Dietary cholesterol from eggs increases the ratio of total cholesterol to high-density lipoprotein cholesterol in humans: a meta-analysis

¹ From the Division of Human Nutrition and Epidemiology, Wageningen University, Wageningen, Netherlands, and the Wageningen Centre for Food Sciences, Wageningen, Netherlands.

² Supported by the Netherlands Heart Foundation (grant number 95.118).

³ Reprints not available. Address correspondence to MB Katan, Division of Human Nutrition and Epidemiology, Wageningen University, Bomenweg 2, 6703 HD Wageningen, Netherlands. E-mail: martijn.katan{at}staff.nutepi.wau.nl.

ABSTRACT  
Background: Several epidemiologic studies found no effect of egg consumption on the risk of coronary heart disease. It is possible that the adverse effect of eggs on LDL-cholesterol is offset by their favorable effect on HDL cholesterol.

Objective: The objective was to review the effect of dietary cholesterol on the ratio of total to HDL cholesterol.

Design: Studies were identified by MEDLINE and Biological Abstracts searches (from 1974 to June 1999) and by reviewing reference lists. In addition, we included data from a more recently published study. Studies were included if they had a crossover or parallel design with a control group, if the experimental diets differed only in the amount of dietary cholesterol or number of eggs and were fed for 14 d, and if HDL-cholesterol concentrations were reported. Of the 222 studies identified, 17 studies involving 556 subjects met these criteria.

Results: The addition of 100 mg dietary cholesterol/d increased the ratio of total to HDL cholesterol by 0.020 units (95% CI: 0.010, 0.030), total cholesterol concentrations by 0.056 mmol/L (2.2 mg/dL) (95% CI: 0.046, 0.065 mmol/L; 1.8, 2.5 mg/dL), and HDL-cholesterol concentrations by 0.008 mmol/L (0.3 mg/dL) (95% CI: 0.005, 0.010 mmol/L; 0.2, 0.4 mg/dL).

Conclusions: Dietary cholesterol raises the ratio of total to HDL cholesterol and, therefore, adversely affects the cholesterol profile. The advice to limit cholesterol intake by reducing consumption of eggs and other cholesterol-rich foods may therefore still be valid.

Key Words: Dietary cholesterol • eggs • total cholesterol • HDL cholesterol • LDL cholesterol • meta-analysis

INTRODUCTION  
One of the dietary recommendations in the prevention of coronary heart disease is to limit egg consumption (1) because eggs have been shown to be a major source of dietary cholesterol (2). Dietary cholesterol increases serum total and LDL-cholesterol concentrations (3–7), which are established risk factors for coronary heart disease (8); however, several epidemiologic studies found no relation between egg consumption and risk of coronary heart disease (9, 10). The absence of such a relation may imply that the recommendation of lowering egg consumption is of little use in the prevention of coronary heart disease. One egg contains 200 mg/cholesterol. Although it is obvious that dietary cholesterol increases total cholesterol concentrations (3, 6, 7), several studies showed that dietary cholesterol increases not only concentrations of LDL cholesterol but also concentrations of HDL cholesterol (3, 6). Because HDL cholesterol may protect against coronary heart disease, the adverse effects of egg consumption on total and LDL-cholesterol concentrations might be attenuated by the favorable effects on HDL-cholesterol concentrations.

The ratio of total to HDL cholesterol involves the opposing effects of LDL and HDL cholesterol on coronary heart disease risk. As a result, the ratio is a better predictor of coronary heart disease risk than are individual lipoprotein concentrations (8, 11, 12). Therefore, it may be more appropriate to study the effect of dietary cholesterol on the ratio of total to HDL cholesterol than on individual lipoprotein concentrations.

We reviewed well-controlled studies to study the effect of dietary cholesterol from egg intake on the ratio of total to HDL-cholesterol concentrations in humans. We added data from an unpublished study of our own.

METHODS  
Selection of studies
We screened MEDLINE (National Library of Medicine, Bethesda, MD) from 1974 through June 1999 and Biological Abstracts from 1989 through June 1999 for experimental studies on the effects of dietary cholesterol and eggs on total cholesterol and lipoproteins. We did not screen MEDLINE before 1974 because measurements of HDL cholesterol, which were part of our main outcome measure, were not available at that time. For the literature searches, the key words egg, eggs, and dietary cholesterol were each intersected with the words serum (plasma) lipoprotein, serum (plasma) cholesterol, HDL, and LDL. We found 1190 citations in MEDLINE and 883 in Biological Abstracts. In addition, we checked the reference lists of several meta-analyses (3, 6, 7, 13, 14) and selected studies. A scan of the titles led to the selection of 221 citations. The abstracts of these citations were examined for compliance with the following inclusion criteria: 1) studies had to be published in English; 2) within a study, the composition of the experimental diets could differ only by the amount of cholesterol or the amount of eggs; 3) subjects had to be weight stable throughout the study; 4) the design had to eliminate the effect of nonspecific drifts of the outcome variable with time, which have been accomplished either by feeding different groups of volunteers different diets side by side (parallel design) or feeding each volunteer several diets in random order (crossover or Latin-square design); 5) feeding periods had to be 14 d to attain equilibrium in concentrations of total cholesterol and lipoproteins; and 6) studies had to report fasting concentrations of total cholesterol and lipoproteins. Studies with before-and-after designs or linear designs without a control group were excluded.

Of the 221 articles passing the title scan, 56 passed the abstract scan. Because most of the 56 abstracts did not provide sufficient information on the basis of our selection criteria, we checked the full text of these articles. Sixteen of the 56 articles (28%) met the inclusion criteria (15–30). Most other studies were not selected because they did not provide information on HDL-cholesterol concentrations or had a linear design without a control group. In addition to the data of these 16 studies, we used data from our own recent study on the response to egg yolk cholesterol as a function of the apolipoprotein A4 1/2 polymorphism (31) (Table 1).

View this table:
TABLE 1.. Characteristics of studies and diets and the effects of dietary cholesterol on serum cholesterol and lipoproteins¹  
The 17 selected studies yielded 24 dietary comparisons and 5 control treatments. The studies included 422 men and 134 women. Ten studies were conducted with men only, 6 included both men and women, and 1 included only women. No studies reported the race of the subjects. The age of the volunteers ranged from 18 to 75 y, mean body mass index (in kg/m²) ranged from 20.8 to 28, and mean baseline cholesterol concentration ranged from 4.06 to 5.92 mmol/L (157 to 229 mg/dL). Not all studies reported mean body mass index (15, 17–19, 22, 28) or baseline cholesterol concentration (22, 23, 27, 30). There were 11 metabolic ward studies, in which all food was provided; 5 of these studies were of free-living subjects who were provided eggs, high cholesterol products, or egg-free substitutes. The change in cholesterol intake ranged from 137 to 897 mg/d. Values for total, LDL-, and HDL-cholesterol plasma concentrations were multiplied by 1.029 to convert to serum values (32).

Statistical analysis
We subtracted the mean concentration of serum cholesterol at the end of the low-cholesterol diet from that at the end of the high-cholesterol diet to calculate the change in serum cholesterol. Six studies reported the means of individual ratios of total to HDL cholesterol (17, 20, 22, 26, 31, 33) and 4 studies reported the means of the individual ratios of HDL- to LDL-cholesterol concentrations (17, 22, 29, 31). Therefore, we used mean concentrations of total, LDL, and HDL cholesterol at the end of each diet to estimate the mean ratios of total to HDL- cholesterol and of HDL- to LDL-cholesterol concentrations. Ratios have larger variation than do individual cholesterol and lipoprotein concentrations. According to the Taylor approximation, this procedure to calculate the ratios causes an underestimation of the true ratio. The size of the underestimation is dependent on the total variation in the numerator and denominator and the correlation between the numerator (x) and denominator (y) as follows:

RESULTS  
All 17 studies reported values for total and HDL cholesterol, but 2 studies did not report values for LDL cholesterol (Table 1; 16, 21). Most studies presented comparisons of 2 diets, but 4 studies presented comparisons of 3 or 4 diets (15, 21, 24, 25). In 2 studies, various groups of subjects were studied side by side. In one study, diabetics were compared with healthy subjects (29), whereas in another study hyperlipemic subjects were compared with subjects with familial-combined hyperlipemia (30).

The ratio of total to HDL cholesterol and the concentrations of total and LDL cholesterol increased relative to control groups or treatments after an increase in dietary cholesterol in all but one of the studies, whereas HDL cholesterol concentrations increased in 19 of the 24 dietary comparisons. The ratio of HDL- to LDL-cholesterol concentrations decreased in all but one of the studies.

If we assume that one egg contains 200 mg/cholesterol (2), consuming one additional egg daily will increase the ratio of total to HDL cholesterol by 0.041 ± 0.011 units ( ± SEE), total cholesterol by 0.111 ± 0.010 mmol/L (4.3 ± 0.4 mg/dL), LDL cholesterol by 0.100 ± 0.008 mmol/L (3.9 ± 0.3 mg/dL), and HDL cholesterol by 0.016 ± 0.003 mmol/L (0.6 ± 0.1 mg/dL) (Figure 1). One additional egg daily will decrease the ratio of HDL- to LDL cholesterol by 0.011 ± 0.002 units (Table 2
View larger version (14K):
FIGURE 1. . Changes in serum LDL-cholesterol () and HDL-cholesterol () concentrations with cholesterol intake in 17 studies providing 24 dietary comparisons.

 

View this table:
TABLE 2.. Predicted changes in serum total cholesterol concentration and lipoproteins induced by a 100-mg/d increase in dietary cholesterol¹  
We then divided the studies into 2 groups: those with a polyunsaturated-to-saturated fat ratio 0.7, indicative of a background diet relatively high in saturated fat, and those with a ratio >0.7, indicative of a background diet relatively low in saturated fat. The response of LDL-cholesterol concentrations to a change in dietary cholesterol was somewhat weaker in the studies with a background diet low in saturated fat than in those with a background diet high in saturated fat (Figure 2). We estimated that each additional 100 mg dietary cholesterol would increase serum LDL cholesterol by 0.036 ± 0.004 mmol/L in the studies with a background diet low in saturated fat and by 0.061 ± 0.006 mmol/L in the studies with a background high in saturated fat (P = 0.03). The fatty acid composition of the background diet did not affect the response of HDL-cholesterol concentrations to dietary cholesterol or the ratios of total to HDL-cholesterol or of HDL- to LDL-cholesterol concentrations.

View larger version (12K):
FIGURE 2. . The effect of a change in cholesterol intake on serum LDL cholesterol in studies with a ratio of polyunsaturated to saturated fat 0.7 () and >0.7 ().

 
We did not detect publication bias as indicated by the absence of heterogeneity in funnel plots (results not shown). We checked whether our results could also be applied to other studies. For this purpose, we selected 19 articles that reported HDL-cholesterol concentrations but had failed to meet other inclusion criteria, eg, design. These 19 studies provided 33 dietary comparisons (38, 40–57). In 20 of these 33 dietary comparisons, the ratio of total to HDL-cholesterol concentrations increased, whereas in the other 13 comparisons the ratio decreased when cholesterol intake increased. Regression analysis showed that an increase of 100 mg dietary cholesterol/d increased the ratio of total to HDL cholesterol by 0.014 ± 0.003 units in these studies, whereas the ratio was increased by 0.020 units in the studies that fulfilled our selection criteria (Figure 3).

View larger version (16K):
FIGURE 3. . The effect of an increase in dietary cholesterol on the ratio of total cholesterol to HDL cholesterol in 17 studies that fulfilled the selection criteria () and 19 studies that did not fulfill our selection criteria ().

 

DISCUSSION  
Our meta-analysis of 17 trials showed that dietary cholesterol increased the ratio of total to HDL-cholesterol concentrations. The effect was highly significant (P < 0.0009) and the 95% CI was narrow. This suggests that the favorable rise in HDL cholesterol with increased cholesterol intake fails to compensate for the adverse rise in total and LDL-cholesterol concentrations and, therefore, that increased intake of dietary cholesterol may raise the risk of coronary heart disease. Our meta-analysis included men and women with a wide age range from North America (15–20, 22–25, 28, 30), Europe (26, 27, 29, 31), and South Africa (21). The narrow CIs (Table 2) indicate that, although only 24 points were assessed, the effect of dietary cholesterol on serum cholesterol and lipoproteins was repeatable in different studies and populations. The consistency of the findings among studies suggests that our conclusions are valid for much of the white populations of affluent countries. However, the absence of data on the race of subjects does not allow for a confident extrapolation to other populations.

In the present study, we used a regression model without an intercept because no change in cholesterol intake will by definition produce no change in the serum cholesterol concentration that could be attributed to dietary cholesterol. However, in those studies that alter the intake of eggs, the intake of dietary cholesterol, and of other egg components that may affect the serum cholesterol concentration, such as fat and lecithin, is changed. These factors may also affect concentrations of serum cholesterol and, thus, for such studies it may not be valid to force the regression line through the origin. To check this, we performed an analysis excluding studies that altered the intake of eggs (16, 18, 21, 28) or did not report whether the change in fat intake was adjusted for in the control diet (22, 26). This did not materially alter the results and thus we included these studies in our analysis.

Stratification of the studies for study design (crossover or Latin-square compared with parallel), setting (metabolic ward compared with free-living), or adjustment of the change in dietary cholesterol for energy intake did not materially alter the results. A high polyunsaturated-to-saturated fat ratio, indicating a background diet relatively low in saturated fat, attenuated the change in LDL-cholesterol concentration induced by an increase in dietary cholesterol. Some other studies also found that a background diet low in saturated fat attenuated the effect of dietary cholesterol on serum total cholesterol and LDL-cholesterol concentration (37, 38, 58), whereas other studies did not (15, 33, 44, 52, 59–61). In some of the latter studies the change in dietary cholesterol might have been too small to show an effect of the fat composition of the background diet on the change in serum cholesterol concentration. The polyunsaturated-to-saturated fat ratio, however, does not take into account the absolute amount of fat in a diet. Thus, a diet with 5% of energy from polyunsaturated fat and 10% of energy from saturated fat has the same ratio as a diet with 10% of energy from polyunsaturated fat and 20% of energy from saturated fat. Differences between studies in the absolute amount of fat may therefore also serve as an explanation for some of the inconsistent results.

We found no publication bias in our meta-analysis by use of funnel plots. In the studies that failed to fulfill our selection criteria, the effect of dietary cholesterol on the ratio of total to HDL cholesterol was somewhat smaller than in those included in our meta-analysis. This might be due to a lack of dietary control resulting in a large error in the amount of dietary cholesterol that was changed. This attenuates the estimated effect of dietary cholesterol on serum cholesterol concentration toward the null (62). However, it may also be due to the lack of adjustment for the change in fat intake that is induced by the change in egg consumption. Only 3 (42, 48, 51) of these 19 studies adjusted for the change in fat intake, whereas 11 of the 17 studies included in our meta-analysis accounted for the change. Nevertheless, the effect of dietary cholesterol on the ratio of total to HDL cholesterol in the studies that failed to fulfill our selection criteria leaned in the same direction as the effect in our meta-analysis. This indicates that the present results are not due to a biased selection of the studies.

Effects in hyperlipemic subjects
Cholesterol-lowering diets are usually prescribed to hyperlipemic subjects with total cholesterol concentrations >5.0 mmol/L (193 mg/dL) (63). However, the mean baseline cholesterol concentrations of subjects in the studies that fulfilled our selection criteria were <5.0 mmol/L (193 mg/dL), except for 2 studies (15, 30). The moderately hyperlipemic subjects in the study of Chenoweth et al (15) showed a 0.15- or 0.20-unit increase in the ratio of total to HDL cholesterol after an increase in dietary cholesterol, whereas the hyperlipemic subjects in the study of Knopp et al (30) showed a 0.22-unit decrease and the subjects with familial combined hyperlipemia showed a 0.21-unit decrease with an increase in dietary cholesterol of 437 mg/d. In the latter study, the percentage increase in the HDL-cholesterol concentration was larger than that in the total cholesterol concentration. The opposite effect between the studies may have been a chance finding due to the large day-to-day variation in cholesterol concentrations. The additional analysis with studies that failed to fulfill our selection criteria included 5 studies with mostly moderately hyperlipemic subjects (41, 52, 53, 55, 56). Because of the limited number of studies, we could not analyze these studies separately. Nevertheless, the results of these studies did not clearly differ from those in subjects with normal cholesterol concentrations. Therefore, the results of the present meta-analysis appear also to be applicable to hyperlipemic subjects.

Effects on total cholesterol and LDL-cholesterol concentrations
The estimated change in total cholesterol was 0.056 mmol/L (2.2 mg/dL) for each 100-mg/d increase in dietary cholesterol. The predicted change is somewhat smaller than the change of 0.064 mmol total cholesterol/L predicted by the formula of Keys and Parlin (5) assuming a change in dietary cholesterol from 300 to 400 mg/d and is considerably smaller than the change of 0.175 mmol total cholesterol/L predicted by the formula of Hegsted et al (4), but agrees well with changes estimated from more recent meta-analyses (3, 6, 7, 14). It is suggested that a simple linear model may predict group mean changes in LDL-cholesterol concentrations rather well over the normal range of dietary cholesterol intakes, as shown in Figure 1. Because diet-induced changes in total cholesterol and lipoproteins vary considerably between individuals (42, 64, 65), our results cannot reliably predict changes in total cholesterol and lipoproteins in individual subjects or patients.

Dietary cholesterol and risk of coronary heart disease
We showed that consuming one additional egg daily will increase the ratio of total to HDL-cholesterol concentrations by 0.040 units, which would imply an increase in the risk of myocardial infarction of 2.1% (11). The calculated increase in risk may be small in an individual patient, but in view of the widespread consumption of diets high in cholesterol it may be substantial at the population level.

Of course, these calculations do not take into account the effects of other nutrients in eggs that may be beneficial in preventing coronary heart disease, eg, vitamin E, folate, other B vitamins, and unsaturated fatty acids (2). Hu et al (10) calculated that in the United States, eggs contribute to the intake of many nutrients, such as retinol (4%), -tocopherol (3%), folate (4%), other B vitamins (3%), monounsaturated fat (3%), and linoleic acid (2%); however, eggs contributed to 32% of total dietary cholesterol. Thus, in view of the relatively small contribution of eggs to the intake of nutrients that may be beneficial in preventing coronary heart disease, the recommendation to limit the consumption of eggs may still be valid for the prevention of coronary heart disease. Other major sources of dietary cholesterol are dairy fats and meat, but these are already considered as increasing the risk of heart disease because of their saturated fat content.

In conclusion, the consumption of cholesterol increases the ratio of total to HDL-cholesterol concentrations, which would predict increased risk of coronary heart disease. Therefore, the advice to limit the consumption of eggs and other foods rich in dietary cholesterol may still be important in the prevention of coronary heart disease.

ACKNOWLEDGMENTS  
We thank Jan Burema and Albert Otten for statistical support.

REFERENCES  

1. Assmann G, Cullen P, Jossa F, Lewis B, Mancini M. Coronary heart disease: reducing the risk. A worldwide view. International Task Force for the Prevention of Coronary Heart Disease. Circulation 1999;100:1930–8.
2. Vorster HH, Beynen AC, Berger GM, Venter CS. Dietary cholesterol—the role of eggs in the prudent diet. S Afr Med J 1995;85: 253–6.
3. Clarke R, Frost C, Collins R, Appleby P, Peto R. Dietary lipids and blood cholesterol: quantitative meta-analysis of metabolic ward studies. BMJ 1997;314:112–7.
4. Hegsted DM, McGandy RB, Myers ML, Stare FJ. Quantitative effects of dietary fat on serum cholesterol in man. Am J Clin Nutr 1965;17:281–95.
5. Keys A, Parlin RW. Serum cholesterol response to changes in dietary lipids. Am J Clin Nutr 1966;19:175–81.
6. Howell WH, McNamara DJ, Tosca MA, Smith BT, Gaines JA. Plasma lipid and lipoprotein responses to dietary fat and cholesterol: a meta-analysis. Am J Clin Nutr 1997;65:1747–64.
7. Hegsted DM, Ausman LM, Johnson JA, Dallal GE. Dietary fat and serum lipids: an evaluation of the experimental data. Am J Clin Nutr 1993;57:875–83.
8. Kinosian B, Glick H, Preiss L, Puder KL. Cholesterol and coronary heart disease: predicting risks in men by changes in levels and ratios. J Invest Med 1995;43:443–50.
9. Dawber TR, Nickerson RJ, Brand FN, Pool J. Eggs, serum cholesterol, and coronary heart disease. Am J Clin Nutr 1982;36:617–25.
10. Hu FB, Stampfer MJ, Rimm EB, et al. A prospective study of egg consumption and risk of cardiovascular disease in men and women. JAMA 1999;281:1387–94.
11. Stampfer MJ, Sacks FM, Salvini S, Willett WC, Hennekens CH. A prospective study of cholesterol, apolipoproteins, and the risk of myocardial infarction. N Engl J Med 1991;325:373–81.
12. Assmann G, Schulte H, von Eckardstein A, Huang Y. High-density lipoprotein cholesterol as a predictor of coronary heart disease risk. The PROCAM experience and pathophysiological implications for reverse cholesterol transport. Atherosclerosis 1996;124(suppl): S11–20.
13. McNamara DJ. Cholesterol intake and plasma cholesterol: an update. J Am Coll Nutr 1997;16:530–34.
14. McNamara DJ. Relationship between blood and dietary cholesterol. Adv Meat Res 1990;6:63–87.
15. Chenoweth W, Ullmann M, Simpson R, Leveille G. Influence of dietary cholesterol and fat on serum lipids in men. J Nutr 1981;111: 2069–80.
16. Buzzard IM, McRoberts MR, Driscoll DL, Bowering J. Effect of dietary eggs and ascorbic acid on plasma lipid and lipoprotein cholesterol levels in healthy young men. Am J Clin Nutr 1982;36:94–105.
17. Applebaum-Bowden D, Haffner SM, Hartsook E, Luk KH, Albers JJ, Hazzard WR. Down-regulation of the low-density lipoprotein receptor by dietary cholesterol. Am J Clin Nutr 1984;39:360–7.
18. Sacks FM, Salazar J, Miller L, et al. Ingestion of egg raises plasma low density lipoproteins in free-living subjects. Lancet 1984;1:647–9.
19. Bowman MP, Van Doren J, Taper LJ, Thye FW, Ritchey SJ. Effect of dietary fat and cholesterol on plasma lipids and lipoprotein fractions in normolipidemic men. J Nutr 1988;118:555–60.
20. Johnson C, Greenland P. Effects of exercise, dietary cholesterol, and dietary fat on blood lipids. Arch Intern Med 1990;150:137–41.
21. Vorster HH, Benade AJ, Barnard HC, et al. Egg intake does not change plasma lipoprotein and coagulation profiles. Am J Clin Nutr 1992;55:400–10.
22. Duane WC. Effects of lovastatin and dietary cholesterol on sterol homeostasis in healthy human subjects. J Clin Invest 1993;92:911–8.
23. Martin LJ, Connelly PW, Nancoo D, et al. Cholesteryl ester transfer protein and high density lipoprotein responses to cholesterol feeding in men: relationship to apolipoprotein E genotype. J Lipid Res 1993;34:437–46.
24. Ginsberg HN, Karmally W, Siddiqui M, et al. A dose-response study of the effects of dietary cholesterol on fasting and postprandial lipid and lipoprotein metabolism in healthy young men. Arterioscler Thromb 1994;14:576–86.
25. Ginsberg HN, Karmally W, Siddiqui M, et al. Increases in dietary cholesterol are associated with modest increases in both LDL and HDL cholesterol in healthy young women. Arterioscler Thromb Vasc Biol 1995;15:169–78.
26. Blanco-Molina A, Castro G, Martin ED, et al. Effects of different dietary cholesterol concentrations on lipoprotein plasma concentrations and on cholesterol efflux from Fu5AH cells. Am J Clin Nutr 1998;68:1028–33.
27. Sehayek E, Nath C, Heinemann T, et al. U-shape relationship between change in dietary cholesterol absorption and plasma lipoprotein responsiveness and evidence for extreme interindividual variation in dietary cholesterol absorption in humans. J Lipid Res 1998;39:2415–22.
28. Flynn MA, Nolph GB, Osio Y, et al. Serum lipids and eggs. J Am Diet Assoc 1986;86:1541–8.
29. Romano G, Tilly KM, Patti L, et al. Effects of dietary cholesterol on plasma lipoproteins and their subclasses in IDDM patients. Diabetologia 1998;41:193–200.
30. Knopp RH, Retzlaff BM, Walden CE, et al. A double-blind, randomized, controlled trial of the effects of two eggs per day in moderately hypercholesterolemic and combined hyperlipidemic subjects taught the NCEP Step I diet. J Am Coll Nutr 1997;16:551–61.
31. Weggemans RM, Zock PL, Meyboom S, Funke H, Katan MB. The apoprotein A4-1/2 polymorphism and the response of serum cholesterol to dietary cholesterol. J Lipid Res 2000;44:1623–8.
32. Laboratory Methods Committee of the Lipids Research Clinics Program. Cholesterol and triglyceride concentrations in serum/plasma pairs. Clin Chem 1977;23:60–3.
33. Kestin M, Clifton PM, Rouse IL, Nestel PJ. Effect of dietary cholesterol in normolipidemic subjects is not modified by nature and amount of dietary fat. Am J Clin Nutr 1989;50:528–32.
34. Taylor JR. An introduction to error analysis. Mill Valley, CA: University Science Books, 1982.
35. Weggemans RM, Zock PL, Urgert R, Katan MB. Differences between men and women in response of serum cholesterol to dietary changes. Eur J Clin Invest 1999;29:827–34.
36. SAS Institute Inc. SAS/STAT user's guide: version 6 edition. Cary, NC: SAS Institute Inc, 1989.
37. The National Diet-Heart Study Research Group. The National Diet-Heart Study final report. Circulation 1968;37(suppl):I1–428.
38. Schonfeld G, Patsch W, Rudel LL, Nelson C, Epstein M, Olson RE. Effects of dietary cholesterol and fatty acids on plasma lipoproteins. J Clin Invest 1982;69:1072–80.
39. Egger M, Davey SG, Schneider M, Minder C. Bias in meta-analysis detected by a simple, graphical test. BMJ 1997;315:629–34.
40. Beynen AC, Katan MB. Effect of egg yolk feeding on the concentration and composition of serum lipoproteins in man. Atherosclerosis 1985;54:157–66.
41. Beynen AC, Katan MB. Reproducibility of the variations between humans in the response of serum cholesterol to cessation of egg consumption. Atherosclerosis 1985;57:19–31.
42. Katan MB, Beynen AC, de Vries JH, Nobels A. Existence of consistent hypo- and hyperresponders to dietary cholesterol in man. Am J Epidemiol 1986;123:221–34.
43. Glatz JF, Turner PR, Katan MB, Stalenhoef AF, Lewis B. Hypo- and hyperresponse of serum cholesterol level and low density lipoprotein production and degradation to dietary cholesterol in man. Ann N Y Acad Sci 1993;676:163–79.
44. Zanni EE, Zannis VI, Blum CB, Herbert PN, Breslow JL. Effect of egg cholesterol and dietary fats on plasma lipids, lipoproteins, and apoproteins of normal women consuming natural diets. J Lipid Res 1987;28:518–27.
45. Vuoristo M, Miettinen TA. Absorption, metabolism, and serum concentrations of cholesterol in vegetarians: effects of cholesterol feeding. Am J Clin Nutr 1994;59:1325–31.
46. Schnohr P, Thomsen OO, Riis HP, Boberg AG, Lawaetz H, Weeke T. Egg consumption and high-density-lipoprotein cholesterol. J Intern Med 1994;235:249–51.
47. Oh SY, Miller LT. Effect of dietary egg on variability of plasma cholesterol levels and lipoprotein cholesterol. Am J Clin Nutr 1985; 42:421–31.
48. Nestel P, Tada N, Billington T, Huff M, Fidge N. Changes in very low density lipoproteins with cholesterol loading in man. Metabolism 1982;31:398–405.
49. Nestel PJ. Fish oil attenuates the cholesterol induced rise in lipoprotein cholesterol. Am J Clin Nutr 1986;43:752–7.
50. Mistry P, Miller NE, Laker M, Hazzard WR, Lewis B. Individual variation in the effects of dietary cholesterol on plasma lipoproteins and cellular cholesterol homeostasis in man. Studies of low density lipoprotein receptor activity and 3-hydroxy-3-methylglutaryl coenzyme A reductase activity in blood mononuclear cells. J Clin Invest 1981;67:493–502.
51. McMurry MP, Connor WE, Cerqueira MT. Dietary cholesterol and the plasma lipids and lipoproteins in the Tarahumara Indians: a people habituated to a low cholesterol diet after weaning. Am J Clin Nutr 1982;35:741–4.
52. Lichtenstein AH, Ausman LM, Carrasco W, Jenner JL, Ordovas JM, Schaefer EJ. Hypercholesterolemic effect of dietary cholesterol in diets enriched in polyunsaturated and saturated fat. Dietary cholesterol, fat saturation, and plasma lipids. Arterioscler Thromb 1994; 14:168–75.
53. Edington JD, Geekie M, Carter R, Benfield L, Ball M, Mann J. Serum lipid response to dietary cholesterol in subjects fed a low-fat, high-fiber diet. Am J Clin Nutr 1989;50:58–62.
54. Brown SA, Morrisett J, Patsch JR, Reeves R, Gotto-AM J, Patsch W. Influence of short term dietary cholesterol and fat on human plasma Lp[a] and LDL levels. J Lipid Res 1991;32:1281–9.
55. Sarkkinen E, Korhonen M, Erkkila A, Ebeling T, Uusitupa M. Effect of apolipoprotein E polymorphism on serum lipid response to the separate modification of dietary fat and dietary cholesterol. Am J Clin Nutr 1998;68:1215–22.
56. Gylling H, Miettinen TA. Cholesterol absorption and synthesis related to low density lipoprotein metabolism during varying cholesterol intake in men with different apoE phenotypes. J Lipid Res 1992;33:1361–71.
57. Boerwinkle E, Brown SA, Rohrbach K, Gotto AM Jr, Patsch W. Role of apolipoprotein E and B gene variation in determining response of lipid, lipoprotein, and apolipoprotein levels to increased dietary cholesterol. Am J Hum Genet 1991;49:1145–54.
58. Fielding CJ, Havel RJ, Todd KM, et al. Effects of dietary cholesterol and fat saturation on plasma lipoproteins in an ethnically diverse population of healthy young men. J Clin Invest 1995;95:611–8.
59. Anderson JT, Grande F, Keys A. Independence of the effects of cholesterol and degree of saturation of the fat in the diet on serum cholesterol in man. Am J Clin Nutr 1976;29:1184–9.
60. McNamara DJ, Kolb R, Parker TS, et al. Heterogeneity of cholesterol homeostasis in man. Response to changes in dietary fat quality and cholesterol quantity. J Clin Invest 1987;79:1729–39.
61. Oh SY, Monaco PA. Effect of dietary cholesterol and degree of fat unsaturation on plasma lipid levels, lipoprotein composition, and fecal steroid excretion in normal young adult men. Am J Clin Nutr 1985;42:399–413.
62. Kleinbaum DG, Kupper LL, Morgenstern H. Applied regression analysis and other multivariable methods. Belmont, CA: Duxbury Press, 1988.
63. Wood D, De-Backer G, Faergeman O, Graham I, Mancia G, Pyorala K. Prevention of coronary heart disease in clinical practice. Summary of recommendations of the Second Joint Task Force of European and other Societies on Coronary Prevention. J Hypertens 1998; 16:1407–14.
64. Denke MA, Frantz ID Jr. Response to a cholesterol-lowering diet: efficacy is greater in hypercholesterolemic subjects even after adjustment for regression to the mean. Am J Med 1993;94:626–31.
65. Goff DC Jr, Shekelle RB, Moye LA, Katan MB, Gotto AM Jr, Stamler J. Does body fatness modify the effect of dietary cholesterol on serum cholesterol? Results from the Chicago Western Electric Study. Am J Epidemiol 1993;137:171–7.