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Long-term vitamin E supplementation fails to reduce lipid peroxidation in people at cardiovascular risk: analysis of underlying factors
© Chiabrando et al; licensee BioMed Central Ltd. 2002
Received: 15 January 2002
Accepted: 19 March 2002
Published: 19 March 2002
Antioxidant supplementation with vitamin E had no effect in the prevention of cardiovascular diseases (CVD) in three recent large, randomized clinical trials. In order to reassess critically the role of vitamin E in CVD prevention, it is important to establish whether these results are related to a lack of antioxidant action.
We examined the in vivo antioxidant effect of vitamin E (300 mg/day for about three years) in 144 participants in the Primary Prevention Project (females and males, aged ≥ 50 y, with at least one major CV risk factor, but no history of CVD). Urinary 8-epi-PGF2α (isoprostane F2α-III or 15-F2t-isoP), a validated biomarker of lipid peroxidation, was measured by mass spectrometry.
Urinary excretion of 8-epi-PGF2α [pg/mg creatinine, median (range)] was 141 (67–498) in treated and 148 (76–561) in untreated subjects (p = 0.10). Taking into account possible confounding variables, multiple regression analysis confirmed that vitamin E had no significant effect on this biomarker. Levels of 8-epi-PGF2α were in the normal range for most subjects, except smokers and those with uncontrolled blood pressure or hyperglycemia.
Prolonged vitamin E supplementation did not reduce lipid peroxidation in subjects with major cardiovascular risk factors. The observation that the rate of lipid peroxidation was near normal in a large proportion of subjects may help explain why vitamin E was not effective as an antioxidant in the PPP study and was ineffective for CVD prevention in large scale trials.
The "oxidative hypothesis" of atherosclerosis proposes that oxidative modification of lipids in low-density lipoproteins (LDL) contributes to atherogenesis [1, 2]. Antioxidants that are effective against lipid peroxidation should therefore reduce atherosclerosis and hence afford protection from cardiovascular diseases (CVD). In contrast to a) epidemiological evidence that antioxidants taken with the diet or as supplements reduce cardiovascular (CV) risk , and b) experimental data supporting its anti-atherogenic properties , vitamin E failed to show any beneficial effect in recent large intervention studies . In two large-scale trials, long-term supplementation with vitamin E (300–400 lU/day) failed to reduce cardiovascular events in post-myocardial infarction patients (GISSI-Prevenzione ) and in subjects at high CV risk (HOPE ). In the trial conducted by our group (Primary Prevention Project, PPP ), vitamin E (300 mg/day) taken over three years also showed no effect on the incidence of cardiovascular events in individuals with one or more major risk factors (see Methods). Therefore, the question whether vitamin E had an effective in vivo antioxidant action in the populations under study in these trials is under debate [9–12].
When these studies were designed, the antioxidant efficacy of vitamin E in humans had not been demonstrated in vivo because of the lack of reliable methods . Measurement of urinary or circulating F2-isoprostanes (iPF2 or F2-isoP) is now accepted as a reliable tool for evaluating the rate of lipid peroxidation in vivo[9, 14–16]. Using urinary excretion of 8-epi-PGF2α (also termed iPF2α-III or 15-F2t-isoP) as a biomarker, it has been shown that short-term administration of vitamin E (600 mg/day for 14 days) reduced in vivo lipid peroxidation in some clinical settings where oxidative stress is abnormally high, e.g., diabetes mellitus (-37%), hypercholesterolemia (-58%) and cystic fibrosis (-42%) [17–19]. In contrast, vitamin E had no antioxidant activity in conditions where lipid peroxidation was normal . No data are available on the antioxidant effect of longer-term supplementation with vitamin E in subjects at moderate/high cardiovascular risk.
Using a highly selective and validated mass spectrometric assay for 8-epi-PGF2α, we measured in vivo lipid peroxidation in PPP trial participants who had taken vitamin E daily for about three years vs those who did not take vitamin E.
Major cardiovascular risk factors in the 144 subjects.
Old age ≥ 65 y
Family history of premature myocardial infraction
Overnight urine was obtained from subjects consecutively presenting at five participating centers for a scheduled follow-up visit after at least one year of randomized treatment. With a sample size of 70 individuals per arm, the study had a 90% power (1-β) to detect, with α = 0.05, a difference of at least 25% in urinary 8-epi-PGF2α between treated and untreated individuals. Two groups of 72 subjects treated or not treated with vitamin E were studied. Clinical and biochemical variables were reassessed yearly and on the occasion of urine collection.
Urinary 8-epi-PGF2α was selectively measured as we have described previously  using immunoaffinity chromatography for selective extraction/purification and a stable isotope dilution assay with gas chromatography-negative ion chemical ionization mass spectrometry for quantitation, with 2H4-8-epi-PGF2α as the internal standard. Urinary excretion of 8-epi-PGF2α was expressed as pg/mg creatinine. Creatinine was measured highly selectively by stable-isotope dilution HPLC-electrospray-tandem mass spectrometry, using 2H3-creatinine as the internal standard. Urine was stored at -20°C until analyzed. Analyses were done on blind-coded samples.
Means were compared by the non-parametric Mann-Whitney U test to avoid assumptions about the distribution of the variables. Levels of 8-epi-PGF2α were expressed as median (range) values. Multiple regression analysis was used to 1) evaluate the effect of vitamin E on urinary excretion of 8-epi-PGF2α, taking into account the following potential confounding variables (age, sex, aspirin treatment, smoking, systolic and diastolic blood pressure, blood glucose, blood cholesterol and obesity), and 2) assess whether any of these variables was independently associated with lipid peroxidation. Linear correlation analysis was also used. Probability values of p ≤ 0.05 (two tails) were considered to be statistically significant.
1. Antioxidant Effect of Vitamin E
Baseline characteristics of the two study groups
VITAMIN E (n = 72)
NO VITAMIN E (n = 72)
59 ± 6
61 ± 7
Body mass index (kg/m2)
27 ± 4
27 ± 4
Systolic blood pressure (mm Hg)
146 ± 16
145 ± 15
Diastolic blood pressure (mm Hg)
88 ± 8
87 ± 7
Blood glucose (mg/dL)
91 ± 32
103 ± 35**
Total blood cholesterol (mg/dL)
243 ± 47
225 ± 45*
Aspirin treatment (yes/no)
Multiple regression analysis: variables associated with urinary excretion of 8-epi-PGF2α
all subjects (n = 144)
nonsmokers (n = 120)
Vitamin E treatment
Systolic blood pressure (mmHg)
Blood glucose (mg/dL)
Diastolic blood pressure (mmHg)
Blood cholesterol (mg/dL)
Smoking was the only strong determinant of lipid peroxidation in the overall sample (Table 3, discussed below). Since it is known that vitamin E does not reduce excessive lipid peroxidation in smokers [22, 23], we investigated whether the presence of smokers in our sample might mask an antioxidant effect of vitamin E in the nonsmokers (n = 120; 63 untreated, 57 treated with vitamin E). The levels of 8-epi-PGF2α in nonsmokers, however, were not significantly reduced by prolonged vitamin E supplementation [122 (67–326) vs 146 (76–316), p = 0.09)]. Multivariate analysis confirmed that vitamin E did not reduce lipid peroxidation in this sample (β = -0.10, p = 0.32, Table 3).
2. Lipid Peroxidation in Subjects at CV Risk
Since vitamin E has thus far proved effective as an in vivo antioxidant in humans when lipid peroxidation is excessive [17–19, 24], but not when it is normal , we addressed the question whether in subjects eligible for primary prevention of CVD, lipid peroxidation was increased enough to decrease appreciably with vitamin E. As a whole, this sample of patients with at least one CVD risk factor did not have an abnormal rate of lipid peroxidation. The levels of urinary 8-epi-PGF2α in untreated nonsmokers [146 (76–316) pg/mg creatinine] were similar to those of controls in other studies where this biomarker was selectively measured by mass spectrometry [20, 22]. They were also similar to those we found in healthy nonsmoking volunteers [139 (71–256) pg/mg creatinine; mean ± SD age, 37 ± 11y; n = 20, unpublished data].
We therefore analyzed more closely factors possibly associated with lipid peroxidation in our sample, which is rather heterogeneous but is fairly representative of a population with major risk factors for cardiovascular diseases.
3. Factors Associated with Lipid Peroxidation in Subjects at CV Risk
Multiple regression analysis of the whole group of 144 subjects showed cigarette smoking was the only strong determinant of excessive lipid peroxidation (β = 0.46; p < 0.0001, Table 3). Urinary excretion of 8-epi-PGF2α was higher in smokers (n = 24; 14 ± 6 cigarettes daily) than nonsmokers (n = 120) [185 (91–561) vs 138 (67–326) pg/mg creatinine; p = 0.003]. Vitamin E did not significantly reduce levels of 8-epi-PGF2α in smoking PPP participants [179 (91–498) vs 199 (138–561) pg/mg creatinine; p = 0.44; n = 15 and 9, respectively].
The presence of smoking, a strong determinant of lipid peroxidation, very likely hampered the detection of other clinically important variables possibly associated with urinary 8-epi-PGF2α in our initial sample. We therefore investigated the relationship between these variables and 8-epi-PGF2α levels in the 120 nonsmokers.
Systolic blood pressure
In nonsmoking participants, blood glucose measured at the time of urine collection (mean ± SD: 108 ± 24 mg/dL, n = 94) did not appear to be related to lipid peroxidation, based on multiple regression analysis (β = 0.17, p = 0.11. Table 3). However, subjects with blood glucose ≥ 140 mg/dL had higher excretion of 8-epi-PGF2α than those with <140 mg/dL [180 (121–326) vs 140 (70–266), n = 10 and 84, respectively, p = 0.009)], likely because only high blood glucose levels may be associated with excessive lipid peroxidation.
In nonsmoking PPP participants, blood cholesterol at the time of urine collection (mean ± SD: 231 ± 40 mg/dL, range 144–351) was not significantly associated with lipid peroxidation (Table 3). Aspirin administration (n = 72) did not affect urinary excretion of 8-epi-PGF2α (Table 3), as already reported [14, 26]. We found no evidence (Table 3) of increased lipid peroxidation in relation to age, sex or obesity.
Long-term supplementation with vitamin E-at a dose largely exceeding that of a vitamin E-rich diet (300 mg/day)-did not substantially reduce lipid peroxidation in people with one or more major cardiovascular risk factors. This may help explain why vitamin E was not effective for CVD prevention in the PPP study. As opposed to other studies showing an antioxidant effect of vitamin E in small, uncontrolled subgroups of patients, our observations were obtained in a sample of subjects that more realistically represent a population with cardiovascular risk factors. In fact, as usually occurs in clinical practice, most candidates for cardiovascular prevention are treated-although not necessarily controlled-for their modifiable risk factors. The lack of antioxidant effect in our sample may be explained by the rather surprising finding that lipid peroxidation was normal in a large proportion of these subjects.
We investigated whether oxidative stress was increased in high-risk subjects, given that this category could, in principle, be more sensitive to antioxidant therapy. However, we found no evidence of a correlation between CV risk score and urinary excretion of 8-epi-PGF2α in untreated subjects, suggesting that lipid peroxidation was not associated with their global CV risk. Although, on average, lipid peroxidation was normal in our population, it was clearly increased in relation to extreme conditions reportedly associated with oxidative stress. Lipid peroxidation was, in fact, significantly higher in smokers, in agreement with consistent evidence of elevated oxidative stress in cigarette smokers, mostly obtained using 8-epi-PGF2α and/or other F2-isoprostanes as biomarkers [21, 22, 27]. We also confirmed previous observations that excessive lipid peroxidation in smokers cannot be reduced by vitamin E [22, 23].
A secondary, but original finding of this study is the direct relationship between urinary excretion of an F2-isoprostane and systolic blood pressure in treated hypertensive patients with different degrees of blood pressure control. Whether this relationship also exists in untreated hypertensive patients should be investigated. An association between oxidative stress and arterial hypertension has been suggested by several clinical and experimental studies [28–32]. The hypothesis that free radical-mediated mechanisms may play a role in the pathophysiology of hypertension has recently gained support from observations that antioxidants lower blood pressure in hypertensive patients [30, 33–36]. However, vitamin E in particular does not seem effective , possibly because it was not antioxidant in these circumstances.
As to other factors reportedly related to in vivo lipid peroxidation, our findings agree with previous evidence. In particular, we confirmed that enhanced urinary excretion of 8-epi-PGF2α is associated with impaired glycemic control in diabetic patients . We did not find a correlation between urinary excretion of 8-epi-PGF2α and blood cholesterol, which, on average, was slightly elevated in our sample. Such a correlation was, in fact, found in subjects with homozygote familial hypercholesterolemia and in subjects with very high blood cholesterol, but not in those with normal cholesterol levels .
Prolonged supplementation with 300 lU/day vitamin E did not reduce lipid peroxidation in subjects with one or more major cardiovascular risk factors. On average, however, lipid peroxidation was near-normal in this population. These data may help explain the overall lack of benefit of vitamin E in recent cardiovascular prevention trials [6–8]. They also suggest the need to reassess whether lipid peroxidation is indeed an epidemiologically relevant determinant of cardiovascular diseases and, consequently, to reconsider the utility of antioxidants as a general preventive measure.
Participating physicians: Marina Bosisio Pioltelli (general practitioner, Monza), Alberto Capra (Ospedale Civile, Voghera), Mario Cristofari (Ospedale di Desio), Gaetana Palumbo (Ospedale S. Carlo Borromeo, Milano) and Susanna Rossi (Ospedale di Rovereto)
Coordinating group: Chiara Chiabrando, Fausto Avanzini, Roberto Fanelli and Maria Carla Roncaglioni (Istituto Mario Negri, Milano)
Claudia Rivalta was supported by the Fondazione "Angela and Angelo Valenti."
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