Obesity Research · Vol. 2, No. 1 · 2015 · pp. 32–38 · e-ISSN 2377-8385

Cardiovascular Diseases in Relation to Anthropometric, Biochemical and Dietary Intake in Women: A Case Control Study

Parvez I. Paracha, Huma Waheed, Saima I. Paracha, Shahid Ullah, Syeda Sidra Bano

Department of Human Nutrition, Agricultural University, Peshawar, PakistanPakistan
Rehman Medical Institute, Hayatabad, Peshawar, PakistanPakistan
National AIDS Control Programme, National Institute of Health, Islamabad, PakistanPakistan
Shahid Ullah, Faculty of Medicine, Nursing and Health Sciences, Flinders University, Ad- elaide, AustraliaAustralia

DOI: https://doi.org/10.17140/oroj-2-106 · Published 2015-04-06 · Licence: https://creativecommons.org/licenses/by/4.0 · © 2015 The Author(s)

Abstract

Background: Cardiovascular diseases in women are increasing at an alarming rate but very little attention has been given due to economic and socio-cultural reasons. A study was undertaken to examine the relationship between cardiovascular diseases and nutritional status in Pakistani women. Methods: A case-control study was carried out in the Outpatients department (OPD) of the Cardiology Unit, Rehman Medical Institute (RMI), Peshawar, Khyber Pakhtunkhwa, Pakistan. The inclusion criteria for selection of cases were females having complaints of myocardial infarction and free from all other infectious and chronic diseases. Forty three cases and 43 controls were selected for the study. Subjects were interviewed for their medical history, dietary intake demographic and socio-economic characteristics. Weight, height measurements and blood samples from both the cases and controls were taken for assessing their nutritional status. Data were analyzed using Student’s t-test, Chi-square test, univariate and multivariate unconditional logistic regression to study the relationship between different variables. Results: The results revealed that the cases had a significantly (p<0.05) higher median age than the controls but there were no significant (p>0.05) differences in the mean weight, height, BMI, serum ferritin and haemoglobin concentrations between the cases and controls. High prevalence of overweight and obesity was found in both cases (67.4%) and controls (81.4%). Cases had a significantly lower mean dietary energy, protein, carbohydrates, and fat intake than the controls but there was no significant difference (p>0.05) in the mean iron intake between the cases and controls. Results of logistic regression showed no significant association between the dependent (CVD) and independent variables (age, diastolic blood pressure, BMI, exercise, family history, family type, family size, haemoglobin, ferritin, carbohydrates and protein). Conclusions: The study does not reveal significant relationship between the CVDs and nutritional status. The prevalence of overweight and obesity in women was found to be alarmingly high and needs to be addressed by appropriate interventions to prevent the incidence of metabolic syndromes and chronic diseases in population.

Keywords: Cardiovascular diseases; Nutritional status; Overweight and obesity; Pakistani women

Introduction

Cardiovascular diseases (CVDs) are one of the leading causes of disability and premature deaths in adults worldwide, low income to middle income countries bear the brunt by accounting for over 80% of the global disease burden and overwhelming health expenditures amounting to billions of dollars 1,2 annually.1,2 The prevalence of CVDs increases with advancing age and varies among racial, ethnic, geographic, and socio-demographic groups. It has been estimated that by the year 2020, the prevalence of CVDs will increase by 75% with predominance in developing counties. CVDs account for 17.3 million deaths per year that are likely to reach 23.6 million deaths per year by 2030.3 The social and economic implications of CVDs in terms of increased burden on the healthcare system, family sufferings, Disability Adjusted Life Years (DALYs) lost, reduced productivity and economic outputs are enormous and well 4,5,6 documented.

Pakistan has been confronted with an increasing risk of cardiovascular diseases due to non-implementation of food safety laws, unhealthy dietary practices, poor sanitation and hygiene practices, population explosion, rapid urbanization, limited resources, lack of physical activity and unhealthy lifestyles.7,8 Women share a greater burden of CVDs than men due to sedentary lifestyles, reproductive stress and poor dietary intake.9 CVDs shorten the life expectancy of women by about 5 years as compared to non-CVDs women.10 In Pakistan, CVDs account for 19% of all the deaths occurring among adults aged 30-70 years.11

Since very limited work has been done on the risk factors associated with cardiovascular diseases in women in this part of the world, a case-control study was undertaken to assess the relationship between CVDs in women and their nutritional status by taking their anthropometric, biochemical, dietary and demographic and socio-economic characteristics.

Materials And Methods

A case-control study was carried out in the Outpatients department (OPD) of the Cardiology Unit, Rehman Medical Institute (RMI), Peshawar, Pakistan. Permission to undertake the study was taken from ethical committee of the hospital. The inclusion criteria used for selection of cases were female adults having complaints of myocardial infarction confirmed by clinical and laboratory tests including ECG, ETT, ECHO and blood pressure by a Cardiologist. The controls were women accompanying patients without having any disease. The cases and controls were representing a sample from different geographical areas as RMI is a reputable health care centre with a specified cardiac unit which attracts patients from all over the province. Both cases and controls were exposed to similar risk factors and the latter resembled with the cases in all respects except for the presence of disease. Informed consent was obtained from the 43 cases and 43 controls enrolled in the study.

Medical history, general characteristics and weightheight measurements of women were taken by following the recommended procedures.12 Body mass index of the subjects was computed and prevalence of overweight and obesity was assessed by following the WHO cut-offs.13 Haemoglobin and serum ferritin concentration of women were determined by digital 14,15 portable Hemocue and ELISA, respectively. A 24-hr dietary recall was used to assess dietary energy, carbohydrate, protein, fat and iron intakes of women.16

Statistical Analysis

Anthropometric, biochemical, dietary, demographic and socio-economic data were analysed by using STATA software version 12.0.17 Descriptive statistics were expressed as mean and standard deviation for discrete and continuous measures, whereas percentages were reported for categorical variables. Median and Inter-quartile range (IQR) was reported for skewed data. An independent sample t test was used to compare the mean differences between the cases and controls in anthropometric measurements (weight, height and body mass index), 7,8 biochemical indicators (haemoglobin and ferritin concentrations) dietary intake (energy, carbohydrate, protein, fat and iron) and demographic-socioeconomic characteristics (age, family size, number of children) at 5% level of significance. A Chi-square test of independence was performed to measure the extent of association between two categorical variables with continuity correction where appropriate and a Mann-Whitney U test was used to compare the differences in medians.

A multivariate analysis was undertaken using unconditional logistic regression logit procedure in STATA Version 1217 for unmatched case-control design. Univariate logistic regression was first performed variable by variable, without any adjustment. This was done to explore the association between each variable and the risk of myocardial infarction. Multivariate modelling approach was undertaken by putting all variables considered clinically important. This was done to adjust for each variable with all of the other variables listed in the model. The estimates were expressed as unadjusted Odds Ratio (OR) from univariate model and adjusted OR from multivariate model. The ORs were considered statistically significant if their 95% Confidence Interval (CI) did not include unity. The more the OR deviated from 1, the stronger was the association between the exposure variable.

Results And Discussion

General characteristics of cases and controls presented in Table 1 indicate that cases had significantly (p<0.05) higher median age and mean systolic blood pressure than the controls, but no significant differences were observed in the mean weight, height, body mass index and diastolic blood pressure between

the cases and controls. Lack of a significant difference in the mean BMI between the cases and controls is somewhat contrary to the general perception that obesity is one of the risk factors for cardiovascular diseases. The categorization of women on the basis of BMI revealed that only about 5% of women in CVDs group were under weight, while 35% and 33% were overweight and obese, respectively. In other words 68% of women in CVDs group were overweight and obese in comparison to about 81% overweight and obese women in non CVDs group (control group) indicating a higher prevalence of overweight and obesity in the non CVDs group (Table 1). Similarly, no significant (p>0.05) association between health status (MI yes-no) and body mass index (high and low) negates the established association between the BMI and CVDs. No significant association between BMI and CVDs also identifies BMI as a poor predictor of health status and its cut-off values for categorization of individuals into underweight, normal, overweight and obesity and applicability among different races and ethnic groups has been questioned seriously.22 However, the difference in mean anthropometric results and association between different categorical variables across different countries could be attributed to differences in genetic and environmental factors that influence the relationships between different variables.

Table 2 shows the mean Heaemoglobin (Hb) and Serum Ferritin (SF) concentrations of CVD cases and controls as well as the prevalence of Anaemia (An), Iron Deficiency (ID) and Iron Deficiency Anaemia (IDA) between the cases and controls. As evident from Table 2, there were no significant (p<0.05) differences in the mean Hb and SF levels between the cases and controls. However, mean SF concentration of cases as well as non-iron deficient group tended to show an increase of 30% and 63%, respectively, over the corresponding iron status groups of controls reflecting a trend of weak relationship due to non-significant results between SF and CVDs (Table 2). Similarly, there was no significant association between the iron status groups (anemic and non-anaemic; iron deficient and non-iron deficient; iron deficient anaemic and iron deficient non-anaemic) and CVDs status (Table 2).

Age (yrs), Median (IQR) 46.5 (40.0-50.0) 50.0 (45.0-56.0) 42.0 (40.0-50.0) <0.01 Weight (kg), Mean ± SD 66.9±13.4 65.8+16.0 68.1±10.8 0.43 Height (kg), Mean ± SD 152.5±4.3 153.30+4.30 152.44±4.4 0.37 Body mass index, Mean ± SD 28.3+5.5 27.3± 6.0 29.3± 4.7 0.10 Systolic, mm/Hg, Mean ± SD 128.0±17.13 132.47±20.94 123.02±11.45 0.01 Diastolic, mm/Hg, Mean ± SD 84.98±12.75 86.16±14.68 83.79±10.51 0.39 Under weight (BMI <18.5) n (%) 2 (2.3) Normal weight (18.5 ≤ BMI <25) n (%) 20 (23.3) 12 (27.9) 8 (18.6) 0.44 Overweight (25 ≤ BMI <30) n (%) 31 (36.0) 15 (34.8) 16 (37.2) 0.99 Obese ≥30 n (%) 33 (38.4) 14 (32.6) 19 (44.2) 0.38 SD=Standard deviation; IQR=Inter quartile range (25th-75th Percentile); p values are based on Mann Whitney U test for age (skewed distribution); Independent sample t-test for systolic, diastolic and BMI variables (symmetric distribution) and Chi-square test for a categorical variable body mass index General characteristics of subjects.

The results related to non-significant association between the CVDs, SF and other iron status indicators are in fair agreement with findings of the earlier researchers23 who also reported no significant association between the increasing risk of CVD and SF. Similarly, no significant association was found between the mortality of CVDs’ patients and SF.24 Conversely, a U-shaped relationship was found between CVD, IHD and SF levels in women and no significant association between CVD 25 26 and SF in men.25 Another study26 revealed that SF ≥200 ng/ml was associated with four fold higher risk of coronary heart dis- 27-30 ease in Iranian men. Likewise, other researchers also reported a significant association between CVDs and SF. The conflicting results in establishing an association between CVDs and SF 18-21 may be attributed to differences in ethnicity, ages, gender, socioeconomic characteristics, study designs and type and severity of CVDs. No significant association (p>0.05) between the health status (MI yes-no) and iron status indicators also suggests that Hb and SF do not share any relationship with CVDs.

Dietary energy, carbohydrates, protein, fat and iron intakes of the cases and controls shown in Table 3 revealed that the cases had significantly lower mean dietary energy, carbohydrates, protein and fat intakes than the controls but there was no significant difference in the mean dietary iron intake between the cases and controls. The lower nutrients intake of cases may have been partly attributed to patients’ stress and illness and partly to confounding variables such as BMI. The lower energy and carbohydrates intake have been reported31 to have protective affects against cardiovascular diseases but in our study the lower nutrients intake by cases could not prevent the occurrence of MI. The differences in results amongst the various studies could be attributed to the differences in intensity of CVDs, study designs, dietary and environmental variations. The present results suggest that hospitalized CVD patients are at a greater risk of malnutrition. The nutrients intake of controls also appeared to be lower when compared with the mean nutrients intake of corresponding age non-hospitalized adult normal women as well with 32-34 those of recommended dietary allowances. Thus, one day 24hr dietary recall of hospitalized patients (cases) and non-patients

Variable Total (n=86) Cases(n=43) Control (n=43) p-value

2 (4.7) - -

Variable Cases (n=43) Controls (n=43) p-value

Hemoglobin (Hb), Mean ± SD 13.52±2.18 (n=43) 13.14±1.18 (n=43) 0.3828 Anaemic (Hb< 12 g/dl), Mean ± SD 10.20±1.66 (n=8) 10.62±0.65 (n=9) 0.5166 Non-anaemic (Hb≥ 12 g/dl), Mean ± SD Serum Ferritin (SF), Mean ± SD 53.75±76.93 (n=43) 41.39 ± 69.79 (n=43) 0.4374 Iron deficient (SF<12 ng/ml), Mean ± SD Non-iron deficient (SF ≥ 12 ng/ml) Mean ± SD Anaemic (Hb<12 g/dl) n (%) 8 (18.60) Non-anaemic (Hb≥ 12 g/dl) n (%) 35 (81.40) Iron deficient (SF<12 ng/ml) n (%) 18 (41.86) Non-iron deficient (SF ≥ 12 ng/ml)n (%) Iron deficient anaemic (SF<12 ng/ml and Hb<12 g/dl) n (%) Non-iron deficient anaemic (SF ≥12 ng/ml (Hb<12 g/dl) n (%) Iron deficient non-anaemic (SF<12 ng/ml) (Hb ≥ 12 g/dl) n (%) Non-iron deficient non-anaemic (SF ≥12 ng/ml) (Hb ≥12 g/dl) n (%)

Table 2. Biochemical status of cases and controls (n=86). Energy (kcal), Mean± SD 699.09±269.77 949.23±275.86 0.0001 CHO (g), Mean± SD 107.17±51.72 141.77±50.51 0.0023 Protein (g), Mean± SD 31.86±10.86 41.76±17.34 0.0022 Fat (g), Mean± SD 23.84±21.18 33.35±12.00 0.0127 Iron (mg), Mean± SD 8.63±5.44

Table 3. Dietary nutrients intake per day of cases and control.

(controls) selected from attendants and accompanied persons of cases may not be suitable to capture their usual dietary intake and therefore, dietary results may be used with caution.

The demographic and socio-economic characteristics of cases and controls presented in Table 4 show that 95% of the women from cases and 86% of the women from the controls had education up to secondary school level and there was no significant association between education and health status groups. Similarly, 93% of cases were housewives in comparison to 84% of women in the control group and no significant association was found between the subjects’ profession and health status groups (Table 4). Likewise, no significant association was found between the economic and health status categorical variables (Table 4). These findings differ from the generally established perception that individuals with lower socio-economic status have increased morbidity and shorter life expectancy than those of higher socio-economic status. Lack of association between the socio-demographic and health status variables suggests that causes of CVDs in women are beyond the socio-demographic domain. The results are in line with those of others35 who studied an association between the socio-demographic characteris-

14.28±1.45 (n= 35) 13.81±1.37 (n=34) 0.1699

2.39±3.41 (n=18) 4.55±3.49 (n=12) 0.1062

90.74±83.34 (n=25) 55.65±77.86 (n=31) 0.1132

9 (20.93) 0.787 34 (79.07) 12 (27.91) 0.175 25(58.14) 31 (72.09)

5 (11.63) 2 (4.65)

13 (30.23) 10 (23.26) 0.339 3 (6.98) 7 (16.28)

22 (51.16) 24 (55.18)

Variable Cases (n=43) Control (n=43) p-value

10.11±4.44 0.4374

tal disorders and reported that increased cardiovascular profile in young adults could not be explained by socio-demographic variables alone. Conversely, there was a compelling body of evidence that populations from lower socio-economic status had higher incidence CVDs and premature deaths as compared to those of the higher socio-economic status.36

Results of logistic regression presented in Table 5 showed no significant association between the dependent (CVD) and independent variables (age, diastolic blood pressure, BMI, exercise, family history, family type, family size, haemoglobin, ferritin, carbohydrates and protein). Non-significant association between CVDs and independent variables suggest the complex nature of the disease that may result from a variety of factors not included in this study, in other words, to establish an association between CVDs and risk factors, a more thorough and comprehensive investigation is required by taking into consideration genetic, environmental (anthropometric, dietary, biochemical, clinical), lifestyle factors, socio-economic characteristics, a larger sample size and robust study design. These arguments are substantiated 35 37 by other researchers37 who reported a significant association between Coronary Artery Disease (CAD) and smoking (OR=1.89;

CI=1.48-1.65); CAD and alcohol (OR=1.37; 95% CI=1.30-1.46); CAD and diabetes (OR=1.37; 95% CI=1.25-1.50); CAD and high fat diet (OR=1.35; 95% CI=1.28-1.43); CAD and BMI>24 kg/m2 (OR=1.09; 95% CI=1.03-1.17). Similarly, others investigators2 have also reported a significant association between Myocardial Infarction (MI) and smoking (OR=2.87, CI=2.58-3.19); MI and diabetes (OR=2.37, CI=2·07-2·7); MI and hypertension (OR=1.91, CI=1.74-2·1); MI and abdominal obesity (OR=1.62,CI=1.45-1.80); MI and psychosocial factors (OR=2.67; CI=2.21-3.22); MI and Apoβ/ApoA1 ratio (3 vs. 1) (OR=1.84; CI=1.58-2.13).

Health and socio-demo- Total graphic characteristics (n=86) Education

Lower secondary 78 (90.7) Higher secondary 8 (9.3)

Profession

Unemployed (Housewife) 76 (88.4) Employed 10 (11.6)

Family Type

Nuclear 49 (57.0) Joint 37 (43.0)

Family History

No 59 (68.6) Yes 27 (31.4)

Socio-economic Status

Moderate rich 58 (67.4) Rich 28 (32.6)

Exercise

No 50 (58.1) Yes 36 (41.9) Percentages are in parentheses. p values are based on Chi-square test

Table 4. Health and demographic-socioeconomic characteristics of cases and controls.

Variable (Categorical) Unadjusted Adjusted

Age, y (≤ 40 vs. > 40) 2.59 (0.97-6.95) SBP, mmHg (≤ 140 vs. > 140) 9.60 (1.14-80.52) DBP, mmHg (≤ 90 vs. > 90) 2.30 (0.71-7.42) BMI (≤ 30 vs. > 30) 0.55 (0.23-1.33) Exercise (No vs. Yes) 0.56 (0.24-1.33) Family History (No vs. Yes) 0.46 (0.18-1.18) Family Type (Nuclear vs. joint) 0.75 (0.32-1.77) Family Size (≤ 5 vs. > 5) 0.71 (0.22-2.25) Haemoglobin (≤ 10 vs. > 10) 1.00 (0.19-5.26) Ferritin (≤100 vs. > 100) 3.53 (0.88-14.09) Carbohydrates (≤ 100 vs. > 100) 0.32 (0.12-0.84) Protein (≤ 50 vs. > 50) 0.21 (0.04-1.07) SBP=Systolic blood pressure; DBP=diastolic blood pressure; BMI=Body mass index; OR=Odds ratio; CI=Confidence interval A= Each risk variable was adjusted for with all of the other risk variable listed in the table.

Table 5. Unconditional logistic regression model of socio-demographic and nutritional factors associated with CVD cases over control.

Limitations Of The Study

The sample size of the study was relatively small which may limit its scope and applications to be generalized. Ideally, controls should have been selected from the general population but controls were selected from accompanying patients who may not necessarily be relatives of the patients. It is customary in this part of the world that friends and relatives from distant places visit hospitals for inquiring about patients’ health but still the selection of controls from the attendants could have introduced a selection bias and distorted some results. Due to funding con-

Cases Controls p-value (n=43) (n=43)

41 (95.4) 37 (86.1) 0.14 2 (4.6) 6 (13.9)

40 (93.0) 36 (83.7) 0.18 3 (7.0) 7 (16.3)

26 (60.5) 23 (53.5) 0.51 17 (39.5) 20 (46.5)

33 (76.7) 26 (60.5) 0.10 10 (23.3) 17 (39.5)

31 (72.1) 27 (62.8) 0.36 12 (27.9) 16 (37.2)

28 (65.1) 22 (51.2) 0.19 15 (34.9) 21 (48.8)

a OR (95% CI) p-value OR (95% CI) p-value

0.06 3.08 (0.87-10.86) 0.08 0.04 24.00 (2.00-288.52) 0.01 0.16 1.36 (0.25-7.41) 0.72 0.18 0.33 (0.10-1.06) 0.06 0.19 0.41 (0.13-1.26) 0.12 0.11 0.41 (0.12-1.38) 0.15 0.51 0.95 (0.31-2.93) 0.94 0.56 1.41 (0.28-7.12) 0.68 0.99 0.88 (0.11-7.16) 0.91 0.07 2.42 (0.41-14.32) 0.33 0.02 0.35 (0.10-1.23) 0.10 0.06 0.40 (0.06-40.53) 0.76

straints, the control sample size (n=43) was kept equal to cases (n=43) that could have limited the statistical power of the study. In addition, all variables of interest could not be included in the study and that could be one of the reasons for not establishing any association between the dependent and independent variables. Keeping in view the above stated limitations, the results may be used with caution further studies are needed in the area to augment the study findings.

Conflicts Of Interest

This is to declare that none of the authors have any conflict of interests.

Individual Contribution

PIP conceptualized, designed and supervised the study; HW conducted field and laboratory work; SIP assisted PIP in manuscript drafting and critically reviewing the paper; SU did the statistical analysis of the data; SSB facilitated HW during data collection and management.

References

  1. GeorgeAMensahHBrownDW. An overview of cardiovascular disease burden in the United States. Health Affairs. 2007; 26: 38-48. doi: 10.1377/hlthaff.26.1.3810.1377/hlthaff.26.1.38 https://doi.org/10.1377/hlthaff.26.1.38
  2. YusufSHawkenSOunpuuS. Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study. Lancet. 2004; 364: 937-952. doi: http://dx.doi.org/10.1016/ S0140-6736(04)17018-9
  3. NagTGhoshA. Cardiovascular disease risk factors in Asian Indian population: A systematic review. J Cardiovasc Dis Res. 2013; 4: 222-228. doi: 10.1016/j.jcdr.2014.01.00410.1016/j.jcdr.2014.01.004 https://doi.org/10.1016/j.jcdr.2014.01.004
  4. ThakurJSPrinjaSCargCCMendisSMenabdeN. Social and economic implications of non-communicable diseases in India. Indian J Comm Med. 2011; 36: 13-22. doi: 10.4103/0970- 0218.9470410.4103/0970-0218.94704 https://doi.org/10.4103/0970-0218.94704
  5. ShadmaniFKKaramiM. Joint effect of modifying selected risk factors on attributable burden of cardiovascular diseases. Int J Prev Med. 2013; 4: 1461-1467
  6. AmiriMMajidHAHairiFMThangiahNBulgibaA. Prevalence and determinants of cardiovascular disease risk factors among the residents of urban community housing projects in Malaysia. BMC Public Health. 2014; 14: 3. doi: 10.1186/1471- 2458-14-S3-S310.1186/1471-2458-14-s3-s3 https://doi.org/10.1186/1471-2458-14-s3-s3
  7. MONHRC. National Nutrition Survey 2011. Ministry of National Health Services, Regulations and Coordination. Government of Pakistan, Islamabad. 2011
  8. PBS. Pakistan Social and Living Standards Measurement Survey (2012-13). Pakistan Bureau of Statistics. Government of Pakistan, Islamabad
  9. JafarTH. Women in Pakistan have a greater burden of clinical cardiovascular risk factors than men. Int J Cardiol. 2006; 106: 348-354. doi: 10.1016/j.ijcard.2005.02.01310.1016/j.ijcard.2005.02.013 https://doi.org/10.1016/j.ijcard.2005.02.013
  10. HageFGMansurSJXingDOparilS. Hypertension in women. Kidney Int Suppl. 2013; 3: 352-356. doi: 10.1038/ kisup.2013.76
  11. WHO. Non-communicable diseases country profiles 2014. World Health Organization. Geneva. 2014
  12. WHO. Measuring changes in iron status. World Health Organization. Geneva. 1983
  13. WHO. Expert committee on physical status the use and interpretation of anthropometry. Tech Rep Ser No. 854. World Health Organization. Geneva. 1995
  14. SchenckHVFalkenssonMLundbergB. Evaluation of Hemocue: a new device for determining haemoglobin. Clin Chem. 1986; 32: 526-529
  15. PolsonRJKennaJGBomfordAWilliamsR. Measurement of ferritin in serum by an indirect competitive enzyme-linked immunosorbant assay. Clin Chem. 1988; 34: 661-664. doi:
  16. ThompsonFESubarAF. Dietary assessment methodology. In: Coulston AM, Boushey CJ, Ferruzzi MG eds. Nutrition in the prevention and treatment of disease. 3rd ed. London: Academic Press. 2013; 5-46
  17. HamiltonLC. Statistics with Stata: Version 12, 8th edition. USA, CENGAGE. 2013
  18. HeYLamTHJiangB. Changes in BMI before and during economic development and subsequent risk of cardiovascular disease and total mortality: A 35-year follow-up study in China. Diabetes Care. 2014; 37(9): 2540-2547. doi: 10.2337/ dc14-0243
  19. WhitlockGLewingtonSSherlikerP. Body-mass index and cause-specific mortality in 900000 adults: collaborative analyses of 57 prospective studies. Lancet. 2009; 373: 1083- 1096. doi: 10.1016/S0140-6736(09)60318-410.1016/s0140-6736(09)60318-4 https://doi.org/10.1016/s0140-6736(09)60318-4
  20. FlegalKMKitBKOrpanaHGraubardBI. Association of all-cause mortality with overweight and obesity using standard body mass index categories: a systematic review and meta-analysis. JAMA. 2013; 309: 71-82. doi: 10.1001/jama.2012.11390510.1001/jama.2012.113905 https://doi.org/10.1001/jama.2012.113905
  21. ChenYCopelandWKVedanthanR. Association between body mass index and cardiovascular disease mortality in East Asians and South Asians: pooled analysis of prospective data from the Asia Cohort Consortium. Br Med J. 2013; 347: f5446. doi: 10.1136/bmj.f544610.1136/bmj.f5446 https://doi.org/10.1136/bmj.f5446
  22. LovegroveJA. CVD risk in South Asians: the importance of defining adiposity and influence of dietary polyunsaturated fat. Proc. Nutr. Soc. 2007; 66: 286-298. doi: 10.1017/ S0029665107005514
  23. GalanPNoisettelNEstaquioC. Serum ferritin, cardiovascular risk factors and ischaemic heart diseases: a prospective analysis in the SU.VI.MAX (SUpplementation en VItamines et Mine´raux AntioXydants) cohort. Public Health Nutr. 2006; 9: 70-74. doi: 10.1079/PHN200582610.1079/phn2005826 https://doi.org/10.1079/phn2005826
  24. SemposCTLookerACGillumREMcGeeDLVuongCVJohnsonCL. Serum ferritin and death from all causes and cardiovascular disease: the NHANES II Mortality Study. National Health and Nutrition Examination Study. Ann Epidemiol. 2000; 10: 441-448. doi: 10.1016/S1047-2797(00)00068-510.1016/s1047-2797(00)00068-5 https://doi.org/10.1016/s1047-2797(00)00068-5
  25. FriedrichNMilmanNVölzkeHLinnebergAJørgensenT. Is serum ferritin within the reference range a risk predictor of cardiovascular disease? A population-based, long-term study comprising 2874 subjects. Br J Nutr. 2009; 102: 594-600. doi: 10.1017/S000711450922085X10.1017/s000711450922085x https://doi.org/10.1017/s000711450922085x
  26. PourmoghaddasASaneiHGarakyaraghiMEsteki-GhashghaeiFGharaatiM. The relation between body iron store and ferritin, and coronary artery disease. ARYA Atheroscler. 2014; 10: 32-36
  27. SullivanJL. Iron and the sex difference in heart disease risk. Lancet. 1981; 1: 1293-1294
  28. KiechlSAichnerFGerstenbrandF. Body iron stores and presence of carotid atherosclerosis. Results from the Bruneck Study. Arterioscler Thromb. 1994; 14: 1625-1630
  29. HaidariMJavadiESanatiAHajilooiMGhanbiliJ. Association of increased ferritin with premature coronary stenosis in men. Clin Chem. 2001; 47: 1666-1672
  30. SilviaWDBiswasSUthappaSShettyP. Ferritin, a potent threat for acute myocardial infarction? J Assoc Physicians India. 2003; 51: 947-950
  31. JeppesenJSchaafPJonesC. Effects of low-fat, high carbohydrate diets on risk factors for ischemic heart disease in postmenopausal women. Am J Clin Nutr. 1997; 65: 1027-1033
  32. MurphyKJCrichtonMThorpAA. Dairy foods and dairy protein consumption is inversely related to markers of adiposity in obese men and women. Nutrients. 2013; 4565-4584
  33. FAO. Nutrients requirement in human nutrition. 2nd edition. Food and Agricultural Organization. Italy. 2004
  34. FNB/NAP. Dietary reference intakes for energy, carbohydrates, fiber, fat, fatty acids, cholesterol, protein and amino acids. Food and Nutrition Board, National Academy Press. Washington, DC. 2005
  35. BirkenaesABSogaardAJEnghJA. Sociodemographic characteristics and cardiovascular risk factors in patients with severe mental disorders compared with the general population. J Clin Psychiatry. 2006; 67: 425-433
  36. KaplanGAKeilJE. Socio-economic factors and cardiovascular diseases: A review of literature. Circulation. 1993; 88: 1973-1998. doi: 10.1161/01.CIR.88.4.197310.1161/01.cir.88.4.1973 https://doi.org/10.1161/01.cir.88.4.1973
  37. YangWXYangZWuYJQiaoSBYangYJChenJL. Factors associated with coronary artery disease in young population (age ≤ 40): analysis with 217 cases. Chinese Med Sci J. 2014; 29: 38-42