Literature DB >> 25995236

The impact of dietary habits and metabolic risk factors on cardiovascular and diabetes mortality in countries of the Middle East and North Africa in 2010: a comparative risk assessment analysis.

Ashkan Afshin1, Renata Micha2, Shahab Khatibzadeh3, Saman Fahimi4, Peilin Shi1, John Powles5, Gitanjali Singh1, Mohammad Yawar Yakoob6, Morteza Abdollahi7, Suad Al-Hooti8, Farshad Farzadfar9, Anahita Houshiar-Rad7, Nahla Hwalla10, Eda Koksal11, Abdulrahman Musaiger12, Gulden Pekcan13, Abla Mehio Sibai10, Sahar Zaghloul14, Goodarz Danaei15, Majid Ezzati16, Dariush Mozaffarian1.   

Abstract

OBJECTIVE/
DESIGN: We conducted a comparative risk assessment analysis to estimate the cardiometabolic disease (CMD) mortality attributable to 11 dietary and 4 metabolic risk factors in 20 countries of the Middle East by age, sex and time. The national exposure distributions were obtained from a systematic search of multiple databases. Missing exposure data were estimated using a multilevel Bayesian hierarchical model. The aetiological effect of each risk factor on disease-specific mortality was obtained from clinical trials and observational studies. The number of disease-specific deaths was obtained from the 2010 Global Burden of Disease mortality database. Mortality due to each risk factor was determined using the population attributable fraction and total number of disease-specific deaths. SETTING/POPULATION: Adult population in the Middle East by age, sex, country and time.
RESULTS: Suboptimal diet was the leading risk factor for CMD mortality in 11 countries accounting for 48% (in Morocco) to 72% (in the United Arab Emirates) of CMD deaths. Non-optimal systolic blood pressure was the leading risk factor for CMD deaths in eight countries causing 45% (in Bahrain) to 68% (in Libya) of CMD deaths. Non-optimal body mass index and fasting plasma glucose were the third and fourth leading risk factors for CMD mortality in most countries. Among individual dietary factors, low intake of fruits accounted for 8% (in Jordan) to 21% (in Palestine) of CMD deaths and low intake of whole grains was responsible for 7% (in Palestine) to 22% (in the United Arab Emirates) of CMD deaths. Between 1990 and 2010, the CMD mortality attributable to most risk factors had decreased except for body mass index and trans-fatty acids.
CONCLUSIONS: Our findings highlight key similarities and differences in the impact of the dietary and metabolic risk factors on CMD mortality in the countries of the Middle East and inform priorities for policy measures to prevent CMD. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

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Year:  2015        PMID: 25995236      PMCID: PMC4442236          DOI: 10.1136/bmjopen-2014-006385

Source DB:  PubMed          Journal:  BMJ Open        ISSN: 2044-6055            Impact factor:   2.692


This study provides country-specific estimates of the cardiometabolic disease mortality attributed to individual dietary and metabolic risk factors informing national priorities for prevention strategies. Dietary data used in this study were from mixed sources, which increases the statistical uncertainty in dietary estimates. A major advantage of the study is that it has incorporated various sources of uncertainty into the analysis and has quantified the overall uncertainty intervals for the mortality estimates. The aetiological effect sizes of diet–disease relationships were obtained from the most recent meta-analyses of the clinical trials and observational studies that had adjusted for major confounders. However, the possibility of residual confounding cannot be excluded. The cardiometabolic disease burden of individual dietary factors might have been underestimated due to the measurement error and adjustment of aetiological effect sizes for potential mediators (eg, blood pressure, body mass index and blood lipids). The number of cardiometabolic deaths attributed to the combined effect of dietary factors might have been overestimated due to the correlation of dietary factors at the population level.

Introduction

Cardiometabolic disease (CMD), including cardiovascular disease (CVD) and type 2 diabetes mellitus (DM), is the leading cause of mortality in the Middle East and North Africa, accounting for nearly one million deaths annually.1 2 Over the past few decades, along with socioeconomic changes, the prevalence of a suboptimal lifestyle (eg, dietary) and metabolic (eg, obesity) risk factors has rapidly increased in this region.2–6 Yet the absence of a valid and reliable methodology for comparative risk assessment, as well as systematic and comparable methods to assess nationally representative risk patterns, has hindered accurate estimation of the impacts of lifestyle and metabolic risk factors on CMD in each country of this region. Several prior efforts have estimated how various risk factors contribute to CMD globally. For instance, the World Health Organization (WHO) estimated the global and regional burdens of disease attributable to multiple risk factors, including four metabolic factors (high blood pressure, high blood cholesterol, high blood glucose and adiposity) and only one dietary factor (low fruits and vegetables combined).7 Other nation-specific analyses—for example, in the USA, Australia, Iran, Japan and Mexico—have similarly estimated the health impact of selected dietary and metabolic risk factors.8–12 The global burden of disease (GBD) 2010 study built on these prior efforts by developing more systematic and comparable methods to collect nationally representative data and evaluating aetiological effect sizes of risk factor–disease relationships.2 A particular advance of GBD 2010 was the new systematic assessment of multiple dietary risk factors for CMD, based not only on national food availability estimates but also individual-level data on dietary consumption.2 13 These prior efforts included estimation of the contribution of suboptimal diet and metabolic risk factors to chronic disease mortality in the overall Middle East and North African region.14 However, detailed national results, including by key subgroups within each country by age and sex, have not as yet been reported. In addition, these prior analyses have not utilised the most current evidence for aetiological effects of diet, which produces substantial overall CMD burdens; nor have they examined how the selection of optimal levels of dietary and metabolic risk factors influences the estimated CMD impact. To address these key gaps in knowledge, we evaluated the CMD mortality attributable to dietary and metabolic risk factors in 20 countries of the Middle East and North Africa, as well as changes in risk factor levels and corresponding attributable mortality between 1990 and 2010.

Methods

The methods and standardised data collection protocol have been described in detail elsewhere.1 2 13 15–20 In brief, we conducted a population-level comparative risk assessment analysis for 15 dietary and metabolic risk factors to estimate the number of deaths that would have been averted in 1990 and 2010 in 20 countries of the Middle East and North Africa if distributions of risk factor exposure had been sustained at an optimal level (table 1). The countries included in our analysis were Afghanistan, Algeria, Bahrain, Egypt, Iran, Iraq, Jordan, Kuwait, Lebanon, Libya, Morocco, Oman, Palestine, Qatar, Saudi Arabia, Syria, Tunisia, Turkey, the United Arab Emirates (UAE) and Yemen.
Table 1

Metabolic and dietary risk factors, their definitions, optimal levels and disease outcomes

Risk factor (definitions)*Optimal levelDisease outcomes†
Metabolic risk factors‡
 High systolic blood pressure115±6 mm HgCHD, ischaemic stroke, haemorrhagic stroke, hypertensive heart disease, aortic aneurysm, rheumatic heart disease, inflammatory heart disease, other CVDs
 High fasting plasma glucose5.3±0.3 mmol/L2CHD, ischaemic stroke, haemorrhagic stroke, DM
 High serum total cholesterol4.0±0.9 mmol/L2CHD, ischaemic stroke
 High body mass index23±1 kg/m2CHD, ischaemic stroke, hypertensive disease, DM
Dietary risk factors§
 Low intake of fruits (except fruit juices and salted or pickled fruits)300±30 g/day47CHD, ischaemic stroke, haemorrhagic stroke
 Low intake of whole grains (food ≥1.0 g fibre per 10 g of carbohydrate)2.5 (50 g)±0.25 servings/dayCHD, ischaemic stroke, haemorrhagic stroke, DM
 Low intake of vegetables and beans (excluding vegetable juices, starchy potatoes, corn and salted or pickled vegetables), plus total beans and legumes, including tofu (excluding soya milk)400±40 g/day¶47CHD, ischaemic stroke, haemorrhagic stroke
 Low intake of seafood ω-3 fats (total dietary eicosapentaenoic acid+docosahexaenoic acid (EPA+DHA) intake)250±25 mg/dayCHD
 Low intake of nuts and seeds4 (1 oz)±0.4 servings/weekCHD, DM
 High intake of sodium2000±200 mg/day**Blood pressure-mediated effect (CHD, ischaemic stroke, haemorrhagic stroke)††
 Low intake of polyunsaturated fatty acids as a replacement for saturated fatty acids or carbohydrate12±1.2% of total calories48CHD
 High intake of trans fats (mainly partially hydrogenated vegetable oils and ruminant products)0.5±0.05% of total calories49CHD
 High intake of processed meats0 serving/dayCHD, DM
 High intake of sugar-sweetened beverages (≥50 kcal/8 oz (226.8 g) serving, excluding 100% fruit and vegetable juices)0 serving/dayBMI,‡‡ DM§§
 High intake of red meat (unprocessed) excluding poultry, fish, eggs and all processed meat1 (100 g)±0.1 serving/weekDM

*Alternative risk factor definitions (metrics) have been defined in the methodology GBD paper for dietary risk factors.13

†Indicates diseases for which convincing or probable evidence of an aetiological association with the risk factor of interest was determined.13

‡Low density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C) and triglycerides were excluded because of the lack of sufficient or unbiased data on global risk factor levels to generate estimates for the Middle East in a comparable and consistent fashion.20

§Total energy, fruit juices, plant ω-3 and dietary cholesterol were excluded because of the absence of studies on potential associations. Milk and dietary calcium were excluded as their evidence did not qualify as convincing or probable for causality.

¶The optimal intake for vegetables is 300±30 g/day that was increased to 400±40 g/d when beans and legumes were added to the total vegetable intake.

**The recent GBD 2010 study used an optimal level for sodium of 1000 mg/day, but due to the subsequent Institute of Medicine report and controversy around it, we used an optimal level of 2000 mg/day.50

††Direct effect of high sodium on CHD, ischaemic stroke and haemorrhagic stroke was considered in the sensitivity analyses using the RRs of sodium intake not mediated through SBP.

‡‡BMI was not studied as an outcome, but BMI-mediated effects were, such as on CHD, ischaemic stroke and diabetes.

§§Direct effect of high sugar-sweetened beverages on DM was estimated based on a meta-analysis of 8 prospective cohorts (310,819 participants, 15,043 incident cases of diabetes), comparing the highest (1-2 servings/d) vs. lowest (<1 serving/mo) category of intake. Three cohorts included adjustment for BMI, most appropriate for our modeling of direct (non-obesity mediated) effects; but these also adjusted for total energy intake, which could cause underestimation of full effects.51

BMI, body mass index; CHD, coronary heart disease; CVD, cardiovascular disease; DM, diabetes mellitus; GBD, global burden of disease.

Metabolic and dietary risk factors, their definitions, optimal levels and disease outcomes *Alternative risk factor definitions (metrics) have been defined in the methodology GBD paper for dietary risk factors.13 †Indicates diseases for which convincing or probable evidence of an aetiological association with the risk factor of interest was determined.13 ‡Low density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C) and triglycerides were excluded because of the lack of sufficient or unbiased data on global risk factor levels to generate estimates for the Middle East in a comparable and consistent fashion.20 §Total energy, fruit juices, plant ω-3 and dietary cholesterol were excluded because of the absence of studies on potential associations. Milk and dietary calcium were excluded as their evidence did not qualify as convincing or probable for causality. ¶The optimal intake for vegetables is 300±30 g/day that was increased to 400±40 g/d when beans and legumes were added to the total vegetable intake. **The recent GBD 2010 study used an optimal level for sodium of 1000 mg/day, but due to the subsequent Institute of Medicine report and controversy around it, we used an optimal level of 2000 mg/day.50 ††Direct effect of high sodium on CHD, ischaemic stroke and haemorrhagic stroke was considered in the sensitivity analyses using the RRs of sodium intake not mediated through SBP. ‡‡BMI was not studied as an outcome, but BMI-mediated effects were, such as on CHD, ischaemic stroke and diabetes. §§Direct effect of high sugar-sweetened beverages on DM was estimated based on a meta-analysis of 8 prospective cohorts (310,819 participants, 15,043 incident cases of diabetes), comparing the highest (1-2 servings/d) vs. lowest (<1 serving/mo) category of intake. Three cohorts included adjustment for BMI, most appropriate for our modeling of direct (non-obesity mediated) effects; but these also adjusted for total energy intake, which could cause underestimation of full effects.51 BMI, body mass index; CHD, coronary heart disease; CVD, cardiovascular disease; DM, diabetes mellitus; GBD, global burden of disease.

Selection of risk factors

We selected 11 dietary and 4 metabolic risk factors for which sufficient evidence was available on the presence and magnitude of probable causal relationships with coronary heart disease (CHD), stroke, other CVDs or DM from high-quality epidemiological studies. The dietary factors included low intake of fruits, whole grains, vegetables and beans, seafood ω-3 fats, nuts and seeds and polyunsaturated fatty acids (PUFA) as a replacement for saturated fatty acids (SFA) or carbohydrate, and high intake of sodium, trans fats, processed meat, sugar-sweetened beverages (SSBs) and unprocessed red meat. Several other important dietary factors (eg, low intake of milk, low intake of dietary calcium and high intake of dietary cholesterol) were also considered but were not included because the evidence on causal effects was less convincing.13 The metabolic risk factors included in our analysis were high systolic blood pressure (SBP), fasting plasma glucose, serum total cholesterol and body mass index (BMI). Table 1 summarises these 15 risk factors, their optimal level, also referred to as theoretical-minimum-risk exposure distributions, and disease outcomes.

Data sources

Dietary factors

We estimated the intake of each dietary factor by sex, age and time in 187 countries using the data from individual-level nutrition surveys and the United Nations Food and Agricultural Organization (FAO) food balance sheets data from each country. To identify nationally representative nutrition surveys from all countries around the world, we conducted systematic searches of multiple databases; collected data on the survey characteristics as well as the mean and SD of measured intakes of the dietary factors of interest by country, sex, age and time; and performed survey quality assessment by review of evidence for selection bias, sample representativeness, response rate and validity of dietary assessment methods. The characteristics of the 15 dietary surveys identified in 20 countries of the Middle East and North Africa and included in this study are provided in the data supplement (see online supplementary table S1). For countries without identified dietary surveys, we utilised the comprehensive FAO food balance sheets, providing data on national food availability per capita for major food groups in 176 countries across all years. Food availability data from the FAO food balance sheets from all years between 1980 and 2010 were extracted and used to create 17 standard food and nutrient groups most closely matching the key dietary factors of interest. Since availability data may overestimate true intakes, we determined and utilised the relationship between individual-level dietary surveys and the FAO food balance sheets, accounting for age and sex patterns in the individual-level intakes, to adjust the estimated intakes in those countries having only FAO data. For each dietary factor, we developed an age-integrating Bayesian hierarchical model that estimated the mean consumption level and its statistical uncertainty for each age-sex-country-year stratum. Primary inputs were the survey-level intake data, including all available country-specific, time-specific, age-specific and sex-specific consumption levels (mean, distribution), data on the numbers of participants in each strata and survey-level indicator covariates (sampling representativeness, dietary assessment method, type of dietary metric); the food disappearance data derived and standardised from the FAO including 17 nutrients or food groups and 4 factors derived from principal components analysis of these 17 variables; lagged distributed national income; and random effects for each country, region (21 GBD regions) and super-region (7 GBD groupings of super-regions). For five countries (Afghanistan, Bahrain, Iraq, Oman and Qatar) with no FAO food balance sheets data, dietary data were imputed based on the regional mean in each age-sex group and the country-specific covariates (see online supplementary figure S1). Model validity across different iterations had been evaluated using cross-validation; and sources of uncertainty were identified and incorporated, including from survey-level versus FAO country data, sampling uncertainty of original data sources, and additional uncertainty associated with suboptimal metrics, subnational samples or household-level surveys. Thus, by combining the individual-level diet surveys and the adjusted FAO data, our dietary estimates in the Global Dietary Database were derived from dietary information available in all countries.

Metabolic risk factors

The distributions of metabolic risk factors were obtained from recently published studies by GBD Metabolic Risk Factors Diseases Collaborating Group.17–20 In these studies, the researchers systematically reviewed published and unpublished studies from 1980 to 2008 and collected data on the mean and SD of each metabolic risk factor from representative surveys in all countries across the world. Data were collected and modelled separately for men and women. A multilevel Bayesian hierarchical model was used to estimate missing data and derive the average risk factor level and their 95% uncertainty interval (UI) for each age-country-year unit.

Aetiological effects of risk factors on mortality

For each dietary factor, we obtained the relative risk (RR) of CHD, stroke and DM mortality (or incidence) per unit of exposure based on the most recent published systematic reviews and meta-analyses of epidemiological studies (see online supplementary table S4).21 For those dietary factor-disease pairs for which no recent systematic review and meta-analysis were available (eg, nuts and CHD, stroke and DM), we conducted de novo meta-analyses.22 The present analyses are based on the most updated available data until November 2014 on the probable or convincing aetiological effects of diet on CMD. The studies used for quantifying the aetiological effect sizes included randomised controlled trials of exposure reduction (ie, nuts, PUFA, ω-3 fatty acids and sodium) and observational studies that estimated the effects of baseline or cumulatively updated exposure. The majority of observational studies used for effect sizes had adjusted for important potential confounders (eg, age, sex, race, education, socioeconomic status, physical activity, smoking, alcohol consumption). Aetiological effects of metabolic risk factors were estimated using the data from large cohort pooling projects.23 For each risk factor-disease pair, we used the same RR for men and women and consistent age-patterns of RRs.23 Effect modification by other factors (eg, race, prevalent disease) was also evaluated and incorporated in the analysis where applicable.

Optimal distributions

To measure the mortality effects of all non-optimal levels of exposure consistently and comparably across dietary and metabolic risk factors, we used an optimal level as the alternative exposure distribution (table 1). The optimal intake for dietary factors with protective effects was defined as the intake levels to which beneficial effects may plausibly continue based on epidemiological studies. For example, the intake of ω-3 fatty acids seems to reduce CHD mortality at intakes up to 250 mg/day, but has relatively little additional mortality benefits at higher intakes.24 In setting an optimal intake for protective factors, we also took into account the levels observed in populations that have high intake.21 For metabolic risk factors and dietary factors with harmful effects, optimal level was defined as the exposure levels associated with the lowest level of harm. For example, optimal intake for processed meat was zero. The SD of the optimal levels was determined using the global mean to SD regression co-efficient.17–20

Disease-specific deaths

The number of deaths due to CHD (ICD-10 codes I20–I25), ischaemic stroke (I63, I65–I67, I69.3), haemorrhagic stroke (I60-62, I69.0-2), hypertensive heart disease (I11–I13), aortic aneurysm (I71), rheumatic heart disease (I01, I02.0, I05–I09), inflammatory heart disease (I33, I42), other CVDs and DM (E10–E14) for the 1990 and 2010 periods was obtained from the GBD 2010 mortality database, which provides estimated annual mortality statistics by country, age, sex and cause of deaths.1 Considering that reliable mortality data from Afghanistan were not available, we excluded Afghanistan from the analysis and only presented the data on the distribution of dietary and metabolic risk factors in this country.

Statistical analysis

For each risk factor, we computed the population-attributable fraction (PAF): Where x is the exposure level, P(x) is the actual distribution of exposure in the population, P′ (x) is the optimal exposure distribution; RR(x) is the RR of mortality at exposure level x, and m is the maximum exposure level. PAF measures the total effects of a risk factor (direct as well as mediated through other factors) and represents the proportional reduction in disease-specific mortality that would occur if risk factor exposure was at the optimal level. We calculated the number of deaths from CHD, ischaemic stroke, haemorrhagic stroke, hypertensive heart disease, aortic aneurysm, rheumatic heart disease, inflammatory heart disease, other CVDs and DM attributable to each risk factor by multiplying its PAF by total disease-specific mortality. Deaths attributable to a single risk factor across different disease outcomes were summed to obtain the total attributable mortality to that particular risk factor. We conducted all analyses separately by country, sex and age groups (25–29, 30–34, 35–39, 40–44, 45–49, 50–54, 55–59, 60–64, 65–69, 70–74, 75–79, and 80+years) and time (1990 and 2010). We also calculated the change in the risk factor level, total CMD mortality and CMD deaths attributable to each risk factor. To calculate the latter, we accounted for the change in population structure by standardising the 1990–2010 population.

Uncertainty and sensitivity analyses

For each risk factor, we estimated the sampling uncertainty of the attributable mortality using the second order Monte Carlo simulation. In this method, for each unit of observation (ie, country-age-sex-year), we drew repeatedly from the normal distribution of exposure (assumed to be normal), a log-normal distribution of disease-specific RRs, a normal distribution of the optimal intake, and a normal distribution of cause-specific mortality. Each set of exposure, disease-specific RR, optimal intake and disease-specific mortality draws was used to calculate the PAF and attributable mortality. We used 1000 draws for each risk factor, and reported 95% UI based on the resulting distributions of 1000 estimated attributable deaths. In addition to the sampling uncertainty, we examined the sensitivity of our results to the choice of the optimal level of each risk factor. All analyses were conducted using R V.2.15.0.

Results

Distribution of dietary and metabolic risk factors by country, sex and age

In 2010, all metabolic risk factors in almost all countries had suboptimal national distributions (figure 1A). The highest national means were seen in Kuwait (BMI 30.2 kg/m2 and serum total cholesterol 5.1 mmol/L), Libya (SBP 132 mm Hg) and Saudi Arabia (fasting plasma glucose 6.4 mmol/L). Similarly, the national intakes of dietary factors in most countries were non-optimal (figure 1B and C). The lowest intakes of protective dietary factors were in Libya (fruits 60.4 g/day and vegetables 134 g/day), Turkey (whole grains 3.2 g/day), Afghanistan (nuts 4.6 g/day), Yemen (PUFA 3.6%E/day) and Lebanon (seafood ω-3 fatty acids 8.3 mg/day). The highest intakes of harmful dietary factors were observed in UAE (processed meat 6.7 g/day), Algeria (red meat 707 g/week), Egypt (trans fat 6.5%E/day), Lebanon (SSBs 185 g/day) and Bahrain (sodium 5404 mg/day). No single country consistently showed a more favourable national profile of all metabolic risk factors or healthier consumption pattern of all dietary factors.
Figure 1

National levels of metabolic risk factors (A) and national intakes of protective (B) and harmful (C) dietary factors in the Middle East and North Africa, by country (2010). Red line represents the optimal level.

National levels of metabolic risk factors (A) and national intakes of protective (B) and harmful (C) dietary factors in the Middle East and North Africa, by country (2010). Red line represents the optimal level. Continued Continued Women consistently had a higher BMI and total cholesterol in almost all age groups across all countries, whereas no appreciable difference was seen in SBP and fasting plasma glucose levels among men and women (see online supplemental figures S2–S5). The consumption patterns of all dietary factors were similar among men and women except for sodium, which was consistently higher among men across all age groups (see online supplementary figures S6–S9). SBP consistently increased by age, whereas BMI, fasting plasma glucose and total cholesterol showed a decreasing trend among the elderly (see online supplementary figures S2–S5). The consumption of dietary factors did not vary by age except for SSB intake which decreased by age (see online supplementary figures S6–S9).

CMD mortality by country, sex and age

In 2010, CMD caused 492 036 deaths (49% of CMD deaths due to CHD, 26% stroke, 19% other CVDs and 6% diabetes) among men and 419 102 deaths among women (40% CHD, 30% stroke, 21% other CVDs and 9% diabetes). Nearly 43% of total CMD (388 000 CMD deaths) occurred prematurely (defined as deaths below the age of 70). The highest rates of CMD mortality (per million adults) were seen in Egypt (5722 deaths) and Syria (4167 deaths), and the lowest rates were seen in Qatar (504 deaths), the UAE (832 deaths) and Bahrain (1103 deaths) (see online supplementary figure S10).

CMD mortality attributable to metabolic risk factors by country

Non-optimal SBP (>115 mm Hg) was the leading metabolic risk for CMD mortality in the region accounting for 48% of CMD deaths (436 190 deaths, 95% UI 422 098 to 451 182) (figure 2). Non-optimal BMI (>23 Kg/m2) and fasting plasma glucose (>5.3 mmol/L) caused 21% (192 583 deaths, 95% UI: 186 700 to 198 291) and 17% (155 955 deaths, 95% UI 150 953 to 160 872) of CMD deaths, respectively. High serum total cholesterol (>4 mmol/L) was responsible for 12% of CMD deaths (108 811 deaths, 95% CI 99 687 to 119 315).
Figure 2

Cardiometabolic deaths attributable to dietary and metabolic risk factors in the Middle East and North Africa among (A) men, (B) women, (C) total adult population (2010). Other cardiovascular diseases (CVDs) include hypertensive heart disease, aortic aneurysm, rheumatic heart disease, inflammatory heart disease, other unspecified CVDs.

Cardiometabolic deaths attributable to dietary and metabolic risk factors in the Middle East and North Africa among (A) men, (B) women, (C) total adult population (2010). Other cardiovascular diseases (CVDs) include hypertensive heart disease, aortic aneurysm, rheumatic heart disease, inflammatory heart disease, other unspecified CVDs. The ranking of metabolic risk factors was slightly different across countries (see online supplementary tables S5–S23). Non-optimal SBP was the leading metabolic risk factor for CMD mortality in all countries except Bahrain. Non-optimal fasting plasma glucose was the leading risk factor for CMD deaths in Bahrain, the second leading metabolic risk factor for CMD deaths in nine countries (ie, Algeria, Libya, Morocco, Oman, Palestine, Qatar, Saudi Arabia, Tunisia and Yemen), the third leading risk factor for CMD deaths in six countries (ie, Iraq, Jordan, Kuwait, Lebanon, Syria and Turkey) and the fourth leading risk factor for CMD deaths in the UAE, Egypt and Iran. Non-optimal BMI was the second or third leading metabolic risk factor for CMD mortality in most countries. Serum total cholesterol ranked the third or fourth leading risk factor for CMD mortality in most countries. The CMD mortality rate due to individual metabolic risk factors varied across countries (table 3). The number of CMD deaths (per million adults) due to non-optimal SBP ranged from 208 deaths (in Qatar) to 2855 deaths (in Egypt). The highest number of CMD deaths attributable to non-optimal fasting plasma glucose was observed in Morocco (1351 deaths per million adults). The highest number of CMD deaths due to non-optimal BMI (1,252 deaths per million adults) and serum total cholesterol (638 deaths per million adults) were seen in Egypt. The lowest number of CMD deaths (deaths per million adults) attributable to non-optimal BMI (170 deaths), fasting plasma glucose (187 deaths) and serum total cholesterol (98 deaths) were seen in Qatar.
Table 3

Cardiometabolic deaths (per million adults) attributable to dietary and metabolic risk factors in 20 countries of the Middle East and North Africa (2010)

High systolic blood pressure (>115 mm Hg)Overweight- obesityHigh fasting plasma glucose (>5.3 mmol/L)High serum total cholesterol (>4 mmol/L)Suboptimal Diet*Low fruits (<300 g/day)Low whole grains (<125 g/day)Low nuts and seeds (<16.2 g/day)Low vegetables and beans (<400 g/d)Low seafood ω-3 fatty acids (<250 mg/day)High sodium (>2000 mg/d)Low PUFA as a replacement for SFA or carbohydrate (<12% E/day)High trans-fatty acids (>0.5%E/day)High processed meat (>0 g/day)High SSBs (>0 g/day)High unprocessed red meat (>14.3 g/day)
High income
 Bahrain43038346515856210210799851021413899424439
(396–464)(355–413)(426–507)(130–188)(536–589)(89–117)(95–120)(88–113)(70–100)(88–116)(86–190)(32–45)(86–111)(36–49)(35–54)(28–51)
 Kuwait8706595193881041238305199237238184106124632921
(804–940)(628–690)(470–569)(347–436)(1003–1076)(215–264)(286–326)(176–220)(215–259)(208–267)(108–257)(92–120)(101–146)(50–76)(22–37)(15–28)
 UAE39228721622749812215010594129836134391812
(342–441)(255–319)(183–252)(185–269)(478–516)(102–143)(131–168)(86–125)(74–117)(104–155)(49–118)(48–75)(27–42)(29–51)(14–23)(9–17)
 Oman8724607132719522191681681751901667591534737
(794–953)(425–498)(652–776)(209–350)(907–999)(192–248)(149–189)(150–187)(145–210)(167–217)(101–229)(63–88)(74–110)(45–61)(39–55)(27–48)
 Qatar208170187982605153534661482129191613
(189–229)(157–183)(170–204)(80–115)(249–271)(44–60)(46–61)(46–61)(38–56)(52–71)(29–66)(17–26)(22–37)(16–24)(13–19)(9–17)
 Saudi Arabia1102582689256101925618120723922513511854502917
(1002–1208)(541–626)(616–760)(200–332)(975–1064)(227–289)(159–204)(183–233)(203–278)(194–258)(83–184)(100–137)(46–62)(41–60)(22–36)(13–22)
Upper middle income
 Algeria1540514672231139541121521331222332211245474657
(1409–1676)(460–583)(615–735)(175–310)(1322–1464)(378–445)(190–242)(191–237)(281–344)(195–252)(199–432)(97–127)(38–52)(40–54)(38–55)(45–70)
 Iran20356705896301976444429311455444388170315962010
(1829–2244)(608–731)(527–653)(496–809)(1890–2064)(400–492)(392–468)(271–354)(408–502)(387–501)(244–534)(143–199)(276–351)(77–115)(14–26)(8–12)
 Jordan1379118711604441487231368256159311343111128628443
(1267–1495)(1115–1263)(1071–1255)(362–540)(1403–1568)(210–254)(338–399)(226–283)(142–179)(271–352)(218–460)(94–130)(104–155)(52–72)(67–102)(32–56)
 Lebanon193710008435671773386358327228562210861981025914
(1695–2198)(904–1103)(735–970)(394–798)(1703–1852)(343–431)(326–391)(284–373)(202–253)(491–639)(130–289)(66–111)(155–239)(81–125)(45–74)(10–18)
 Libya211397710154091866577303298483374402112165675026
(1936–2301)(895–1066)(922–1121)(323–516)(1782–1946)(523–633)(268–341)(261–341)(437–530)(319–429)(253–545)(92–135)(134–199)(55–80)(39–63)(19–33)
 Tunisia2028817872455181948931228834236344512480734522
(1812–2230)(716–939)(776–991)(325–631)(1715–1920)(425–554)(272–353)(245–332)(277–413)(305–425)(277–600)(100–151)(68–94)(59–88)(34–55)(16–28)
 Turkey1897956636551195447364431128735644211491933510
(1759–2044)(897–1012)(578–693)(457–671)(1863–2042)(429–518)(605–684)(274–348)(258–319)(307–410)(275–601)(96–132)(79–103)(76–109)(25–45)(8–12)
Lower middle income
 Egypt28551252490638293881476846234851552626310351004110
(2653–3048)(1177–1328)(437–541)(515–790)(2829–3047)(742–887)(727–810)(417–510)(307–394)(454–578)(328–713)(230–298)(959–1113)(82–120)(28–54)(8–12)
 Iraq210210589855531990553311332379429367207192815529
(1885–2334)(956–1170)(887–1098)(433–717)(1897–2081)(491–617)(270–355)(290–376)(312–458)(365–493)(226–498)(176–245)(153–231)(68–96)(43–69)(22–37)
 Morocco15709171352241158641727923730921936385487910255
(1417–1729)(800–1057)(1225–1488)(168–332)(1499–1679)(372–462)(245–315)(211–265)(256–366)(190–251)(227–493)(71–99)(42–55)(68–90)(83–122)(41–71)
 Palestine16827228492411629603195219402304331117140474319
(1547–1829)(667–780)(768–934)(178–311)(1544–1708)(536–673)(165–230)(191–249)(333–479)(262–345)(205–445)(99–138)(107–174)(38–57)(33–52)(15–24)
 Syria210994374358522946285103774506214562292181113810
(1882–2365)(852–1037)(632–859)(439–774)(2190–2384)(558–700)(470–552)(333–424)(378–527)(550–689)(283–618)(198–261)(179–264)(87–134)(26–50)(7–12)
 Yemen17945866653201827555523309408358266194136684219
(1618–1962)(491–685)(589–744)(233–414)(1759–1895)(487–622)(479–567)(267–354)(345–479)(303–414)(168–361)(162–228)(104–172)(55–81)(33–52)(13–24)

*Calculated based on the joint PAF of individual dietary factors.

PAF, population-attributable fraction.

CMD mortality attributable to dietary factors by country

Low intake of fruits (112 960 deaths, 95% UI 108 958 to 117 346) and low intake of whole grains (104 234, 95% UI 101 156 to 107 283) were the leading dietary risk factors for CMD mortality in the region accounting for 12% and 11% of total CMD deaths, respectively (table 2). Among harmful dietary factors, high intake of sodium was responsible for the highest number of CMD deaths (86 010 deaths, 95% CI 53 811 to 116 434).
Table 2

Cardiometabolic deaths attributable to dietary and metabolic risk factors in the Middle East and North Africa (2010)*

TotalMenWomen22–44 years45–70 years70+ years
Total cardiometabolic deaths†911 137492 036419 10165 259322 978522 900
Metabolic risk factors
High systolic blood pressure (>115 mm Hg)
 Deaths (n)436 190235 076201 11424 290184 937226 964
 95% UI(422 098–451 182)(224 182–245 132)(191 457–210 826)(22 525–26 087)(179 090–190 918)(214 238–240 271)
 % of total CMD deaths47.947.84837.257.343.4
Overweight-obesity (BMI>23 Kg/m2)
 Deaths (n)192 58391 556101 02716 91595 03180 636
 95% UI(186 700–198 291)(88 165–95 007)(96 351–105 225)(16 029–17 905)(91 790–97 962)(75 535–85 263)
 % of total CMD deaths21.118.624.125.929.415.4
High fasting plasma glucose (>5.3 mmol/L)
 Deaths (n)155 95580 35975 595720463 82184 929
 95% UI(150 953–160 872)(76 283–84 255)(72 288–78 995)(6634–7793)(60 916–66 649)(80 859–88 990)
 % of total CMD deaths17.116.3181119.816.2
High serum total cholesterol (>4 mmol/L)
 Deaths (n)108 81156 84751 96511 60054 78142 430
 95% UI(99 687–119 315)(51 793–63 276)(44 642–60 432)(10 465–12 714)(51 040–58 706)(34 434–51 956)
 % of total CMD deaths12121218178
Dietary risk factors
Suboptimal diet§
 Deaths (n)435 174254 717180 45741 337194 647199 191
 95% UI(418 779–450 860)(245 203–264 260)(173 144–187 239)(39 786–42 917)(187 605–201 173)(190 583–207 953)
 % of total CMD deaths47.851.843.163.360.338.1
Low fruits (<300 g/day)
 Deaths (n)112 96066 74046 22014 81551 87746 268
 95% UI(108 958–117 346)(63 489–70 403)(43 827–48 790)(13 750–15 961)(49 226–54 627)(43 409–49 229)
 % of total CMD deaths12141123169
Low whole grains (<125 g/day)
 Deaths (n)104 23461 75142 48313 25748 82542 152
 95% UI(101 156–107 283)(59 378–64 259)(40 784–44 187)(12 518–14 015)(46 701–51 011)(40 008–44 333)
 % of total CMD deaths11131020158
High sodium (>2000 mg/day)¶
 Deaths (n)86 01053 01932 991646846 52333 020
 95% UI(53 811–116 434)(32 988–71 435)(20 548–45 029)(2386–10 746)(31 057–60 575)(19 716–45 953)
 % of total CMD deaths911810146
Low seafood ω-3 fatty acids (<250 mg/day)**
 Deaths (n)84 74952 47232 27710 42440 77533 550
 95% UI(80 298–89 032)(48 687–55 864)(29 957–34 519)(9464–11 391)(37 971–43 693)(30 623–36 704)
 % of total CMD deaths911816136
Low vegetables and beans (<400 g/day)
 Deaths (n)76 44946 21230 237984634 03732 567
 95% UI(72 913–79 598)(43 504–48 785)(28 094–32 184)(8952–10 701)(31 950–36 121)(30 161–34 992)
 % of total CMD deaths89715116
Low nuts and seeds (<16.2 g/day)††
 Deaths (n)69 89142 74027 151869333 74527 454
 95% UI(66 870–73 190)(40 060–45 412)(25 425–28 902)(7987–9471)(31 510–35 915)(25 493–29 586)
 % of total CMD deaths89713105
High trans-fatty acids (>0.5%E/day)
 Deaths (n)67 78041 01126 769802132 80626 953
 95% UI(64 326–71 343)(38 388–43 869)(24 722–28 860)(7237–8801)(30 417–35 140)(24 511–29 509)
 % of total CMD deaths78612105
Low PUFA as a replacement for SFA or carbohydrate (<12% E/day)
 Deaths (n)35 57421 95413 620429817 05414 222
 95% UI(33 584–37 604)(20 368–23 803)(12 542–14 726)(3855–4742)(15 680–18 521)(12 840–15 657)
 % of total CMD deaths453753
High processed meat (>0 g/day)
 Deaths (n)18 60911 6436966252491046981
 95% UI(17 355–19 947)(10 490–12 785)(6303–7607)(2180–2934)(8163–10 057)(6057–7849)
 % of total CMD deaths222431
High sugar-sweetened beverages (>0 g/day)
 Deaths (n)929149774315141345423336
 95% UI(7144–11 360)(3803–6107)(3336–5297)(1119–1730)(3474–5572)(2529–4133)
 % of total CMD deaths111211
High unprocessed red meat (>14.3 g/day)
 Deaths (n)45952379221648723081800
 95% UI(4192–5027)(2097–2657)(1937–2517)(410–566)(2055–2565)(1516–2128)
 % of total CMD deaths0.50.50.50.70.70.3

*The Middle East and North Africa region includes 20 countries: Afghanistan, Algeria, Bahrain, Egypt, Iran, Iraq, Jordan, Kuwait, Lebanon, Libya, Morocco, Oman, Palestine, Qatar, Saudi Arabia, Syria, Tunisia, Turkey, United Arab Emirates and Yemen. Contrary to the WHO Eastern Mediterranean region classification, it excludes Djibouti, Somalia, South Sudan and Sudan. Afghanistan was excluded from the analysis due to lack of reliable mortality data.

†Total cardiometabolic deaths include CHD (ICD-10 codes I20–I25), ischaemic stroke (I63, I65–I67, I69.3), haemorrhagic/other non-ischaemic stroke (I60–62, I69.0–2), hypertensive heart disease (I11–I13), aortic aneurysm (I71), rheumatic heart disease (I01, I02.0, I05–I09), inflammatory heart disease (I33, I42), other CVDs and diabetes mellitus (E10–E14).

‡The mortality burden of different risk factors is not mutually exclusive. There might be interaction among these factors, plus the effect of one factor may be mediated through another, such as a part of the BMI effect through fasting glucose or effects of fruits through systolic blood pressure. These effects, therefore, cannot be summed.

§Calculated based on the PAF of individual dietary factors.

¶In comparison with a prior study evaluating the CMD burden due to individual dietary factors in the whole region,2 we used a higher optimal level for sodium (2000 mg/day vs 1000 mg/day) to take into account the recent conclusions of the US Institute of Medicine.50

**There was an aetiological relationship of fish with CHD and stroke, in contrast to ω-3 fatty acids that had effect on CHD only.

††We also used a more modest aetiological effect size for nuts and CHD relationship based on the results of a new meta-analysis.22

BMI, body mass index; CHD, coronary heart disease; CMD, cardiometabolic disease; CVD, cardiovascular disease; PAF, population-attributable fraction; PUFA, polyunsaturated fatty acids; UI, uncertainty interval.

Cardiometabolic deaths attributable to dietary and metabolic risk factors in the Middle East and North Africa (2010)* *The Middle East and North Africa region includes 20 countries: Afghanistan, Algeria, Bahrain, Egypt, Iran, Iraq, Jordan, Kuwait, Lebanon, Libya, Morocco, Oman, Palestine, Qatar, Saudi Arabia, Syria, Tunisia, Turkey, United Arab Emirates and Yemen. Contrary to the WHO Eastern Mediterranean region classification, it excludes Djibouti, Somalia, South Sudan and Sudan. Afghanistan was excluded from the analysis due to lack of reliable mortality data. †Total cardiometabolic deaths include CHD (ICD-10 codes I20–I25), ischaemic stroke (I63, I65–I67, I69.3), haemorrhagic/other non-ischaemic stroke (I60–62, I69.0–2), hypertensive heart disease (I11–I13), aortic aneurysm (I71), rheumatic heart disease (I01, I02.0, I05–I09), inflammatory heart disease (I33, I42), other CVDs and diabetes mellitus (E10–E14). ‡The mortality burden of different risk factors is not mutually exclusive. There might be interaction among these factors, plus the effect of one factor may be mediated through another, such as a part of the BMI effect through fasting glucose or effects of fruits through systolic blood pressure. These effects, therefore, cannot be summed. §Calculated based on the PAF of individual dietary factors. ¶In comparison with a prior study evaluating the CMD burden due to individual dietary factors in the whole region,2 we used a higher optimal level for sodium (2000 mg/day vs 1000 mg/day) to take into account the recent conclusions of the US Institute of Medicine.50 **There was an aetiological relationship of fish with CHD and stroke, in contrast to ω-3 fatty acids that had effect on CHD only. ††We also used a more modest aetiological effect size for nuts and CHD relationship based on the results of a new meta-analysis.22 BMI, body mass index; CHD, coronary heart disease; CMD, cardiometabolic disease; CVD, cardiovascular disease; PAF, population-attributable fraction; PUFA, polyunsaturated fatty acids; UI, uncertainty interval. Like metabolic risk factors, the ranking dietary factors varied across the countries (see online supplementary tables S5–S23). Low intake of fruits was the leading dietary risk factor for CMD mortality in 10 countries, the second leading risk factor for mortality in 5 countries (Egypt, Iran, Kuwait, Lebanon and Turkey) and the third leading dietary factor for mortality in Bahrain and the UAE. Low intake of whole grains was the leading dietary risk factor for CMD mortality in four countries (Jordan, Kuwait, Turkey and the UAE). The leading dietary risk factor for mortality in Iran was low intake of vegetables and beans, and the leading dietary risk factor for mortality in Lebanon and Qatar was low intake of seafood ω-3 fatty acids. Among harmful dietary factors, high intake of sodium was responsible for the highest number of CMD deaths in most countries except Egypt where high intake of trans fat was the leading dietary risk factor for mortality. The absolute CMD burden of each individual dietary factor was also different across countries (table 3). The highest number of CMD deaths due to low intake of fruits (814 deaths per million adults, 95% CI 742 to 887), whole grains (768 per million adults, 95% CI 727 to 810) and nuts (462 deaths, 95% CI 417 to 510) were observed in Egypt; the highest number of CMD deaths attributable to low intake of seafood ω-3 fatty acids (621 per million adults, 95% CI 550 to 689) was observed in Syria; and the highest number of CMD deaths attributable to low intake of vegetables and beans (483 per million adults, 95% CI 437 to 530) was observed in Libya. The lowest number of CMD deaths attributable to all dietary factors (except for unprocessed red meat) was observed in Qatar. Cardiometabolic deaths (per million adults) attributable to dietary and metabolic risk factors in 20 countries of the Middle East and North Africa (2010) *Calculated based on the joint PAF of individual dietary factors. PAF, population-attributable fraction.

CMD mortality attributable to metabolic and dietary risk factors by age and sex

The number of CMD deaths due to dietary and metabolic risk factors increased by age mainly due to the increase in the number of CMD deaths in the older age groups. However, the proportion of CMD deaths attributable to these risk factors decreased by age. Nearly 50% of CMD deaths due to metabolic and dietary risk factors occurred before the age of 70. Among metabolic risk factors, non-optimal total cholesterol had the highest proportion of premature CMD deaths (61% of all cholesterol-attributable deaths) and non-optimal fasting plasma glucose had the lowest proportion of premature CMD deaths (46%) (see online supplementary figure S11). The proportion of CMD deaths due to BMI was greater among women while no appreciable difference was seen in CMD mortality due to other metabolic risk factors (table 2). On the other hand, men consistently had a slightly larger proportion of CMD deaths due to most dietary factors.

Change in risk factor distributions, CMD mortality and CMD burden due to risk factors between 1990 and 2010

During the 1990–2010 period, the adult population of the Middle East and North Africa has increased by 94% (from 115 914 968 to 224 905 818); the total number of CMD deaths has increased by 58% (from 576 999 to 911 137); the number of CMD deaths per million adults has decreased by 19%; and the age-specific CMD mortality decreased in all age groups. Among metabolic risk factors, the regional mean of BMI has increased by 7%, whereas the regional mean of other metabolic risk factors has not changed significantly. Among protective dietary factors, regional intakes of nut and seafood ω-3 fatty acids have increased by 16% and 13%, respectively, while the whole grains consumption has decreased by 21%. Among harmful dietary factors, trans fat intake and sodium intake increased by 20% and 7% while consumption of processed meat and unprocessed red meat was decreased by 5% and 6%, respectively (see online supplementary figure S12). Furthermore, the CMD mortality attributable to all metabolic risk factors has decreased except for BMI, which has increased by 18%. Similarly, CMD mortality attributable to all dietary factors has decreased except for the high intake of trans fat, which has increased by 10% (see online supplementary tables S2 and S3).

Sensitivity analyses

In a sensitivity analysis, change of optimal levels for SBP (from 115 to 110 mm Hg), BMI (from 23 to 21 kg/m2), fasting plasma glucose (from 5.3 to 4.9 mmol/L) and total cholesterol (from 4.0 to 3.8 mmol/L) increased the attributable mortality by 20–30%. Also, change of optimal level for sodium from 2000 to 1000 mg/day increased the attributable mortality by 30% (see online supplementary figure 13). To remove the contribution of differences in age structure, we standardised the number of CMD deaths attributable to each risk factor using the WHO standard population.25 Age-standardisation increased the CMD mortality due to all risk factors in all countries signifying the relatively young population of the countries in 2010. This increase was of larger magnitude in specific countries including Qatar, the UAE, Kuwait and Bahrain. Additionally, we used the age-standardised proportional mortality to remove the contribution of difference in underlying CMD mortality. Using age-standardised proportional mortality resulted in significant changes in the relative CMD burden of risk factors across countries. This sensitivity analysis provides an estimate of the contribution of each risk factor to the between-country heterogeneity of CMD burden independent of age structure and underlying country-specific CMD mortality. However, we believe that non-standardised mortality rates provide decision-makers in each country with a better estimate of the true CMD burden of each risk factor in their country based on the total CMD mortality due to all risk factors and should be used for planning prevention strategies in these countries.

Discussion

We systematically evaluated and quantified the impact of 11 dietary and 4 metabolic risk factors on CMD mortality by age and sex in 20 countries of the Middle East and North Africa in 1990 and 2010. Our results demonstrate that suboptimal diet and high SBP were the leading risk factors for CMD mortality accounting for 50–70% of CMD deaths in the countries of the region. Non-optimal BMI and fasting plasma glucose were the third and fourth leading risk factors for CMD mortality in most countries. Among individual dietary factors, low intake of fruits and whole grains were responsible for the highest number of CMD deaths. Our investigation also highlights key similarities and differences in CMD burden due to these risk factors across countries and informs evidence-based priorities for prevention strategies as well as the subsequent implementation research in the region. An unhealthy lifestyle (eg, poor diet and physical inactivity), poor detection and inadequate treatment are the key contributors to the non-optimal levels of metabolic risk factors in this region.26–32 Additionally, sociocultural changes including economic development, urbanisation and modernisation have been shown to contribute to this problem through the increased availability, affordability and consumption of unhealthful foods and adoption of a sedentary lifestyle.6 14 33 34 Building on previous reports on the high prevalence of metabolic risk factors in this region,6 35–39 our study demonstrates the high CMD mortality due to these risk factors in all countries of the region and highlights the need for adoption and implementation of effective interventions to reduce the burden of these risk factors. Our analysis also quantified the contribution of diet (ie, SSBs and sodium) to the burden of metabolic risk factors and highlighted the gap in knowledge about the contribution of other factors to the CMD burden of metabolic risk factors. Suboptimal diet is driven by a range of factors acting at the individual level (eg, education, income and nutritional knowledge), community level (eg, accessibility to supermarket, and food availability at local stores) and national level (eg, food and agricultural policies, food marketing).40 As will be discussed further below, the relative influence of each of these determinants varies across individual dietary factors. For example, the FAO food balance sheet data show that availability is a major barrier to the adequate intake of fruits in this region.36 Although the per capita availability of fruits has increased in the high and upper middle income countries of the region, it has decreased in the lower-middle income countries of the region.36 Furthermore, the amount of fruit available per person (∼200 g/day) is still below the recommended level in most countries.41 This is partly due to a lack of natural resources (eg, water and fertile soil) which makes most countries of the region food insufficient.38 41 However, some countries such as Jordan have been able to increase fruit production by adopting targeted agricultural policies.42 Furthermore, our consumption data show that the true intake of fruits (∼125 g/day) is much lower than the amount available per person. This highlights the need for interventions to improve the accessibility and affordability of fruits in the countries of the region. Like fruits, although the per capita availability of seafood has increased in most countries of the region over the past two decades, the amount available per person is still low, particularly in the lower-middle income countries.36 41 The FAO Globefish Highlights report shows that fisheries and aquaculture production is relatively underdeveloped in the countries of the region, making them dependent on and vulnerable to the global seafood market. In contrast to fruits and seafood, low intake of whole grains seems to be driven by factors other than availability. While the per capita availability of cereal has increased in most countries of the region over the past two decades, the proportion of total energy derived from cereals has decreased in the countries of the region.36 Furthermore, the increase in the cereal consumption is mainly driven by the increased level of refined grains.41 A recent review on drivers of nutrition transition in this region suggests that changes in food environment (eg, increased availability of fast food restaurants and aggressive food marketing), food price and lifestyle (eg, higher participation of women in the workforce) which resulted from urbanisation, modernisation and economic development are the most important factors that contributed to this shift.41 The WHO has recommended nine voluntary targets for global non-communicable disease (NCD) prevention and 25 indicators for monitoring the countries’ progress towards these targets.43 While in this study we showed that suboptimal diet is the leading risk factor for CMD morality in most countries of the region, the WHO recommendations only include one dietary target (30% reduction in sodium intake) and five dietary indicators (intake of fruits and vegetables, sodium and SFAs and two dietary policy indicators including restricting marketing of unhealthy products to children and trans fat regulation).43 Furthermore, most countries of the region have not adopted the basic national policies recommended by the WHO.44 This clearly highlights the gap in the WHO dietary recommendations for prevention of NCDs in this region and underlines the urgent need for revision of these recommendations. On the basis of our findings, attention to dietary factors should be expanded beyond the fruits and vegetables sodium and saturated fat to other dietary factors (eg, whole grains, seafood ω-3 fats and nuts). Furthermore, considering the difference in burden of dietary risk factors across the countries, the priority setting for dietary interventions should be nation specific. Our analysis has several strengths. We focused on nation-specific impacts of dietary and metabolic risk factors on CMD informing national priorities for prevention strategies. We obtained and used the most updated aetiological effect sizes of diet–disease relationships. We assessed the sensitivity of our results to various assumptions about the optimal distribution of dietary and metabolic risk factors by taking into account evidence from epidemiological studies and the feasibility of achieving the optimal distribution at the population level. We accounted for heterogeneity in the current level of risk factors, effect of risk factors on CMD mortality, and current cause-specific mortality by country, age, sex and time. Potential limitations should also be considered in the interpretation of our findings. Dietary data were from mixed sources including nationally representative individual-level nutrition surveys and FAO food balance sheets. As with all measures, assessment methods for diet were not perfect. Also, nutrition data for five countries (ie, Afghanistan, Bahrain, Iraq, Oman and Qatar) were imputed based on the regional mean in each age-sex group and country-specific covariates. Each of these issues increases the statistical uncertainty in dietary measurements. The major advantage of our study is that we incorporated these sources of uncertainty into our analysis and quantified the overall UI for the mortality estimates. We used RRs from meta-analyses of the observational studies that had adjusted for major confounders; however, the possibility of residual confounding cannot be excluded. In particular, correlation among diet factors may affect our estimated aetiological effect for individual dietary factors. To examine the magnitude of the residual confounding due to correlation of dietary factors, we performed three sensitivity analyses. First, using our estimated aetiological effects of each individual dietary factor, we computed the RR for combinations of dietary factors and compared that with the RRs observed in prospective cohort studies evaluating associations of overall dietary patterns with incident CVD events. Second, we compared our estimated RR with the RR estimated from three randomised controlled feeding trials evaluating effects of overall dietary patterns on CVD risk factors (ie, DASH, DASH-sodium and OmniHeart).28 29 45 Third, we compared our estimated RR with the RR from the PREDIMED trial, a large randomised clinical trial evaluating effects of an overall dietary pattern on the incidence of CVD.46 These sensitivity analyses demonstrated that our estimated RRs corresponded very closely to the observed RRs, confirming that our RRs are not substantially affected by correlation of dietary factors.21 We used the joint population attributable fraction to estimate the number of CMD deaths attributable to the combined effect of dietary factors and assumed that the intakes of individual dietary factors were independent within each country-age-sex group. This could overestimate the CMD burden of suboptimal diet. On the other hand, the CMD burden of suboptimal diet might be underestimated in this study due to measurement error and adjustment for potential mediators (eg, blood pressure, BMI, blood lipids). In addition, we focused on CMD mortality, while dietary and metabolic risk factors would increase the risk of specific cancers as well. Thus, our estimates might be a conservative estimate of the burden of disease due to these risk factors at the regional or country level. In summary, we found that metabolic and dietary risk factors were major contributors to CMD mortality in countries of the Middle East and North Africa; however, their relative importance varied across countries. Our findings inform the need for adoption, implementation and evaluation of evidence-based national government policies to improve diet and prevent CMD in countries of the region.
  40 in total

1.  The state of health in the Arab world, 1990-2010: an analysis of the burden of diseases, injuries, and risk factors.

Authors:  Ali H Mokdad; Sara Jaber; Muna I Abdel Aziz; Fadia AlBuhairan; Abduljabbar AlGhaithi; Nawal M AlHamad; Suad N Al-Hooti; Adel Al-Jasari; Mohammad A AlMazroa; Ahmed Mohamed AlQasmi; Shirina Alsowaidi; Majed Asad; Charles Atkinson; Alaa Badawi; Talal Bakfalouni; AbdelAziz Barkia; Stan Biryukov; Charbel El Bcheraoui; Farah Daoud; Mohammad Hossein Forouzanfar; Diego Gonzalez-Medina; Randah R Hamadeh; Mohamed Hsairi; Seifeddin Saleh Hussein; Nadim Karam; Shams Eldin Ali Hassan Khalifa; Tawfik A M Khoja; Faris Lami; Katherine Leach-Kemon; Ziad A Memish; Ali A Mokdad; Mohsen Naghavi; Jamal Nasher; M Bassam Hijawi Qasem; Mohammad Shuaib; Al Anoud M Al Thani; Mohamed H Al Thani; Mohammed Zamakhshary; Alan D Lopez; Christopher J L Murray
Journal:  Lancet       Date:  2014-01-20       Impact factor: 79.321

2.  Estimating the global and regional burden of suboptimal nutrition on chronic disease: methods and inputs to the analysis.

Authors:  R Micha; S Kalantarian; P Wirojratana; T Byers; G Danaei; I Elmadfa; E Ding; E Giovannucci; J Powles; S Smith-Warner; M Ezzati; D Mozaffarian
Journal:  Eur J Clin Nutr       Date:  2011-09-14       Impact factor: 4.016

3.  Primary prevention of cardiovascular disease with a Mediterranean diet.

Authors:  Ramón Estruch; Emilio Ros; Jordi Salas-Salvadó; Maria-Isabel Covas; Dolores Corella; Fernando Arós; Enrique Gómez-Gracia; Valentina Ruiz-Gutiérrez; Miquel Fiol; José Lapetra; Rosa Maria Lamuela-Raventos; Lluís Serra-Majem; Xavier Pintó; Josep Basora; Miguel Angel Muñoz; José V Sorlí; José Alfredo Martínez; Miguel Angel Martínez-González
Journal:  N Engl J Med       Date:  2013-02-25       Impact factor: 91.245

Review 4.  Fish intake, contaminants, and human health: evaluating the risks and the benefits.

Authors:  Dariush Mozaffarian; Eric B Rimm
Journal:  JAMA       Date:  2006-10-18       Impact factor: 56.272

5.  A comparative risk assessment of burden of disease and injury attributable to 67 risk factors and risk factor clusters in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010.

Authors:  Stephen S Lim; Theo Vos; Abraham D Flaxman; Goodarz Danaei; Kenji Shibuya; Heather Adair-Rohani; Markus Amann; H Ross Anderson; Kathryn G Andrews; Martin Aryee; Charles Atkinson; Loraine J Bacchus; Adil N Bahalim; Kalpana Balakrishnan; John Balmes; Suzanne Barker-Collo; Amanda Baxter; Michelle L Bell; Jed D Blore; Fiona Blyth; Carissa Bonner; Guilherme Borges; Rupert Bourne; Michel Boussinesq; Michael Brauer; Peter Brooks; Nigel G Bruce; Bert Brunekreef; Claire Bryan-Hancock; Chiara Bucello; Rachelle Buchbinder; Fiona Bull; Richard T Burnett; Tim E Byers; Bianca Calabria; Jonathan Carapetis; Emily Carnahan; Zoe Chafe; Fiona Charlson; Honglei Chen; Jian Shen Chen; Andrew Tai-Ann Cheng; Jennifer Christine Child; Aaron Cohen; K Ellicott Colson; Benjamin C Cowie; Sarah Darby; Susan Darling; Adrian Davis; Louisa Degenhardt; Frank Dentener; Don C Des Jarlais; Karen Devries; Mukesh Dherani; Eric L Ding; E Ray Dorsey; Tim Driscoll; Karen Edmond; Suad Eltahir Ali; Rebecca E Engell; Patricia J Erwin; Saman Fahimi; Gail Falder; Farshad Farzadfar; Alize Ferrari; Mariel M Finucane; Seth Flaxman; Francis Gerry R Fowkes; Greg Freedman; Michael K Freeman; Emmanuela Gakidou; Santu Ghosh; Edward Giovannucci; Gerhard Gmel; Kathryn Graham; Rebecca Grainger; Bridget Grant; David Gunnell; Hialy R Gutierrez; Wayne Hall; Hans W Hoek; Anthony Hogan; H Dean Hosgood; Damian Hoy; Howard Hu; Bryan J Hubbell; Sally J Hutchings; Sydney E Ibeanusi; Gemma L Jacklyn; Rashmi Jasrasaria; Jost B Jonas; Haidong Kan; John A Kanis; Nicholas Kassebaum; Norito Kawakami; Young-Ho Khang; Shahab Khatibzadeh; Jon-Paul Khoo; Cindy Kok; Francine Laden; Ratilal Lalloo; Qing Lan; Tim Lathlean; Janet L Leasher; James Leigh; Yang Li; John Kent Lin; Steven E Lipshultz; Stephanie London; Rafael Lozano; Yuan Lu; Joelle Mak; Reza Malekzadeh; Leslie Mallinger; Wagner Marcenes; Lyn March; Robin Marks; Randall Martin; Paul McGale; John McGrath; Sumi Mehta; George A Mensah; Tony R Merriman; Renata Micha; Catherine Michaud; Vinod Mishra; Khayriyyah Mohd Hanafiah; Ali A Mokdad; Lidia Morawska; Dariush Mozaffarian; Tasha Murphy; Mohsen Naghavi; Bruce Neal; Paul K Nelson; Joan Miquel Nolla; Rosana Norman; Casey Olives; Saad B Omer; Jessica Orchard; Richard Osborne; Bart Ostro; Andrew Page; Kiran D Pandey; Charles D H Parry; Erin Passmore; Jayadeep Patra; Neil Pearce; Pamela M Pelizzari; Max Petzold; Michael R Phillips; Dan Pope; C Arden Pope; John Powles; Mayuree Rao; Homie Razavi; Eva A Rehfuess; Jürgen T Rehm; Beate Ritz; Frederick P Rivara; Thomas Roberts; Carolyn Robinson; Jose A Rodriguez-Portales; Isabelle Romieu; Robin Room; Lisa C Rosenfeld; Ananya Roy; Lesley Rushton; Joshua A Salomon; Uchechukwu Sampson; Lidia Sanchez-Riera; Ella Sanman; Amir Sapkota; Soraya Seedat; Peilin Shi; Kevin Shield; Rupak Shivakoti; Gitanjali M Singh; David A Sleet; Emma Smith; Kirk R Smith; Nicolas J C Stapelberg; Kyle Steenland; Heidi Stöckl; Lars Jacob Stovner; Kurt Straif; Lahn Straney; George D Thurston; Jimmy H Tran; Rita Van Dingenen; Aaron van Donkelaar; J Lennert Veerman; Lakshmi Vijayakumar; Robert Weintraub; Myrna M Weissman; Richard A White; Harvey Whiteford; Steven T Wiersma; James D Wilkinson; Hywel C Williams; Warwick Williams; Nicholas Wilson; Anthony D Woolf; Paul Yip; Jan M Zielinski; Alan D Lopez; Christopher J L Murray; Majid Ezzati; Mohammad A AlMazroa; Ziad A Memish
Journal:  Lancet       Date:  2012-12-15       Impact factor: 79.321

Review 6.  Effects on coronary heart disease of increasing polyunsaturated fat in place of saturated fat: a systematic review and meta-analysis of randomized controlled trials.

Authors:  Dariush Mozaffarian; Renata Micha; Sarah Wallace
Journal:  PLoS Med       Date:  2010-03-23       Impact factor: 11.069

7.  National, regional, and global trends in systolic blood pressure since 1980: systematic analysis of health examination surveys and epidemiological studies with 786 country-years and 5·4 million participants.

Authors:  Goodarz Danaei; Mariel M Finucane; John K Lin; Gitanjali M Singh; Christopher J Paciorek; Melanie J Cowan; Farshad Farzadfar; Gretchen A Stevens; Stephen S Lim; Leanne M Riley; Majid Ezzati
Journal:  Lancet       Date:  2011-02-03       Impact factor: 79.321

Review 8.  National, regional, and global trends in fasting plasma glucose and diabetes prevalence since 1980: systematic analysis of health examination surveys and epidemiological studies with 370 country-years and 2·7 million participants.

Authors:  Goodarz Danaei; Mariel M Finucane; Yuan Lu; Gitanjali M Singh; Melanie J Cowan; Christopher J Paciorek; John K Lin; Farshad Farzadfar; Young-Ho Khang; Gretchen A Stevens; Mayuree Rao; Mohammed K Ali; Leanne M Riley; Carolyn A Robinson; Majid Ezzati
Journal:  Lancet       Date:  2011-06-24       Impact factor: 79.321

9.  National and subnational mortality effects of metabolic risk factors and smoking in Iran: a comparative risk assessment.

Authors:  Farshad Farzadfar; Goodarz Danaei; Hengameh Namdaritabar; Julie Knoll Rajaratnam; Jacob R Marcus; Ardeshir Khosravi; Siamak Alikhani; Christopher Jl Murray; Majid Ezzati
Journal:  Popul Health Metr       Date:  2011-10-11

Review 10.  A review of adult obesity prevalence, trends, risk factors, and epidemiologic methods in Kuwait.

Authors:  Stalo Karageorgi; Osama Alsmadi; Kazem Behbehani
Journal:  J Obes       Date:  2013-12-17
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  46 in total

1.  Characterising Long Term Care Needs among Chinese Older Adults with Cognitive Impairment or ADL Limitations.

Authors:  Yi Yang
Journal:  J Cross Cult Gerontol       Date:  2020-03

2.  Nutritional Knowledge, Attitude and Practice of North West Households in Iran: Is Knowledge likely to Become Practice?

Authors:  Sakineh Nouri Saeidlou; Fariba Babaei; Parvin Ayremlou
Journal:  Maedica (Bucur)       Date:  2016-12

3.  Dairy Food Intake and All-Cause, Cardiovascular Disease, and Cancer Mortality: The Golestan Cohort Study.

Authors:  Maryam S Farvid; Akbar F Malekshah; Akram Pourshams; Hossein Poustchi; Sadaf G Sepanlou; Maryam Sharafkhah; Masoud Khoshnia; Mojtaba Farvid; Christian C Abnet; Farin Kamangar; Sanford M Dawsey; Paul Brennan; Paul D Pharoah; Paolo Boffetta; Walter C Willett; Reza Malekzadeh
Journal:  Am J Epidemiol       Date:  2017-04-15       Impact factor: 4.897

4.  Dietary Protein Sources and All-Cause and Cause-Specific Mortality: The Golestan Cohort Study in Iran.

Authors:  Maryam S Farvid; Akbar F Malekshah; Akram Pourshams; Hossein Poustchi; Sadaf G Sepanlou; Maryam Sharafkhah; Masoud Khoshnia; Mojtaba Farvid; Christian C Abnet; Farin Kamangar; Sanford M Dawsey; Paul Brennan; Paul D Pharoah; Paolo Boffetta; Walter C Willett; Reza Malekzadeh
Journal:  Am J Prev Med       Date:  2017-02       Impact factor: 5.043

Review 5.  Coronary Heart Disease in the Middle East and North Africa: Current Status and Future Goals.

Authors:  Mahmoud I Traina; Wael Almahmeed; Ahmad Edris; E Murat Tuzcu
Journal:  Curr Atheroscler Rep       Date:  2017-05       Impact factor: 5.113

Review 6.  Diabetes epidemic sweeping the Arab world.

Authors:  Bisher Abuyassin; Ismail Laher
Journal:  World J Diabetes       Date:  2016-04-25

Review 7.  Dietary Issues and Challenges on Cardiometabolic Health in Korea: From a Viewpoint of a National Nutrition Surveillance System.

Authors:  Kyong Won Lee; Kyong Park; Seung-Min Lee; Hyunjung Lim; Min-Jeong Shin
Journal:  Clin Nutr Res       Date:  2017-01-23

8.  Editorial: Public Health Nutrition in the Middle East.

Authors:  Nahla Hwalla; Connie M Weaver; Rania A Mekary; Sibelle El Labban
Journal:  Front Public Health       Date:  2016-03-01

9.  A Lebanese dietary pattern promotes better diet quality among older adults: findings from a national cross-sectional study.

Authors:  Lamis Jomaa; Nahla Hwalla; Leila Itani; Marie Claire Chamieh; Abla Mehio-Sibai; Farah Naja
Journal:  BMC Geriatr       Date:  2016-04-19       Impact factor: 3.921

10.  Chronic disease prevalence among elderly Saudi men.

Authors:  Nazmus Saquib; Juliann Saquib; Abdulrahman Alhadlag; Mohamad Anas Albakour; Bader Aljumah; Mohammed Sughayyir; Ziad Alhomidan; Omar Alminderej; Mohamed Aljaser; Abdulrahman Al-Mazrou
Journal:  Int J Health Sci (Qassim)       Date:  2017 Nov-Dec
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