Skip to main content
PLOS ONE logoLink to PLOS ONE
. 2014 Mar 26;9(3):e92609. doi: 10.1371/journal.pone.0092609

Comparison of Vegetarian Diets and Omnivorous Diets on Plasma Level of HDL-c: A Meta-Analysis

Zili Zhang 1,#, Jian Wang 1,#, Sifan Chen 2, Zhaoyu Wei 3, Zhengtu Li 1, Siwen Zhao 4, Wenju Lu 1,*
Editor: Alberico Catapano5
PMCID: PMC3966789  PMID: 24671216

Abstract

Low plasma level of high density lipoprotein cholesterol (HDL-c) was an independent risk factor for cardio vascular disorder, and associated with poor outcomes in pulmonary arterial hypertension. To compare the effects of vegetarian diets and omnivorous diets on HDL-c in plasma, we identified cross-sectional and cohort studies related to HDL-c listed on PubMed and ISI Web of Knowledge as well as the corresponding references (until Nov, 2013). Twelve studies with a total of 4177 individuals were selected for meta-analysis. This meta-analysis indicates that vegetarian diets did not alter plasma HDL-c concentrations, as it wasn’t initially expected by the authors [Standardized Mean Difference (SMD) = 0.02 mmol/l; 95% confidence interval (CI): −0.19 to 0.22 mmol/l]. In Asia and Latin America countries, no significant differences in HDL-c levels between vegetarians and omnivores were found (SMD = −0.09 mmol/l; 95% CI: −0.43 to 0.25 mmol/l). In Europe and North America countries, the plasma level of HDL-c was also not different between the two diets (SMD = 0.09 mmol/l; 95% CI: −0.19 to 0.36 mmol/l). In light of this meta-analysis, we conclude that there is no evidence that plasma HDL-c levels differs in vegetarians and omnivores, even after adjusting for cultural circumstances.

Introduction

Dyslipidemia is a condition often associated with coronary heart diseases, peripheral vascular diseases, atherosclerosis, and stroke [1][3]. It is a common public health problem worldwide, and imposes a significant demand on medical care and health services because of its high prevalence in the general population. In United States of America, dyslipidemia and its related diseases account for over 885,000 deaths and $634.2 billion in related costs annually [4]. Compared to omnivorous subjects, vegetarians have diminished risk of developing dyslipidemia. This may be due to their lower saturated fats consumption and higher fiber intake, which results in a reduction in the concentration of low density lipoprotein cholesterol (LDL-c), a major cardiovascular disease risk factor [5]. Greater fruits, nuts, and cereals consumption may also contribute to atherosclerosis prevention by increasing the intake of anti-oxidants, vitamins, and micronutrients [6]. Moreover, a recently study when vegans were compared to omnivorous subjects also shown functional aspects of high density lipoprotein (HDL) and defective chylomicron removal and VLDL (very low-density lipoprotein) remnants from the plasma may be affected by dietary habits [7]. It is said that high triglyceride (TG), low LDL-c, and low HDL-c levels are predictive for the increased risk of dyslipidemia and are considered to be the major risk factors, followed by smoking and high blood pressure [8][10]. Especially, it was estimated that 11% of the US men had low HDL-c levels [11]. At present, the clinical management of dyslipidemia risk involves targeting multiple risk factors to achieve the maximum decrease in risk and HDL-c has been an important target for intervention efforts. HDL is responsible for reverse transportation of cholesterol, carrying basically the cholesterol from tissues to the liver. It has been known for quite a long time that the plasma concentration of HDL-c correlated inversely with the incidence of cardio vascular disorder (CVD) and coronary heart disease (CHD) and that low HDL-c was an independent CVD risk factor (particularly when HDL-c <1.0344 mmol/l) [8], [12], [13]. According to the Vahit Study, a 1 mg/dl HDL reduction results in 3%−4% increase in coronary artery disease (CAD) prevalence. It is now a common practice to measure HDL-c level [13] and compute the ratio of LDL-c to HDL-c or the cholesterol to HDL-c for a better assessment of CHD risk [14]. Importantly, a recent study demonstrated that low plasma level of HDL-c was associated with higher mortality and clinical worsening in pulmonary arterial hypertension patients [15].

Nowadays, with the development of society and economy, specialists began to pay much attention to the relationship of different diets and plasma cholesterol levels. In this study, vegetarian diets and omnivorous diets have been considered, and we wanted to compare whether there is a difference in HDL-c concentrations between the two kinds of diets. In view of conflicting results and the limited sample sizes in individual studies, we performed a meta-analysis for this comparison. In addition, stratified analysis was made by some cultural similarities in order to find whether different cultural background represents a factor influencing the plasma level of HDL-c.

Methods

Literature Search

A systematic search of the literature was carried out by using Pub Med and ISI Web of Knowledge resources (until Nov, 2013). The keywords used for the search included “lacto” or “vegetarian” or “non meat eaters” or “omnivorous diet” or “omnivores” or “meat- eating” or “no vegetarian” concatenated with “blood lipid levels” or “plasma lipids” or “HDL-c” or “plasma lipoproteins”. Two reviewers firstly identified eligible articles by the abstracts available. Then, if the abstract met the inclusion criteria, the full article text was obtained ( Figure 1 ).

Figure 1. Results of search for eligible studies.

Figure 1

Study Selection

Full articles were obtained if they met the following inclusion criteria: 1) published in English and on humans; 2) adult humans ≥18 years of age, free-living people, and all volunteers have been on the diets for more than 2 months; 3) control groups included; 4) one or more of the following lipids and lipoproteins assessed: HDL-c, TC, LDL-c, and TG. In addition, subject group characteristics, sex, age, BMI, sample size, location, recruitment procedure, and classifying information should be included. We found 12 studies that were consistent with our inclusion criteria ( Table 1 ). Discarded citations included reviews, insufficient detail on classification, and other descriptive or intervention studies.

Table 1. Characteristics of literatures included in the meta-analysis and observational studies evaluating the effects of diets in HDL (mmol/l)1.

Study Country Cultural2 Design3 Median BMI Vegetarians Omnivores Weight
age Vegetarians Omnivores No. ofsubjects Mean±SD No. ofsubjects Mean±SD (%)
Thorogood et al. (1987) UK Euro-Amer Cohort 38.2 1550 1.50±1.36 1198 1.49±1.20 12.0
Alexander et al. (1999) USA Euro-Amer Cross 44.0 27.2±5.2 31.4±7.4 74 1.15±0.27 45 1.03±0.26 8.7
Krajcovicova et al. (2000) Slovak Euro-Amer Cross 48.0 22.8±1.5 24.2±2.3 54 1.42±0.15 59 1.31±0.23 8.7
Li et al. (2001) Australia Euro-Amer Cross 37.5 23.6±2.8 26.4±3.4 43 1.03±0.24 60 1.09±0.25 8.4
Hoffmann et al. (2001) Germany Euro-Amer Cross 45.0 111 1.66±0.43 138 1.50±0.30 10.3
Robinson et al. (2002) UK Euro-Amer Cross 30.0 24.7±5.2 24.7±5.2 43 1.21±0.33 43 1.47±0.47 7.9
Teixeira Rde et al. (2007) Brazil Asia-Latin Cross 49.5 22.6±3.1 26.7±5.1 67 1.17±0.26 134 1.18±0.31 9.8
De Biase et al. (2007) Brazil Asia-Latin Cross 35.8 23.5±4.5 25.4±5.2 19 1.43±0.38 22 1.45±0.47 5.8
Papadaki et al. (2008) Greece Euro-Amer Cross 45.0 30.8±4.3 31.3±4.6 10 1.01±0.21 10 1.07±0.24 3.8
Chen et al. (2010) China Asia-Latin Cross 52.0 22.9±2.9 23.3±3.5 173 1.44±0.34 190 1.61±0.38 10.8
K. Femandes et al. (2011) Brazil Asia-Latin Cross 40.0 24.0±3.6 24.4±3.6 29 1.15±0.32 58 1.04±0.19 7.7
C. Juliana et al. (2013) Brazil Asia-Latin Cross 37.0 23.0±1.6 23.5±1.2 18 1.09±0.20 29 1.16±0.31 6.1
1

Data were expressed as Mean ± SD; To convert from mg/dl to mmol/L, multiply by 0.02586;

2

Euro-Amer (Europe and North America): UK, USA, Slovak, Australia, Germany, and Greece; Asia-Latin (Asia and Latin America): Brazil and China.

3

Cross: cross-sectional studies; Cohort: cohort studies.

Data Extraction

Two investigators independently extracted data and reached a consensus on all of the items. After the initial search procedures were completed, remaining citations were examined to determine whether they met the inclusion criteria. For articles that met the criteria, the following information was collected: country of origin of author, year of publication, country of origin of subjects, selection and characteristics of each diet group, demographics, and the mean HDL-c levels of a group of subjects while on that diet. Nutrient intake did not change within a study; any drift in the HDL-c level with time occurred simultaneously in both diet groups and therefore did not affect the differences in final levels.

Data Synthesis and Analysis

The strength of the association of HDL-c levels in different diets was measured as followed: Mean ± SDs (mmol/l) with 95% CI and % weight for all trials. To convert from mg/dl to mmol/l, multiply by 0.02586. Stratified analyses were also performed by some cultural similarities. A statistical test for heterogeneity was performed based on the Q-test [16] ( Figure 2 ), a P value greater than 0.05 indicates a lack of heterogeneity among studies. The summary SMD (Standardized Mean Difference) estimate was calculated by the random-effects model (the Der Simonian and Laird method was used) [17]. Funnel plots and Egger’s linear regression test were used to provide diagnosis of the potential publication bias [17] (Figure S1; Figure S2). Sensitivity analyses were performed to assess the stability of the results ( Figure 3 ). All analyses were done with Stata software (version 10.0; StataCorp LP, College Station, TX), using two-sided P values.

Figure 2. Forest plot of HDL-c levels among different diets.

Figure 2

The squares and horizontal lines correspond to the study-specific SMD and 95% CI. The area of the squares reflects the study-specific weight (inverse of the variance). The diamond represents the pooled SMD and 95% CI. % weighted for random-effects.

Figure 3. Sensitivity analyses of 12 studies, the part between two short lines shows the 95% CI of one study, each small circle indicates mean differences.

Figure 3

Results

Results of the Literature Search

In the initial stage, 612 studies were included, of which 415 were excluded on the basis of screening using inclusion and discarded criteria. The remaining 197 abstracts were reviewed, and full reports were evaluated, of which 22 potentially relevant articles were included. Of the remaining studies, 10 additional studies were excluded, of these 12 trials published all-year time span that met specific inclusion criteria after a close examination ( Figure 1 ). Reports were excluded because age did not accord with, they did not report HDL-c levels, did not detail on classification, did not report human studies, and were not in English or English translations were unavailable. These studies included 4177 individuals, 2191 vegetarians and 1986 omnivores. The reviews were all observational studies (including cross-sectional studies and cohort studies).

Study Characteristics

We identified 12 trials with 4177 individuals [5], [18][28]. Two types of diets were considered, and there were vegetarian diets and omnivorous diets. Vegetarians were classified as lacto-ovo vegetarians (people who consume eggs, milk, and dairy products), lacto-vegetarians (people who consume milk and dairy products, but not eggs), and ovo-vegetarians (people who consume eggs, but not milk or dairy products). Vegetarians consume no meat, or no more than six times per year, and they had to have been practicing their diets for more than 2 months prior to the study [29]. They have been recruited from the Vegetarian Society, Seventh-Day Adventist Churches, Adventist Seminary Institute, and monasteries. Omnivores were defined as people who eat food of both plant and animal origin [5]. They were from the surrounding communities, friends, relatives of vegetarians, and healthy public-service personnel or the Oxford arm of the European Prospective Investigation into Cancer and Nutrition (EPIC-Oxford) through advertisements, radio, posters, and others. In the present study, all volunteers ranged from 30 to 52 years old, without family history of overt vascular diseases (such as myocardial infarction, cerebrovascular, and angina etc), hyperlipoproteinemia, dyslipidemia, and related diseases.

Effect of Vegetarian Diets and Omnivorous Diets on HDL-c Profile

In our study, the baseline characteristics of two groups were almost similar (Table1). Results of this meta-analysis suggested that individuals consuming vegetarian diets, as a group, had the same HDL-c level as omnivores ( Figure 2 ) (SMD = 0.02 mmol/l; 95% CI: −0.19 to 0.22 mmol/l). We assessed the association of plasma HDL-c levels between vegetarian and omnivores which stratified by some cultural similarities. In Asia and Latin America countries, it was suggested that there was no significant difference in plasma HDL-c level between vegetarians and omnivores (SMD = −0.09 mmol/l; 95% CI: −0.43 to 0.25 mmol/l), and in Europe and North America countries, the phenomenon was also consistent between the two diets (SMD = 0.09 mmol/l; 95% CI: −0.19 to 0.36 mmol/l). In light of this meta-analysis, we conclude that there is no evidence that plasma HDL-c levels differs in vegetarians and omnivores, even after adjusting for cultural circumstances.

Furthermore, we found no evidence of publication bias, and there was a good of heterogeneity among studies. However, there was a modest degree of sensitivity analyses because of two studies deviating a little far from SMD [23], [25], and they were kept for having no influence on heterogeneity (Figure S1 and Figure S2). Differences in response between men and women were not all reported in the 12 studies, and therefore were not considered in the present report. But the present study’s results were almost applicable to both sexes, because there was no heterogeneity between them. Only 2 original studies [20], [30] excluded for gender classification, 2 references were studies of women [21], [31] and 1 of men [25], but there was an almost equal number of men or women in the two groups (in vegetarian group men and women were 673 and 1348, respectively; and in omnivores were 687 and 1016, respectively).

Discussion

The present meta-analysis study provides evidence indicating that there was no significant difference in HDL-c levels between vegetarians and omnivores. Moreover, stratified analyses performed by cultural similarities also revealed that the plasma HDL-c levels were constant regardless of cultural circumstances. These results were against to our original expectation.

Initially, we hypothesized that omnivores consuming excess animal protein and saturated fatty acid had unbalanced diet and low HDL-c level, which was consistent with the notion of that omnivorous diets was associated with higher incidence of chronic cardiovascular diseases. However, based on the data produced in our meta-analysis study, the lack of meat in the diet seems not providing advantages to the vegetarians. In the included individual studies, because the only criteria to differentiate vegetarian and omnivore was meat consumption, the consumption of other animal products was ignored. As a mater of fact, majority of the vegetarians also consumes eggs, milk, and other dairies, and perhaps in larger amounts, thus reducing the contrast with omnivores. Egg yolk is one of the greatest cholesterol-containing foodstuffs; whereas milk and dairy products importantly contribute to the high saturated fat and also cholesterol content of the daily food intake. Omnivores usually take more proportion of lean meat instead of fat meat as their food; the lean meat itself does not increase plasma cholesterol levels [32][34]. Alcohol also increases HDL-c concentration and perhaps omnivores tend to consume more alcohol than vegetarians [35], [36]. In addition, vegetarians tend to take lower saturated fat and higher polyunsaturated fat than omnivores. Meta-analyses of metabolic ward studies [37] and controlled dietary trials [38] have revealed that saturated fat increases HDL-c, and so does polyunsaturated fat, although to a lesser extent. So, it is difficult to predict HDL-c level simply based on different diet groups. Consistently, previous reports [39], [40] also showed that diet and exercise interventions have no significant effect on HDL-c, but do affect measurements of other types of blood lipids.

Apart from environmental factors such as lifestyle and nutrition, about 70% of the variations in plasma HDL-c levels in humans are genetically determined [41], [42]. It is widely postulated that variations in plasma HDL-c concentration are determined by both the rate at which HDL-c is produced and the rate of catabolism of HDL particles [43], [44]. There are several known molecules that play a role in regulating plasma HDL-c concentration, including hepatic lipase (HL), lecithin cholesterol acyltransferase (LCAT), cholesteryl ester transfer protein (CETP), and phospholipid transfer protein (PLTP). It is now generally accepted serum HDL-c concentrations are regulated in part by members of the lipase enzyme family, especially HL, in which loss-of-function mutations are hypothesized to result in elevated HDL-c level. The lipases have highly conserved structural domains, and these enzymes function to metabolize triglycerides and phospholipids [43], [45]. It is important in the processing of lipids carried within lipoproteins and probably also in the uptake of lipoprotein particles into cells [46]. Although synthesized in nonendothelial cells, the secreted enzymes translocate to the surface of endothelial cells, where they carry out their metabolic function.

Lastly, we realize that there are several limitations in our study: 1. In our meta-analysis, we could not obtain information from all studies on the blood pressure, weight status, insulin or diabetes conditions which were main risk factors for dyslipidemia, and lacking of those original data limited our further evaluation of potential interactions. 2. Our results were based on unadjusted estimates, while more precise analysis should be conducted if more detailed individual data were available. 3. It was difficult to quantitatively describe the foods, especially all data were self-reported. 4. It was important to distinguish the differences between vegan diets and vegetarian diets. A vegan consumed no meat, eggs, and dairy products, but the latter included dairy products and eggs in the diets, which could produce different physiological effects.

In summary, our meta-analysis indicated that vegetarians and omnivores presented almost consistent HDL-c plasma levels regardless of different cultural background. A well designed population-based study with large sample sizes, detailed exposure information, and stratification for age, sex, location, race, and BMI is warranted to validate these findings.

Supporting Information

Figure S1

Begg’s funnel plot for publication bias test. Each point represents a separate study for the indicated association SMD, standardized mean difference. Horizontal line means standard error.

(TIF)

Figure S2

Egger’s publication bias plot. Standardized effect estimates versus precision along with the regression line and the 95% CI about the intercept. Failure of this 95% CI to include zero indicates asymmetry in the funnel plot and may give evidence of publication bias. Guidelines include x = 0 and y = 0.

(TIF)

Checklist S1

PRISMA Checklist.

(DOC)

Funding Statement

This work was supported by NIH (R01-HL093020), National Natural Science Foundation of China (81070043, 81173112, 81170052, 81220108001), Guangdong Natural Science Foundation Team Grant (1035101200300000), and Guangzhou Department of Education Yangcheng Scholarship (10A058S, 12A001S). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

References

  • 1. NCEP (2001) Executive Summary of The Third Report of The National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, And Treatment of High Blood Cholesterol In Adults (Adult Treatment Panel III). JAMA 285: 2486–2497. [DOI] [PubMed] [Google Scholar]
  • 2. Rosengren A, Hagman M, Wedel H, Wilhelmsen L (1997) Serum cholesterol and long-term prognosis in middle-aged men with myocardial infarction and angina pectoris. A 16-year follow-up of the Primary Prevention Study in Goteborg, Sweden. Eur Heart J 18: 754–761. [DOI] [PubMed] [Google Scholar]
  • 3. Pekkanen J, Linn S, Heiss G, Suchindran CM, Leon A, et al. (1990) Ten-year mortality from cardiovascular disease in relation to cholesterol level among men with and without preexisting cardiovascular disease. N Engl J Med 322: 1700–1707. [DOI] [PubMed] [Google Scholar]
  • 4. Rosamond W, Flegal K, Furie K, Go A, Greenlund K, et al. (2008) Heart disease and stroke statistics–2008 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee. Circulation 117: e25–146. [DOI] [PubMed] [Google Scholar]
  • 5.Vinagre JC, Vinagre CC, Pozzi FS, Zacari CZ, Maranhao (2013) RC Plasma kinetics of chylomicron-like emulsion and lipid transfers to high-density lipoprotein (HDL) in lacto-ovo vegetarian and in omnivorous subjects. Eur J Nutr. [DOI] [PubMed]
  • 6. Craig WJ, Mangels AR (2009) Position of the American Dietetic Association: vegetarian diets. J Am Diet Assoc 109: 1266–1282. [DOI] [PubMed] [Google Scholar]
  • 7. Vinagre JC, Vinagre CG, Pozzi FS, Slywitch E, Maranhao RC (2013) Metabolism of triglyceride-rich lipoproteins and transfer of lipids to high-density lipoproteins (HDL) in vegan and omnivore subjects. Nutr Metab Cardiovasc Dis 23: 61–67. [DOI] [PubMed] [Google Scholar]
  • 8. Castelli WP, Doyle JT, Gordon T, Hames CG, Hjortland MC, et al. (1977) HDL cholesterol and other lipids in coronary heart disease. The cooperative lipoprotein phenotyping study. Circulation 55: 767–772. [DOI] [PubMed] [Google Scholar]
  • 9. Matsuzawa Y, Funahashi T, Kihara S, Shimomura I (2004) Adiponectin and metabolic syndrome. Arterioscler Thromb Vasc Biol 24: 29–33. [DOI] [PubMed] [Google Scholar]
  • 10. Zimmet P, Magliano D, Matsuzawa Y, Alberti G, Shaw J (2005) The metabolic syndrome: a global public health problem and a new definition. J Atheroscler Thromb 12: 295–300. [DOI] [PubMed] [Google Scholar]
  • 11. Harper CR, Jacobson TA (1999) New perspectives on the management of low levels of high-density lipoprotein cholesterol. Arch Intern Med 159: 1049–1057. [DOI] [PubMed] [Google Scholar]
  • 12. Grundy SM, Cleeman JI, Daniels SR, Donato KA, Eckel RH, et al. (2005) Diagnosis and management of the metabolic syndrome: an American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement. Circulation 112: 2735–2752. [DOI] [PubMed] [Google Scholar]
  • 13. Gordon T, Castelli WP, Hjortland MC, Kannel WB, Dawber TR (1977) High density lipoprotein as a protective factor against coronary heart disease. The Framingham Study. Am J Med 62: 707–714. [DOI] [PubMed] [Google Scholar]
  • 14. Assmann G, Cullen P, Jossa F, Lewis B, Mancini M (1999) Coronary heart disease: reducing the risk: the scientific background to primary and secondary prevention of coronary heart disease. A worldwide view. International Task force for the Prevention of Coronary Heart disease. Arterioscler Thromb Vasc Biol 19: 1819–1824. [DOI] [PubMed] [Google Scholar]
  • 15. Heresi GA, Aytekin M, Newman J, DiDonato J, Dweik RA (2010) Plasma levels of high-density lipoprotein cholesterol and outcomes in pulmonary arterial hypertension. Am J Respir Crit Care Med 182: 661–668. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16. DerSimonian R, Laird N (1986) Meta-analysis in clinical trials. Control Clin Trials 7: 177–188. [DOI] [PubMed] [Google Scholar]
  • 17. Egger M, Davey Smith G, Schneider M, Minder C (1997) Bias in meta-analysis detected by a simple, graphical test. BMJ 315: 629–634. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18. Li D, Sinclair A, Mann N, Turner A, Ball M, et al. (1999) The association of diet and thrombotic risk factors in healthy male vegetarians and meat-eaters. Eur J Clin Nutr 53: 612–619. [DOI] [PubMed] [Google Scholar]
  • 19. Robinson F, Hackett AF, Billington D, Stratton G (2002) Changing from a mixed to self-selected vegetarian diet–influence on blood lipids. J Hum Nutr Diet 15: 323–329. [DOI] [PubMed] [Google Scholar]
  • 20. Teixeira Rde C, Molina Mdel C, Zandonade E, Mill JG (2007) Cardiovascular risk in vegetarians and omnivores: a comparative study. Arq Bras Cardiol 89: 237–244. [DOI] [PubMed] [Google Scholar]
  • 21. Papadaki A, Vardavas C, Hatzis C, Kafatos A (2008) Calcium, nutrient and food intake of Greek Orthodox Christian monks during a fasting and non-fasting week. Public Health Nutr 11: 1022–1029. [DOI] [PubMed] [Google Scholar]
  • 22. De Biase SG, Fernandes SF, Gianini RJ, Duarte JL (2007) Vegetarian diet and cholesterol and triglycerides levels. Arq Bras Cardiol 88: 35–39. [DOI] [PubMed] [Google Scholar]
  • 23. Krajcovicova M, Blazicek P, Babinska K, Kopcova J, Klvanova J, et al. (2000) Traditional and alternative nutrition–levels of homocysteine and lipid parameters in adults. Scand J Clin Lab Invest 60: 657–664. [DOI] [PubMed] [Google Scholar]
  • 24. Alexander H, Lockwood LP, Harris MA, Melby CL (1999) Risk factors for cardiovascular disease and diabetes in two groups of Hispanic Americans with differing dietary habits. J Am Coll Nutr 18: 127–136. [DOI] [PubMed] [Google Scholar]
  • 25. Hoffmann I, Groeneveld MJ, Boeing H, Koebnick C, Golf S, et al. (2001) Giessen Wholesome Nutrition Study: relation between a health-conscious diet and blood lipids. Eur J Clin Nutr 55: 887–895. [DOI] [PubMed] [Google Scholar]
  • 26. Thorogood M, Carter R, Benfield L, McPherson K, Mann JI (1987) Plasma lipids and lipoprotein cholesterol concentrations in people with different diets in Britain. Br Med J (Clin Res Ed) 295: 351–353. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27. Fernandes Dourado K, de Arruda Camara ESCF, Sakugava Shinohara NK (2011) Relation between dietary and circulating lipids in lacto-ovo vegetarians. Nutr Hosp 26: 959–964. [DOI] [PubMed] [Google Scholar]
  • 28. Chen CW, Lin CT, Lin YL, Lin TK, Lin CL (2011) Taiwanese female vegetarians have lower lipoprotein-associated phospholipase A2 compared with omnivores. Yonsei Med J 52: 13–19. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29. Barnard ND, Scialli AR, Bertron P, Hurlock D, Edmonds K, et al. (2000) Effectiveness of a low-fat vegetarian diet in altering serum lipids in healthy premenopausal women. Am J Cardiol 85: 969–972. [DOI] [PubMed] [Google Scholar]
  • 30. Famodu AA, Osilesi O, Makinde YO, Osonuga OA (1998) Blood pressure and blood lipid levels among vegetarian, semi-vegetarian, and non-vegetarian native Africans. Clin Biochem 31: 545–549. [DOI] [PubMed] [Google Scholar]
  • 31. Li D (2001) Relationship between the concentrations of plasma phospholipid stearic acid and plasma lipoprotein lipids in healthy men. Clin Sci (Lond) 100: 25–32. [PubMed] [Google Scholar]
  • 32. Watts GF, Ahmed W, Quiney J, Houlston R, Jackson P, et al. (1988) Effective lipid lowering diets including lean meat. Br Med J (Clin Res Ed) 296: 235–237. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33. Sinclair AJ, O’Dea K, Dunstan G, Ireland PD, Niall M (1987) Effects on plasma lipids and fatty acid composition of very low fat diets enriched with fish or kangaroo meat. Lipids 22: 523–529. [DOI] [PubMed] [Google Scholar]
  • 34. Scott LW, Dunn JK, Pownall HJ, Brauchi DJ, McMann MC, et al. (1994) Effects of beef and chicken consumption on plasma lipid levels in hypercholesterolemic men. Arch Intern Med 154: 1261–1267. [PubMed] [Google Scholar]
  • 35. Baer DJ, Judd JT, Clevidence BA, Muesing RA, Campbell WS, et al. (2002) Moderate alcohol consumption lowers risk factors for cardiovascular disease in postmenopausal women fed a controlled diet. Am J Clin Nutr 75: 593–599. [DOI] [PubMed] [Google Scholar]
  • 36. van der Gaag MS, van Tol A, Vermunt SH, Scheek LM, Schaafsma G, et al. (2001) Alcohol consumption stimulates early steps in reverse cholesterol transport. J Lipid Res 42: 2077–2083. [PubMed] [Google Scholar]
  • 37. Clarke R, Frost C, Collins R, Appleby P, Peto R (1997) Dietary lipids and blood cholesterol: quantitative meta-analysis of metabolic ward studies. BMJ 314: 112–117. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38. Mensink RP, Zock PL, Kester AD, Katan MB (2003) Effects of dietary fatty acids and carbohydrates on the ratio of serum total to HDL cholesterol and on serum lipids and apolipoproteins: a meta-analysis of 60 controlled trials. Am J Clin Nutr 77: 1146–1155. [DOI] [PubMed] [Google Scholar]
  • 39. Kelley GA, Kelley KS, Roberts S, Haskell W (2012) Comparison of aerobic exercise, diet or both on lipids and lipoproteins in adults: a meta-analysis of randomized controlled trials. Clin Nutr 31: 156–167. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40. Yoshikawa H, Takeyama H, Nishiwaki H, Kamiya T, Yamada K (1976) [A case of leukemic reticulosis, myelogenous type with consumption coagulopathy and mediastinal tumor involving the thymus (author’s transl)]. Rinsho Ketsueki 17: 553–561. [PubMed] [Google Scholar]
  • 41. Heller DA, de Faire U, Pedersen NL, Dahlen G, McClearn GE (1993) Genetic and environmental influences on serum lipid levels in twins. N Engl J Med 328: 1150–1156. [DOI] [PubMed] [Google Scholar]
  • 42. Hamsten A, Iselius L, Dahlen G, de Faire U (1986) Genetic and cultural inheritance of serum lipids, low and high density lipoprotein cholesterol and serum apolipoproteins A-I, A-II and B. Atherosclerosis. 60: 199–208. [DOI] [PubMed] [Google Scholar]
  • 43. Qin S, Kawano K, Bruce C, Lin M, Bisgaier C, et al. (2000) Phospholipid transfer protein gene knock-out mice have low high density lipoprotein levels, due to hypercatabolism, and accumulate apoA-IV-rich lamellar lipoproteins. J Lipid Res 41: 269–276. [PubMed] [Google Scholar]
  • 44. Rader DJ, Ikewaki K (1996) Unravelling high density lipoprotein-apolipoprotein metabolism in human mutants and animal models. Curr Opin Lipidol 7: 117–123. [DOI] [PubMed] [Google Scholar]
  • 45. McCoy MG, Sun GS, Marchadier D, Maugeais C, Glick JM, et al. (2002) Characterization of the lipolytic activity of endothelial lipase. J Lipid Res 43: 921–929. [PubMed] [Google Scholar]
  • 46. Choi SY, Komaromy MC, Chen J, Fong LG, Cooper AD (1994) Acceleration of uptake of LDL but not chylomicrons or chylomicron remnants by cells that secrete apoE and hepatic lipase. J Lipid Res 35: 848–859. [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Figure S1

Begg’s funnel plot for publication bias test. Each point represents a separate study for the indicated association SMD, standardized mean difference. Horizontal line means standard error.

(TIF)

Figure S2

Egger’s publication bias plot. Standardized effect estimates versus precision along with the regression line and the 95% CI about the intercept. Failure of this 95% CI to include zero indicates asymmetry in the funnel plot and may give evidence of publication bias. Guidelines include x = 0 and y = 0.

(TIF)

Checklist S1

PRISMA Checklist.

(DOC)


Articles from PLoS ONE are provided here courtesy of PLOS

RESOURCES