Next Article in Journal
The Long Term Impact of Micronutrient Supplementation during Infancy on Cognition and Executive Function Performance in Pre-School Children
Next Article in Special Issue
Fried Food Consumption and Cardiovascular Health: A Review of Current Evidence
Previous Article in Journal
Proanthocyanidins Prevent High Glucose-Induced Eye Malformation by Restoring Pax6 Expression in Chick Embryo
Previous Article in Special Issue
Red Blood Cell Docosapentaenoic Acid (DPA n-3) is Inversely Associated with Triglycerides and C-reactive Protein (CRP) in Healthy Adults and Dose-Dependently Increases Following n-3 Fatty Acid Supplementation
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Dietary Patterns, Alcohol Consumption and Risk of Coronary Heart Disease in Adults: A Meta-Analysis

1
Department of Nutrition, Zhejiang Hospital, Hangzhou 310013, China
2
Department of Digestion, Zhejiang Hospital, Hangzhou 310013, China
*
Author to whom correspondence should be addressed.
Nutrients 2015, 7(8), 6582-6605; https://0-doi-org.brum.beds.ac.uk/10.3390/nu7085300
Submission received: 27 May 2015 / Revised: 22 July 2015 / Accepted: 24 July 2015 / Published: 7 August 2015
(This article belongs to the Special Issue Nutrition and CVD)

Abstract

:
Previous studies reported the potential associations between dietary patterns and the risk of coronary heart disease (CHD) in adulthood, however a consistent perspective has not been established to date. Herein, we carried out this meta-analysis to evaluate the associations between dietary patterns and the risk of CHD. MEDLINE and EBSCO were searched for relevant articles published up to April 2015. A total of 35 articles (reporting 37 original studies) met the inclusion criteria and were included in the present meta-analysis. The decreased risk of CHD was shown for the highest compared with the lowest categories of healthy/prudent dietary patterns (odds ratio (OR) = 0.67; 95% confidence interval (CI): 0.60, 0.75; p < 0.00001) and alcohol consumption (OR = 0.68; 95% CI: 0.59, 0.78; p < 0.00001). There was evidence of an increased risk of CHD in the highest compared with the lowest categories of the unhealthy/Western-type dietary patterns (OR = 1.45; 95% CI: 1.05, 2.01; p = 0.02). The results of this meta-analysis indicate that different dietary patterns may be associated with the risk of CHD.

1. Introduction

Although the incidence and mortality of coronary heart disease (CHD) have decreased in the United States and Western Europe since 1970s, it remains the leading cause of death globally, with 7.2 million deaths occurring worldwide every year [1,2,3]. In China, the prevalence of CHD surpassed 80 million by 2010, and every year it causes death in over one million people [4,5]. It is well-known that CHD is considered as a multifactorial chronic disease that may be associated with hypertension, dyslipidemia, impaired glucose tolerance, smoking, genetic factors, and dietary factors [6,7,8].
In the past few decades, many studies particularly focused on diet modification as an important determinant in the development of CHD and found associations between the intakes of individual foods or nutrients and the risk of CHD. However, in reality, people generally do not take nutrients alone but consume meals containing many combinations of foods and nutrients [9]. Consequently, the analysis of dietary patterns has been increasingly used in nutritional epidemiology, taking into account the combined effects of foods, and potentially facilitating nutritional recommendations [10].
Recently, an emerging body of evidence has suggested that there has been considerable attention in epidemiological research on the associations between overall dietary patterns and the risk of CHD [11,12,13,14,15,16,17,18,19,20,21,22,23]. Nevertheless, the results of dietary patterns and CHD risk are inconsistent. Although some studies reported positive associations between Western/unhealthy dietary patterns and the risk of CHD [14,19,22], others showed no significant association [12]. Therefore, we conducted a meta-analysis of studies published up to April 2015, to further identify the potential associations between dietary patterns and the risk of CHD.

2. Methods

2.1. Literature Search Strategy

An electronic literature search was conducted in MEDLINE and EBSCO to identify human studies written in English or Chinese, published up to April 2015, with the following keywords: dietary pattern, dietary patterns, alcohol drinking, alcohol consumption, cardiovascular disease, ischemic heart disease, myocardial infarction, coronary heart disease and coronary diseases. In addition, we manually searched all references cited in original studies and reviews identified.

2.2. Study Included Criteria

Two independent reviewers (L. Shu and X.-Y. Zhang) read the abstracts of the papers retrieved in the initial search to identify studies that examined the associations between dietary patterns and the risk of CHD. When all reviewers agreed, the papers were reviewed against inclusion and exclusion criteria for this meta-analysis. To be eligible, dietary pattern studies had to fulfill the following criteria: (1) The study was published as an original article reporting the relationship of different dietary patterns and the risk of CHD. (2) Food or dietary patterns in studies were examined by principal component analysis (PCA) and/or factor analysis (FA). (3) Odds ratios or hazard ratios, and percentage for CHD (or data can be calculated) had been provided. (4) CHD was diagnosed based on clinical manifestations (including myocardial infarction or angina, or myocardial ischemia, or cardiac failure and arrhythmia, or a death certificate cause of death as CHD), electrocardiogram, and coronary aeteriography. Alcohol studies were included in this meta-analysis if they met the following criteria: (1) the study was published as an original article; (2) the association between alcohol intake and risk of CHD had been reported in studies; (3) the different alcohol consumption categories have been described in studies; and (4) CHD was diagnosed based on clinical manifestations, electrocardiogram, and coronary arteriography.

2.3. Data Extraction

Information extracted from each study included authors, geographic region, study design, sample size, the number of CHD, dietary assessment method, identification of dietary patterns, and factors that were adjusted in the including studies.

2.4. Definition of “High Intake”

Dietary patterns were identified by principal component analysis or factor analysis. Factor scores for each pattern were categorized into tertiles, quartiles, or quintiles (the lowest category and the highest category represented low and high intake, respectively, to each dietary pattern.) The different forms of alcohol consumption were converted into grams of ethanol per day. Alcohol consumption of >25 g/day for men or >12.5 g/day for women was defined as a high intake of alcohol or heavy alcohol drinking; alcohol consumption of <12.5 g/day for men or <7.5 g/day for women was defined as a low intake of alcohol, and alcohol consumption of >12.5 g/day and <25 g/day for men or >7.5 g/day and <12.5 g/day for women was defined as a moderate alcohol consumption [24].

2.5. Quality Assessment

The Newcastle–Ottawa Quality Assessment scale was used for quality assessment [25]. Eight questions were assessed and each satisfactory answer received one point (may receive two points in comparability categories), resulting in a maximum score of nine. Only those studies in which most the questions were deemed satisfactory (i.e., with a score of six or higher) were considered to be of high methodological quality.

2.6. Assessment of Heterogeneity

Heterogeneity of the study results was estimated by the chi-squared test. p Values less than 0.05 were considered to be significant. In this meta-analysis, a random-effects model was used to account for possible heterogeneity between studies, while a fixed-effects model was adopted in the absence of heterogeneity [26].

2.7. Statistical Analysis

Statistical analyses were performed using Review Manager, version 5.0 (Nordic Cochrane Centre, Copenhagen, Denmark) and STATA software, version 12.0 (Stata Corp, College Station, TX, USA). The original studies reported the results of dietary patterns or alcohol consumption in terms of quintiles, quartiles, and tertiles of dietary factor scores and the risk of CHD. We used meta-analysis to evaluate the risk of CHD in the highest versus the lowest categories of healthy/prudent, unhealthy/Western-type dietary patterns and alcohol consumption. Random-effect models were used to calculate the pooled odd ratio (OR) for dietary patterns in highest categories compared with lowest categories. Raw data from individual studies were weighted and combined to produce an overall OR. Publication bias was assessed by inspection of the funnel plot and by formal testing for “funnel plot” asymmetry using Begg’s test and Egger’s test [27]. All statistical tests were two-sided and p values less than 0.05 were considered significant.

3. Results

3.1. Overview of Included Studies for the Systematic Meta-Analysis

An electronic literature search in the database of MEDLINE and EBSCO identified 560 studies, 525 of which were excluded based on the reasons listed in Figure 1: meta-analysis, reviews or systematic reviews (n = 173); title and abstract did not contain the data on classification of dietary pattern or alcohol consumption (n = 278); did not provide sufficient dichotomous data on dietary pattern and CHD (n = 25); focused on single nutrients or food (n = 18); did not provide the data about percent of CHD or number of each group (n = 20); reported data using different alcohol consumption categories (n = 10); and reported the same data (n = 1). At last, 35 articles [8,11,13,14,15,16,17,18,19,20,21,22,23,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49] (reporting 37 original studies) met the inclusion criteria and were included in this meta-analysis. Descriptive information of each included study was presented in Table 1.
Figure 1. Flow chart of article screening and selection process.
Figure 1. Flow chart of article screening and selection process.
Nutrients 07 05300 g001
Table 1. Characteristics of 35 studies included in the meta-analysis (1991–2015).
Table 1. Characteristics of 35 studies included in the meta-analysis (1991–2015).
Author and Publication YearLocationStudy DesignTotal Number of SubjectsAge (Year)/SexDiet Assessment MethodDietary Patterns IdentifiedFactors Adjusted for in Analyses
Osler et.al., 2002 [8]DanishCohort583430–60 years bothFFQ“prudent food” “Western food”Smoking, exercise, education, BMI and alcohol intake
Fung et.al., 2001 [11]USCohort69,01738–63 years womenFFQ“Prudent” “Western”Age, period, smoking, BMI, hormone replacement therapy, aspirin use, caloric intake, family history, history of hypertension, multivitamin and vitamin E supplement use, physical activity
Iqbal et.al., 2008 [13]52 countriesCase-control5761/10,64641–70 years bothFFQOriental, Western, prudentAge, sex, region, education, BMI, physical activity, smoking
Hoffmann et.al., 2004 [14]GermanyCase-control200/25530–80 years womenFFQ“Western”Age, cigarette smoking, hormone replacement therapy, hypertension, education level, physical activity level and sport
Stricker et.al., 2012 [15]DutchCohort40,01150–69 years bothFFQ“Prudent” “Western”Age, gender, physical activity, smoking status, education, systolic- and diastolic blood pressure and energy intake
Weikert et.al., [16] (CORA) 2005GermanyCase-control200/25530–80 years womenFFQ“Simplified food pattern”Age, cigarette smoking, education attainment, BMI, physical activity level, total energy intake, hormone replacement therapy, hypertension, dyslipidemia, and diabetes
Weikert et.al., [16] (EPIC-Potsdam) 2005GermanyCohort26,79535–65 years bothFFQ“Simplified food pattern”Age, cigarette smoking, education attainment, BMI, physical activity level, total energy intake, hormone replacement therapy, hypertension, dyslipidemia, and diabetes
Lipoeto et.al., 2004 [17]IndonesiaCase-control93/189men and womenFFQ“Animal foods”Age, physical activity and stress level, total energy
Tucker et.al., 2005 [18]USCohort50134–80 years men7-day diet records“Low SF and high FV”Age,, total energy intake, BMI, smoking, alcohol use, physical activity score, dietary supplement use
McNaughton et.al., 2009 [19]UKCohort731435–55 years bothFFQ“Dietary pattern 1” “Dietary pattern 2”Age, sex, energy misreporting, ethnicity, smoking, alcohol, physical activity, blood pressure and BMI
Fitzgerald et.al., 2012 [20]USCohort34,827≥45 years womenFFQ“DASH”Randomization status, age, smoking, time-varying postmenopausal status, time-varying hormone therapy use, alcohol intake, energy intake, physical activity, cigarettes per day, BMI, and highest education level
Martínez-Gonzlez et.al., 2011 [21]SpainCohort13,60934–43 years bothFFQ“Mediterranean”Age, sex, family history of coronary heart disease, total energy intake, physical activity, smoking, BMI, diabetes at baseline, use of aspirin, history of hypertension and history of hypercholesterolemia
Maruyama et.al., 2013 [22]JapanCohort64,03740–79 years bothFFQ“Vegetable” “Animal food” “Dairy product”Age, BMI, smoking category, walking time, hours of sports, perceived mental stress, total energy intake, history of hypertension and diabetes
Hu et.al., 2000 [23]USCohort44,87440–75 years menFFQ“Prudent”, “Western”Age, BMI, time period, cigarette smoking, parental history of myocardial infarction before age 60, multivitamin and vitamin E supplement use, alcohol consumption, history of hypertension, physical activity, total energy intake, and profession
Guallar-Castillón et.al., 2012 [28]SpainCohort40,75729–69 years bothDietary history“Mediterranean”, “Westernized”BMI, waist circumference, education, smoking, physical activity at work, physical activity at home, physical activity during leisure time, diabetes, hypertension, hypercholesterolemia, cancer, oral contraceptives, menopausal status, hormone replacement therapy, total energy intake, and stratified by age at recruitment, sex, and center.
Martínez-González et.al., 2002 [29]SpainCase-control171/171≤80 years bothFFQPriori pattern” “Mediterranean” “Post hoc pattern”Smoking, BMI, high blood pressure, high blood cholesterol, diabetes, leisure-time activity, family history of CHD before 60y, aspirin intake and socioeconomic status
Shimazu et.al., 2007 [30]JapanCohort40,54740–79 years bothFFQ“Japanese pattern” “Animal food”Age, sex, smoking status, walking duration, education, total energy intake, BMI, and history of hypertension
Arriola et.al., 2010 [31]SpainCohort41,43829–69 years bothDietary history questionnaireAlcohol intakeCentre, smoking status, height and educational level, stratified by age, physical activity index, waist/hip ratio, vitamin E, antithrombotic and antihemorrhagic drugs and energy intake
Beulens et.al., 2007 [32]USCohort11,71140–75 years menFFQAlcohol intakeAge, smoking, BMI, physical activity, diabetes, hypercholesterolemia, family history of MI, aspirin use, lipid-lowering therapy, energy intake, and energy-adjusted quintiles of saturated fat, trans fatty acids, sodium, potassium, magnesium, folate, vitamin E, n-3 fatty acids, and dietary fiber.
Bos et.al., 2010 [33]DutchCohort10,53049–70 years womenFFQAlcohol intakeAge, smoking, BMI, menopausal status, physical activity, education level, hypercholesterolemia, diabetes, antihypertensive medication, daily energy intake, vitamin E, vitamin C, saturated fat, and fiber intake
Fernández-Jarne et.al., 2003 [34]SpainCase-control171/171Mean 62 years BothFFQTotal alcohol intakeTotal energy intake, smoking, BMI, high blood pressure, high blood cholesterol, diabetes, leisure-time physical activity, aspirin use, family history of coronary heart disease, marital status, occupation, study level, olive oil consumption, ratio of monounsaturated to saturated fat, folic acid, and total fiber intake.
Fuchs et.al., 2004 [35]USCohort14,50645–64 years menDietary questionnaireAlcohol intakeAge, cigarette-years of smoking, BMI, LDL- and HDL-cholesterol level, waist/hip ratio, educational level, income, sport index, diabetes mellitus, systolic blood pressure, use of antihypertensive medication.
Ikehara et.al., 2009 [36]JapanCohort19,35640–69 years menSelf-administered questionnaireAlcohol consumptionAge, smoking status, body mass index, history of hypertension and diabetes, sports of leisure time, levels of mental stress, presence of flushing and job, marital status, medical checkups and area.
Ikehara et.al., 2008 [37]JapanCohort83,68240–79 years bothSelf-administered questionnaireEthanol intakeAge, smoking status, BMI, history of hypertension and diabetes, frequency of exercise, perceived mental stress, education level, and intake of vegetables, fish, and fruit
Ikehara et.al., 2013 [38]JapanCohort47,10040–69 years womenSelf-reported questionnaireAlcohol consumptionAge, smoking status, body mass index, history of diabetes, sports at leisure time, flushing after drinking alcohol, mental stress, menopausal status and area, history of hypertension
Mukamal et.al., 2006 [39]USCohort38,07740–75 years menFFQAlcohol consumptionAge, smoking status, body mass index, the presence or absence of diabetes, hypertension, hypercholesterolemia, and a parental history of myocardial infarction, use or nonuse of aspirin, physical activity, intake of energy, and energy-adjusted intake of folate, vitamin E, saturated fat, trans fat, and fiber.
Keil et.al., 1997 [40]GermanyCohort62/107145–64 years both7-day recallAlcohol intakeAge, smoking, hypertension, BMI
Kono et.al., 1991 [41]JapanCase-control89/27140–69 years bothSelf-administered questionnaireAlcohol intakeAge, smoking, strenuous exercise, BMI, systemic hypertension, diabetes mellitus, heart disease in parent, job class
Schröder et.al., 2007 [42]SpainCase-control224/127025–74 years bothQuestionnaireAlcohol intakeAge, smoking, educational level, leisure-time physical activity, total cholesterol, LDL- and HDL-cholesterol, diabetes, hypercholesterolemia drug treatment, and diagnosed hypertension
Wells et.al., 2004 [43]New ZealandCase-control1381/189235–74 years bothQuestionnaireAlcohol intakeAge group, history of CHD, tobacco smoking, leisure-time physical activity, current antihypertensive drug treatment, family history of premature cardiovascular disease, BMI, diabetes, socioeconomic status, income and low education.
Kitamura et.al., 1998 [44]JapanCohort847640–59 years menInterviewAlcohol intakeAge, serum total cholesterol, cigarette smoking, BMI, left ventricular hypertrophy, and history of diabetes mellitus.
Mukamal et.al., 2006 (n = 2) [45]USCohort4410≥65 years bothSelf-administered questionnaireAlcohol useAge, sex, race, education, marital status, smoking, exercise intensity, depression score, frequent aspirin use, BMI, and diabetes mellitus.
Solomon et.al., 2000 [46]USCohort510330–55 years womenFFQAlcohol consumptionAge, time period, body mass index, cigarette smoking, parental history of MI before age 60 years, hypertension, hypercholesterolemia, menopausal status/postmenopausal hormone use, aspirin use, multivitamin use, vitamin E supplement use, and physical activity level.
Bazzano et.al., 2009 [47]ChinaCohort64,597≥40 years menInterviewer-administered questionnaireAlcohol consumptionAge, body-mass index, average systolic blood pressure, physical activity, cigarette smoking, diabetes education, urban or rural residence, and living in North China
Hvidtfeldt et.al., 2010 [48]DenmarkCohort266,986≥39 years bothFFQ or diet history questionnaireAlcohol intakeAge, year of baseline questionnaire
Rajpathak et.al., 2010 [49]USCohort319850–79 years womenFFQAlcohol intakeAge, race/ethnicity, BMI, smoking, hypertension, high cholesterol, hormone use, regular aspirin use, quintiles of physical activity, duration of DM, intake of saturated fat, PUFA, fiber.
BMI: body mass index; CHD: coronary heart disease; LDL-cholesterol: low-density lipoproteins cholesterol; HDL-cholesterol: high-density lipoproteins cholesterol; WHR: waist hip ratio; FFQ: food frequency questionnaire.

3.2. Healthy Dietary Pattern

The healthy/prudent dietary patterns were characterized by high consumption of vegetables, fruits, whole grains, olive oil, fish, soy, poultry and low fat dairy. The examined studies labeled it as “Prudent” [8,11,13,15,23], “Simplified food” [16], “Low SF and high FV” [18], “Dietary pattern 1” [19], “DASH” [20], “Mediterranean” [21,28,29], “Vegetable and fruit” [22], and “Japanese pattern” [30]. Figure 2 showed an obvious evidence of a decreased risk of CHD in the highest compared with the lowest categories of “healthy/prudent dietary patterns (OR = 0.67; CI: 0.60, 0.75; p < 0.00001). A random-effects model was used to assess the data included in our analyses. The heterogeneity was apparent in all the studies (p = 0.004; I2 = 57%).
Figure 2. Forest plot of the highest compared with the lowest categories of intake of the healthy/prudent dietary patterns and coronary heart disease (CHD) risk.
Figure 2. Forest plot of the highest compared with the lowest categories of intake of the healthy/prudent dietary patterns and coronary heart disease (CHD) risk.
Nutrients 07 05300 g002

3.3. Western-Type Dietary Pattern

The unhealthy/Western-type dietary patterns were characterized by high consumption of red and/or processed meat, refined grains, sweets, high-fat dairy products, butter, potatoes and high-fat gravy, and low intakes of fruits and vegetables. The studies under consideration labeled it as “Western” [8,9,13,14,15,23,28], “Animal foods” [17,22,30] and “Dietary pattern 2” [19]. The association between unhealthy/Western-type dietary patterns and the risk of CHD was shown in Figure 3. There was evidence of an increased risk of CHD in the highest compared with the lowest categories of unhealthy/Western-type dietary patterns (OR = 1.45; CI: 1.05, 2.01; p = 0.02) where all studies were combined in the random-effects model. There was significant heterogeneity (I2 = 96%, p < 0.00001).
Figure 3. Forest plot of the highest compared with the lowest categories of intake of the unhealthy/Western-type dietary patterns and CHD risk.
Figure 3. Forest plot of the highest compared with the lowest categories of intake of the unhealthy/Western-type dietary patterns and CHD risk.
Nutrients 07 05300 g003

3.4. Alcohol Consumption

The alcohol consumption was characterized by moderate intakes of wines, alcohol-containing beers, and white spirits. Nineteen studies (reporting twenty original studies) have identified moderate alcohol consumption. The data from nineteen studies were assessed using the random-effects model, and there was significant heterogeneity (I2 = 83%, p < 0.00001). Figure 4 showed an obvious evidence of a decreased risk of CHD in the moderate drinking compared with non-drinking category intake of the alcohol consumption levels (OR = 0.68; 95% CI: 0.59, 0.78; p < 0.00001).
Figure 4. Forest plot of the moderate drinking compared with the non-drinking category of intake the alcohol-drinking pattern and CHD risk.
Figure 4. Forest plot of the moderate drinking compared with the non-drinking category of intake the alcohol-drinking pattern and CHD risk.
Nutrients 07 05300 g004

3.5. Publication Bias

Inspection of funnel plots did not reveal evidence of asymmetry (Appendix A). Begg’s tests for publication bias were not statistically significant (highest compared with lowest category: healthy/prudent dietary pattern, Begg’s test p = 0.285; unhealthy/Western-type dietary pattern, Begg’s test p = 0.276; and alcohol consumption, Begg’s test p = 0.218).

3.6. Quality Assessment

The quality of each study in terms of population and sampling methods, description of exposure and outcomes, and statistical adjustment of data, is summarized in Appendix B. Thirty-one of thirty-five studies received a score of six or higher on the Newcastle–Ottawa Quality assessment scale and were considered to be of high methodological quality [8,11,13,14,15,16,18,19,20,21,23,28,30,31,32,33,34,36,37,38,39,40,41,42,43,44,45,46,47,48,49].

3.7. Sensitivity Analysis

When the results were analyzed by removing non-American and non-European studies [17,22,30,36,37,38,41,44,47], the difference in the risk of CHD was shown in Western-type dietary pattern and alcohol consumption (Western-type: OR = 1.53; 95% CI: 1.05, 2.22; p < 0.01; alcohol consumption: OR = 0.68; 95% CI :0.51, 0.80; p < 0.05). When sample size <10,000 was removed [8,14,16,17,18,19,29,34,40,41,42,43,44,45,46], the difference in the risk of CHD was shown in Western-type dietary pattern (OR = 1.77; 95% CI: 1.08, 2.28; p < 0.01). Similarly, when the results were analyzed by removing the studies adjusted for total energy intake [16,17,18,20,21,22,23,28,30,31,32,34,39], the difference in the risk of CHD for those in the highest category compared with the lowest categories of Western-type dietary pattern was detected. Moreover, when the results were analyzed by removing the studies adjusted for sex, no difference in the risk of CHD was found. Finally, when the results were analyzed by removing case-control studies, the difference in the risk of CHD was shown in alcohol consumption (OR = 0.74; 95% CI: 0.66, 0.83; p < 0.01). As these variables have a strong effect on association between different dietary patterns and risk of CHD, their differences may partially explain the observed heterogeneity between studies (Table B2).

4. Discussion

Limited epidemiological research has reported the associations between dietary patterns and the risk of CHD. To our knowledge, this is the latest meta-analysis evaluating the evidence for dietary patterns and CHD risk. In the present study, we have an update on the earlier systematic review (Li et al., and Hou et al., 2014) [50,51] and further explore the association between moderate alcohol consumption and the risk of CHD. The results of this meta-analysis demonstrate that the healthy/prudent dietary patterns and moderate alcohol consumption may decrease the risk of CHD, whereas unhealthy/Western-type dietary patterns may increase the risk of CHD. Our findings have confirmed the associations between different dietary patterns and the risk of CHD, and provided information that may be translated into public health action for primary prevention of CHD.
In our analyses, the healthy/prudent dietary patterns were associated with a reduced risk of CHD. Our results were in agreement with some previous studies, which reported an inverse association between healthy/prudent dietary patterns and the risk of CHD [11,23]. The apparently protective effect of vegetables, and fruits may be related to high concentration of antioxidant substances (e.g., vitamin C, vitamin E, and other carotenoids compounds). A previous meta-analysis of fruit and vegetables consumption and risk of CHD concluded that high intakes of fruit and vegetables were associated with a decreased risk of CHD [52]. Besides, several studies have also indicated that antioxidants such as vitamin E can slow the rate of oxidation, protecting endothelial cells and vascular [53], thereby reducing the risk of CHD. Furthermore, earlier studies have found that higher intake of folate may decrease the concentration of homocysteine, which may increase the risk of CHD [53,54]. Recently, Pereira et al. reported an inverse association between dietary fiber and the risk of CHD [55]. To our knowledge, the possible mechanism is that dietary fiber can modify blood lipid profiles, lower blood pressure, as well as reduce blood glucose concentrations by slowing intestinal absorption [56]. In addition, some clinical and biological investigations have also found that the micro- and macro-constituents of fruit and vegetables may decrease the risk of hypertension, dyslipidemia and diabetes, which are considered as having an important role in the development or progression of CHD [57,58].
The unhealthy/Western-type dietary patterns were associated with an increased risk of CHD in this meta-analysis. Our results were consistent with previous studies [17,19], which indicated that red meat and processed meat consumption were associated with an increased risk of CHD. To our knowledge, there are several plausible explanations for the positive association between Western-type dietary patterns and CHD risk. Firstly, high consumption of red and processed meat is associated with raised total cholesterol, LDL-cholesterol and blood pressure, and greater BMI [59]. As mentioned above, these metabolic changes are related with the risk factors for CHD. Secondly, high temperature commercial cooking or frying, commonly used in preparing processed meats, may generate heterocyclic amines or polycyclic aromatic hydrocarbons, which may increase the risk of CHD and DM [60,61]. Finally, processed meats contain a high content of salt, nitrates and their byproducts (e.g., peroxynitrite), which may be associated with an increased risk of CHD [62].
An inverse association was shown for moderate alcohol consumption and the risk of CHD in our analyses. Previously, a meta-analysis of alcohol consumption and the risk of CHD indicated that moderate alcohol-drinking (≤1.5 drinks/day) was associated with a decreased risk of CHD [63]. In fact, alcohol consumption has been consistently considered an important risk for some chronic diseases, including hypertension and diabetes. Nevertheless, our results found the favorable effect of moderate alcohol consumption on the development of CHD. As we all know, moderate alcohol consumption can raise the concentration of serum high density lipoprotein cholesterol, which may protect against atheroma formation in coronary arteries [64,65]. In addition, it is also associated with the increased vascular wall prostacyclin, thus preventing thrombus formation in coronary arteries [66]. Furthermore, some studies have found that light to moderate alcohol consumption can lower the levels of fasting insulin [67], which is related to the decreased risk of CHD.

Strengths and Limitations

This meta-analysis has its own strengths and limitations. Firstly, this is the latest meta-analysis reporting the associations between dietary patterns and the risk of CHD. We not only have an update on an earlier systematic review (Li et al. and Hou et al., 2014) [50,51], but also further explore the association between moderate alcohol consumption and the risk of CHD. Secondly, the cases of CHD were confirmed based on clinical manifestations, electrocardiogram, and coronary arteriography, avoiding misdiagnosis. Thirdly, no signs of publication bias were evident in the funnel plot, and the statistical test for publication bias was non-significant. However, some limitations should also be mentioned, when interpreting the results of this meta-analysis. Firstly, the principal limitation of this study was the use of potentially biased evidence. Moreover, there was an inconsistent adjustment for potential confounders among the included studies, and we did not exclude the possibility of confounding in this meta-analysis. As a result, the data included in our analyses might suffer from differing degrees of completeness and accuracy. Secondly, ten of thirty-six studies are case-control studies in this meta-analysis. Thus, selection bias is inevitable in our analyses.

5. Conclusions

In conclusion, results from this meta-analysis indicate that healthy/prudent dietary patterns and moderate alcohol consumption are associated with a decreased risk of CHD, while unhealthy/Western-type patterns are associated with an increased risk of CHD. In addition, these findings also suggest that a change of diet is essential for the prevention of CHD. Herein, it makes sense to elucidate the potential associations between dietary patterns and the risk of CHD, and provide scientific rationale for formulating dietary guidelines. Further studies are required to confirm the causal associations between dietary patterns and the risk of CHD.

Acknowledgments

This study was supported by provinces and the ministry of education (Grant NO.2014PYA002). The authors thank all participants from Department of Nutrition, Zhejiang Hospital, Zhejiang, China.

Author Contributions

X.-Y.Z., L.S. and P.-F.Z. conceived and designed the experiments. C.-J.S., X.-L.Y., D.L. and W.G. conducted research. X.-Y.Z. and L.S. analyzed data and wrote the paper. All authors read and approved the final manuscript.

Conflicts of Interest

The authors declared no conflict of interest.

Appendix A

Figure A1. Funnel plots for coronary heart disease(CHD) in the highest compared with the lowest category of intake of the “healthy” dietary pattern in all studies.
Figure A1. Funnel plots for coronary heart disease(CHD) in the highest compared with the lowest category of intake of the “healthy” dietary pattern in all studies.
Nutrients 07 05300 g005
Figure A2. Funnel plots for CHD in the highest compared with the lowest category of intake of the “Western-type” dietary pattern in all studies.
Figure A2. Funnel plots for CHD in the highest compared with the lowest category of intake of the “Western-type” dietary pattern in all studies.
Nutrients 07 05300 g006
Figure A3. Funnel plots for CHD in the moderate drinking compared with non-drinking category intake of “alcohol consumption” pattern in all studies.
Figure A3. Funnel plots for CHD in the moderate drinking compared with non-drinking category intake of “alcohol consumption” pattern in all studies.
Nutrients 07 05300 g007

Appendix B

Table B1. Assessment of study quality.
Table B1. Assessment of study quality.
StudiesSelectionComparabilityOutcomeScore
12345A5B678
Cohort
Fung et al., 2001 [11]****************
Fitzgerald et al., 2012 [20]****************
Guallar-Castillón et al., 2012 [28]**************
Hu et al., 2000 [23]******************
Martínez-Gonzlez et al., 2011 [21]**************
Maruyama et al., 2013 [22]**********
Osler et al., 2002 [8]******************
Shimazu et al., 2007 [30]****************
Stricker et al., 2012 [15]****************
Tucker et al., 2005 [18]************
Weikert et al., 2005 [16]******************
McNaughton et al., 2009 [19]****************
Arriola et al., 2010 [31]***************
Solomon et al., 2000 [46]****************
Beulens et al., 2007 [32]****************
Bos et al., 2010 [33]******************
Fuchs et al., 2004 [35]**********
Ikehara et al., 2008 [37]**************
Ikehara et al., 2009 [36]**************
Ikehara et al., 2013 [38]**************
Keil et al., 1997 [40]**************
Mukamal et al., 2006 [39]************
Mukamal et al., 2006 (n = 2) [45]************
Bazzano et al., 2009 [47]****************
Hvidtfeldt et al., 2010 [48]**************
Rajpathak et al., 2010 [49]**************
Kitamura et al., 1998 [44]************
Case-control
Iqbal et al., 2008 [13]**************
Martínez-González et al., 2002 [29]**********
Weikert et al. (CORA) 2005 [16]**************
Lipoeto et al., 2004 [17]**********
Hoffmann et al., 2004 [14]**************
Fernández-Jarne et al., 2003 [34]******************
Kono et al., 1991 [41]**************
Schröder et al., 2007 [42]**********
Wells et al., 2004 [43]****************
* For case-control studies, 1, indicates cases independently validated; 2, cases are representative of population; 3, community controls; 4, controls have no history of blood pressure disease; 5A, study controls for age; 5B, study controls for additional factor (s); 6, ascertainment of exposure by blinded interview or record; 7, same method of ascertainment used for cases and controls; and 8, non response rate the same for cases and controls. For cohort studies, 1 indicates exposed cohort truly representative; 2, non exposed cohort drawn from the same community; 3, ascertainment of exposure; 4, outcome of interest not present at start; 5A, cohorts comparable on basis of age; 5B, cohorts comparable on other factor(s); 6, quality of outcome assessment; 7, follow-up long enough for outcomes to occur; and 8, complete accounting for cohorts.
Table B2. Dietary patterns, alcohol consumption and coronary heart disease: sensitivity analysis.
Table B2. Dietary patterns, alcohol consumption and coronary heart disease: sensitivity analysis.
Study CharacteristicCategoryHealthy Dietary Pattern (95% CI)Western-Style Dietary Pattern (95% CI)Alcohol Consumption (95% CI)
Age>500.65 (0.56, 0.76)1.31 (0.91, 1.88)0.72 (0.60, 0.86)
<500.75 (0.63, 0.90)1.49 (0.90, 2.45)0.59 (0.45, 0.79)
Sample sizeLarge (>10,000)0.71 (0.64, 0.79)1.21 (0.87, 1.67)0.72 (0.62, 0.83)
Small (<10,000)0.56 (0.37, 0.86)1.77 (1.08, 2.88)0.64 (0.46, 0.87)
RaceWhite0.67 (0.58, 0.77)1.53 (1.05, 2.22)0.68 (0.51, 0.80)
Asian and Other0.75 (0.60, 0.92)1.15 (0.63, 2.11)0.76 (0.57, 1.06)
Study designCase-control0.48 (0.28, 0.84)4.49 (0.73, 25.75)0.51 (0.37, 1.07)
Cohort0.72 (0.64, 0.81)1.08 (0.79, 1.48)0.74 (0.66, 0.83)
Total energyAdjusted0.67 (0.56, 0.80)1.05 (0.73, 1.51)0.78 (0.68, 0.90)
Unadjusted0.65 (0.61, 0.70)1.99 (1.27, 3.13)0.76 (0.55, 0.78)

References

  1. Mackay, J.; Mensah, G. The Atlas of Heart Disease and Stroke. Available via World Health Organization. Available online: http://www.who.int/cardiovascular_diseases/resources/atlas/en/ (accessed on 29 September 2004).
  2. Levi, F.; Lucchini, F.; Negri, E.; La Vecchia, C. Trends in mortality from cardiovascular and cerebrovascular diseases in Europe and other areas of the world. Heart 2002, 88, 119–124. [Google Scholar] [CrossRef] [PubMed]
  3. Xu, J.; Lee, E.T.; Peterson, L.E.; Devereux, R.B.; Rhoades, E.R.; Umans, J.G.; Best, L.G.; Howard, W.J.; Paranilam, J.; Howard, B.V. Differences in risk factors for coronary heart disease among diabetic and nondiabetic individuals from a population with high rates of diabetes: The Strong Heart Study. J. Clin. Endocrinol. Metab. 2012, 97, 3766–3767. [Google Scholar] [CrossRef] [PubMed]
  4. He, J.; Gu, D.; Wu, X.; Reynolds, K.; Duan, X.; Yao, C.; Wang, J.; Chen, C.S.; Chen, J.; Wildman, R.P.; et al. Major causes of death among men and women in China. N. Engl. J. Med. 2005, 353, 1124–1134. [Google Scholar] [CrossRef] [PubMed]
  5. World Health Organization. World Health Statistics Annual, 2010. Available via World Health Organization. Available online: http://www.who.int/whosis/whostat/2010/en/index.html (accessed on 13 June 2011).
  6. Frankel, S.; Elwood, P.; Sweetnam, P.; Yarnell, J.; Smith, G.D. Birthweight, body-mass index in middle age, and incident coronary heart disease. Lancet 1996, 348, 1478–1480. [Google Scholar] [CrossRef]
  7. McKeigue, P.M.; Lithell, H.O.; Leon, D.A. Glucose tolerance and resistance to insulin-stimulated glucose uptake in mean aged 70 years in relation to size at birth. Diabetologia 1998, 41, 1133–1138. [Google Scholar] [CrossRef] [PubMed]
  8. Osler, M.; Helms Andreasen, A.; Heitmann, B.; Høidrup, S.; Gerdes, U.; Mørch Jørgensen, L.; Schroll, M. Food intake patterns and risk of coronary heart disease: A prospective cohort study examining the use of traditional scoring techniques. Eur. J. Clin. Nutr. 2002, 56, 568–574. [Google Scholar] [CrossRef] [PubMed]
  9. Lancaster, K.J.; Smiciklas-Wright, H.; Weitzel, L.B.; Mitchell, D.C.; Friedmann, J.M.; Jensen, G.L. Hypertension-related dietary patterns of rural older adults. Prev. Med. 2004, 38, 812–818. [Google Scholar] [CrossRef] [PubMed]
  10. Hu, F.B. Dietary pattern analysis: A new direction in nutritional epidemiology. Curr. Opin. Lipidol. 2002, 13, 3–9. [Google Scholar] [CrossRef] [PubMed]
  11. Fung, T.T.; Willett, W.C.; Stampfer, M.J.; Manson, J.E.; Hu, F.B. Dietary patterns and the risk of coronary heart disease in women. Arch. Intern. Med. 2001, 161, 1857–1862. [Google Scholar] [CrossRef] [PubMed]
  12. Guo, J.; Li, W.; Wang, Y.; Chen, T.; Teo, K.; Liu, L.S.; Yusuf, S. Influence of dietary patterns on the risk of acute myocardial infarction in China population: The INTERHEART China study. Chin. Med. J. (Engl.) 2013, 126, 464–470. [Google Scholar] [PubMed]
  13. Iqbal, R.; Anand, S.; Ounpuu, S.; Islam, S.; Zhang, X.; Rangarajan, S.; Chifamba, J.; Al-Hinai, A.; Keltai, M.; Yusuf, S.; et al. Dietary patterns and the risk of acute myocardial infarction in 52 countries: Results of the INTERHEART study. Circulation 2008, 118, 1929–1937. [Google Scholar] [CrossRef] [PubMed]
  14. Hoffmann, K.; Zyriax, B.C.; Boeing, H.; Windler, E. A dietary pattern derived to explain biomarker variation is strongly associated with the risk of coronary artery disease. Am. J. Clin. Nutr. 2004, 80, 633–640. [Google Scholar] [PubMed]
  15. Stricker, M.D.; Onland-Moret, N.C.; Boer, J.M.; van der Schouw, Y.T.; Verschuren, W.M.; May, A.M.; Peeters, P.H.; Beulens, J.W. Dietary patterns derived from principal component- and k-means cluster analysis: Long-term association with coronary heart disease and stroke. Nutr. Metab. Cardiovasc. Dis. 2013, 23, 250–256. [Google Scholar] [CrossRef] [PubMed]
  16. Weikert, C.; Hoffmann, K.; Dierkes, J.; Zyriax, B.C.; Klipstein-Grobusch, K.; Schulze, M.B.; Jung, R.; Windler, E.; Boeing, H. A homocysteine metabolism-related dietary pattern and the risk of coronary heart disease in two independent German study populations. J. Nutr. 2005, 135, 1981–1988. [Google Scholar] [PubMed]
  17. Lipoeto, N.I.; Agus, Z.; Oenzil, F.; Wahlqvist, M.; Wattanapenpaiboon, N. Dietary intake and the risk of coronary heart disease among the coconut-consuming Minangkabau in West Sumatra, Indonesia. Asia Pac. J. Clin. Nutr. 2004, 13, 377–378. [Google Scholar] [PubMed]
  18. Tucker, K.L.; Hallfrisch, J.; Qiao, N.; Muller, D.; Andres, R.; Fleg, J.L. The combination of high fruit and vegetable and low saturated fat intakes is more protective against mortality in aging men than is either alone: The Baltimore Longitudinal Study of Aging. J. Nutr. 2005, 135, 556–561. [Google Scholar] [PubMed]
  19. McNaughton, S.A.; Mishra, G.D.; Brunner, E.J. Food patterns associated with blood lipids are predictive of coronary heart disease: The Whitehall II study. Br. J. Nutr. 2009, 102, 619–624. [Google Scholar] [CrossRef] [PubMed]
  20. Fitzgerald, K.C.; Chiuve, S.E.; Buring, J.E.; Ridker, P.M.; Glynn, R.J. Comparison of associations of adherence to a Dietary Approaches to Stop Hypertension (DASH)-style diet with risks of cardiovascular disease and venous thromboembolism. J. Thromb. Haemost. 2012, 10, 189–198. [Google Scholar] [CrossRef] [PubMed]
  21. Martinez-Gonzalez, M.A.; Garcia-Lopez, M.; Bes-Rastrollo, M.; Toledo, E.; Martínez-Lapiscina, E.H.; Delgado-Rodriguez, M.; Vazquez, Z.; Benito, S.; Beunza, J.J. Mediterranean diet and the incidence of cardiovascular disease: A Spanish cohort. Nutr. Metab. Cardiovasc. Dis. 2011, 21, 237–244. [Google Scholar] [CrossRef] [PubMed]
  22. Maruyama, K.; Iso, H.; Date, C.; Kikuchi, S.; Watanabe, Y.; Wada, Y.; Inaba, Y.; Tamakoshi, A. Dietary patterns and risk of cardiovascular deaths among middle-aged Japanese: JACC Study. Nutr. Metab. Cardiovasc. Dis. 2013, 23, 519. [Google Scholar] [CrossRef] [PubMed]
  23. Hu, F.B.; Rimm, E.B.; Stampfer, M.J.; Ascherio, A.; Spiegelman, D.; Willett, W.C. Prospective study of major dietary patterns and risk of coronary heart disease in men. Am. J. Clin. Nutr. 2000, 72, 912–921. [Google Scholar] [PubMed]
  24. US Government. Alcoholic Beverages: Dietary Guidelines for Americans 2005; US Government Printing Office: Washington, DC, USA, 2005.
  25. Stang, A. Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses. Eur. J. Epidemiol. 2010, 25, 603–605. [Google Scholar] [CrossRef] [PubMed]
  26. Higgins, J.P.; Thompson, S.G.; Deeks, J.J.; Altman, D.G. Measuring inconsistency in meta-analyses. BMJ 2003, 327, 557–560. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Begg, C.B.; Mazumdar, M. Operating characteristics of a rank correlation test for publication bias. Biometrics 1994, 50, 1088–1101. [Google Scholar] [CrossRef] [PubMed]
  28. Guallar-Castillon, P.; Rodriguez-Artalejo, F.; Tormo, M.J.; Sánchez, M.J.; Rodríguez, L.; Quirós, J.R.; Navarro, C.; Molina, E.; Martínez, C.; Marín, P.; et al. Major dietary patterns and risk of coronary heart disease in middle-aged persons from a Mediterranean country: The EPIC-Spain cohort study. Nutr. Metab. Cardiovasc. Dis. 2012, 22, 192–199. [Google Scholar] [CrossRef] [PubMed]
  29. Martinez-Gonzalez, M.A.; Fernandez-Jarne, E.; Serrano-Martinez, M.; Marti, A.; Martinez J, A.; Martin-Moreno, J.M. Mediterranean diet and reduction in the risk of a first acute myocardial infarction: An operational healthy dietary score. Eur. J. Nutr. 2002, 41, 153–160. [Google Scholar] [CrossRef] [PubMed]
  30. Shimazu, T.; Kuriyama, S.; Hozawa, A.; Ohmori, K.; Sato, Y.; Nakaya, N.; Nishino, Y.; Tsubono, Y.; Tsuji, I. Dietary patterns and cardiovascular disease mortality in Japan: A prospective cohort study. Int. J. Epidemiol. 2007, 36, 600–609. [Google Scholar] [CrossRef] [PubMed]
  31. Arriola, L.; Martinez-Camblor, P.; Larranaga, N.; Basterretxea, M.; Amiano, P.; Moreno-Iribas, C.; Carracedo, R.; Agudo, A.; Ardanaz, E.; Barricarte, A.; et al. Alcohol intake and the risk of coronary heart disease in the Spanish EPIC cohort study. Heart 2010, 96, 124–130. [Google Scholar] [CrossRef] [PubMed]
  32. Beulens, J.W.; Rimm, E.B.; Ascherio, A.; Spiegelman, D.; Hendriks, H.F.; Mukamal, K.J. Alcohol consumption and risk for coronary heart disease among men with hypertension. Ann. Intern. Med. 2007, 146, 10–19. [Google Scholar] [CrossRef] [PubMed]
  33. Bos, S.; Grobbee, D.E.; Boer, J.M.; Verschuren, W.M.; Beulens, J.W. Alcohol consumption and risk of cardiovascular disease among hypertensive women. Eur. J. Cardiovasc. Prev. Rehabil. 2010, 17, 119–126. [Google Scholar] [CrossRef] [PubMed]
  34. Fernandez-Jarne, E.; Martinez-Losa, E.; Serrano-Martinez, M.; Prado-Santamaria, M.; Brugarolas-Brufau, C.; Martinez-Gonzalez, M.A. Type of alcoholic beverage and first acute myocardial infarction: A case-control study in a Mediterranean country. Clin. Cardiol. 2003, 26, 313–318. [Google Scholar] [CrossRef] [PubMed]
  35. Fuchs, F.D.; Chambless, L.E.; Folsom, A.R.; Eigenbrodt, M.L.; Duncan, B.B.; Gilbert, A.; Szklo, M. Association between alcoholic beverage consumption and incidence of coronary heart disease in whites and blacks: The Atherosclerosis Risk in Communities Study. Am. J. Epidemiol. 2004, 160, 466–474. [Google Scholar] [CrossRef] [PubMed]
  36. Ikehara, S.; Iso, H.; Yamagishi, K.; Yamamoto, S.; Inoue, M.; Tsugane, S. Alcohol consumption, social support, and risk of stroke and coronary heart disease among Japanese men: The JPHC Study. Alcohol. Clin. Exp. Res. 2009, 33, 1025–1032. [Google Scholar] [CrossRef] [PubMed]
  37. Ikehara, S.; Iso, H.; Toyoshima, H.; Date, C.; Yamamoto, A.; Kikuchi, S.; Kondo, T.; Watanabe, Y.; Koizumi, A.; Wada, Y.; et al. Alcohol consumption and mortality from stroke and coronary heart disease among Japanese men and women: The Japan collaborative cohort study. Stroke 2008, 39, 2936–2942. [Google Scholar] [CrossRef] [PubMed]
  38. Ikehara, S.; Iso, H.; Yamagishi, K.; Kokubo, Y.; Saito, I.; Yatsuya, H.; Inoue, M.; Tsugane, S. Alcohol consumption and risk of stroke and coronary heart disease among Japanese women: The Japan Public Health Center-based prospective study. Prev. Med. 2013, 57, 505–510. [Google Scholar] [CrossRef] [PubMed]
  39. Mukamal, K.J.; Chiuve, S.E.; Rimm, E.B. Alcohol consumption and risk for coronary heart disease in men with healthy lifestyles. Arch. Intern. Med. 2006, 166, 2145–2150. [Google Scholar] [CrossRef] [PubMed]
  40. Keil, U.; Chambless, L.E.; Doring, A.; Filipiak, B.; Stieber, J. The relation of alcohol intake to coronary heart disease and all-cause mortality in a beer-drinking population. Epidemiology 1997, 8, 150–156. [Google Scholar] [CrossRef] [PubMed]
  41. Kono, S.; Handa, K.; Kawano, T.; Hiroki, T.; Ishihara, Y.; Arakawa, K. Alcohol intake and nonfatal acute myocardial infarction in Japan. Am. J. Cardiol. 1991, 68, 1011–1014. [Google Scholar] [CrossRef]
  42. Schroder, H.; Masabeu, A.; Marti, M.J.; Cols, M.; Lisbona, J.M.; Romagosa, C.; Carión, T.; Vilert, E.; Marrugat, J. Myocardial infarction and alcohol consumption: A population-based case-control study. Nutr. Metab. Cardiovasc. Dis. 2007, 7, 609–615. [Google Scholar] [CrossRef] [PubMed]
  43. Wells, S.; Broad, J.; Jackson, R. Alcohol consumption and its contribution to the burden of coronary heart disease in middle-aged and older New Zealanders: A population-based case-control study. N. Z. Med. J. 2004, 117, 793. [Google Scholar]
  44. Kitamura, A.; Iso, H.; Sankai, T.; Naito, Y.; Sato, S.; Kiyama, M.; Okamura, T.; Nakagawa, Y.; Iida, M.; Shimamoto, Y.; et al. Alcohol intake and premature coronary heart disease in urban Japanese men. Am. J. Epidemiol. 1998, 147, 59–65. [Google Scholar] [CrossRef] [PubMed]
  45. Mukamal, K.J.; Chung, H.; Jenny, N.S.; Kuller, L.H.; Longstreth, W.T.; Mittleman, M.A.; Burke, G.L.; Cushman, M.; Psaty, B.M.; Siscovick, D.S. Alcohol consumption and risk of coronary heart disease in older adults: The Cardiovascular Health Study. J. Am. Geriatr. Soc. 2006, 54, 30–37. [Google Scholar] [CrossRef] [PubMed]
  46. Solomon, C.G.; Hu, F.B.; Stampfer, M.J.; Colditz, G.A.; Speizer, F.E.; Rimm, E.B.; Willett, W.C.; Manson, J.E. Moderate alcohol consumption and risk of coronary heart disease among women with type 2 diabetes mellitus. Circulation 2000, 102, 494–499. [Google Scholar] [CrossRef] [PubMed]
  47. Bazzano, L.A.; Gu, D.; Reynolds, K.; Chen, J.; Wu, X.; Chen, C.S.; Duan, X.; Chen, J.; He, J. Alcohol consumption and risk of coronary heart disease among Chinese men. Int. J. Cardiol. 2009, 135, 78–85. [Google Scholar] [CrossRef] [PubMed]
  48. Hvidtfeldt, U.A.; Tolstrup, J.S.; Jakobsen, M.U.; Heitmann, B.L.; Grønbaek, M.; O'Reilly, E.; Bälter, K.; Goldbourt, U.; Hallmans, G.; Knekt, P.; et al. Alcohol intake and risk of coronary heart disease in younger, middle-aged, and older adults. Circulation 2010, 121, 1589–1597. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  49. Rajpathak, S.N.; Freiberg, M.S.; Wang, C.; Wylie-Rosett, J.; Wildman, R.P.; Rohan, T.E.; Robinson, J.G.; Liu, S.; Wassertheil-Smoller, S. Alcohol consumption and the risk of coronary heart disease in postmenopausal women with diabetes: Women’s Health Initiative Observational Study. Eur. J. Nutr. 2010, 49, 211–218. [Google Scholar] [CrossRef] [PubMed]
  50. Hou, L.; Li, F.; Wang, Y.; Ou, Z.; Xu, D.; Tan, W.; Dai, A. Association between dietary patterns and coronary heart disease: A meta-analysis of prospective cohort studies. Int. J. Clin. Exp. Med. 2015, 8, 781–790. [Google Scholar] [PubMed]
  51. Li, F.; Hou, L.N.; Chen, W.; Chen, P.L.; Lei, C.Y.; Wei, Q.; Tan, W.L.; Zheng, S.B. Associations of dietary patterns with the risk of all-cause, CVD and stroke mortality: A meta-analysis of prospective cohort studies. Br. J. Nutr. 2014, 113, 16–24. [Google Scholar] [CrossRef] [PubMed]
  52. Dauchet, L.; Amouyel, P.; Hercberg, S.; Dallongeville, J. Fruit and vegetable consumption and risk of coronary heart disease: A meta-analysis of cohort studies. J. Nutr. 2006, 136, 2588–2593. [Google Scholar] [PubMed]
  53. Clarke, R. Lowering blood homocysteine with folic acid based supplements: Meta-analysis of randomized trials. Indian Heart J. 2000, 52 (Suppl. S7), S59–S64. [Google Scholar] [PubMed]
  54. Elkelboom, J.W.; Lonn, E.; Genest, J., Jr.; Hankey, G.; Yusuf, S. Homocysteine and cardiovascular disease: A critical review of the epidemiologic evidence. Ann. Intern. Med. 1999, 131, 363–375. [Google Scholar] [CrossRef]
  55. Pereira, M.A.; O’ Reilly, E.; Augustsson, K.; Fraser, G.E.; Goldbourt, U.; Heitmann, B.L.; Hallmans, G.; Knekt, P.; Liu, S.; Pietinen, P.; et al. Dietary fiber and risk of coronary heart disease: A pooled analysis of cohort studies. Arch. Intern. Med. 2004, 164, 370–376. [Google Scholar] [CrossRef] [PubMed]
  56. Wu, Y.; Qian, Y.; Pan, Y.; Li, P.; Yang, J.; Ye, X.; Xu, G. Association between dietary fiber intake and risk of coronary heart disease: A meta-analysis. Clin. Nutr. 2015, 34, 603–611. [Google Scholar] [CrossRef] [PubMed]
  57. Van Duyn, M.A.; Pivonka, E. Overview of the health benefits of fruit and vegetable consumption for the dietetics professional: Selected literature. J. Am. Diet. Assoc. 2000, 10, 1511–1521. [Google Scholar] [CrossRef]
  58. Bazzano, L.A.; Serdual, M.K.; Liu, S. Dietary intake of fruits and vegetables and risk of cardiovascular disease. Curr. Atheroscler. Rep. 2003, 5, 492–499. [Google Scholar] [CrossRef] [PubMed]
  59. Steffen, L.M.; Kroenke, C.H.; Yu, X.; Pereira, M.A.; Slattery, M.L.; Van Horn, L.; Gross, M.D.; Jacobs, D.R., Jr.; et al. Associations of plant food, dairy product, and meat intakes with 15-y incidence of elevated blood pressure in young black and white adults: The Coronary Artery Risk Development in Young Adults (CARDIA) Study. Am. J. Clin. Nutr. 2005, 82, 1169–1177. [Google Scholar] [PubMed]
  60. Lakshmi, V.M.; Schut, H.A.; Zenser, T.V. 2-Nitrosoamino-3-methylimidazo [4,5-f] quinoline activated by the inflammatory response forms nucleotide adducts. Food Chem. Toxicol. 2005, 43, 1607–1617. [Google Scholar] [CrossRef] [PubMed]
  61. Bogen, K.T.; Keating, G.A. U.S. dietary exposures to heterocyclic amines. J. Expo. Anal. Environ. Epidemiol. 2001, 11, 155–168. [Google Scholar] [CrossRef] [PubMed]
  62. He, F.J.; MacGregor, G.A. Effect of modest salt reduction on blood pressure: A meta-analysis ofrandomized trials. Implications for public health. J. Hum. Hypertens. 2002, 16, 761–770. [Google Scholar] [CrossRef] [PubMed]
  63. Rimm, E.B.; Williams, P.; Fosher, K.; Criqui, M.; Stampfer, M.J. Moderate alcohol intake and lower risk of coronary heart disease: Meta-analysis of effects on lipids and haemostatic factors. BMJ 1999, 319, 1523–1528. [Google Scholar] [CrossRef] [PubMed]
  64. Castelli, W.P.; Doyle, J.T.; Gordon, T.; Hames, C.G.; Hjortland, M.C.; Hulley, S.B.; Kagan, A.; Zukel, W.J. Alcohol and blood lipids. The Cooperative Lipoprotein Phenotyping Study. Lancet 1977, 2, 153–155. [Google Scholar] [CrossRef]
  65. Hulley, S.B.; Gordon, S. Alcohol and high-density lipoprotein cholesterol: Causal inference from diverse study designs. Circulation 1981, 64, 57–63. [Google Scholar]
  66. Moncada, S.; Randomski, N.W. The problems and the promise of prostaglandin influences in atherogenesis. Ann. N. Y. Acad. Sci. 1985, 454, 121–130. [Google Scholar] [CrossRef] [PubMed]
  67. Lazarus, R.; Sparrow, D.; Weiss, S.T. Alcohol intake and insulin levels: The Normative Aging Study. Am. J. Epidemiol. 1997, 145, 909–916. [Google Scholar] [CrossRef] [PubMed]

Share and Cite

MDPI and ACS Style

Zhang, X.-Y.; Shu, L.; Si, C.-J.; Yu, X.-L.; Liao, D.; Gao, W.; Zhang, L.; Zheng, P.-F. Dietary Patterns, Alcohol Consumption and Risk of Coronary Heart Disease in Adults: A Meta-Analysis. Nutrients 2015, 7, 6582-6605. https://0-doi-org.brum.beds.ac.uk/10.3390/nu7085300

AMA Style

Zhang X-Y, Shu L, Si C-J, Yu X-L, Liao D, Gao W, Zhang L, Zheng P-F. Dietary Patterns, Alcohol Consumption and Risk of Coronary Heart Disease in Adults: A Meta-Analysis. Nutrients. 2015; 7(8):6582-6605. https://0-doi-org.brum.beds.ac.uk/10.3390/nu7085300

Chicago/Turabian Style

Zhang, Xiao-Yan, Long Shu, Cai-Juan Si, Xiao-Long Yu, Dan Liao, Wei Gao, Lun Zhang, and Pei-Fen Zheng. 2015. "Dietary Patterns, Alcohol Consumption and Risk of Coronary Heart Disease in Adults: A Meta-Analysis" Nutrients 7, no. 8: 6582-6605. https://0-doi-org.brum.beds.ac.uk/10.3390/nu7085300

Article Metrics

Back to TopTop