolic risk factors and insulin resistance, except for
demonstrated benefit in terms of decreased triglycerides, needs further investigation among South Asians. Data
also show that intake of monounsaturated fatty acids (MUFAs) ranged from 4.7% to 16.4%en in developing
countries, and supplementing it from olive, canola, mustard, groundnut, and rice bran oils may reduce metabolic
risk. In addition, in some developing countries, intake of n-6 PUFAs (obtained from sunflower, safflower, corn,
soybean, and sesame oils) and trans-fatty acids (TFAs) is increasing. These data show imbalanced consumption
of fats and oils in developing countries, which may have potentially deleterious metabolic and glycemic
consequences, although more research is needed. In view of the rapid rise of T2DM in developing countries,
more aggressive public health awareness programs coupled with governmental action and clear country-specific
guidelines are required, so as to promote widespread use of healthy oils, thus curbing intake of SFAs and TFAs,
and increasing intake of n-3 PUFAs and MUFAs. Such actions would contribute to decelerating further
escalation of ‘‘epidemics’’ of obesity, the metabolic syndrome, and T2DM in developing countries.
Address correspondence to: Anoop Misra, MD, Director and Head, Department of Diabetes and Metabolic Diseases, Fortis Flt. Lt. Rajan Dhall Hospital, Vasant Kunj,
New Delhi 110070, INDIA. E-mail: anoopmisra@metabolicresearchindia.com
Abbreviations: AA 5 arachidonic acid, ALA 5 alpha-linolenic acid, AMDR 5 acceptable macronutrient distribution range, CHD 5 coronary heart disease, DALY 5
disability-adjusted life-years, DHA 5 docosahexaenoic acid, EPA 5 eicosapentaenoic acid, FAO 5 Food and Agricultural Organization, FBS 5 Food Balance Sheet,
HDL-c 5 high-density lipoprotein cholesterol, ICMR 5 Indian Council of Medical Research, IGT 5 impaired glucose tolerance, LA 5 linoleic acid, LDL-c 5 low-
density lipoprotein cholesterol, MAL 5 maximum limit, MIL 5 minimum level, MUFA 5 monounsaturated fatty acid, NCD 5 noncommunicable disease, PHVO 5
partially hydrogenated vegetable oil, PUFA 5 polyunsaturated fatty acid, P/S 5 PUFA-to-SFA ratio, T2DM 5 type 2 diabetes mellitus, TC 5 total cholesterol, TFA 5
trans-fatty acid, TG 5 triglyceride, TPFA 5 trans polyunsaturated fatty acid, SFA 5 saturated fatty acid, WHO 5 World Health Organization
Dr. Misra has received travel and lodging support from MPOB for conferences organized by them.
Journal of the American College of Nutrition, Vol. 29, No. 3, 289S–301S (2010)
Published by the American College of Nutrition
289S
Role of Fats in Type 2 Diabetes in Developing Countries
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Fig. 1. Relationship between nutrition transition, urbanization, and the rise in obesity and the metabolic syndrome in developing countries. (Adapted
from [6].)
INTRODUCTION Recent evidence shows that specific fatty acids affect cell
metabolism, modifying the balance between fatty acid
Developing countries are undergoing rapid nutrition oxidation and lipogenesis. Changes in the quantity and quality
transition [1]. From a healthy, traditional, high-fiber, low-fat, of dietary fats may modify insulin sensitivity [5]. Table 1
low-calorie diet, a shift is being made toward consumption of summarizes the metabolic abnormalities (constituting the
refined carbohydrates, high total fat, and red meats, along with metabolic syndrome) in patients with impaired insulin
low intakes of fiber [2]. It is important to note that widespread sensitivity [6,7]. High intake of total fat is associated with
availability and commercial use of low-cost unhealthy fasting hyperinsulinemia [8,9] and a lower insulin sensitivity
vegetable oils have increased dietary intake of fats and index [10]. Data from epidemiologic studies in developed
trans-fatty acids (TFAs) [3]. These faulty dietary habits have nations show that total fat intake was higher in patients with
contributed to increases in obesity, the metabolic syndrome, T2DM than in normoglycemic controls [11]. Furthermore, a
and type 2 diabetes mellitus (T2DM) [4]. Fig. 1 shows the high fat intake has been shown to predict the development of
relationship between nutrition transition, urbanization, and the impaired glucose tolerance (IGT) in a group of healthy
rise in obesity, the metabolic syndrome, and T2DM in subjects [12] and progression from IGT to T2DM in patients
developing countries. The following discussion focuses on with IGT [13]. Impaired glucose-insulin-lipid metabolism may
rapid escalation of noncommunicable diseases (NCDs), occur consequent to a decrease in insulin sensitivity, starting a
specifically, obesity, the metabolic syndrome, and T2DM, in cascade of metabolic events causing T2DM and a clustering of
the context of trends in consumption and dietary preferences of other cardiovascular risk factors. The overall bulk of data,
fats and oils and their relationships with NCDs in developing except for a few studies [14–22], shows an association of
countries. excess fat intake with obesity and glucose-insulin metabolic
Table 1. Abnormalities Associated with Insulin Resistance Asian diets, particularly in relation to insulin resistance and
NCDs, readers are referred to a recent comprehensive review
Glucose metabolism [24].
1. Fasting hyperinsulinemia
2. Elevated fasting glucose levelsa
3. Impaired glucose tolerance (elevated 2 hours post oral
glucose load levels) RISE OF NCDs IN DEVELOPING
Lipids and uric acid COUNTRIES
1. Raised triglyceridesa
2. Low levels of HDL-ca The prevalence of NCDs is rapidly increasing worldwide,
3. Increased small, dense LDL particles leading to increased morbidity and mortality. It is important to
4. Increased postprandial lipemia
5. Increased plasma uric acid concentrations note that about 60% of global burden of increase in NCDs is
expected to occur in developing countries, and most of the
Blood pressure regulationa
associated mortality is obesity-related and attributable to T2DM
1. Elevated sympathetic nervous system activity
2. Augmented renal sodium retention and coronary heart disease (CHD) [25]. Continuing undernutri-
3. Hypertension tion and infectious diseases, along with escalating overnutrition
Others (overweight/obesity), have created a ‘‘double burden’’ of
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Fig. 2. Per capita supply per day of fat from vegetable oils and animal fats in developed and developing countries. (Source: [42].)
INCREASING SUPPLY AND African children (1–9 years) in 1999, higher mean total fat
CONSUMPTION OF FATS AND OILS IN intake was reported in urban areas (26.5%en) compared with
DEVELOPING COUNTRIES rural areas (21%en) [44]. A study from 4 regions of Kenya
(716 urban and 292 rural women) showed high total fat intake
The following section provides data on supply and trends in (34.5%en) in urban areas and relatively high intake (27.7%en)
intake of dietary fats in some developing countries. It should even in rural areas. The Food Balance Sheet (FBS) data show
be noted that data from many of the developing countries are that in China, the per capita supply per day of energy intake
limited; however, most reported data show an increase in increased from 22.2%en in 1995–1997 to 27.2%en in 2001–
consumption of total fat in both rural and urban areas. 2003 [42]. In 2006, 57.9% of urban and 38.7% of rural Chinese
Fig. 2 shows the trends (1961–2003) in per capita supply consumed more than 30%en from fats compared with 19.8%
per day of fat from vegetable oils and animal fats in developed and 12.1%, respectively, in 1989 [45]. It is important to note
and developing countries [42]. Over the past 4 decades, the that the increase in total fat intake in China can be ascribed to
supply of animal fat in developing countries has increased, an increase in the intake of fat from animal foods [46]. In
while the supply in developed countries has decreased [42]. India, fat intake increased in rural (24 to 34 g/d) and urban (36
Global production for the domestic supply of vegetable oils to 41g/d) populations during 1973–2004 [47,48]. A study on
increased significantly between 1961 and 1963 and between urban slum dwellers in North India showed a median total fat
2001 and 2003, especially in developing countries, accounting intake of 24.7%en in men and 28.7%en in women [49]. In
for 68.8% of the total quantity of vegetable oils from 2001 to European regions, %en from dietary fat in Hungary, Lithuania,
2003, while developed countries produced 31.2% [43]. Latvia, and Estonia was estimated as 37.9%, 44%, 42%, and
Increased availability and consumption of vegetable oils have 36%, respectively [50,51]. It is interesting to note that fat
been significantly contributed by globalization and open intake (%en) decreased from 39.6 to 31.6 in the nationally
market economies adapted during the past decade by many representative sample of the Russian Federation between 1992
developing countries. and 2000 [52]. Finally, in metropolitan areas in Brazil, %en
Table 2 gives an overview of the mean intake of total fat from dietary fats increased from 25.8% in 1974–1975 to 30.5%
(%energy, [%en]) from some developing countries. In South in 2002–2003 [53].
PUFAs
11.3
5.9
4.0
5.5
4.4
5.8
3.3
5.1
4.0
WITH OBESITY, THE METABOLIC
NA
NA
SYNDROME, AND T2DM IN
DEVELOPING COUNTRIES
MUFAs
16.4
12.0
12.6
15.0
4.7
7.2
8.1
6.0
7.7
NA
NA
As was previously stated, high-fat diets promote weight
gain and insulin resistance and may play a role in the
development of T2DM [10–13,54]. However, secular data are
SFAs
14.1
25.4
11.2
10.6
14.0
5.7
4.1
7.4
5.0
6.0
8.8
limited regarding relationships between total fat intake and
obesity and the metabolic syndrome, and no data are available
Total Fat
26.7
21.1
35.6
37.9
20
Table 3 gives a summary of the relationship of total fat intake
to weight gain in some developing countries. The high intake of
traditional diets (rich in whole milk, fats, and oils) was associated
Age (y)
57
24–74
20–75
35–44
19–69
30–85
40–59
18–54 with greater risk of abdominal obesity in adult Mongolian
NA
49
2349
135
115
105
503
839
200
224
423
and total fat intake after adjusting for sex, age, and other multiple
confounders [58]. Clearly, more research is needed in developing
Mexican Health and Nutrition Survey (MHNS)
DEVELOPING COUNTRIES
Survey from 1992–94
[91]
[63]
[92]
[93]
[94]
[64]
[95]
[50]
1997
2002
2006
2007
2005
2004
1994
2005
Tanzania
Hungary
Mexico
Taiwan
Nigeria
India
Energy intake from fat was positively associated with BMI in males and
Energy density associated with energy intake and overweight; fat was not
High carbohydrate (80%en) and low fat intake (8%en). The latter may
women) intakes. No dietary variables were associated with obesity
in selected developing countries (4.1% in Tanzania [rural and
Migration from rural to urban increased percent energy from fat and
en 5 energy, NA 5 data not available, TC 5 total cholesterol, HDL-c 5 high-density lipoprotein-cholesterol, LDL-c 5 low-density lipoprotein-cholesterol, BMI 5 body mass index.
acid) is popularly used in home cooking in India. Annually,
about 800,000 tones are produced, and much of it is made by
a predictor of overweight.
countries.
Table 3. Relationship of Total Dietary Fat Intake to Weight Gain (Data from Selected Developing Countries)
[101]
[102]
[103]
[104]
[97]
[98]
[99]
13 villages and
3 subdistricts
1854
5783
530
337
120
40–79
20–59
25–74
3–12
.10
.15
NA
NA
Thailand, rural
Table 4. Fatty Acid Composition of Various Fats and Oils (g/100 g) Used in Developing Countries
Canolabd Canada 6 62 22 10
Flax seedd China, India, Ethiopia 10 21 16 53
Sesamebc Bulgaria, South India 15 42 42 1.0
Palmoleina Malaysia, Indonesia, Columbia 42 46 11 ,0.5
Palm kernela Malaysia, Indonesia, Columbia 82 15 2 ,0.5
PHVO 5 partially hydrogenated vegetable oil, SFAs 5 saturated fatty acids, MUFAs 5 monounsaturated fatty acids, LA 5 linoleic acids, ALA 5 alpha-linolenic acid,
PUFAs 5 polyunsaturated fatty acids.
Percentages may not add to 100% because of rounding and other constituents not listed. Where percentages vary, average values are used.
a
High in saturated fatty acid.
b
High in monounsaturated fatty acids.
c
High in linoleic acid.
d
High in alpha-linolenic acid.
e
Contains 2% trans-fatty acids.
f
Contains 53% trans-fatty acids.
Source: [62].
high n-6:n-3 PUFAs diet showed a trend toward loss of insulin LCn-3 PUFA supplementation in British Caucasians and Indo-
sensitivity, significant lowering of total membrane n-3 PUFAs, Asian Sikhs in the United Kingdom. After supplementation,
and a trend toward lower eicosapentaenoic acid (EPA) and concentrations of plasma TG, apo B-48, platelet phospholipids,
docosahexaenoic acid (DHA) levels [67]. In another study on and arachidonic acid (AA) decreased, while high-density
Indo-Asians by the same group, Brady et al. [68] reported that lipoprotein-cholesterol (HDL-c), EPA, and DHA levels
high dietary intake of n-6 PUFAs did not attenuate the beneficial significantly increased in Indo-Asians compared with British
effects of fish oil supplementation on plasma TG levels. Caucasians, but insulin sensitivity was not improved [70]. A
30-day dietary intervention study with salmon oil (rich in LCn-
3 PUFAs) in Mexican subjects showed a significant decrease
n-3 Polyunsaturated Fatty Acids
in TG levels and an increase in HDL-c levels in the
Fish, fish oils, and some vegetable oils (flaxseed, mustard, hypertriglyceridemic group, along with a significant decrease
canola) are good sources of n-3 PUFAs [69]. In Costa Rica, the in TC and TG and an increase in HDL-c in the hypercholes-
intake of n-3 PUFAs was 0.35 g, 0.41 g, and 0.44 g/d in rural, terolemic group [71]. In an important study in India, it was
semiurban, and urban areas, respectively [63]. In Korea, intake shown that 0.75% energy (2.2 g) ALA from vegetable oils (like
of n-3 PUFAs was 2.1 g/d and 1.5 g/d in men and women, flaxseed, mustard, and canola) may be required to increase the
respectively [64]. In diets of Asian Indian adolescents, n-3 LCn-3 PUFAs to about the same extent as 0.1% energy (0.3 g)
PUFAs contributed to 0.7%en [65]. from LCn-3 PUFAs derived from fish oils [72]. A study on
Only a few intervention studies have been conducted on T2DM and hypertensive patients (n 5 50) in Iran showed a
South Asians and other ethnic groups in developing countries decrease in TG and apo B-100 levels and no detrimental
using n-3 rich oils or diets. Short-term intervention studies effects on apo A-1, glucose, insulin, and glycosylated
with n-3 PUFAs in migrant South Asians have not yielded hemoglobin levels after 10 weeks of supplementation with
definitive results. Lovegrove et al. [70] compared the impact of 2 g/d n-3 PUFA capsules (520 mg EPA and 480 mg DHA) as
compared with controls (1 g/d of 300 mg SFA, 100 mg MUFA, fats (margarines, shortenings, gel) account for 60%, 20%, and
and 600 mg LA) [73]. Overall, although the effects of n-3 10% of total usage, respectively. Limited data obtained in
PUFAs on triglyceride and HDL-c levels are convincing, their India on various types of biscuits and Indian sweets purchased
effects on insulin sensitivity and hyperglycemia are not clear at from local bakeries show that TFA content ranges between
present; long-term follow-up studies with higher doses and 30% and 40% and between 6% and 26% of total fatty acids,
large sample sizes may be required. respectively. Use of margarine spreads (made with PHVO)
increases the TFA content of the product [83].
Monounsaturated Fatty Acids In an urban slum population of North India, particularly in
men, the consumption of TFAs was greater than 1% of the
The MUFAs are present in the following oils: olive (76%),
energy [49]. Further, TFA intake (%en) was 1.1 among
mustard (70%), almond (69%), canola (62%), and groundnut
adolescents and young adults in North India [24]. TFAs
(50%). Other oils such as palm (44%) sesame (42%), and rice
accounted for 33% of fatty acids in products used in Iranian
bran (41%) also have fair quantities of MUFA. In developing
homes, with an average per-person intake of 14 g/1000 kcal
countries, MUFA intake ranged from 4.7% (Tanzania) to
[84]. In Costa Rica, 63% of subjects (n 5 1167) consumed at
16.4% (Cameroon) (Table 2). Asian Indians belonging to low
least 1% energy from TFAs [85]. TFA consumption increased
socio-economic status (SES) in India consumed less MUFA
from rural (3.5 g/d) to semiurban (3.86 g/d) to urban areas
(%en): males, 4.7; females, 5.7 [49]. Low MUFA intake has
(4.17 g/d) in Costa Rica [63]. Analysis of trans polyunsatu-
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Fats and Fatty World Health World Health Organization/Food and Indian Dietary Guidelines (Indian Council
Acids (%en) Organization, 2003 [25] Agricultural Organization, 2008 [87] of Medical Research 1989, 2009) [62,88]
Total fat 15–30 AMDR: 20–35 15–30
MAL: 35
MIL: 15
SFAs ,10 MAL: 10 ,10
PUFAs 6–10 AMDR: 6–11 ,8
MAL: 11
MIL(to prevent deficiency): 3
MIL(to prevent chronic disease): 6
n-6 PUFAs (LA) 5–8 AMDR: 2.5–9 3–7
Average LA requirement: 2
Individual LA level: 2.5
n-3 PUFAs 1–2 AMDR (n-3a): 0.5–2 .1
Minimum requirement (ALA): $0.5
AMDR (EPA + DHA) g/d: 0.250–2b
MALc , g/d: 3
MUFAs By differenced By differenced,e NA
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Saturated Fatty Acids recommends a 2%en average LA requirement for adults, with
an acceptable macronutrient distribution range (AMDR) of
Both International (WHO/FAO, 2003; WHO/FAO, 2008)
2.5% to 9%en [87]. According to the ICMR (India, 1989)
and ICMR (India, 1989) guidelines suggest that the intake of
guidelines, %en from n-6 PUFAs should be between 3% and
SFA should not exceed a maximum limit (MAL) of 10%en to
7% [62]; this has not been mentioned in the recent ICMR
keep cholesterol levels in a normal range and to reduce the risk
report [88] (Table 5).
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