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Factorial study of the effect of n–3 fatty acid supplementation and atorvastatin on the kinetics of HDL apolipoproteins A-I and A-II in men with abdominal obesity^1,2,3

¹ From the Metabolic Research Centre, School of Medicine and Pharmacology, University of Western Australia, Perth, Australia

² Supported by grants from the National Health and Medical Research Council and the National Heart Foundation of Australia. Support was also provided by the Raine Medical Research Foundation, the Royal Perth Hospital Medical Research Foundation, and Pfizer. DCC was supported by a postdoctoral fellowship from the Raine/National Heart Foundation of Australia. PHRB is a fellow of the NHMRC of Australia and is partially supported by the National Institutes of Health (NIBIB grant P41 EB-001975). Omacor capsules and corn oil were a generous gift from Provona Biocare, Oslo, Norway.

³ Reprints not available. Address correspondence to PHR Barrett, Metabolic Research Centre, School of Medicine and Pharmacology, Royal Perth Hospital, Box X2213 GPO, Perth, WA 6847, Australia. E-mail: pbarrett{at}cyllene.uwa.edu.au.

	ABSTRACT

TOP ABSTRACT INTRODUCTION SUBJECTS AND METHODS RESULTS DISCUSSION REFERENCES

 
Background: Disturbed HDL metabolism in insulin-resistant, obese subjects may account for an increased risk of cardiovascular disease. Fish oils and atorvastatin increase plasma HDL cholesterol, but the underlying mechanisms responsible for this change are not fully understood.

Objective: We studied the independent and combined effects of fish oils and atorvastatin on the metabolism of HDL apolipoprotein A-I (apo A-I) and HDL apo A-II in obese men.

Design: We conducted a 6-wk randomized, placebo-controlled, 2 x 2 factorial intervention study of the effects of fish oils (4 g/d) and atorvastatin (40 mg/d) on the kinetics of HDL apo A-I and HDL apo A-II in 48 obese men with dyslipidemia with intravenous administration of [d₃]-leucine. Isotopic enrichments of apo A-I and apo A-II were measured with gas chromatography–mass spectrometry with kinetic parameters derived from a multicompartmental model (SAAM II).

Results: Fish oils and atorvastatin significantly decreased plasma triacylglycerols and increased HDL cholesterol and HDL₂ cholesterol (P < 0.05 for main effects). A significant (P < 0.02) main effect of fish oils was observed in decreasing the fractional catabolic rate of HDL apo A-I and HDL apo A-II. This was coupled with a significant decrease in the corresponding production rates, accounting for a lack of treatment effect on plasma concentrations of apo A-I and apo A-II. Atorvastatin did not significantly alter the concentrations or kinetic parameters of HDL apo A-I and HDL apo A-II. None of the treatments altered insulin resistance.

Conclusions: Fish oils, but not atorvastatin, influence HDL metabolism chiefly by decreasing both the catabolism and production of HDL apo A-I and HDL apo A-II in insulin-resistant obese men. Addition of atorvastatin to treatment with fish oils had no additional effect on HDL kinetics compared with fish oils alone.

Key Words: Cardiovascular disease • n–3 fatty acids • 3-hydroxy-3-methylglutaryl coenzyme A reductase • HMG CoA reductase inhibitor • HDL • lipoprotein metabolism

	INTRODUCTION

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Obesity, an important risk factor for cardiovascular disease and type 2 diabetes, is a growing problem in developed and developing populations (1). Abdominal obesity is typically seen in overweight men and is strongly associated with hypertriglyceridemia and low HDL cholesterol, which may chiefly account for the increased risk of atherosclerosis in these men (2).

With the use of stable isotopes and multicompartmental modeling, we previously showed that in men with insulin resistance the dysregulation of apolipoprotein (apo) B metabolism may be caused by a combination of overproduction of VLDL apo B and decreased catabolism of apo B–containing particles (3). Apo A-I and apo A-II are the main apolipoproteins of HDL. Compelling evidence supports the antiatherogenic role of apo A-I in preventing cardiovascular disease, with less consistent data available for apo A-II (4, 5). Expansion of the VLDL-triacylglycerol pool in insulin resistance enhances cholesteryl ester transfer protein (CETP)–mediated heteroexchange of neutral lipids among lipoproteins, thereby increasing HDL-triacylglycerol content. Subsequent hydrolysis by hepatic lipase results in a thermodynamically unstable HDL particle that is catabolized rapidly by the liver and kidney (6). Consistent with this, we and others previously showed an increased catabolism of HDL-apo A-I and HDL-apo A-II particles in insulin-resistant subjects (7-10).

Effective management of dyslipidemia in abdominal obesity often requires lipid-regulating pharmacotherapy (11). Data from several clinical trials support the use of fish oils (rich source of n–3 fatty acids) and 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors (statins) to treat dyslipidemia in insulin resistance and obesity (12-15). Combination of n–3 fatty acids with a statin may also constitute a safe and effective treatment for obesity-related dyslipidemia (16, 17). We have previously reported that both n–3 fatty acids and atorvastatin effectively lowered plasma triacylglycerol and increased HDL-cholesterol concentrations (17). Our kinetic data suggest that n–3 fatty acids decrease VLDL-apo B secretion (18), whereas atorvastatin increases hepatic clearance of all apo B–containing lipoproteins (19). By decreasing plasma triacylglycerols, n–3 fatty acids and statins may alter the metabolic fate of HDL particles. However, the kinetic effects of n–3 fatty acids and atorvastatin, used alone or in combination, on HDL-apo A-I and HDL-apo A-II kinetics in abdominally obese subjects have not yet been investigated.

In the present study, we examined the independent and combined effects of n–3 fatty acid supplementation and atorvastatin on HDL-apo A-I and HDL-apo A-II kinetics in insulin-resistant men with abdominal obesity. We hypothesized that n–3 fatty acids and atorvastatin would decrease the fractional catabolic rate (FCR) of both HDL apo A-I and HDL apo A-II.

	SUBJECTS AND METHODS

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Subjects
Forty-eight obese men were recruited (17). Abdominal obesity was defined as waist circumference >100 cm. All subjects had plasma triacylglycerol >1.2 mmol/L and cholesterol >5.2 mmol/L. None of the subjects had diabetes mellitus, apolipoprotein E2/E2 genotype, macroproteinuria, creatinemia, hypothyroidism, or abnormal liver enzymes. Subjects consumed <1 fish meal/wk, <30 g alcohol/d, and no fish-oil supplements. None reported a history of cardiovascular disease or was taking agents that affect lipid metabolism. All provided written consent, and the study was approved by the Royal Perth Hospital Ethics Committee.

Study design
This study is a component of a large placebo-controlled 2 x 2 factorial-designed intervention trial with fish-oil supplementation and atorvastatin on lipoprotein metabolism that commenced in 1998 (17-20). Volunteers entered a randomized, doubled-blind, placebo-controlled intervention trial that involved a 3-wk run-in period with body weight variations of <2%. After the run-in period they were randomly assigned to 1 of 4 treatment groups for 6 wk: atorvastatin (40 mg/d), fish oils [4 Omacor capsules (Provona Biocare, Oslo, Norway), consisting of 45% eicosapentaenoic acid and 39% docosahexaenoic acid, taken orally at night, ie, 4 g/d], atorvastatin plus fish oils, or atorvastatin placebo plus 4 g/d placebo corn oil. Compliance with fish oils and atorvastatin were checked by tablet count at weeks 3 and 6.

Clinical protocols
Subjects were admitted to the metabolic ward after a 14-h fast. They were studied in a semirecumbent position and allowed only water for 10 h. Venous blood was collected for biochemical analyses. Plasma volume was determined by multiplying body weight by 0.045 (in L/kg), with adjustment for decrease in relative plasma volume associated with obesity as described by Riches et al (21). Dietary intake was assessed for energy and major nutrients by using at least two 24-h dietary diaries at the beginning and end of the study. Diets were analyzed with the use of DIET 4 NUTRIENT CALCULATION SOFTWARE (Xyris Software, Highgate Hill, Queensland, Australia). Physical activity was assessed by a 7-d recall questionnaire as described by Blair (22).

A single bolus of [d₃]-leucine (5 mg/kg body weight) was administered intravenously into an antecubital vein by a 21G butterfly needle (3). Blood samples were taken at baseline; at 5, 10, 20, 30, 40 min; and at 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, and 10 h after isotope injection. Additional fasting blood samples were collected in the morning on the following 4 d (24, 48, 72, and 96 h). All procedures were repeated after 6 wk.

Biochemical analyses
Laboratory methods for measurements of lipid and lipoprotein were previously detailed (7). HDL₂ (1.063–1.125 g/L) and HDL₃ (1.125–1.21 g/L) were isolated by ultracentrifugation (200 000 x g for 24 h at 20 °C) from 0.5 mL plasma, and cholesterol concentrations were measured. Plasma nonesterified fatty acids were measured with a kit (Randox, CO Antrim, United Kingdom). Plasma insulin was measured by radioimmunoassay (DiaSorini, Saluggia, Italy). Plasma glucose concentration was measured by the hexokinase method. Plasma lathosterol concentration was assayed by using gas chromatography–mass spectrometry. Insulin resistance was estimated by using the homeostasis model assessment formula (23). Apolipoprotein E genotype was determined as previously described (3).

Isolation and measurement of isotopic enrichment of HDL apo A-I and HDL apo A-II
Laboratory methods for isolation and measurement of isotopic enrichment were previously detailed (7, 8). Briefly, apo B was precipitated from 250 µL plasma by using heparin (25 µL) and 12.5 µL 2.0 M MnCl₂. A volume of 60 µL 64% CsCl was added to 200 µL heparin and manganese-treated plasma to adjust the density to 1.21 g/mL. HDL was subsequently isolated from 230 µL of this sample by ultracentrifugation (200 000 x g for 24 h at 20 °C; Optima XL-100K; Beckman Coulter, Fullerton, Australia). Apo A-I and apo A-II were isolated by using polyacrylamide gel electrophoresis and transferred to polyvinylidene difluoride membrane. The apo A-I and apo A-II bands were excised from the membrane, hydrolyzed with 200 µL 6 M HCL at 110 °C for 16 h, and dried for derivatization by using the oxazolinone method as previously described (7). Apo A-I and apo A-II isotopic enrichment was measured with gas chromatography–mass spectrometry.

Model of apo A-I and apo A-II metabolism and calculation of kinetic parameters
The multicompartmental model used to describe HDL-apo A-I leucine tracer-to-tracee ratios is shown in Figure 1. The SAAM II program (SAAM Institute, Seattle, WA) was used to fit the model to the observed tracer data. The model includes a 4-compartment subsystem (compartments 1–4) that describe plasma leucine kinetics. This subsystem is connected to an intrahepatic delay compartment 5 that accounts for the time required for the synthesis and secretion of apo A-I into plasma. Compartments 6 and 7 describe the kinetics of apo A-I in the plasma HDL fraction and in a nonplasma compartment, respectively. HDL-apo A-I metabolic markers, including production rate and FCR, were derived after a fit of the model to the plasma leucine and apolipoprotein AI tracer:tracee data. The same model and calculation of kinetic parameters was used for HDL apo A-II.

View larger version (7K): [in this window] [in a new window]   FIGURE 1. Compartment model describing the tracer kinetics of HDL apolipoprotein A-I (apo A-I) and HDL apo A-II. The model includes a 4-compartment subsystem (compartments 1–4) that describes plasma leucine kinetics. This subsystem is connected to an intrahepatic delay compartment (compartment 5), which accounts for the time required for the synthesis and secretion of apo A-I into plasma. Compartments 6 and 7 describe the kinetics of apo A-I (or apo A-II) in the plasma HDL fraction and in a nonplasma compartment, respectively.

	RESULTS

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Subject characteristics
The pretreatment clinical and biochemical characteristics of the obese subjects randomly assigned to the 4 treatment groups are shown in Table 1. On average, they were middle-aged, centrally obese, normotensive, and insulin resistant (3). No significant group differences were observed in any of the variables. Of the 48 obese subjects, 31 were E3/E3 homozygotes, 2 were E2/E3 heterozygotes, 13 were E3/E4 heterozygotes, and 2 were E4/E4 homozygotes. No statistically significant differences were observed in the frequency distribution of E alleles among the groups. Tablet and capsule counts confirmed that compliance with random assignment to active intervention or placebo was >95%.

Table 2

Table 3

	DISCUSSION

TOP ABSTRACT INTRODUCTION SUBJECTS AND METHODS RESULTS DISCUSSION REFERENCES

 
This is the first study to examine the independent and combined effects of n–3 fatty acid supplementation and a statin on HDL-apo A-I and HDL-apo A-II metabolism in nondiabetic, insulin-resistant obese subjects. We provide new evidence that n–3 fatty acids influence the kinetics of HDL by decreasing both catabolism and production of apo A-I and apo A-II without significantly altering in their pool sizes. These effects were achieved with no significant alteration in insulin resistance, body weight, or dietary intake. In contrast, atorvastatin did not significantly alter synthesis or the turnover of HDL apo A-I and HDL apo A-II. Combination treatment did not provide an additional effect on HDL metabolism compared with n–3 fatty acids alone.

Effect of fish-oil supplementation on HDL metabolism
By using stable isotope techniques, only one study has examined the effects of n–3 fatty acid supplementation on HDL-apo A-I metabolism (24). Frenais et al (24) reported that in 5 diabetic patients HDL-apo A-I FCR and production rate were significantly decreased after treatment with n–3 fatty acid supplementation. The concentration of HDL apo A-I was not significantly changed. Our data extend the previous study by using a significantly larger sample size and examining the effect of n–3 fatty acid supplementation on both HDL-apo A-I and HDL-apo A-II metabolism. We report a new finding that, similar to HDL-apo A-I kinetics, n–3 fatty acids decreased the FCR and production of HDL apo A-II. Although n–3 fatty acids did not alter pool sizes of apo A-I or apo A-II in plasma, our data clearly show that n–3 fatty acids exhibit significant effects on HDL turnover. We have previously shown that n–3 fatty acids lower plasma triacylglycerols by a reduction in VLDL-apo B production (18). As described earlier, this in turn decreases CETP-mediated heteroexchange of neutral lipids among lipoproteins, thereby delaying the uptake of HDL by the liver (6). This notion is consistent with our present findings. The precise reason for decreased production of apo A-I and apo A-II with fish oils in abdominal obesity remains unclear. Given that n–3 fatty acids are peroxisome proliferator-activated receptor- agonists (25), one would expect fish oils to increase apo A-I and apo A-II production. However, note that n–3 fatty acids are only "weak" agonists, and their effect on the gene expression of apo A-I and apo A-II might be limited (26). We have previously shown that subjects with insulin resistance without diabetes have accelerated catabolism of HDL apo A-I with elevated production rates of apo A-I compared with lean control subjects (7). Consistent with this, we found that changes in the FCRs of apo A-I and apo A-II were significantly associated with their corresponding changes in production rates in the fish-oil and the combined treatment groups. Taken together, it is likely that fish oils decreased the FCRs of apo A-I and apo A-II and that a decreased production rate may be a "balancing feedback" mechanism of reduced uptake of HDL particles, but this requires further investigation.

Effect of atorvastatin on HDL metabolism
Previous studies have only examined the effect of statins on HDL-apo A-I metabolism (7, 27, 28). Consistent with the present findings, all have consistently failed to show significant changes in the production and catabolic rates of HDL apo A-I. By decreasing plasma triacylglycerol concentrations, statins may, indirectly, decrease CETP-mediated heteroexchange of neutral lipids and subsequently delay the uptake of HDL by the liver (6). However, atorvastatin could also possibly enhance hepatic HDL receptors for the uptake of larger HDL particles in plasma (29). Such a mechanism may therefore account for the lack of treatment effect in the FCRs of apo A-I and apo A-II particles but this requires further investigation.

In contrast to fish oils, atorvastatin treatment did not alter HDL-apo A-I and HDL-apo A-II production. Although statin-induced inhibition of the Rho-signaling pathway may increase the expression and production of apo A-I in vitro (30, 31), no in vivo effect on production was seen in this study. A recent study by Mauger et al (32) compared the effect of simvastatin (80 mg) and atorvastatin (40 mg) on HDL-apo A-I kinetics in overweight persons with dyslipidemia. They found that simvastatin significantly increased HDL-apo A-I production compared with atorvastatin, provocatively suggesting statin-specific or dose effects on HDL-apo A-I metabolism. Although several studies have examined the effects of statin on HDL-apo A-I kinetics, no studies have investigated its effect on the flux of HDL apo A-II. Given that both apo A-I and apo A-II share similar metabolic pathways, the lack of effect of atorvastatin on HDL apo A-II was not unexpected.

Effect of fish oils plus atorvastatin on HDL metabolism
Our previous findings showed that the combination of n–3 fatty acids and atorvastatin effectively normalized the kinetic abnormalities in apo B metabolism by decreasing VLDL-apo B production and increasing the FCR of VLDL, intermediate-density lipoprotein, and LDL apo B (20). In this study, we further explore the potential effect of the combination treatment on HDL metabolism. The present data suggest that the combination treatment did not provide additional effect on HDL metabolism compared with fish oils alone.

Fish oils plus atorvastatin did not alter plasma HDL-apo AI or HDL-apo AII concentrations; however, the positive and additive effect of each agent on HDL cholesterol, specifically the HDL₂ subfraction, was observed. Although the basis for this effect is unclear, it may be attributable to the greater reductions in plasma triacylglycerols and VLDL-apo B pool sizes with combination treatment than with either of the monotherapies that result in less CETP-mediated exchange of neutral lipids between lipoproteins, as discussed earlier.

The study has limitations. Our study was restricted to men, and, given the sex differences in HDL metabolism, our results may not apply to women; however, this requires investigation. HDL particles are subjected to modifications by several lipase and lipid transfer proteins, particularly, lipoprotein lipase, hepatic lipase, CETP, and phospholipid transfer protein (33). Measurements of their activities in plasma may help to formally corroborate our findings. Moreover, examination of the effect of both agents on the kinetics of HDL₂, HDL₃, LpA-I, LpA-I:LpA-II, and pre-ß HDL may also be important to elucidate their precise mechanisms of action on HDL metabolism.

Elevated triacylglycerols and low HDL cholesterol are significant risk factors for coronary disease (34, 35). Correction of these abnormalities with n–3 fatty acids and atorvastatin may have clinical significance, consistent with evidence that these agents decrease the risk of coronary disease. Taken together with our previous findings on apo B metabolism, we provide a kinetic basis for changes in lipids and lipoproteins with n–3 fatty acids and atorvastatin. Despite this, it appears that such changes in apo B and HDL metabolism are largely independent of each other. With the exception of the associations between VLDL-apo B secretion and apo A-I and apo A-II FCRs, apo B metabolic limits were not associated with HDL apoprotein metabolism. The results of the present study indicate that in obese subjects with insulin resistance and dyslipidemia, n–3 fatty acids influence the metabolism of HDL metabolism by decreasing both catabolism and production of apo A-I and apo A-II. Combination treatment of fish oils with other therapeutic agents that selectively increase apo A-I and apo A-II production may be particularly important in the prevention of cardiovascular disease in this group of patients. Given that statins regulate lipoprotein metabolism chiefly by decreasing hepatic cholesterol biosynthesis, their impact on HDL metabolism might be limited. Despite this, our previous data clearly show its favorable effect on the catabolism of apo B lipoproteins. Hence, further studies should also examine the additive effect of fibrates, insulin sensitizers, or CETP inhibitors together with fish oils or a statin regimen.

	ACKNOWLEDGMENTS

 
We thank the nursing staff of the Clinical Research Studies Unit of the School of Medicine and Pharmacology (Royal Perth Hospital, Perth, Australia) for providing expert clinical assistance.

DCC, GFW, and PHRB contributed to the conception and design of the study. GFW and DCC supervised the experiment and the data collection. DCC and MNN performed the statistical analysis. PHRB and MNN performed the modeling of the data. All authors contributed to the writing of the manuscript. None of the authors had a conflict of interest with any aspect of this research.

	REFERENCES

TOP ABSTRACT INTRODUCTION SUBJECTS AND METHODS RESULTS DISCUSSION REFERENCES

 

1. Grundy SM. Obesity, metabolic syndrome, and cardiovascular disease. J Clin Endocrinol Metab 2004;89:2595–600.[Free Full Text]
2. Bjorntorp P. "Portal" adipose tissue as a generator of risk factors for cardiovascular disease and diabetes. Artherosclerosis 1990;10:493–6.[Free Full Text]
3. Chan DC, Watts GF, Redgrave TG, Mori TA, Barrett PHR. Apolipoprotein B-100 kinetics in visceral obesity: associations with plasma apolipoprotein C-III concentration. Metabolism 2002;29:1041–6.
4. Assmann G, Nofer JR. Atheroprotective effects of high-density lipoproteins. Annu Rev Med 2003;54:321–41.[Medline]
5. Tailleux A, Duriez P, Fruchart JC, Clavey V. Apolipoprotein A-II, HDL metabolism and atherosclerosis. Atherosclerosis 2002;164:1–13.[Medline]
6. Rashid S, Barrett HBR, Uffelman KD, Watanabe T, Adeli K, Lewis GF. Lipolytically modified triglyceride-enriched HDLs are rapidly cleared from the circulation. Arterioscler Thromb Vasc Biol 2002;22:483–7.[Abstract/Free Full Text]
7. Watts GF, Barrett PHR, Ji J, et al. Differential regulation of lipoprotein kinetics by atorvastatin and fenofibrate in subjects with the metabolic syndrome. Diabetes 2003;52:803–11.[Abstract/Free Full Text]
8. Ji J, Watts GF, Johnson AG, et al. High-density lipoprotein (HDL) transport in the metabolic syndrome: application of a new model for HDL particle kinetics. J Clin Endocrinol Metab 2006;91:973–9.[Abstract/Free Full Text]
9. Brinton EA, Eisenberg S, Breslow JL. Human HDL cholesterol levels are determined by apoA-I fractional catabolic rate, which correlates inversely with estimates of HDL particle size. Effects of gender, hepatic and lipoprotein lipases, triglyceride and insulin levels, and body fat distribution. Arterioscler Thromb Vasc Biol 1994;14:707–20.
10. Terry RB, Yurgalevitch S, Thompson PD. High-density apolipoprotein A-I and A-II kinetics in relation to regional adiposity. Metabolism 1992;41:1386–92.[Medline]
11. Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults. Executive Summary of the Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III). JAMA 2001;285:2486–97.[Free Full Text]
12. Harris WS. n–3 Fatty acids and serum lipoproteins: human studies. Am J Clin Nutr 1997;65:1645S–54S.[Abstract/Free Full Text]
13. Mori TA, Beilin LJ. Long-chain omega 3 fatty acids, blood lipids and cardiovascular risk reduction. Curr Opin Lipidol 2001;12:11–7.[Medline]
14. Brown AS, Bakker-Arkema RG, Yellen L, et al. Treating patients with documented atherosclerosis to National Cholesterol Education Program-recommended low-density-lipoprotein cholesterol goals with atorvastatin, fluvastatin, lovastatin and simvastatin. J Am Coll Cardiol 1998;32:665–72.[Abstract/Free Full Text]
15. Stein EA, Lane M, Laskarzewski P. Comparison of statins in hypertriglyceridemia. Am J Cardiol 1998;81:B66–9.[Medline]
16. Bhatnagar D, Mackness MI, Durrinton PN. Treatment of mixed hyperlipidaemia using a combination of omega-3 fatty acids and HMG CoA reductase inhibitor. Eur Heart J 2001;3:D53–8.
17. Chan DC, Watts GF, Mori TA, Barrett PHR, Beilin LJ, Redgrave TG. Factorial study of the effects of atorvastatin and fish oil on dyslipidemia in visceral obesity. Eur J Clin Invest 2002;32:429–36.[Medline]
18. Chan DC, Watts GF, Mori TA, Barrett PHR, Redgrave TG, Beilin LJ. Randomized controlled trial of the effect of n–3 fatty acids supplementation on apolipoprotein B-100 and chylomicron remnant metabolism in visceral obesity. Am J Clin Nutr 2003;77:300–9.[Abstract/Free Full Text]
19. Chan DC, Watts GF, Barrett PHR, Mori TA, Redgrave TG, Beilin LJ. Mechanism of action of an HMGCoA reductase inhibitor on apolipoprotein B-100 kinetics in visceral obesity. J Clin Endocrinol Metab 2002;87:2283–9.[Abstract/Free Full Text]
20. Chan DC, Watts GF, Barrett PHR, Beilin LJ, Redgrave TG, Mori TA. Regulatory effects of HMGCoA reductase inhibitor and fish oils on apolipoprotein B100 kinetics with insulin resistant obese male subjects with dyslipidaemia. Diabetes 2002;51:2377–86.[Abstract/Free Full Text]
21. Riches FM, Watts GF, Naoumova RP, Kelly JM, Croft KD, Thompson GR. Hepatic secretion of very-low-density lipoprotein apolipoprotein B-100 studied with a stable isotope technique in men with visceral obesity. Int J Obes Relat Metab Disord 1998;22:414–23.[Medline]
22. Blair SN. How to assess exercise habits and physical fitness. In: Matarazzo JD, ed. Behavioral health. New York, NY: Wiley, 1984:424–47.
23. Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Treacher DF, Turner RC. Homeostasis model assessment: insulin resistance and B-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia 1985;28:412–9.[Medline]
24. Frenais R, Ouguerram K, Maugeais C, et al. Effect of dietary omega-3 fatty acids on high-density lipoprotein apolipoprotein AI kinetics in type II diabetes mellitus. Atherosclerosis 2001;157:131–5.[Medline]
25. Price PT, Nelson CM, Clarke SD. Omega-3 polyunsaturated fatty acid regulation of gene expression. Curr Opin Lipidol 2000;11:3–7.[Medline]
26. Dallongeville J, Baugé E, Tailleux A, et al. Peroxisome proliferator-activated receptor is not rate-limiting for the lipoprotein-lowering action of fish oil. J Biol Chem 2001;276:4634–9.[Abstract/Free Full Text]
27. Bilz S, Wagner S, Schmitz M, Bedynek A, Keller U, Demant T. Effects of atorvastatin versus fenofibrate on apoB-100 and apoA-I kinetics in mixed hyperlipidemia. J Lipid Res 2004;45:174–85.[Abstract/Free Full Text]
28. Bach-Ngohou K, Ouguerram K, Frenais R, et al. Influence of atorvastatin on apolipoprotein e and AI kinetics in patients with type 2 diabetes. J Pharmacol Exp Ther 2005;315:363–9.[Abstract/Free Full Text]
29. Vaziri ND, Liang K. Effects of HMG-CoA reductase inhibition on hepatic expression of key cholesterol-regulatory enzymes and receptors in nephrotic syndrome. Am J Nephrol 2004;24:606–13.[Medline]
30. Geneieve M, Duez H, Blanquart C, et al. Statin-induced inhibition of the Rho-signaling pathway activates PPAR and induces HDL apoA-I. J Clin Invest 2001;107:1423–32.[Medline]
31. Bonn V, Cheung RC, Chen B, Taghibiglou C, Van Iderstine SC, Adeli K. Simvastatin, an HMG-CoA reductase inhibitor, induces the synthesis and secretion of apolipoprotein AI in HepG2 cells and primary hamster hepatocytes. Atherosclerosis 2002;163:59–68.[Medline]
32. Mauger JF, Couture P, Paradis ME, Lamarche B. Comparison of the impact of atorvastatin and simvastatin on apoA-I kinetics in men. Atherosclerosis 2005;178:157–63.[Medline]
33. Borggreve SE, De Vries R, Dullaart RP. Alterations in high-density lipoprotein metabolism and reverse cholesterol transport in insulin resistance and type 2 diabetes mellitus: role of lipolytic enzymes, lecithin:cholesterol acyltransferase and lipid transfer proteins. Eur J Clin Invest 2003;33:1051–69.[Medline]
34. Cullen P. Evidence that triglycerides are an independent coronary heart disease risk factor. Am J Cardiol 2000;86:943–9.[Medline]
35. Franceschini G. Epidemiologic evidence for high-density lipoprotein cholesterol as a risk factor for coronary artery disease. Am J Cardiol 2000;88:9N–13N.

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