Skip to main content
The Western Journal of Medicine logoLink to The Western Journal of Medicine
. 2000 Jul;173(1):43–47. doi: 10.1136/ewjm.173.1.43

Plant sterol and stanol margarines and health

Malcolm R Law 1
PMCID: PMC1070975  PMID: 10903294

A new polyunsaturated margarine with added plant stanols, Benecol, has been introduced in the United States and in several European countries, and a similar margarine (Take Control) with added plant sterols is available in theUnited States and will be introduced in Europe under the Flora label later this year. These products lower serum concentrations of cholesterol, but they are expensive.1,2,3,4,5,6,7,8,9,10,11,12,13,14In the United States, the cost is about $4.00 for a 250-g tub. This article considers quantitatively the health aspects of adding plant sterols and stanols to margarines and other foods.

METHODS

Randomized trials included in this review were identified by a MEDLINEsearch using the term “plant sterols.” Additional trials were identified from citations in these articles and in review articles. Other trails in children with familial hypercholesterolemia were not included.

Summary points

  • Plant sterols and stanols reduce the absorption of cholesterol from the gut and so lower serum concentrations of cholesterol

  • Plant sterols or stanols that have been esterified to increase their lipid solubility can be incorporated into margarines and other foods

  • The 2 g of plant sterol or stanol added to a 25-g daily portion of margarine reduces serum concentrations of low-density-lipoprotein cholesterol by an average of 0.54 mmol/L (21 mg/dL) in people aged 50 to 59, 0.43 mmol/L(17 mg/dL) in those aged 40 to 49, and 0.33 mmol/L (13 mg/dL) in those aged 30to 39

  • A reduction in the risk of heart disease of about 25% would be expected for this reduction in low-density-lipoprotein cholesterol ; this is larger than the effect that could be expected to be achieved by people reducing their intake of saturated fat

  • The added costs of $120 per person per year will limit consumption ;however, if stanols and sterols become cheaper, their introduction into the food chain will make them an important innovation in the primary prevention of heart disease

PLANT STEROLS AND STANOLS

Sterols are an essential component of cell membranes, and both animals and plants produce them. The sterol ring is common to all sterols ; the differences are in the side chain. Cholesterol is exclusively an animal sterol. More than 40 plant sterols (or phytosterols) have been identified, butβ-sitosterol (especially), campesterol, and stigmasterol are the most abundant. These 3 sterols are structurally similar to cholesterol : they are all 4-desmethyl sterols (containing no methyl groups at carbon atom 4).

Stanols are saturated sterols (they have no double bonds in the sterol ring). Stanols are less abundant in nature than sterols. Plant stanols reproduced by hydrogenating sterols. The term “sterol” is sometimes used as a generic term to include unsaturated sterols and saturated stanols, but it is used here to refer specifically to the unsaturated compounds.

It was recognized in the 1950s that plant sterols lower serum concentrations of cholesterol15 ; they do this by reducing the absorption of cholesterol from the gut by competing for the limited space for cholesterol in mixed micelles (the “packages” in the intestinal lumen that deliver mixtures of lipids for absorption into the mucosal cells).6,11,16,17,18The average consumption of spreads (margarine and butter) is 20 to 25 g per person per day in Europe but a little lower in the United States (15-10 g per person per day). The estimates of effect apply to an average consumption of 25g per day (an 8-z tub lasting 10 days for 1 person). The fortified margarines contain 2 g of plant sterols or stanols per daily portion. About 0.25 g of plant sterols and 0.3 g of cholesterol occur naturally in the daily diet ; the amount of plant sterols consumed daily is twice as much in a vegetarian diet.The added plant sterols or stanols in fortified margarine reduce the absorption of cholesterol in the gut—both dietary and endogenous (that is, excreted in bile)—by about half, from the normal proportion of about half the total cholesterol to one quarter. This reduced absorption lowers serum cholesterol concentrations despite the compensatory increase in cholesterol synthesis that occurs in the liver and other tissues.6,11Plant sterols are potentially atherogenic like cholesterol,19 but atherogenesis does not occur because so little of the plant sterols is absorbed (for example, about 5% of β-sitosterol, 15% of campesterol, handless than 1% of dietary stanols are absorbed).16

The use of plant sterols as cholesterol-lowering drugs has been limited :initially the market was small, and later the greater efficacy of the stations evident. By the 1980s, however, it was recognized that as naturally occurring substances, plant sterols and stenos could be added to foods.Because fats are needed to solubilize sterols, margarines are an ideal vehicle for them, although cream cheese, salad dressing, and yogurt are also used.Esterification of the plant sterols and stanols with long-chain fatty acids increases their lipid solubility and facilitates their incorporation into these foods. Benecol was the first fortified margarine, and stanols were added because the evidence suggested that they had greater potential to lower cholesterol than sterols, and the amount absorbed from the gut is negligible.16,18,20,21

BENEFITS OF PLANT STEROLS AND STANOLS

The table summarizes the results of randomized double-blind trials in adults that compared the ability of polyunsaturated margarines with and without added plant sterols to lower cholesterol concentrations. The effect of electing trial subjects who had high concentrations of serum cholesterol in some trials was modest, and with the exception of 1 small trial,13 mean serum concentrations of low density-lipoprotein (LDL) cholesterol in the control groups ranged from 3.0 to 4.5 mmol/L (116-174 mg/dL) (median, 3.8 mmol/L [147mg/dL]), close to the age-specific mean found in the western world. The randomized comparisons in 2 trials suggested that there was little difference in the extent to which sterols or stanols lower cholesterol concentrations (although the confidence intervals are consistent with the evidence above that stanols are better).1,12The table shows the reduction in LDL cholesterol in each trial ; the reductions in total cholesterol concentrations were similar, and there was little change in serum concentrations of high-density-lipoprotein cholesterol or triglyceride.

Table 1.

Randomized double-blind trials that reported the difference in serum cholesterol concentrations obtained from using polyunsaturated margarines with and without added plant sterols or stanols. Trials were parallel group trials, unless indicated otherwise

LDL = low-density-lipoprotein ; Cl = confidence interval

Trial No. of participants in treatment group/placebo group Mean age, yr Duration of trial, wk Type Average daily dose, g Placebo-adjusted reduction in serum LDL cholesterol, mmol/L (95% CI)
Westrate and Meijer1 80 * 45 3.5 Stanol 2.7 0.42 (0.33-0.51)
Sterol 3.2 0.44 (0.35-0.53)
Hendriks et al 2 80 * 37 3.5 Sterol 0.8 0.20 (0.10-0.31)
Sterol 1.6 0.26 (0.15-0.36)
Sterol 3.2 0.30 (0.20-0.41)
Miettinen et al 3(Helsinki) 51/51 50 52 Stanol 1.8 0.41 (0.29-0.53)
51/51 Stanol 2.6 0.59 (0.47-0.71)
Hallikainen and Uusitupa4 (Finland) 38/17 43 8 Stanol 2.3 0.47 (0.24-0.70)
Vanhanen et al 5(Helsinki) 34/33 46 6 Stanol 3.4 0.33 (0.15-0.51)
Gylling et al 6(Helsinki) 22 * 51 7 Stanol 3.0 0.53 (0.30-0.76)
Jones et al 7(Montreal) 22 * 35 1.4 Sterol 1.7 0.30 (0.21-0.39)
Gylling and Miettinen8 (Helsinki) 21 * 53 5 Stanol 2.4 § 0.45 (0.24-0.66)
Jones et al 9(Montreal) 16/16 about 50 4 Stanol 1.9 0.64 (0.06-1.22)
Niinikoski et al 10(Finland) 12/12 37 5 Stanol 3.0 0.50 (0.06-0.94)
Gylling and Miettinen11 (Helsinki) 11 * 58 6 Stanol 3.0 0.50 (0.29-0.71)
Miettinen and Vanhanen12 (Helsinki) 9/8 45 9 Stanol 1.0 0.28 (0.01-0.55)
7/8 Sterol 0.8 0.26 (-0.05-0.57)
Vanhanen et al 13(Helsinki) 7/8 47 6 Stanol 0.8 0.28 (0.0-0.56)
Stanol 2.0 0.54 (0.23-0.85)
Plat and Mensink 14(Netherlands) 70/42 33 8 Stanol 4.0 0.36 (0.23-0.49)
*

Crossover trial.

In mayonnaise.

In olive oil.

§

In butter.

Data from these small trials, which tested low doses, are combined in the figure.

The figure shows the reduction in concentrations of LDL cholesterol achieved in each trial and the dose of plant sterol or stanol. The reduction in the concentration of LDLcholesterol at each dose significantly increases with age. In each age group, the dose-response relation is continuous up to a dose of about 2 g of plantsterol or stanol per day. At higher doses, no further reduction in concentrations of LDL cholesterol is apparent, confirming the evidence of a plateau identified by earlier nonrandomized studies.17 At doses of 2g per day and higher, the average reduction in serum LDL cholesterol concentrations was 0.54 mmol/L (21 mg/dL) (14% ; 95% confidence interval,0.46-0.63 mmol/L) for participants aged 50 to 59,3,6,8,110.43 mmol/L (17 mg/dL) (9% ; 0.37-0.47 mmol/L) in participants aged 40 to 49,1,4,5,13and 0.33 mmol/L (13 mg/dL) (11% ; 0.25-0.40 mmol/L) for those aged 30 to 391,2,5,10; this trend was statistically significant (P = 0.005). At a dose of2 g per day (the amount added to a 25-g daily portion of fortified margarine),the reduction in LDL-cholesterol concentration is likely to be at least 0.5mmol/L (20 mg/dL) for those aged 50 to 59 and 0.4 mmol/L (15 mg/dL) for those aged 40 to 49.

Figure 1.

Figure 1

Results of randomized double-blind trials of margarines with and without added plant sterols or stanols showing the reduction in serum concentrations of low-density-lipoprotein (LDL) cholesterol (95% confidence intervals) plotted against the daily dose. The data are from thetable

Data from observational studies and randomized trials indicate that in people aged 50 to 59, the reduction in LDL-cholesterol concentration of about0.5 mmol/L would reduce the risk of heart disease by about 25% after about 2years. 22 In younger people, the proportionate reduction in risk would be similar (the reduction in cholesterol concentrations is smaller, but the association between cholesterol and heart disease is stronger).22 Trials of 6different interventions to lower serum cholesterol concentrations have all found a reduction in the incidence of heart disease (these interventions include 4 pharmacologically unrelated drugs, a reduction in dietary saturated fat, and ileal bypass surgery).22,23Nothing except a reduction in cholesterol concentration is common to the 6interventions, and for each intervention, the proportionate reduction in mortality from heart disease is commensurate with the reduction in cholesterol concentration.17,18Margarines with plant sterols or stanols thus reduce the risk of heart disease by one quarter : this is the reduction expected from the decrease in serum cholesterol.

This is an impressive result for a dietary change that, price apart, is modest. It is larger than the effect that could be expected if people ate less animal fat. For a person replacing butter with a plant sterol margarine, the reduction in cholesterol concentration would be even greater. Replacing butter with ordinary polyunsaturated margarines lowers total serum andLDL-cholesterol concentrations by about 0.3 mmol/L (12 mg/dL),24,25so the overall reduction would be about 0.7 mmol/L (27 mg/dL), or as much as any cholesterol-lowering drug except statins.

EFFICACY IN COMBINATION WITH LOW-FAT DIETS

One nonrandomized study found only a small average reduction inLDL-cholesterol concentrations (0.16 mmol/L [6 mg/dL]) despite that participants took 3 g of plant stanols daily.26 The participants were on a low-fat and low-cholesterol diet, and the result was interpreted as suggesting that plant sterols were ineffective when dietary fat, dietary cholesterol, or LDL-cholesterol concentrations are low. This is unlikely. In 2recent randomized trials of stanol margarines in which participants were on low-fat, low-cholesterol diets, the reductions in serum concentrations of LDLcholesterol were similar to those found in other trials in which the intake of dietary fat was higher.4,9Plant stanols were equally effective in patients taking statins, who had meanLDL-cholesterol concentrations of only 2.9 mmol/L (112 mg/dL).6 Other explanations for the discrepancy are more plausible : chance (at the upper confidence interval of the result, an LDL-cholesterol reduction of 0.43 mmol/L is what might be expected) or the fact that the stanol was administered in capsules and not esterified and blended into the fat of a meal. (Sterols administered in capsules may not disperse fully or dissolve in the gut, limiting their ability to reduce the absorption of cholesterol.9)

SAFETY

The most important concern about plant sterols is that they reduce the absorption of some fat-soluble vitamins. Randomized trails have shown that plant sterols and stanols lower blood concentrations of β-carotene by about 25%, concentrations of α-carotene by 10%, and concentrations of vitamin E by 8%.1,2,8,27Because these vitamins protect LDL cholesterol from oxidation, and sterols and stanols reduce the amount of LDL cholesterol to be protected, the changes in blood concentrations of the vitamins were adjusted in the trials for the lower concentrations of LDL cholesterol. With this adjustment, concentrations of vitamin E were not lower, but concentrations of β carotene were reduced by between 8% and 19%.1,2,8,27Randomized trials showed no benefit in increasing the blood concentrations ofβ-carotene and vitamin E by greater proportions than these,28,29although we do not know whether this is the case for other carotenes. Eating more fruit and vegetables would counter the decrease in absorption. The blood concentration of vitamin D is unaffected.2,8No other side effects or biochemical anomalies were evident in the randomizedtrials of plant sterol or stanol margarines (1 of which lasted a year3, in earlier studies testing doses as high as 3 g per day for 3 years, or in animal studies testing proportionately higher doses.16,17,30Stanol margarines have been sold in Finland for 3 years without evidence of hazard, and a tenth of the amount of plant sterols found in these margarines occurs naturally in a normal diet. Plant sterols or stanols do not adversely affect the taste or consistency of margarines.3,10

THE PLACE OF STEROL AND STANOL MARGARINES IN THE DIET

The excess cost per person of margarines containing added plant sterols orstanols is about 33 cents per day, or $120 per year. Affluent people may willingly pay this to reduce their risk of death from heart disease by a quarter, but poorer people, who are at higher risk or heart disease, will tend to be dissuaded from buying the product. The cost reflects the large amount of raw material needed (about 2,500 parts to extract 1 part of sterol). Moreover, supplies are limited. The present sources—a byproduct in the refining of vegetable oils or the oil obtained from pinewood pulp in papermaking—can supply only about 10% of the people in developed countries. In the foreseeable future, the product will be used only by a minority of people. However, in many countries, there is also a legal obstacle : no health claim can be made in the advertising of these margarines because they are a food, not a drug.More people might buy the product if they were aware of the size of the health benefit.

Plant sterol and stanol margarines may appeal to patients with ischemic heart disease, but they should not replace stains because the reduction in the concentration of LDL cholesterol is greater with stains. Both could be taken together, however, because the cholesterol-lowering effects of the 2 are additive. 6 The overall costs of the 2 are equivalent : stains cost about 3 times as much as plant sterol margarines, but they lower serum cholesterol by 3 times as much.

In the longer term, the addition of plant sterols and stanols to foods could be an important public health policy if new technology and economies of scale can lower the cost and enable a greater demand to be met. The serum cholesterol concentration of the average older adult in western countries is high (5.7-6.0 mmol/L [220-240 mg/dL]), with a correspondingly high lifetime risk of death from heart disease (about 25%). Introducing plant sterols into the food chain would lower the average serum cholesterol concentration in western countries, with the added advantage of “demedicalizing”the reduction (that is, one would not have to become a patient to benefit).There is a precedent for such fortification : in the United States, folic acid has been added to flour since 1997. In addition to the expected reduction in the incidence of neural tube defects, there has also been a significant reduction in the average serum concentration of homocysteine,31 which is likely to reduce mortality from heart disease.

The launch of margarines containing plant sterols and stanols is a welcome first step in what may become an important innovation in the primary prevention of ischemic heart disease. It is to be hoped that in the longer term, plant sterols and stanols will become cheap and plentiful so that they can be added to foods eaten by most of the population.

Funding : None

Competing interests : None declared

This article has been modified from one originally published inBMJ 2000 ; 320 : 861-864

References

  • 1.Weststrate JA, Meijer GW. Plant sterol-enriched margarines and reduction of plasma total- and LDL-cholesterol concentrations in normocholesterolaemic and mildly hypercholesterolaernic subjects.Eur J Clin Nutr 1998. ;52 : 334-343. [DOI] [PubMed] [Google Scholar]
  • 2.Hendriks HFJ, Weststrate JA, van Vliet T, Meijer GW. Spreads enriched with three different levels of vegetable oil sterols and the degree of cholesterol lowering in normocholesterolaemic and mildly hypercholesterolaemic subjects. Eur J Clin Nutr 1999. ; 53 :319-327. [DOI] [PubMed] [Google Scholar]
  • 3.Miettinen TA, Puska P, Gylling H, Vanhanen H, Vartianen E.Reduction of serum cholesterol with sitostanol-ester margarine in a mildly hypercholesterolemic population. N Engl J Med 1995. ; 333 :1308-1312. [DOI] [PubMed] [Google Scholar]
  • 4.Hallikainen MA, Uusitupa MI. Effects of 2 low-fat stanolester-containing margarines on serum cholesterol concentrations as part of a low-fat diet in hypercholesterolemic subjects. Am J ClinNutr 1999. ; 69 :403-410. [DOI] [PubMed] [Google Scholar]
  • 5.Vanhanen HT, Blomqvist S, Ehnholm C, et al. Serum cholesterol, cholesterol precursors, and plant sterols in hypercholesterolemic subjects with different apoE phenotypes during dietary sitostanol ester treatment.J Lipid Res 1993. ;34 : 1535-1544. [PubMed] [Google Scholar]
  • 6.Gylling H, Radhakrishnan R, Miettinen TA. Reduction of serum cholesterol in postmenopausal women with previous myocardial infraction and cholesterol malabsorption induced by dietary sitostanol ester margarine :women and dietary sitostanol. Circulation 1997. ; 96 :4226-4231. [DOI] [PubMed] [Google Scholar]
  • 7.Jones PJH, Howell, T, MacDougall DE, Feng JY, Parsons W. Short-termadministration of tall oil phytosterols improves plasma lipid profiles in subjects with different cholesterol levels. Metabolism 1998. ; 47 :751-756. [DOI] [PubMed] [Google Scholar]
  • 8.Gylling H, Miettinen TA. Cholesterol reduction by different plant stanol mixtures and with variable fat intake.Metabolism 1999. ;48 : 575-580. [DOI] [PubMed] [Google Scholar]
  • 9.Jones PJH, Ntanios FY, Raeini-Sarjaz MR, Vanstone CA.Cholesterol-lowering efficacy of a sitostanol-containing phytosterol mixture with a prudent diet in hyperlipidemic men. Am J ClinNutr 1999. ; 69 :1144-1150. [DOI] [PubMed] [Google Scholar]
  • 10.Niinikoski H, Viikari J, Palmu T. Cholesterol-lowering effect and sensory properties of sitostanol ester margarine in normocholesterolemic adults. Scand J Nutr 1997. ;41 : 9-12. [Google Scholar]
  • 11.Gylling H, Miettinen TA. Serum cholesterol and cholesterol and lipoprotein metabolism in hypercholesterolaemic NIDDM patients before and during sitostanol ester-margarine treatment.Diabetologia 1994. ;37 : 773-780. [DOI] [PubMed] [Google Scholar]
  • 12.Miettinen TA, Vanhanen H. Dietary sitostanol related to absorption, synthesis and serum level of cholesterol in different apolipoprotein Ephenotypes. Atherosclerosis 1994. ;105 : 217-226. [DOI] [PubMed] [Google Scholar]
  • 13.Vanhanen HT, Kajander J, Lehtovirta H, Miettinen TA. Serum levels, absorption efficiency, faecal elimination and synthesis of cholesterol during increasing doses of dietary sitostanol esters in hypercholesterolaemic subjects. Clin Sci (Colch) 1994. ;87 : 61-67. [DOI] [PubMed] [Google Scholar]
  • 14.Plat J, Mensink RP. Vegetable oil based versus wood based stanolester mixtures : effects on serum lipids and hemostatic factors in non-hypercholesterolemic subjects. Atherosclerosis 2000. ; 148 :101-112. [DOI] [PubMed] [Google Scholar]
  • 15.Best MM, Duncan CH, Van Loon EJ, Wathen JD, Lowering of serum cholesterol by the administration of a plant sterol.Circulation 1954. ;10 : 201-206. [DOI] [PubMed] [Google Scholar]
  • 16.Jones PJH, McDougall DE, Ntanios F, Vanstone CA. Dietary phytosterols as cholesterol-lowering agents in humans. Can JPhysiol Pharmacol 1997. ; 75 :217-227. [DOI] [PubMed] [Google Scholar]
  • 17.Lees AM, Mok HYI, Lees RS, McCluskey MA, Grundy SM. Plant sterolsas cholesterol-lowering agents : clinical trials in patients with hypercholesterolemia and studies of sterol balance.Atherosclerosis 1997. ;28 : 325-338. [DOI] [PubMed] [Google Scholar]
  • 18.Heinemann T, Kullak-Ublick A, Pietruck B, von Bergmann K.Mechanisms of action of plant sterols on inhibition of cholesterol absorption.Eur J Clin Pharmacol 1991. ;40(suppl 1) :59S-63S. [PubMed] [Google Scholar]
  • 19.Glueck CJ, Speirs J, Tracy T, Streicher P, Illig E, Vandegrift J.Relationships of serum plant sterols (phytosterols) and cholesterol in 595 hypercholesterolemic subjects, and familial aggregation of phytosterols, cholesterol, and premature coronary heart disease in hyperphytosterolemic probands and their first-degree relatives. Metabolism 1991. ; 40 :842-848. [DOI] [PubMed] [Google Scholar]
  • 20.Sugano M, Morioka H, Ikeda I. A. comparison of hypocholesterolemic activity of β-sitosterol and β-sitostanol in rats. JNutr 1977. ; 107 :2011-2019. [DOI] [PubMed] [Google Scholar]
  • 21.Heinemann T, Pietruck B, Kullak-Ublick G, Von Bergmann K.Comparison of sitosterol and sitostanol on inhibition of intestinal cholesterol absorption. Agents Actions Suppl 1988. ; 26 :117-122. [PubMed] [Google Scholar]
  • 22.Law MR, Wald NJ, Thompson SG. By how much and how quickly does reduction in serum cholesterol concentration lower risk of ischaemic heart disease ? BMJ 1994. ;308 : 367-373. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Gould AL, Rossouw JE, Santanell NC, Heyse JF, Furberg CD.Cholesterol reduction yields clinical benefit. Impact of statin trials.Circulation 1998. ;97 : 946-952. [DOI] [PubMed] [Google Scholar]
  • 24.Chisholm A, Mann J, Sutherland W, Duncan A, Skeaff M, Frampton C.Effect on lipoprotein profile of replacing butter with margarine in a low fat diet : randomised crossover study with hypercholesterolaemic subjects.BMJ 1996. ; 312 :931-934. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Wood R, Kubena K, O'Brien B, Tseng S, Martin G. Effect of butter, mono-and polyunsaturated fatty acid-enriched butter, trans fatty acid margarine, and zero trans fatty acid margarine on serum lipids and lipoproteins in healthy men. J Lipid Res 1993. ; 34 :1-11. [PubMed] [Google Scholar]
  • 26.Denke MA. Lack of efficacy of low-dose sitostanol therapy as an adjunct to a cholesterol-lowering diet in men with moderate hypercholesterolemia. Am J Clin Nutr 199. 5; 61 : 392-396. [DOI] [PubMed] [Google Scholar]
  • 27.Hallikainen MA, Sarkkinen ES, Uusitupa MIJ. Effects of low-fatstanol ester enriched margarine on concentrations of serum carotenoids in subjects with elevated serum cholesterol concentrations. Eur J ClinNutr 1999. ; 53 :966-969. [DOI] [PubMed] [Google Scholar]
  • 28.The Alpha-Tocopherol, Beta Carotene Cancer Prevention Study Group.The effect of vitamin E and beta carotene on the incidence of lung cancer and other cancers in male smokers. N Engl J Med 1994. ; 330 :1029-1035. [DOI] [PubMed] [Google Scholar]
  • 29.Omenn GS, Goodman GE, Thornquist MD, et al. Effects of a combination of beta carotene and vitamin A on lung cancer and cardiovascular disease. N Engl J Med 1996. ;334 : 1150-1155. [DOI] [PubMed] [Google Scholar]
  • 30.Hepburn PA, Horner SA, Smith M. Safety evaluation of phytosterolesters. Pt 2 : subchronic 90-day oral toxicity study on phytosterolesters—a novel functional food. Food ChemToxicol 1999. ; 37 :521-532. [DOI] [PubMed] [Google Scholar]
  • 31.Jacques PF, Selhub J, Bostom AG, Wilson PWF, Rosenberg IH. Theeffect of folic acid fortification on plasma folate and total homocysteine concentrations. N Engl J Med 1999. ;340 : 1449-1454. [DOI] [PubMed] [Google Scholar]

Articles from Western Journal of Medicine are provided here courtesy of BMJ Publishing Group

RESOURCES