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J Community Health (2013) 38:919925

DOI 10.1007/s10900-013-9702-0

ORIGINAL PAPER

Ischemic Heart Disease and Its Related Factors in Mongolia:


A Nationwide Survey
Tsogzolbaatar Enkh-Oyun Kazuhiko Kotani
Dambadarjaa Davaalkham Yasuko Aoyama
Satoshi Tsuboi Taeko Oguma Yosikazu Nakamura

Published online: 16 May 2013


Springer Science+Business Media New York 2013

Abstract Ischemic heart disease (IHD) remains one of Keywords Ischemic heart disease  Mongolia 
the most important disorders associated with disability and Prevalence  Cross-sectional study
mortality worldwide, and is one of the major causes of
cardiovascular diseases in Mongolia. The objective of the
current study was to determine the prevalence of IHD and Introduction
its related factors in a general population in Mongolia. We
conducted a nationwide cross-sectional survey between Ischemic heart disease (IHD) is characterized by ischemia of
March and September, 2009. General participants were the heart tissues due to atherosclerosis of the coronary
recruited from urban to rural regions in a multistage ran- arteries [1, 2]. Several risk factors have been identified,
dom cluster sampling method. The diagnosis of IHD was including age, male gender, smoking, alcohol use, lower
based on the Rose questionnaire (World Health Organiza- intake of fruit and vegetables, physical inactivity, and car-
tion) and electrocardiographic findings. A total of 369 diometabolic disorders [1, 2]. In 2004, IHD was the leading
(16.2 %) subjects with IHD were diagnosed among 2,280 cause of mortality in the world accounting for 12.2 % of all
participants. The prevalence of subjects with IHD was deaths [1]. The WHO projected that by 2030 the percentage
significantly increased by age: from 9.9 % in individuals of deaths due to IHD will increase up to 14.2 % and will
age 4044 years compared to 17.7 % in those over remain the leading cause of mortality [1]. Three-fourths of
60 years. Smoking habits (former and current) and non- global deaths due to IHD occurred in low- and middle-
frequent intake of fruits and vegetables were significantly income countries, with increasing longevity, urbanization,
positively associated with IHD in men, while heavy alcohol and lifestyle changes [2]. The mortality of IHD is also the
drinking habits and lower education period of time were leading cause of total mortality in Mongolia, and one report
significantly positively associated with IHD in women. documented that the mortality of IHD in men in age group
IHD was found to be prevalent, especially among people 4565 years was 3.1 times higher than in women in the same
aged over 40 years, in Mongolia. Statistical factors related age group [3]. However, there has been little information on
to IHD were found to be significantly different based on the epidemiology of IHD in Mongolia. More data for the
sex. The current data may provide relevant information to prevention of IHD, such as the real prevalence and its related
prevent IHD in the Mongolian population. risk factors of IHD, are needed.
As a recent topic, socioeconomic status (SES) can play a
role in the development of IHD [4, 5]. Previous studies have
T. Enkh-Oyun (&)  K. Kotani  Y. Aoyama  S. Tsuboi  shown that a lower SES is associated with IHD [6, 7]. From a
T. Oguma  Y. Nakamura
Department of Public Health, Jichi Medical University,
the results of a Chinese study that investigated the associa-
3311-1 Yakushiji, Shimotsuke City, Tochigi 329-0498, Japan tion of SES with myocardial infarction, low levels of edu-
e-mail: enkhoyun_t@yahoo.com cation were more commonly found in cases with myocardial
infarction compared to controls [7]. The SES indicators,
D. Davaalkham
Department of Epidemiology and Biostatistics, Health Sciences
such as education levels, were predictive for the incidence of
University of Mongolia, Ulaanbaatar, Mongolia heart failure among patients with IHD in Israel [6]. A

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relationship between SES and health is of particular interest of eight chapters with a total of 80 closed-ended and open-
in Mongolia, which is globalizing at an accelerated pace and ended questions. This questionnaire included their SES,
has rapid changes of the socioeconomic environment. alcohol and tobacco use, nutrition, physical activity, and
However, there have been no studies on the relationship health status. Subjects answers to the questionnaires were
between SES and IHD in Mongolia. confirmed by interviews. Physical examinations were
Again, no epidemiologic surveys exist focusing on IHD conducted following an overnight fast.
and its related factors among the general Mongolian pop-
ulation [3], although several surveys have been conducted Physical Examinations
for subjects with background diseases to IHD, such as
hypertension, in Mongolia [811]. Because the surveys that Height was measured in centimeters (without shoes), and
were recruited from living people exclude sufferers from weight was in kilograms (with heavy clothing removed).
sudden death caused by IHD, this often makes difficult the Body mass index was calculated as weight in kilograms
exact statistics related to IHD. In order to develop strate- divided by the square of height in meters. Overweight and
gies for the prevention of IHD, although we acknowledge obesity were defined according to the WHO definition of a
omitting the specific cases from sudden death caused by BMI greater than or equal to 25 as overweight and a BMI
IHD, it is crucial for us to have nationwide updated data for greater than or equal to 30 as obesity. Two blood pressure
subjects with IHD in the Mongolian population. The recordings were obtained from the right arm of participants
objective of the current study was, therefore, to determine in a sitting position after 10 min of rest, and mean values
the prevalence of the IHD and its related factors in a were calculated. Percentage of hypertension was defined as
general population of Mongolia. follows: systolic blood pressure C140 and diastolic blood
pressure C90 mmHg or currently on medication for
hypertension. In fasting blood samples, concentrations of
Methods total cholesterol and glucose were measured. According to
the WHO criteria using a fasting concentration [13],
We conducted a nationwide cross-sectional study among impaired glucose tolerance (IGT) was defined as a glucose
the general population in Mongolia. A total of 2,280 people level of equal to 6.16.9 mmol/L, diabetes mellitus was
were enrolled in this study. The study was approved by the defined as a glucose level of higher than 7.0 mmol/L, and
Ethics Committee of the Ministry of Health, Mongolia in hypercholesterolemia was defined as total cholesterol of
20th of January in 2009 and these subjects gave their higher than 5.0 mmol/L, respectively.
written consent.
SES Variables
Data Collection
Education variables, such as the start of and total years of
A total of 2,280 randomly selected Mongolian people aged education, were collected, and categorized per the Mon-
over 40 years from 8 rural soums (counties/villages) and 4 golian education system, dividing into 5 categories as
provincial centers of 4 provinces, and 14 khoroos of 4 elementary (\7 years), incomplete secondary (79 years),
districts of Ulaanbaatar city participated in the survey. Data complete secondary (1012 years), vocational [13, 14], and
was collected from March 2009 through August 2009. The university graduates ([14 years). Monthly income was
survey was designed to cover all geographical areas of categorized into the 3 types of lower, middle, and upper
Mongolia, and a four-stage cluster sampling process was levels according to the average salaries per month (Mon-
carried out to randomly select participants from the target golian National Statistic Office 2009).
population. Given the urban versus rural differences in Socioeconomic position was measured and defined as
lifestyle and disease status, the target population was social classes based on the longest held occupation, using a
stratified into urban and rural areas and samples were Registrar Generals Classification [14], where Class I cor-
drawn proportionally from each based on the target popu- responded to the upper social class. Participants were
lation in each area. Before the study, we distributed an placed into 6 groups of social class I (professional, e.g.,
information sheet which explained the purpose of the study physicians, engineers), social class II (managerial e.g.,
to subjects, who were randomly selected by the registration teachers, sales managers, social class III (semi-skilled non
of general practitioners. Subjects were invited to local manual, e.g., bricklayer), social class IV (partly skilled e.g.,
general practitioner centers in the urban districts, local postmen), social class V (unskilled e.g., porters, laborers),
rural soum clinics, and provincial centers. and non-employed VI (retired, unemployed, housewives).
A standard questionnaire of the WHO STEPS Surveil- Persons classified as housewives, students, retired with no
lance Manual was used [12]. The questionnaire consisted information on last occupation or persons whose stated

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occupation could not be classified, and were placed in a odds ratios for evaluating the association between inde-
social class VI which means non employed group. pendent variables and IHD. Adjustments were carried out
for the independent variables which significantly associ-
IHD Diagnosis ated with IHD by Chi square test; that is, age, education,
smoking habits, alcohol consumption and fruit/vegetable
The Rose questionnaire and electrocardiography (ECG) consumption habits. The trend in odds was evaluated by
were applied to the diagnosis of IHD [15]. In comparison using the likelihood ratio test for trend. All probability
with clinical judgment, the Rose questionnaire has been values were two-tailed, and all confidence intervals were
found to have 7881 % sensitivity and 9497 % specificity estimated at the 95 % level. The Statistical Package for the
[1, 16, 17]. Twelve-lead ECGs were taken by trained Social Sciences (SPSS Version 18.0) was used for analysis.
individuals using Cardiomax electrocardiographs. The A statistical significance was set at P \ 0.05.
electrocardiograms from the study participants were ana-
lyzed by the cardiologists with their corresponding Min-
nesota codes [18]. Results

Statistical Analysis Table 1 shows that descriptive statistics of IHD. The


prevalence of IHD was 16.2 % in the study population
The association between the measured variables and aged 40 years and over. The prevalence of IHD did not
prevalence of IHD was analyzed by the Chi square test. differ by sex. There was an increase of IHD correlated with
Logistic regression analyses were used to calculate the age in both sexes (in particular, statistical significance of

Table 1 Descriptive statistics of study population


Entire IHD, P value Total Men with P value Total Women with P value
population, n n (%) men, n IHD, n (%) women, n IHD, n (%)

Total 2,280 369 (16.2) 851 134 (15.7) 1,429 235 (16.4)
Age group (years) 0.003 0.062 0.003
4044 424 42 (9.9) 144 16 (11.1) 280 26 (9.3)
4549 525 87 (16.6) 189 34 (18.0) 336 53 (15.8)
5054 499 88 (17.6) 181 22 (12.2) 318 66 (20.8)
5559 362 69 (19.1) 141 31 (22.0) 221 38 (17.2)
60? 470 83 (17.7) 196 31 (15.8) 274 52 (19.0)
Residence 0.109 0.087 0.519
Urban 1,267 191 (15.1) 479 66 (13.8) 788 125 (15.9)
Rural 1,013 178 (17.6) 372 68 (18.3) 641 110 (17.2)
Monthly income 0.211 0.495 0.401
Lower 967 162 (16.8) 333 56 (16.8) 634 106 (16.7)
Middle 584 103 (17.6) 226 38 (16.8) 358 65 (18.2)
Upper 729 104 (14.3) 292 40 (13.7) 437 64 (14.6)
Education (year) 0.030 0.196 0.078
Elementary 230 47 (20.4) 68 10 (14.7) 162 37 (22.8)
Incomplete secondary 531 97 (18.3) 253 48 (19.0) 278 49 (17.6)
Complete secondary 606 102 (16.8) 221 39 (17.6) 385 63 (16.4)
Vocational 357 53 (14.8) 82 9 (11.0) 275 44 (16.0)
University 556 70 (12.6) 227 28 (12.3) 329 42 (12.8)
Occupation 0.195 0.154 0.654
Social class I 690 93 (13.5) 261 29 (11.1) 429 64 (14.9)
Social class II 431 67 (15.5) 117 20 (17.1) 314 47 (15.0)
Social class III 115 23 (20.0) 31 6 (19.4) 84 17 (20.2)
Social class IV 90 15 (16.7) 72 12 (16.7) 18 3 (16.7)
Social class V 199 34 (17.1) 88 12 (13.6) 111 22 (19.8)
Social class VI 755 137 (18.1) 282 55 (19.5) 473 82 (17.3)

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the trend was observed in women as well as men). The associated with IHD in men. Men who did not consume
education year indicator was significantly associated with vegetables or fruit had higher prevalence of IHD (25.6 and
the prevalence of IHD in the whole study population, and 20.1 %) compared to those who did consume them. Obesity,
this was noted to be particularly significant in women. hypertension, hypercholesterolemia, and glucose disorders
Women with only an elementary education had a higher were not significantly associated with the prevelence of IHD.
prevalence of IHD (22.8 %) compared with women who Table 3 shows the odds ratios for IHD as dependent
had university degrees (12.8 %). variable. Single variate analyses showed that smoking
Smoking was significantly associated with IHD in men habits (former and current smokers) (odds ratio
(Table 2). IHD was more prevalent in current and ex-smokers [OR] = 1.84; 95 % confidence interval [CI] 0.983.44 and
(19.3 and 18.2 %) than in non-smokers (10.0 %). In contrast, OR = 2.15; 95 % CI 1.373.40) and non-frequent intake
alcohol consumption was significantly associated with IHD in of fruits (OR = 1.66; 95 % CI 1.142.40) and vegetables
women. IHD prevalence was higher in heavy drinkers (20.6) (OR = 1.99; 95 % CI 0.571.64), were significantly posi-
but of lower prevalence in low moderate drinkers (11.0 %). tively associated with IHD in men. These results were
Insufficient intake of fruit and vegetables were significantly attenuated in a multivariate regression analysis, and only

Table 2 The prevalence of IHD by related factors


Entire IHD, P value Total Men with P value Total Women with P value
population, n n (%) men, n IHD, n (%) women, n IHD, n (%)

Walking habits ([10 min/day) 0.428 0.377 0.759


Yes 1,935 308 (15.9) 709 108 (15.2) 1,226 200 (16.3)
No 345 61 (17.7) 142 26 (18.3) 203 35 (17.2)
Vegetable consumption habits 0.149 0.021 1.000
Yes 2,090 331 (15.8) 773 114 (14.7) 1,317 217 (16.5)
No 190 38 (20.0) 78 20 (25.6) 112 18 (16.1)
Fruit consumption habits 0.119 0.009 1.000
Yes 1,605 247 (15.4) 532 70 (13.2) 1,073 177 (16.5)
No 675 122 (18.1) 319 64 (20.1) 356 58 (16.3)
Alcohol consumption habits 0.008 0.093 0.017
Non 911 154 (16.9) 211 32 (15.2) 700 122 (17.4)
Low moderate 429 49 (11.4) 101 13 (12.9) 328 36 (11.0)
High moderate 380 58 (15.3) 144 15 (10.4) 236 43 (18.2)
Heavy 560 108 (19.3) 395 74 (18.7) 165 34 (20.6)
Smoking habits 0.081 0.002 0.893
Non smoker 1,600 241 (15.1) 311 31 (10.0) 1,289 210 (16.3)
Current smoker 548 104 (19.0) 430 83 (19.3) 118 21 (17.8)
Ex smoker 132 24 (18.2) 110 20 (18.2) 22 4 (18.2)
Hypercholesterolemia 0.543 0.466 0.845
Yes 382 66 (17.3) 157 28 (17.8) 225 38 (16.9)
No 1,895 303 (16.0) 694 106 (15.3) 1,201 197 (16.4)
Obesity traits 0.975 0.866 0.793
Normal 814 133 (16.3) 315 47 (14.9) 499 86 (17.2)
Overweight 852 136 (16.0) 322 53 (16.5) 530 83 (15.7)
Obesity 614 100 (16.3) 214 34 (15.9) 400 66 (16.5)
Glucose disorder 0.300 0.264 0.401
Normal value 1,929 322 (16.7) 715 119 (16.6) 1,263 203 (16.7)
Impaired glucose tolerance 168 22 (13.1) 65 6 (9.2) 106 16 (15.5)
Diabetes 183 25 (13.7) 71 9 (12.7) 57 16 (14.3)
Hypertension 0.288 0.920 0.260
No 826 130 (15.7) 349 54 (15.5) 477 76 (15.9)
Previously diagnosed 861 152 (17.7) 292 48 (16.4) 569 104 (18.3)
Diagnosed by study 593 87 (14.7) 210 32 (15.2) 383 55 (14.4)

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Table 3 Odds ratio for the IHD as dependent variable and related factors as independent variables
Entire population Men Women
Unadjusted OR Multivariate OR Unadjusted OR Multivariate OR Unadjusted OR Multivariate OR
(95 % CI) (95 % CI) (95 % CI) (95 % CI) (95 % CI) (95 % CI)

Age group (years)


4044 1.0 1.0 1.0 1.0 1.0 1.0
4549 1.81 (1.222.68)* 1.78 (1.202.66)* 1.76 (0.933.32) 1.82 (0.953.51) 1.83 (1.113.01)* 1.84 (1.113.05)*
5054 1.95 (1.312.89)* 1.96 (1.622.92)* 1.11 (0.562.19) 1.11 (0.552.24) 2.56 (1.574.16)* 2.61 (1.604.28)*
5559 2.14 (1.423.24)* 2.18 (1.423.30)* 2.26 (1.174.34)* 2.39 (1.224.72)* 2.03 (1.193.46)* 2.10 (1.223.62)*
60? 1.95 (1.312.90)* 1.87 (1.232.83)* 1.50 (0.792.87) 1.75 (0.893.44) 2.29 (1.383.79)* 2.10 (1.223.62)*
Education (years)
Elementary 1.0 1.0 1.0 1.0 1.0 1.0
Incomplete 0.87 (0.591.28) 0.89 (0.591.35) 1.36 (0.652.85) 1.58 (0.723.47) 0.72 (0.451.17) 0.75 (0.451.27)
secondary
Complete 0.79 (0.541.16) 0.88 (0.581.37) 1.24 (0.582.64) 1.61 (0.713.67) 0.66 (0.421.04) 0.70 (0.411.19)
secondary
Vocational 0.68 (0.441.05) 0.75 (0.441.27) 0.72 (0.271.88) 1.04 (0.353.07) 0.64 (0.391.05) 0.59 (0.311.10)
University 0.56 (0.370.84)* 0.64 (0.381.09) 0.82 (0.371.78) 1.30 (0.493.50) 0.49 (0.300.81)* 0.50 (0.260.97)*
Smoking habits
Non smoker 1.0 1.0 1.0 1.0 1.0 1.0
Current 1.32 (1.031.70)* 1.19 (0.911.56) 2.01 (1.093.69)* 2.15 (1.373.40)* 1.11 (0.681.82) 0.97 (0.591.61)
smoker
Ex smoker 1.25 (0.791.99) 1.10 (0.681.78) 2.16 (1.393.36)* 1.84 (0.983.44)* 1.14 (0.383.40) 0.99 (0.323.08)
Alcohol consumption habits
Non 1.0 1.0 1.0 1.0 1.0 1.0
Low moderate 0.63 (0.450.89)* 0.69 (0.480.98)* 0.83 (0.411.65) 0.81 (0.401.66) 0.58 (0.390.67)* 0.66 (0.440.99)*
High moderate 0.89 (0.641.23) 0.98 (0.701.39) 0.65 (0.341.25) 0.67 (0.341.32) 1.06 (0.721.55) 1.26 (0.841.89)
Heavy 1.18 (0.891.54) 1.20 (0.891.60) 1.29 (0.822.03) 1.27 (0.792.05) 1.23 (0.801.88) 1.38 (0.892.16)
Vegetable consumption habits
Yes 1.0 1.0 1.0 1.0 1.0 1.0
No 1.33 (0.911.93) 1.15 (0.771.74) 1.99 (1.163.44)* 1.79 (0.963.33) 0.97 (0.571.64) 0.84 (0.481.49)
Fruit consumption habits
Yes 1.0 1.0 1.0 1.0 1.0 1.0
No 1.21 (0.961.54) 1.01 (0.781.31) 1.66 (1.142.4)* 1.36 (0.902.05) 0.99 (0.711.36) 0.87 (0.611.24)
Odds ratio [OR] (95 % confidential interval [CI]) adjusted for age, education, smoking, alcohol consumption habits and vegetable, fruit
consumption habits
* P value \0.05

current smoking habits (adjusted OR = 2.13; 95 % CI Mongolia, as well as attempting to determine associated
1.373.40) remained significant risk factors for IHD in risk factors, including SES indicators. The prevalence of
men. In multiple logistic regression models, increasing age IHD was 16.2 % in this population. There were population-
(OR = 2.10; 95 % CI 1.223.62), heavy rather than low based studies in Tehran, Iran (age C30, n = 5,984) [19]
moderate alcohol drinking habits (OR = 0.66; 95 % CI and in India (age C20, n = 1,047) [20] using the same
0.440.099) and lower levels of higher education methodology as ours, namely the Rose questionnaire and
(OR = 0.50; 95 % CI 0.260.97) were significantly asso- ECG studies. The prevalence of our surveys is lower than
ciated with IHD in women. the 21.8 % reported in the Tehran study and higher than the
7.1 % reported in the Indian study [19, 20]. Given these
previous data, IHD appears to have a relatively high
Discussion prevalence in Mongolia. As for age, increasing trends were
observed with age and prevalence of IHD, and subjects
The current study was the first survey conducted nation- over age 60 had the highest prevalence of IHD, regardless
wide on the prevalence of IHD in the general population of of sex. This result is consistent with the previous studies in

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Tehran and India [19, 20]. As for the sex difference in the women, but not in men. In Mongolian tradition, in terms of
prevalence of IHD, the previous studies reported that education, many parents are more concerned about daugh-
women had a higher prevalence of IHD than men: women: ters than sons in the teenage years, and girls therefore have a
22.3 % and men: 18.8 % in the Tehran study [19] and wider range of opportunities to obtain higher education. This
women: 8.9 %, men: 6.2 % in Indian study [20]. Although may partly affect the sex difference observed in the current
the prevalence of IHD was slightly higher in men (16.4 %) study.
compared with women (15.7 %) in our survey, the preva- There are several limitations in our study. The cross-
lence was nearly equal between the sexes. This trend in sectional design might allow for less ability to determine
Mongolia seems rather inconsistent to general trends of the the causal relationship between IHD and its related factors.
prevalence of IHD, suggesting the need for further The prevalence of IHD might not exactly reflect all cases of
investigation. IHD because cases of sudden death caused by IHD would
The current study found a significant association have eliminated those individuals from inclusion in the
between smoking and IHD in men. Smoking is well known study. Future studies with a prospective design and
to be a causatively associated with IHD, and cigarette enrollment of all cases with IHD are therefore warranted.
smokers are 24 times more likely to develop IHD than
nonsmokers [21]. The highest incidence of smoking is
generally observed among men in lower-middle-income Conclusion
countries, and among Mongolian adults, 24.3 % were
found to be smokers (43 % men, 5.2 % women) in 2009 In conclusion, IHD was found to have a high prevalence,
[22]. The fraction of IHD attributable to smoking was especially among people over 40 years of age, in Mongo-
estimated to be 25 % in Mongolian men [23], and the anti- lia. Significant factors related to IHD were found to have
smoking policy is thought to be effective for preventing some differences according to gender. The current data
IHD events in this population. In addition, non-frequent may provide relevant information to help prevent IHD in
fruit and vegetable consumption were significantly asso- the Mongolian population.
ciated with IHD in men. This supports the previous reports,
while these reports also show that the findings were
observed in both sexes [29, 30]. Mongolian men were more
unlikely to eat fruit and/or vegetables than women [22, 31], References
and this trend, in particular regarding fruit consumption,
was notable in the current study. Such sex differences of 1. Mathers, C., Fat, D. M., Boerma, J. T., & World Health Orga-
nization. (2008). The global burden of disease: 2004 update.
dietary habits in Mongolian people may explain the sex- Geneva, Switzerland: World Health Organization.
based differences observed in the current study. 2. Gaziano, T. A., Bitton, A., Anand, S., Abrahams-Gessel, S., &
Among women, low moderate drinking of alcohol was Murphy, A. (2010). Growing epidemic of coronary heart disease
associated with a lower prevalence of IHD. This was con- in low- and middle-income countries. Current Problems in
Cardiology, 35(2), 72115.
sistent with the previous studies [24, 25]. Light to moderate 3. State Implementing Agency of Health GoM. (2012). Health
drinking can have a beneficial impact on morbidity and indicator 2011. Ulaanbaatar: Munkhiin Useg Press.
mortality of IHD [26]. The association between alcohol and 4. Adler, N. E., & Ostrove, J. M. (1999). Socioeconomic status and
IHD among women, rather than men, may be due to factors health: What we know and what we dont. Annals of the New
York Academy of Sciences, 896, 315.
such as menopausal states and stronger effects of alcohol on 5. Hemingway, H., Shipley, M., Brunner, E., Britton, A., Malik, M.,
women [27, 28]. In addition, among women, those with & Marmot, M. (2005). Does autonomic function link social
lower levels of education were noted to have significantly position to coronary risk? The Whitehall II study. Circulation,
higher prevalence of IHD. The association of education years 111(23), 30713077.
6. Benderly, M., Haim, M., Boyko, V., & Goldbourt, U. (2013).
on the prevalence of IHD is the first to be shown in Mongolia. Socioeconomic status indicators and incidence of heart failure
This result is likely similar to the studies conducted in Israel, among men and women with coronary heart disease. Journal of
China and the USA [6, 32]. The mechanisms of involvement Cardiac Failure, 19(2), 117124.
of educational attainment in the development of IHD remain 7. Guo, J., Li, W., Wang, Y., et al. (2012). Influence of socioeco-
nomic status on acute myocardial infarction in the Chinese
unclear, but as an example, persons of lower SES are thought population: The INTERHEART China study. Chinese Medical
to confront more barriers to modifying risk behaviors over Journal (England), 125(23), 42144220.
time such as quitting smoking, improving diet, increasing 8. Bolormaa, N., Narantuya, L., De Courten, M., Enkhtuya, P., &
physical activity and adhering to medications [33]. In our Tsegmed, S. (2008). Dietary and lifestyle risk factors for non-
communicable disease among the Mongolian population. Asia-
study, odds ratios for IHD in women decreased linearly as Pacific Journal of Public Health, 20 Suppl, 2330.
level of education increased. The association between edu- 9. Sharma, S. K., Zou, H., Togtokh, A., et al. (2010). Burden of
cation and IHD in our current study was clearly observed in CKD, proteinuria, and cardiovascular risk among Chinese,

123
J Community Health (2013) 38:919925 925

Mongolian, and Nepalese participants in the International Society 22. Ministry of Health Mongolia W, Milllenium Challenge Account
of Nephrology screening programs. American Journal of Kidney Mongolia, Public Health Institute. (2010). Mongolian STEPs
Diseases, 56(5), 915927. seurvey on the prevalence of noncommunicable disease and
10. Uurtuya, S., Kotani, K., Taniguchi, N., et al. (2010). Comparative injury risk factors-2009. Ulaanbaatar, Mongolia: WHO.
study of atherosclerotic parameters in Mongolian and Japanese 23. Martiniuk, A. L., Lee, C. M., Lam, T. H., et al. (2006). The
patients with hypertension and diabetes mellitus. Journal of fraction of ischaemic heart disease and stroke attributable to
Atherosclerosis and Thrombosis, 17(2), 181188. smoking in the WHO Western Pacific and South-East Asian
11. Mungun-Ulzii, K., Erdenekhuu, N., Altantsetseg, P., Zulgerel, D., regions. Tobacco Control, 15(3), 181188.
& Huang, S. L. (2010). Asymptomatic Mongolian middle-aged 24. Roerecke, M., & Rehm, J. (2011). Ischemic heart disease mor-
women with high homocysteine blood level and atherosclerotic tality and morbidity rates in former drinkers: A meta-analysis.
disease. Heart and Vessels, 25(1), 713. American Journal of Epidemiology, 173(3), 245258.
12. WHO. (2005). WHO STEPS surveillance manual. The WHO 25. World Health Organization. (2011). Management of substance
STEPwise approach to chronic disease risk factor surveillance. abuse team. Global status report on alcohol and health. Geneva,
Geneva: WHO Press. Switzerland: World Health Organization.
13. WHO, IDF. (2006). Definition and diagnosis of diabetes mellitus 26. World Health Organization. (2011). Global status report on
and intermediate hyperglycemia. Geneva: WHO Press. noncommunicable diseases 2010. Geneva, Switzerland: World
14. Ramsay, S. E., Whincup, P. H., Morris, R., Lennon, L., & Health Organization.
Wannamethee, S. G. (2008). Is socioeconomic position related to 27. Tolstrup, J., Jensen, M. K., Tjonneland, A., Overvad, K., Muk-
the prevalence of metabolic syndrome? Influence of social class amal, K. J., & Gronbaek, M. (2006). Prospective study of alcohol
across the life course in a population-based study of older men. drinking patterns and coronary heart disease in women and men.
Diabetes Care, 31(12), 23802382. British Medical Journal, 332(7552), 12441248.
15. Rose, G. A. (1962). The diagnosis of ischaemic heart pain and 28. Mumenthaler, M. S., Taylor, J. L., OHara, R., & Yesavage, J. A.
intermittent claudication in field surveys. Bulletin of the World (1999). Gender differences in moderate drinking effects. Alcohol
Health Organization, 27, 645658. Research and Health, 23(1), 5564.
16. Mathers, C. D., Truelsen, T., Begg, S., & Satoh, T. (2004). 29. Dauchet, L., Amouyel, P., Hercberg, S., & Dallongeville, J.
Global burden of ischaemic heart disease in the year 2000. (2006). Fruit and vegetable consumption and risk of coronary
Geneva: World Health Organization. heart disease: A meta-analysis of cohort studies. Journal of
17. Heyden, S., Bartel, A. G., Tabesh, E., et al. (1971). Angina Nutrition, 136(10), 25882593.
pectoris and the Rose questionnaire. Archives of Internal Medi- 30. Hall, J. N., Moore, S., Harper, S. B., & Lynch, J. W. (2009).
cine, 128(6), 961964. Global variability in fruit and vegetable consumption. American
18. Prineas, R. J., Crow, R. S., & Blackburn, H. W. (2010). The Journal of Preventive Medicine, 36(5), 402409.e5.
Minnesota code manual of electrocardiographic findings: Stan- 31. Millenium Challenge Account Mongolia MoH. (2011). Confer-
dards and procedures for measurement and classification (2nd ence book of the first national forum of prevention and control of
ed.). London: Springer. non-communicable diseases and injury. In The prevention and
19. Hadaegh, F., Harati, H., Ghanbarian, A., & Azizi, F. (2009). control of non-communicable diseases and injury. Ulaanbaatar,
Prevalence of coronary heart disease among Tehran adults: Mongolia, p. 350.
Tehran Lipid and Glucose Study. Eastern Mediterranean Health 32. Centers for Disease C, Prevention. (2011). Prevalence of coro-
Journal, 15(1), 157166. nary heart diseaseUnited States, 20062010. Morbidity and
20. Joshi Pradeep, I. M., Saran, R. K., & Natu, S. M. (2013). A study Mortality Weekly Report, 60(40), 13771381.
of coronary heart disease and the associated risk factors in Luc- 33. Fiscella, K., & Tancredi, D. (2008). Socioeconomic status and
know district, India. International Journal of Biology Medical coronary heart disease risk prediction. Journal of American
Research, 4(1), 29662972. Medical Journal, 300(22), 26662668.
21. CDC home. (2012). Centers for disease control and prevention:
Smoking and Tobacco useHeart Disease and Stroke. http://www.
cdc.gov/tobacco/. Accesed 1 Mar 2013.

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