Atherosclerosis and Lipoproteins |
From the Division of Cardiology (Y.J., H.Y.P.), Yonsei Cardiovascular Genome Center, College of Medicine, and the Department of Food and Nutrition (J.H.L., O.Y.K.), College of Human Ecology, Yonsei University, Seoul, Korea, and the R&D Center (S.Y.L.), Pulmuone Tech Co, Ltd, Seoul, Korea.
Correspondence to Jong Ho Lee, PhD, 120-749 Department of Food and Nutrition, College of Human Ecology, Yonsei University, 134 Shinchon-Dong, Sudaemun-Gu, Seoul, Korea. E-mail jleeb{at}yonsei.ac.kr
| Abstract |
|---|
|
|
|---|
concentrations decreased by
28%. Also, lipid-corrected concentrations of
-carotene, retinol, tocopherols, and lycopene increased by 11% to 40%, and the percentage composition of n-6 fatty acids of serum phospholipid increased by 14% in the whole-grain group. The replacement of refined rice with whole grain and legume powder as a source of carbohydrate in a meal showed significant beneficial effects on glucose, insulin, and homocysteine concentrations and lipid peroxidation in CAD patients. These effects are likely to substantially reduce the risk factors for CAD and diabetes.
Key Words: whole grain and legume powder insulin demand malondialdehyde homocysteine 8-epi-prostaglandin F2
| Introduction |
|---|
|
|
|---|
Higher intake of many constituents of whole grains, including dietary fiber, vitamin E, and polyunsaturated fatty acids, has been independently associated with reduced risk of CAD.2,5 In addition to reduced insulin resistance, the beneficial effects of whole-grain consumption on lipid peroxidation through antioxidative action may be another possible explanation in the significant inverse relation of whole-grain intake to the risk of CAD. Furthermore, recent reports of an association between insulin resistance and hyperhomocysteinemia may suggest that whole-grain consumption decreased plasma homocysteine (Hcy).6,7 A review of epidemiological literature found a clear inverse association between whole-grain intake and the risk of ischemic heart disease death.4 However, surprisingly, only a few prospective studies, such as the Nurses Health Study, which showed that increased intake of whole grains might protect against cardiovascular disease (CVD)5 and the research showing that higher intake of whole grain foods was associated with a lower risk of ischemic stroke among women,8 have examined whether intake of whole grain decreased chronic disease risk.
In addition to whole grains, other plant products, such as vegetables and legumes, also have various kinds of phytochemicals and antioxidants. A higher intake of fruits and vegetables has been found to be protective against CVD, and an increase in their intake has been emphasized.9 Two hundred fifty observational studies on cancer and CVD have also shown that the increasing consumption of fruits and vegetables carries a large public health benefit.10 In a randomized cross-design study, phytochemicals in soybeans were found to reduce lipid peroxidation in vivo and to increase the resistance of LDL to oxidation.11 Therefore, to test the hypothesis that a higher intake of whole grain with vegetables and legumes reduces diabetes and cardiovascular risk factors in CAD patients, we specifically examined the effect of the isocaloric replacement of refined rice (220 kcal) with whole grain and legume powder (66.6% whole grains, 22.2% legumes, 5.6% seeds, and 5.6% vegetables) in CAD patients.
| Methods |
|---|
|
|
|---|
50% occlusion of
1 major coronary artery, old myocardial infarction, or angina pectoris, but any possible nonatherogenic occlusions, such as osteal stenosis and spasm, were excluded. Subjects with baseline lipid profiles with LDL cholesterol levels
3.36 mmol/L or triglyceride levels
1.81 mmol/L or total cholesterol levels
5.17 mmol/L were selected. For patients taking cholesterol-lowering medications, those with total cholesterol
3.88 mmol/L were included. All subjects were of stable weight for 1 year before the study. The macronutrient composition of each subjects usual diet was that of a typical diet with cooked refined rice, which is consumed by a substantial number of Koreans; this diet derives about 64% of energy from carbohydrates, 19% from fat, and 17% from protein. Of the CAD subjects, those with a diagnosis of diabetes, renal disease, liver disease, or thyroid disease were excluded. Subjects on vitamin supplements were also excluded. All subjects were outpatients; they underwent a clinical examination and interview and gave their written informed consent to participate in the study, which was approved by the Medical Ethics Committee of Yonsei Medical University. The present study was carried out in 2 phases: a 4-week run-in phase consisting of the usual diet with cooked refined rice and a 16-week intervention phase consisting of the usual diet or consumption of whole grain and legume powder. During the run-in period, 2 subjects, having maintained neither energy intake nor <1% variation in mean body weight, dropped out. The remaining 76 were randomly subdivided into 2 groups and were assigned to consume either their usual diet (cooked refined rice) or the whole grain and legume powder for breakfast during the 16-week intervention.
Dietary Education and Nutrient Composition of Whole Grain and Legume Powder
All subjects were given written and verbal instructions by a dietitian on how to complete 3-day (2 weekdays and 1 weekend) dietary records every 2 weeks throughout the whole study period. On the sheet, subjects were instructed to record the amount of foods before ingestion and any remaining after ingestion by weighing the foods. During the 4-week run-in period, all participants were advised to continue their usual diet of cooked refined rice. Baseline measurements were also performed at the start of the run-in phase. After the run-in period, the subjects in the control group maintained their usual diet of cooked refined rice, and the subjects in the whole-grain group consumed 70 g of whole grain and legume powder, replacing cooked refined rice as a carbohydrate source for breakfast for 16 weeks. All subjects in the whole-grain group consumed this powder by dissolving it in a glass of water. To check participants compliance during the whole study period, the dietitian interviewed them during weekly visits. They were interviewed to discern whether they were following the program well, including dietary intake and weight changes. During the study period, all participants were also encouraged to maintain their usual lifestyle and were reminded not to make any changes to their usual dietary habits, except for the whole-grain powder substitution in whole-grain group.
Whole grains and legume powder were composed of 66.6% whole grains, 22.2% legumes, 5.6% seeds, and 5.6% vegetables. The diet consisted of brown rice (22.2%), glutinous brown rice (11.1%), barley (22.2%), black beans (22.2%), sesame (5.6%), and Jobs tears (11.1%), which were all roasted and coarsely ground. Little amounts of pumpkin, onion, kale, crown daisy, chestnuts, dried sea mustard, and mushroom were also added to the powder. These were added not only for a coloring effect but also for enrichment of phytochemicals and antioxidants. This was in response to consumers concerns about their health. When compared with 150 g of cooked refined rice, 70 g of whole grain and legume powder was as isocaloric as 220 kcal, but it contained a different composition of nutrients. Cooked refined rice (150 g) provided 46.6 g carbohydrate, 3.8 g protein, 0.73 g fat, 0.15 g fiber, 0.42 mg vitamin E, 0.05 mg vitamin B1, 0.02 mg vitamin B2, 0.5 mg niacin, 0.09 mg vitamin B6, 4.62 µg folate, 0.63 g saturated fatty acid, 0.84 g monounsaturated fatty acid, and 0.90 g polyunsaturated fatty acid, whereas 70 g of whole grain and legume powder provided 35.6 g carbohydrate, 9.2 g protein, 5.0 g fat, 4.2 g fiber, 28.4 retinol equivalent vitamin A, 41.0 µg ß-carotene, 0.62 mg vitamin E, 0.2 mg vitamin B1, 0.1 mg vitamin B2, 2.0 mg niacin, 0.6 mg vitamin B6, 7.1 µg folate, 0.76 g saturated fatty acid, 1.27 g monounsaturated fatty acid, and 2.39 g polyunsaturated fatty acid. Nutrient intake data were calculated as mean values from a 3-day food record with use of the database of the computerized Korean food code, which is based on food composition tables for the year 2000 by the National Rural Living Science Institute in Korea. For more information about usual intake, a semiquantitative food frequency questionnaire was used together with a 3-day dietary record.
BMI, Blood Collection, Blood Pressure Measurement, and Lipid Profile
Body mass index (BMI) was calculated as weight (in kilograms) divided by height (in meters squared). Venous blood specimens were collected after a 12-hour fast in EDTA-treated or plain tubes. The tubes were immediately covered with aluminum foil and placed on ice in the dark until they arrived at the laboratory room. Blood pressure was read from the left arm while the subjects remained seated. An average of 3 measurements was recorded for each subject. The fasting total serum cholesterol and serum triglyceride levels were measured enzymatically, and the HDL cholesterol fraction was measured after precipitation of LDL and VLDL with dextran sulfate-magnesium. LDL cholesterol was estimated indirectly by using the Friedewald formula, ie, LDL=total cholesterol-[HDL+(triglycerides/5)], for subjects with serum triglyceride levels <4.52 mmol/L.
OGTT and HOMA
Subjects received a 75 g glucose solution after an overnight fast to investigate the effect of whole grain and legume powder on glucose and insulin responses. Venous specimens were collected before and 30, 60, 90, and 120 minutes after loading. The glucose criteria, newly developed and modified by the National Diabetes Data Group and the World Health Organization Expert Committee on Diabetes Mellitus, were used to categorize subjects as diabetic: symptoms with a casual plasma glucose >11.1 mmol/L or fasting glucose
7.0 mmol/L and oral glucose tolerance test (OGTT) with a 2-hour postload value
11.1 mmol/L.12 Glucose was measured by a glucose oxidase method with use of the Beckman Glucose Analyzer (Beckman Instruments). Insulin was measured by radioimmunoassays with commercial kits from Immuno Nucleo Corp. Each response of glucose and insulin was calculated with the area under each response curve. Insulin resistance and ß-cell function were also calculated with the homeostasis model assessment (HOMA).13 The formulas are as follows: insulin resistance=[fasting insulin (µU/mL)xfasting glucose (mmol/L)]/22.5, and ß-cell function=20xfasting insulin (µU/mL)/[fasting glucose (mmol/L)-3.5].
Plasma Total Hcy and Serum Retinol, Carotenoids, and Tocopherols
Plasma total Hcy was analyzed with a Bio20 Autoloader Amino Acid Analyzer (Pharmacia Biotech), including a postcolumn ninhydrin reaction system according to the modified method of Anderson, Ueland, and colleagues.14,15 Reversed-phase high-performance liquid chromatography (HPLC) was used to determine retinol, carotenoids, and tocopherols in serum simultaneously, as described by Yeum et al,16 Vogel et al,17 and Fotouchi et al.18 The HPLC system consisted of an Alliance Waters 2690 separation module, Waters 996 photodiode array detector, Waters 474 scanning fluorescence detector, C18 Symmetry 3.9x15-cm column, and PDA Millennium for version 2.15 data station (Waters). The Waters 474 scanning fluorescence detector was set at 294 nm for the detection of tocopherols. Levels of retinol, carotenoids, and tocopherols in serum were reported as corrected levels and expressed as the sum of the serum lipid (in millimoles per liter).19
Plasma Malondialdehyde and Folate
Plasma malondialdehyde (MDA) was assayed according to the fluorometric method described by Buckingham.20 Plasma folate level was analyzed with the kit from Immuno Nucleo Corp Pharmaceuticals.21
Urine Collection and 8-Epi-PGF2
Urine was collected after a 12-hour fast in polyethylene bottles containing 1% butylated hydroxytoluene before blood collection. The tubes were immediately covered with aluminum foil and stored at -70°C until extraction. Urinary 8-epi-prostaglandin F2
(8-epi-PGF2
) was quantified with gas chromatography (Hewlett Packard 6890) and mass selective detector (Hewlett Packard 3973), according to the modified method of Pratico et al22 and Mori et al.23 For gas chromatography/mass spectrometry, pentafluorobenzyl derivatives, as opposed to the pentafluorobenzyl ester, were used; after which, trimethylsilyl derivative, as opposed to bis-trimethylsilyl ester, was used. The gas chromatography/mass spectrometry was programmed to go from 190°C to 310°C at 10°C/min; retention time was 8.5 minutes. Quantification of 8-epi-PGF2
was performed by using the peak area ratio. Urinary creatinines were determined by the alkaline picrate (Jaffe) reaction,24 and urinary 8-epi-PGF2
levels were expressed as picomoles per millimole creatinine.
Serum Phospholipid Fatty Acid Composition
Serum phospholipid composition was analyzed with the modified method of Folch et al,25 with the use of gas chromatography (Hewlett Packard 6890). The temperatures of injection and detector ports were set at 280°C/min, and retention time was 40 minutes. A flame ionization detector was used, and helium was used as the carrier gas at 0.7 mL/min. Peaks were identified by comparison with a known standard mixture (Supelco). Individual fatty acids were calculated as a relative percentage with the elevated fatty acids set at 100% with Chemstation software. Total n-3 (18:3 n-3, 20:3 n-3, 20:5 n-3, 22:5 n-3, and 22:6 n-3) and n-6 (18:2 n-6, 18:3 n-6, 20:3 n-6, 20:4 n-6, 22:4 n-6, and 22:5 n-6) fatty acids were measured in plasma phospholipids.
Statistical Analysis
Statistical analysis was performed with Win SPSS (Statistical Package for the Social Science, SPSS Inc). For descriptive purposes, mean values were presented on untransformed and unadjusted variables. Results were expressed as mean±SE. Effects of the diet on end points were tested by a paired t test in each group before and after consumption. According to whether the subject turns out to have new-onset diabetes, fasting levels of glucose and insulin, their response areas, and insulin resistances were tested by using the Wilcoxon signed rank sum test in each group or by using the Wilcoxon rank sum test between the 2 groups. To determine a more accurate effect of whole grain and legume powder, net differences (change in whole-grain group versus change in control group) were evaluated. To compare differences in frequencies,
2 tests were used. A value of P<0.05 was considered statistically significant.
| Results |
|---|
|
|
|---|
|
Body Weight, Energy and Nutrient Intake, and Lipid Profile
There was <1% variation in mean body weight between week 0 and 16 in the 2 groups that maintained their usual energy intake. Frequent interviews with the subjects did not suggest any important changes in the physical activity patterns of the individual subjects during the study. As expected, BMI and total energy intake were similar before and after treatment in both groups. However, diastolic blood pressure decreased and energy percentage of protein intake increased significantly in the whole-grain group (Tables 1 and 2). Concentration of HDL cholesterol increased significantly in the whole-grain group. However, there were no significant differences in other lipid profiles (Table 1). With the substitution of whole grain and legume powder for refined rice, estimates of fiber and vitamin E intake increased significantly (Table 2). Compared with net differences of these parameters, percent energy intake of protein, vitamin E intake, and HDL cholesterol level in the whole-grain group showed significant increases. However, percent energy intake of carbohydrate significantly decreased in this group. There were no significant differences in net differences of the other parameters.
|
Glucose and Insulin
Glucose and insulin concentrations of the control group did not change significantly between 0 and 16 weeks, whereas serum glucose concentrations of the whole-grain group significantly decreased (Table 2). To investigate the effect of whole-grain powder on glucose and insulin response, OGTT was examined, and 9 of the subjects in the control group and 12 of the subjects in the whole-grain group were found to have new-onset diabetes. However, there was no significant difference in diabetic proportion between the 2 groups.
The effects of whole-grain and legume consumption on serum concentrations of insulin and glucose are shown in Table 3. All subjects were subdivided into 2 categories: nondiabetic subjects and subjects with new-onset diabetes according to OGTT. In the nondiabetic category, the whole-grain group showed significant decreases in fasting glucose level, response areas of glucose and insulin, and insulin resistances and a significant increase in the percentage of ß-cell function from the HOMA equation compared with the values in the control group. Net differences of these values also showed a similar pattern with results above. In the group with new-onset diabetes, the fasting level and response area of glucose in the whole-grain group significantly decreased, and net differences of these values also showed significance (Table 3).
|
MDA, 8-Epi-PGF2
, Total Hcy, Vitamins, and Carotenoids
Plasma MDA and urinary 8-epi-PGF2
concentrations decreased by
28% in the whole-grain group, but there was no significant change in the control group (Table 4). With whole-grain and legume consumption, plasma Hcy concentration decreased by 32%, and unlike the usual case, plasma folate concentration merely showed a tendency to decrease. Net differences of these values also showed significant decreases in the whole-grain group.
|
Lipid-corrected concentrations of
-carotene, retinol,
-tocopherol,
-tocopherol, and lycopene increased by 11% to 40% in the whole-grain group but did not change significantly in the control group (Table 4). Lipid-corrected concentrations of ß-carotene and cryptoxanthin did not change significantly in either group. Only in the case of retinol and
-carotene did net differences show a significant increase in the whole-grain group.
Serum Phospholipid Fatty Acids
The fatty composition of serum phospholipids at baseline was not significantly different between the 2 groups (Table 4). In the whole-grain group, the percent composition of n-6 fatty acids of serum phospholipid increased significantly; however, there was no significance in the net difference between the 2 groups.
| Discussion |
|---|
|
|
|---|
Whole-grain products, because of their physical form and high content of fiber, tend to be slowly digested and absorbed and, thus, have relatively low glycemic indexes.5 In diabetic and nondiabetic subjects, higher intakes of foods with a low glycemic index have been reported to have an association with lower concentrations of insulin. Reduced insulin demand, representing improvement of insulin sensitivity, may be 1 of the protective mechanisms for CAD and diabetes in association with a higher intake of whole grain.1,5 The present study also shows that consumption of whole grain and legume powder reduces insulin demand and hyperinsulinemia in CAD patients with and without diabetes. In fact, an epidemiological study reported that every 6-g increase in daily fiber consumption was associated with a 25% reduction in ischemic heart disease mortality.2 In addition, reduced risk for CAD has been reported in people who consumed a diet containing at least 37 g of dietary fiber per day.2
Whole-grain and legume consumption that decreases insulin resistance or insulin demand, over a long term, may reduce plasma Hcy concentration. This suggestion is related to the report of an association between insulin resistance and hyperhomocysteinemia.7 Recently, elevated total Hcy concentration, an independent risk factor for atherosclerosis,26 has also been suggested to be a possible biological link between insulin resistance and atherothrombosis.6 Although serum concentration of folate did not change significantly, plasma Hcy concentration decreased in the whole-grain group. It might be related to the improvement of insulin resistance, according to decrease in fasting glucose and decreased tendencies of fasting insulin and their respective response.
In addition to being a good source of dietary fiber, whole grains may have beneficial combinations of many micronutrients, antioxidants, and phytochemicals.4,5 Whole grains, legumes, and vegetables are important dietary sources of antioxidant vitamins and unsaturated fatty acids. The intake of polyunsaturated fatty acids and vitamin E is associated with protection from CAD, and carotenoids may also have such protective effects.2 A tendency toward an increase in the percent composition of n-6 fatty acids and in serum concentrations of lipid-corrected carotenoids, especially,
-tocopherol and retinol, in the whole-grain group of the present study may result from an increased intake of these nutrients from whole grains. In addition, other antioxidant intakes from whole grain and legume powder and reduced oxidative stress, such as decreased plasma Hcy concentration, could also spare serum tocopherols and some carotenoids.
Whole grains, legumes, and vegetables contain many antioxidants, including vitamins, trace minerals, and nonnutrients, such as phenolic acids, lignans, and phytoestrogens, and antinutrients, such as phytic acid.4,9,13 Antioxidants in whole grains can slow the rate of oxidation of oxidizable substrates.3,4 Measurement of products of lipid peroxidation, such as plasma MDA27 and urinary 8-epi-PGF2
,28,29 may offer a noninvasive approach to the assessment of oxidative stress and the efficacy of antioxidant therapies. The decrease of plasma MDA and urinary 8-epi-PGF2
concentrations in the whole-grain group might be due to the antioxidative effects of many antioxidants in whole grains and other plant products. In addition, reduced plasma Hcy concentration in the whole-grain group might contribute to the decrease in lipid peroxidation. Recently, Voutilainen et al26 published a study about an enhancement of in vivo lipid peroxidation at elevated fasting plasma total Hcy concentration.
In summary, the present study showed significant beneficial effects of consumption of whole grains and other plant products as a form of coarse powder on glucose, insulin, and Hcy concentrations and lipid peroxidation in CAD patients. These effects are likely to substantially reduce the risk factors of CAD and diabetes in CAD patients. The biological mechanism, whereby whole grain and legume powder may exert their protective effect is not clear in the present study, but it is likely to be due to multiple mechanisms, such as fiber, antioxidants, and many constituents of whole grain and legume powder. Therefore, grains should be consumed in a minimally refined form, and frequent consumption of vegetables and legumes should be recommended to reduce cardiovascular risk factors and the incidence of diabetes in CAD patients.
| Acknowledgments |
|---|
Received May 14, 2001; accepted September 28, 2001.
| References |
|---|
|
|
|---|
2. Anderson JW, Hanna TJ. Impact of nondigestible carbohydrates on serum lipoproteins and risk for cardiovascular disease. J Nutr. 1999; 29: 1457s1466s.
3. Jacobs DR, Meyer KA, Kushi LH, Folsom AR. Whole-grain intake may reduce the risk of ischemic heart disease death in postmenopausal women: the Iowa Womens Health Study. Am J Clin Nutr. 1998; 68: 248257.[Abstract]
4. Slavin J, Jacobs D, Marquart L. Whole-grain consumption and chronic disease: protective mechanisms. Nutr Cancer. 1997; 27: 421.
5.
Liu S, Stampfer MJ, Hu FB, Giovannucci E, Rimm E, Manson JE, Hennekens CH, Willett WC. Whole-grain consumption and risk of coronary heart disease: results from the Nurses Health Study. Am J Clin Nutr. 1999; 70: 412419.
6. Giltay EJ, Hoogeveen EK, Elbers JMH, Gooren LJG, Asscheman H, Stehouwer CDA. Insulin resistance is associated with elevated plasma total homocysteine levels in healthy, non-obese subjects. Atherosclerosis. 1998; 139: 197198.[Medline] [Order article via Infotrieve]
7. Fonseca VA, Mudaliar S, Schmidt B, Fink LM, Kern PA, Henry RR. Plasma homocysteine concentrations are regulated by acute hyperinsulinemia in nondiabetic but not type 2 diabetic subjects. Metabolism. 1998; 47: 686689.[Medline] [Order article via Infotrieve]
8.
Liu S, Manson JE, Stampfer MJ, Rexrode KM, Hu FB, Rimm EB, Willett WC. Whole grain consumption and risk of ischemic stroke in women: a prospective study. JAMA. 2000; 284: 15341540.
9.
Liu S, Manson JE, Lee IM, Cole SR, Hennekens CH, Willett WC, Buring JE. Fruit and vegetable intake and risk of cardiovascular disease: the Womens Health Study. Am J Clin Nutr. 2000; 72: 899900.
10. Negri E, La Vecchia C, Franceshci S, DAvanzo B, Parazzini F. Vegetable and fruit consumption and cancer risk. Int J Cancer. 1991; 48: 350354.[Medline] [Order article via Infotrieve]
11. Block G, Patterson B, Subar A. Fruit, vegetables and cancer prevention: a review of the epidemiological evidence. Nutr Cancer. 1992; 18: 129.[Medline] [Order article via Infotrieve]
12. The Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. Diabetes Care. 1997; 20: 11831197.[Medline] [Order article via Infotrieve]
13. Haffner SM, Kennedv E, Gonsalez C, Stern MP, Miettinen H. A prospective analysis of the HOMA model. Diabetes Care. 1996; 19: 11381141.[Abstract]
14. Anderson A, Battstr L, Isaksson A, Israelsson B, Hultberg B. Determination of homocysteine in plasma by ion-exchange chromatography. Scand J Clin Lab Invest. 1989; 49: 445449.[Medline] [Order article via Infotrieve]
15. Ueland PM, Refsum H, Stabler SP, Mailnow MR, Anderson A, Allen RH. Total homocysteine in plasma or serum: method and clinical applications. Clin Chem. 1993; 39: 17641779.[Abstract]
16. Yeum K-J, Lee-Kim YC, Yoon S, Lee KY, Park IS, Lee KS, Kim BS, Tang G Russell RM, Krinsky NI. Similar metabolites formed from ß-carotene by human gastric mucosal homogenates, lipoxygenase or linoleic acid hydroperoxide. Arch Biochem Biophys. 1995; 321: 167174.[Medline] [Order article via Infotrieve]
17.
Vogel S, Contosis JH, Tucker KL, Wilson PWF, Schafer EJ, Lammi-Keefe CJ. Plasma retinol and plasma and lipoprotein tocopherol and carotenoid concentrations in healthy elderly participants of the Framingham Heart Study. Am J Clin Nutr. 1997; 66: 950958.
18. Fotouchi N, Meydani M, Santos MS, Meydani S, Hennekens CH, Gaziano JM. Carotenoid and tocopherol concentrations in plasma, peripheral blood mononuclear cells, and red blood cells after long-term ß-carotene supplementation in men. Am J Clin Nutr. 1996; 63: 953958.
19. Thurnham DI, Davis JA, Crump BJ, Situnayake RD, Davis M. The use of different lipids to express serum tocopherol: lipid ratios of the measurement of vitamin E status. Ann Clin Biochem. 1986; 23: 514520.[Medline] [Order article via Infotrieve]
20.
Buckingum KW. Effect of dietary polyunsaturated/saturated fatty acid ratio and dietary vitamin E on lipid peroxidation in the rat. J Nutr. 1985; 115: 14251435.
21. Reynolds TM, Brain A. A simple internally-standardized isocratic HPLC assay for vitamin B6 in human serum. J Lipid Chromatogr. 1992; 15: 897914.
22.
Pratico D, Lawson JA, Fitzgerald GA. Cyclooxygenase-dependent formation of the isoprostane, 8-epi-prostaglandin F2
. J Biol Chem. 1995; 270: 9801008.
23. Mori TA, Croft KD, Puddey IB, Beilin LJ. An improved method for the measurement of urinary and plasma F2-isoprostanes using gas chromatography-mass spectrometry. Anal Biochem. 1999; 268: 1125.
24. Liobat-Estelles M, Sevillano-Cabeja A, Campins-Falco P. Kinetic chemometric studies of the determination of creatinine using the Jaffe reaction, I: kinetics of the reaction; analytical conclusion. Analyst. 1989; 11: 597602.
25. Folch J, Lees M, Stanley GHS. A simple method for the isolation and purification of total lipids from animal tissue. J Biol Chem. 1975; 226: 497509.
26.
Voutilainen S, Morrow JD, Roberts LJ, Alfthan G, Alho H, Nyyssen K, Salone JT. Enhanced in vivo lipid peroxidation at elevated plasma total homocysteine levels. Arterioscler Thromb Vasc Biol. 1999; 19: 12631266.
27. Meraji S, Ziouzenkova O, Resch U, Khoschsorur A, Tatzer F, Esterbauer H. Enhanced plasma level of lipid peroxidation in Iranians could be improved by antioxidants supplementation. Eur J Clin Nutr. 1997; 51: 318325.[Medline] [Order article via Infotrieve]
28.
Reilly MP, Delanty N, Roy L, Rokach J, Callaghan PO, Crean P, Lawson JA, Fitzgerald GA. Increased formation of the isoprostanes IPF2-I and 8-epi-prostaglandin F2
, in acute coronary angioplasty: evidence for oxidant stress during coronary reperfusion in human. Circulation. 1997; 96: 33143320.
29.
Delanty N, Reilly M, Pratico D, FitzGerald DJ, Lawson JA, Fitzgerald GA. 8-Epi-prostaglandin F2
: specific analysis of an isoeicosanoid as an index of oxidant stress in vivo. Br J Clin Pharmacol. 1996; 42: 1519.[Medline]
[Order article via Infotrieve]
This article has been cited by other articles:
![]() |
V. E Ohrvik, J. C Olsson, B. E Sundberg, and C. M Witthoft Effect of 2 pieces of nutritional advice on folate status in Swedish women: a randomized controlled trial Am. J. Clinical Nutrition, April 1, 2009; 89(4): 1053 - 1058. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. K. Chung, J. S. Chae, Y. J. Hyun, J. K. Paik, J. Y. Kim, Y. Jang, H. M. Kwon, Y. D. Song, H. C. Lee, and J. H. Lee Influence of Adiponectin Gene Polymorphisms on Adiponectin Level and Insulin Resistance Index in Response to Dietary Intervention in Overweight-Obese Patients With Impaired Fasting Glucose or Newly Diagnosed Type 2 Diabetes Diabetes Care, April 1, 2009; 32(4): 552 - 558. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. A. Timm and J. L. Slavin Dietary Fiber and the Relationship to Chronic Diseases American Journal of Lifestyle Medicine, June 1, 2008; 2(3): 233 - 240. [Abstract] [PDF] |
||||
![]() |
D. R Jacobs Jr, L. F. Andersen, and R. Blomhoff Whole-grain consumption is associated with a reduced risk of noncardiovascular, noncancer death attributed to inflammatory diseases in the Iowa Women's Health Study Am. J. Clinical Nutrition, June 1, 2007; 85(6): 1606 - 1614. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Andersson, S. Tengblad, B. Karlstrom, A. Kamal-Eldin, R. Landberg, S. Basu, P. Aman, and B. Vessby Whole-Grain Foods Do Not Affect Insulin Sensitivity or Markers of Lipid Peroxidation and Inflammation in Healthy, Moderately Overweight Subjects J. Nutr., June 1, 2007; 137(6): 1401 - 1407. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. L Lutsey, L. M Steffen, H. A Feldman, D. H Hoelscher, L. S Webber, R. V Luepker, L. A Lytle, M. Zive, and S. K Osganian Serum homocysteine is related to food intake in adolescents: the Child and Adolescent Trial for Cardiovascular Health Am. J. Clinical Nutrition, June 1, 2006; 83(6): 1380 - 1386. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. K Jensen, P. Koh-Banerjee, M. Franz, L. Sampson, M. Gronbaek, and E. B Rimm Whole grains, bran, and germ in relation to homocysteine and markers of glycemic control, lipids, and inflammation 1 Am. J. Clinical Nutrition, February 1, 2006; 83(2): 275 - 283. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. K. Koh, M. J. Quon, S. H. Han, W.-J. Chung, J. Y. Ahn, J.-a Kim, Y. Lee, and E. K. Shin Additive Beneficial Effects of Fenofibrate Combined With Candesartan in the Treatment of Hypertriglyceridemic Hypertensive Patients Diabetes Care, February 1, 2006; 29(2): 195 - 201. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. R Sahyoun, P. F Jacques, X. L Zhang, W. Juan, and N. M McKeown Whole-grain intake is inversely associated with the metabolic syndrome and mortality in older adults Am. J. Clinical Nutrition, January 1, 2006; 83(1): 124 - 131. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Lairon, N. Arnault, S. Bertrais, R. Planells, E. Clero, S. Hercberg, and M.-C. Boutron-Ruault Dietary fiber intake and risk factors for cardiovascular disease in French adults Am. J. Clinical Nutrition, December 1, 2005; 82(6): 1185 - 1194. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Durga, L. J. H. van Tits, E. G. Schouten, F. J. Kok, and P. Verhoef Effect of Lowering of Homocysteine Levels on Inflammatory Markers: A Randomized Controlled Trial Arch Intern Med, June 27, 2005; 165(12): 1388 - 1394. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. K. Roberts and R. J. Barnard Effects of exercise and diet on chronic disease J Appl Physiol, January 1, 2005; 98(1): 3 - 30. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. R. Peterson, P. Herrero, K. B. Schechtman, S. B. Racette, A. D. Waggoner, Z. Kisrieva-Ware, C. Dence, S. Klein, J. Marsala, T. Meyer, et al. Effect of Obesity and Insulin Resistance on Myocardial Substrate Metabolism and Efficiency in Young Women Circulation, May 11, 2004; 109(18): 2191 - 2196. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. D Liese, A. K Roach, K. C Sparks, L. Marquart, R. B D'Agostino Jr, and E. J Mayer-Davis Whole-grain intake and insulin sensitivity: the Insulin Resistance Atherosclerosis Study Am. J. Clinical Nutrition, November 1, 2003; 78(5): 965 - 971. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. K. Koh, J. Y. Ahn, S. H. Han, D. S. Kim, D. K. Jin, H. S. Kim, M.-S. Shin, T. H. Ahn, I. S. Choi, and E. K. Shin Pleiotropic effects of angiotensin II receptor blocker in hypertensive patients J. Am. Coll. Cardiol., September 3, 2003; 42(5): 905 - 910. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. R Jacobs Jr and L. M Steffen Nutrients, foods, and dietary patterns as exposures in research: a framework for food synergy Am. J. Clinical Nutrition, September 1, 2003; 78(3): 508S - 513. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. B Hu Plant-based foods and prevention of cardiovascular disease: an overview Am. J. Clinical Nutrition, September 1, 2003; 78(3): 544S - 551. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Liu Whole-grain foods, dietary fiber, and type 2 diabetes: searching for a kernel of truth Am. J. Clinical Nutrition, March 1, 2003; 77(3): 527 - 529. [Full Text] [PDF] |
||||
![]() |
D. R. Jacobs Jr and L. M. Steffen Wheat Bran, Whole Grain, and Food Synergy Diabetes Care, September 1, 2002; 25(9): 1652 - 1653. [Full Text] [PDF] |
||||
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
ATVB Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 2001 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |