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Original Research Communication |
1 From the UMR INSERM unit 557/INRA unit 1125, Institut Scientifique et Technique de la Nutrition et de lAlimentation, ISTNA (LIM, GPdC, SB, MM, MZ, CF, SH, and PG) and Unité de Surveillance et dEpidémiologie Nutritionnelle, InVS (LIM and SH), Conservatoire National des Arts et Metiers, Paris; the Laboratoire de Physiologie, Faculté de Médecine, Dijon, France (J-CG); the Laboratoire de Laboratoire de Biologie du Stress Oxydant, Faculté de Pharmacie, Grenoble, France (VD and AF); and the Laboratoire de Biochimie Médicale et Pédiatrique, INSERM unit 308, Faculté de Médecine, Vandoeuvre-lès-Nancy, France (J-PN).
2 Supported in part by a grant from Kelloggs Produit Alimentaire, Rosny sous Bois, France. Bio-Rad, Vitry sur Seine, France, and Carlo Erba, Val de Reuil, France, provided materials for analyzing blood samples.
3 Address reprint requests to LI Mennen, ISTNA/CNAM, 5 rue du Vertbois, 75003 Paris, France. E-mail: s_mennen{at}vcnam.cnam.fr.
| ABSTRACT |
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Objective: We evaluated the determinants of tHcy in healthy French adults.
Design: tHcy was measured by HPLC and fluorometric detection in 1139 women and 931 men aged 3560 y. Subjects were participants of the Supplementation with Antioxidant Vitamins and Minerals Study, which investigates the effects of antioxidant supplementation on chronic diseases. Red blood cell folate (RBCF), plasma vitamins B-6 and B-12, and cardiovascular disease risk factors were also measured. The habitual diet was assessed in 616 subjects. Cross-sectional analyses were adjusted for age, smoking, energy intake, and concentration or intake of folate and vitamin B-6, where appropriate.
Results: The mean (±SD) tHcy concentration was 8.74 ± 2.71 µmol/L in women and 10.82 ± 3.49 µmol/L in men. In women, tHcy was positively related to age (P = 0.001), apolipoprotein B (P < 0.01), serum triacylglycerol (P < 0.01), fasting glucose (P = 0.02), and coffee and alcohol consumption (both P < 0.01) and inversely related to RBCF (P = 0.11) and plasma vitamin B-12 (P = 0.08) and vitamin B-6 (P = 0.01) intakes. In men, tHcy was positively associated with body mass index (P = 0.03), blood pressure (P < 0.02), serum triacylglycerol (P < 0.01), fasting glucose (P = 0.01), and energy intake (P < 0.01) and inversely associated with physical activity (P = 0.04), RCBF (P = 0.02), plasma vitamin B-12 (P = 0.09), and dietary fiber (P < 0.01), folate (P = 0.03), and vitamin B-6 (P = 0.09) intakes.
Conclusion: To control tHcy, decreasing coffee and alcohol consumption may be important in women, whereas increasing physical activity, dietary fiber, and folate intake may be important in men.
Key Words: Homocysteine habitual diet folate cardiovascular disease risk men women coffee Supplementation with Antioxident Vitamins and Minerals Study France
| INTRODUCTION |
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T methylenetetrahydrofolate reductase (EC 1.7.99.5) polymorphism; carriers of the T allele have higher tHcy concentrations than do noncarriers (3). Age and sex are 2 other important determinants of tHcy; it is known that tHcy increases steadily with age and that tHcy is higher in men than in women (49). Major lifestyle determinants of tHcy in apparently healthy subjects are dietary and plasma folate, vitamin B-6 and B-12, smoking, coffee consumption, and physical activity (410). Evidence also exists that tHcy is related to classic cardiovascular disease risk factors such as blood pressure, body mass index, and blood lipids (4, 7, 10, 11). The determinants of tHcy, however, likely are to vary among cultures and countries. Previous studies on lifestyle determinants of tHcy have taken place in Anglo-Saxon countries (United States, Canada, and northern Europe), and one has been performed in Southeast Asia. No information is available on the relation of tHcy and cardiovascular disease and lifestyle factors in middle and southern Europe, where lifestyle habits and cardiovascular disease morbidity are quite different from those in Anglo-Saxon countries. Although the incidence of cardiovascular disease is lower in France than in northern Europe, it remains the major cause of morbidity and mortality. For effective prevention of this disease, it is important to know which are the modifiable determinants of the cardiovascular disease risk factors, including tHcy. In the present study, therefore, we evaluated tHcy in a large French population of healthy men and women between 35 and 60 y of age.
| SUBJECTS AND METHODS |
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± SD: 46.4 ± 6.7 y) and men aged 4560 y (51.1 ± 4.7 y), and none of them use vitamin supplements. Subjects were invited to participate by a multimedia campaign in the whole of France. Potential subjects received detailed information on the study and performed a self-test of acceptability of the daily supplement. A total of 12735 subjects were included at baseline in 1994 and are being followed up for 8 y. Details on recruitment and study design were described earlier (12). For the present analyses, only those subjects were included for whom homocysteine concentrations were measured (n = 2070), which was a random sample of the total population, with a sex ratio of 50%. For 616 subjects in this group, detailed information on the habitual diet was also available. The Supplementation with Antioxidant Vitamins and Minerals Study was approved by the ethical committee for studies on human subjects (CCPPRB no. 706) of Paris-Cochin Hospital and the Comité National Informatique et Liberté (CNIL no. 334641), which advocates that all medical information is confidential and anonymous.
Dietary assessment
The subjects kept a 24-h dietary record randomly every 2 mo, for a total of 6 records/y (2 weekend days and 4 weekdays), so that each day of the week and all seasons were covered for the mean intake of all participants. Information was collected with the use of the Minitel Telematic Network. The Minitel is a small terminal widely used in France as an adjunct to the telephone. At the beginning of the study, participants received free of charge a tiny central processing unit specifically developed for the study and loaded with specialized software that allows subjects to fill out the computerized dietary record off-line and to transmit data during brief telephone connections. The software allowed the subjects to have an interactive discussion with the coordinating center and ask questions, which were answered within a day by one of the investigators. These capabilities and an instruction manual for codification of foods guided the participants during the completion of the records. The manual contains photographs showing portions in 3 sizes, and along with the 2 intermediate and 2 extreme positions, 7 choices are available to indicate the consumed portion. Photos of portion sizes were previously validated with the use of 780 subjects in a pilot study (13). Data on variables such as cooking methods, seasoning, types of foods (fresh, frozen, canned, etc), and place and time of consumption were also collected.
Measurements of risk indicators
All measurements were performed at the end of the second study year. Weight and height and waist and hip circumferences were measured while the subjects were wearing underwear, and body mass index was calculated by dividing weight by the square of height (kg/m2). Blood pressure was measured one time at each arm with a standard mercury sphygmomanometer in subjects who had been lying down for 10 min. The mean of these 2 measurements was taken for analyses. Information about smoking habits was obtained by means of a questionnaire. Blood samples were obtained in Vacutainer tubes (Becton Dickinson, Le pont de Claix, France) from subjects who had been fasting for 12 h. Fasting glucose, total cholesterol, and serum triacylglycerol were all measured by an enzymatic method (Technicon DAX, Eragny sur Oise, France). Apolipoprotein (apo) A-I and apo B were measured by using a nephelemetric assay (BNA; Behring, Paris la Défence, France) and lipoprotein(a) with an immunonephelimetric assay (Array Beckman, Roissy Charles de Gaulle, France). Blood samples for measurement of plasma tHcy were collected in EDTA-containing tubes, which were centrifuged within the hour after the blood sampling at room temperature for 10 min at 3000 x g. The plasma fraction was then transferred to cryotubes, which were kept at -20° C until measurement 6 mo later. tHcy was measured as described earlier (14) by HPLC and fluorometric detection with a Bio-Rad kit (Hercule SA, Vitry sur Seine, France). The concentration of red blood cell folate was estimated by microbiological assay, pyridoxal 5'-phosphate (PLP) by HPLC and fluorometric detection, and vitamin B-12 (n = 309) by an automated chemiluminescence method (Chiron Diagnostics, East Walpole, MA). Laboratory quality assurance included analysis of serum from standard pools with each run and, if available, international standards.
Data analyses
Intakes of energy, protein (animal and vegetable), carbohydrate, total fat, fiber (soluble and nonsoluble), and alcohol were calculated from food consumption with the use of the French computerized food-composition table CIQUAL (15). We used data from those subjects who completed 6 records in the year before the blood sample for homocysteine measurement was taken.
Associations between homocysteine concentrations and cardiovascular disease risk factors and dietary factors were evaluated by using analyses of covariance adjusted for age, smoking, and folate and PLP concentrations or folate and vitamin B-6 intakes, where appropriate. Independent continuous variables were divided in quartiles, which were created separately for men and women. Fasting glucose and serum triacylglycerol were log transformed to obtain a normal distribution.
| RESULTS |
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| DISCUSSION |
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The present data used a cross-sectional design, which implies that no conclusions can be drawn on the causal effect of the determinants of tHcy. It may be that tHcy is a indicator of ongoing cardiovascular disease, which could explain the relation with other risk factors for cardiovascular disease (16). Dietary habits, however, were estimated in the year before tHcy was measured. It is, therefore, more likely that diet may have a causal effect on tHcy. This is especially the case for dietary folate and vitamin B-12 intake, because it is known from intervention studies that they decrease tHcy (17).
The dietary data were only available in a subsample of the total population in which tHcy was measured. This could have biased the relation between tHcy and dietary factors. However, the general characteristics were similar in the subsample to those in the total population (data not shown), which indicates that the subsample was not a distinct group. It has to be noted, however, that our subjects were not representative of the total French population. They were rather healthy, and not many subjects with very high levels of the cardiovascular disease risk factors were included, which may have underestimated the observed associations.
The difference between men and women in the relation of tHcy with age was probably caused by the fact that the age range in the women was much larger than in the men. Even though no statistically significant relation was found in the men, tHcy was highest in the oldest category, and the truncated distribution may have been too small to show an association. The differences between men and women in the associations of tHcy with systolic and diastolic blood pressure and body mass index are more difficult to explain. Although Morris et al (18) showed that differences in tHcy concentrations may be explained by the differences in estrogen status, we did not observe a difference in tHcy between pre- and postmenopausal women. Nygard et al (4) observed statistically significant associations between tHcy and blood pressure, total cholesterol, and serum triacylglycerol in both men and women. However, they did not divide the variables in quartiles but used fixed limits to create categories of cardiovascular disease risk factors. It was not possible to follow the same strategy in our population because too few subjects had elevated risk factors. Curiously, de Bree et al (11), who also used quartiles in their statistical analyses, observed an association between tHcy and total and HDL cholesterol in women but not in men. They did not find an effect of blood pressure. Jacques et al (8) showed positive relations between body mass index in quartiles and tHcy, but they did not separate their analyses between women and men, which means it is possible that their observed relation was caused by a strong relation in men only, as we observed in our study.
Differences in the use of categories for the explaining variable may also be an explanation for the contradictory results on the association of tHcy with physical activity. Again, Nygard et al (4) used a 4-category variable, from no exercise to heavy training, to describe physical activity and found lower tHcy concentrations in those with the highest physical activity. We used a separation in 3 classes and observed only an effect in men, whereas Saw et al (9) distinguished only between having or not having weekly exercise, and found no effect on tHcy. This indicates that to show a relation of tHcy with physical activity, these habits should be questioned in detail, so that accurate separations can be made between different categories.
Many studies observed higher concentrations of tHcy in smokers than in nonsmokers (4, 6, 710), although Rasmussen et al (7) could not confirm this in elderly women and Lussier-Cacan et al (5) did not find any association at all. It is known, however, that smokers eat less fruit and vegetables and may thus have a lower intake of folate and vitamin B-6 (19). Indeed, we observed lower concentrations of folate and PLP in smokers than in nonsmokers (data not shown). It seems therefore logical that the positive trend between smoking and tHcy in men in our study disappeared after adjustment for folate and PLP concentrations. This phenomenon was also found in the study by Saw et al (9), indicating that the effects of smoking may thus be biased by concomitant dietary factors.
The relations between dietary habits and tHcy were investigated previously. Stolzenberg-Solomon et al (20) found an inverse relation between tHcy and dietary protein intake in 260 male and female retired schoolteachers. Jacques et al (8) observed inverse associations between tHcy and intakes of folate, vitamin B-6, and riboflavin, but they did not separate their analyses for men and women. In the study by Rasmussen et al (7), subjects with a high folate intake had a lower tHcy concentration, but this was stronger in younger than in older women. Neither of these 2 studies presented information on intake of fruit and vegetables or dietary fiber. Oshaug et al (21) evaluated tHcy in relation to diet in 310 healthy male offshore workers. Vegetable intake but not fruit intake was inversely associated with tHcy, as was the consumption of skimmed milk and bread. No adjustment was made for intake of folate, vitamin B-6, or vitamin B-12. In the present study the inverse relation between fruit and vegetable intake and tHcy disappeared after adjustment for folate intake, indicating that the folate content of fruit and vegetables determines the relation with tHcy. This, however, was not the case for dietary fiber, indicating that dietary fiber may have a separate effect on tHcy in men, independent of folate intake. Residual confounding may be another explanation for this, as men may have had more difficulties in correct recording of food intake than do women. Confounding by folate intake may also be important for the relation with total energy intake, as we observed in men; folate intake is positively associated with total energy intake and inversely with tHcy and may thus diminish a positive relation between total energy intake and tHcy. This explains why the relation between these factors becomes stronger after adjustment for folate intake. Although vitamin B-6 intake was strongly related to tHcy, no relation of tHcy with PLP was observed. PLP is the bioactive form of vitamin B-6, and when enough vitamin B-6 is ingested, as in an apparently healthy adult population, the concentration of PLP will reach a plateau. At this concentration PLP will not reflect vitamin B-6 intake, because PLP is produced in response to biological needs. Furthermore, intervention studies showed that adding vitamin B-6 supplementation to folic acid supplementation did not further lower blood homocysteine (17). Indeed, the strength of the relation between tHcy and vitamin B-6 intake diminished after adjustment for folate intake, and it is possible that residual confounding is the explanation of the observed relation. The lack of association between vitamin B-12 intake and tHcy in both men and women confirms the result of Jacques et al (8). In contrast, the relation between riboflavin or folate (in women) and tHcy was no longer significant after multiple adjustment. This may be because of the lower number of subjects in the present study for which dietary data were available.
Many studies observed a higher tHcy with a higher coffee consumption and to a lesser extent with a lower tea consumption (79, 20, 22). A recent intervention study showed that consumption of a high dose of chlorogenic acid, a major polyphenol in coffee, or consumption of black tea increases tHcy 45 h after intake (23). The present study could confirm this only for coffee consumption in women. However, none of the aforementioned studies separated their analyses for women and men. The fact that no relation between tHcy and tea was seen can be ascribed to the low tea consumption in our study, which is typical for a French population.
In conclusion, the determinants of tHcy are not the same for women as for men. To prevent cardiovascular disease, a decrease in coffee and alcohol consumption seems to be important in women, whereas an increase in physical activity and dietary fiber and folate intakes and a decrease in total energy intake may be important in men. Intervention studies should be performed to confirm these observations.
| REFERENCES |
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