Adipose tissue arachidonic acid content is associated with the expression of 5-lipoxygenase in atherosclerotic plaques
© Nielsen et al.; licensee BioMed Central Ltd. 2013
Received: 6 January 2013
Accepted: 22 January 2013
Published: 25 January 2013
The content of arachidonic acid in adipose tissue is positively associated with the risk of myocardial infarction, whereas the content of eicosapentaenoic acid in adipose tissue has been reported to be negatively associated with the risk of myocardial infarction. Both arachidonic acid and eicosapentaenoic acid are substrates for the synthesis of pro-inflammatory leukotrienes and leukotrienes derived from eicosapentaenoic acid are generally much less potent. In this study we hypothesized that a high content of arachidonic acid in adipose tissue would reflect a high formation of arachidonic acid derived leukotrienes and a high expression of 5-lipoxygenase in atherosclerotic plaques. Likewise, we hypothesized that a high content of eicosapentaenoic acid in adipose tissue would reflect a low formation of arachidonic acid derived leukotrienes and a low expression of 5-lipoxygenase in plaques.
In a cross sectional study we included 45 consecutive subjects undergoing femoral thrombendarterectomy. The expression of 5-lipoxygenase in plaques was assessed by a semi-automated image analysis computer programme after immunohistochemical staining with mono-clonal 5-lipoxygenase antibodies. Leukotriene B4 and cysteinyl leukotriene formation from stimulated femoral artery plaques was quantified using ELISA methods. The fatty acid content of adipose tissue biopsies from the thigh was analyzed using gas chromatography. Associations between variables were assessed by Pearson correlations and were further explored in a multivariable linear regression model adjusting for potential confounders.
A high content of arachidonic acid in adipose tissue was associated with a higher expression of 5-lipoxygenase in plaques (r = 0.32, p = 0.03), but no significant associations with leukotriene B4 (r = 0.22, p = 0.14) and cysteinyl leukotriene (r = −0.11, p = 0.46) formation was seen. No significant associations were found between the content of eicosapentaenoic acid in adipose tissue and 5-lipoxygenase expression or leukotriene formation in plaque.
Adipose tissue arachidonic acid contents correlated positively with the expression of 5-lipoxygenase in plaques. This association might represent a causal link between adipose tissue arachidonic acid and the risk of myocardial infarction but confirmatory studies are needed.
KeywordsAdipose tissue Arachidonic acid Eicosapentaenoic acid Atherosclerotic plaques 5-Lipoxygenase Leukotriene B4 Cysteinyl leukotrienes
Adipose tissue is widely used in epidemiological studies as a biomarker of long term intake of PUFA . A high adipose tissue content of marine omega-3 PUFA has been associated with a lower risk of acute coronary syndrome [10, 11], while on the contrary, a high content of ARA in adipose tissue has been associated with a higher risk of myocardial infarction [2–4]. The mechanistic explanation of these findings is unsettled, but impacts on plaque inflammation and thus plaque stability could be an important factor. In the present study, we hypothesized that the content of EPA in adipose tissue reflect lower levels of 5-lipoxygenase and 4-series leukotrienes in femoral atherosclerotic plaques, and that the content of ARA in adipose tissue, on the other hand, is associated with higher levels of 4-series leukotrienes and 5-lipoxygenase in plaques. Since EPA and ARA in adipose tissue must be liberated into the circulation and probably also incorporated into atherosclerotic plaques in order to affect the lipoxygenase pathway in the arterial wall, our secondary aim was to assess the correlation between the content of these fatty acids in adipose tissue, plasma, and atherosclerotic femoral plaques, respectively.
71 (54 – 81)
Sex (% men)
Body mass index*, kg/m2
25 (18 – 30)
EPA + DHA intake* (g/day)
0.68 (0.16 – 1.69)
Current smokers, %
Medical history and medications
Cardiovascular disease†, %
Diabetes mellitus, %
Aspirin treatment, %
Anti-hypertensive medication, %
Statin treatment, %
NSAID use‡, %
Total cholesterol*, mmol/l
3.8 (3.1 – 4.6)
5.9 (5.3 – 8.7)
P-hsCRP§, mg/l (n = 37)e
1.8 (0.3 – 6.4)
85 (56 – 107)
Atherosclerotic plaques were all advanced lesions. They were generally highly fibrotic and heavily calcified and 71% were without any lipid core. Inflammatory cells were present in very low numbers. The median expression of 5-lipoxygenase in the plaques was 0.19% and median LTB4 and cysteinyl leukotriene formation from stimulated plaques were 3.4 ng/g and 7.3 ng/g, respectively. A statistically significant correlation between 5-lipoxygenase expression and LTB4 formation (r = 0.32, 95% CI: 0.03; 0.56, p = 0.03), but not cysteinyl leukotriene formation (r = 0.06, 95% CI: -0.24; 0.35, p = 0.71), was observed.
Associations between the content of ARA and EPA in adipose tissue and the expression of 5-lipoxygenase and formation of leukotrienes in plaques
Correlations between PUFA content in adipose tissue and 5-lipoxygenase pathway constituents in plaque and urine
Adipose tissue arachidonic acid (% of total fatty acids)
Adipose tissue eicosapentaenoic acid (% of total fatty acids)
5-lipoxygenase expression (% of plaque area)
0.03 to 0.56
−0.16 to 0.41
Leukotriene B4 (ng/g)
−0.08 to 0.42
−0.05 to 0.50
Cysteinyl leukotrienes (ng/g)
−0.39 to 0.19
−0.27 to 0.31
Leukotriene E4 (pg/mg creatinine)
−0.28 to 0.31
−0.40 to 0.18
Associations between the content of linoleic acid and docosahexaenoic acid in adipose tissue and the expression of 5-lipoxygenase and formation of leukotrienes in plaques
Since both linoleic acid and docosahexaenoic acid could indirectly affect the content of ARA and EPA in adipose tissue and plaques, we included these PUFA in an exploratory analysis. No substantial nor statistically significant correlations were observed between the content of docosahexaenoic acid in adipose tissue and 5-lipoxygenase expression in plaque (r = 0.04, 95% CI: -0.26; 0.33, p = 0.80), LTB4 in plaques (r = 0.18, 95% CI: -0.12; 0.45, p = 0.23), cysteinyl leukotrienes in plaques (r = 0.01, 95% CI: -0.28; 0.30, p = 0.96) or urine LTE4 levels (r = −0.04, 95% CI: -0.34; 0.25, p = 0.75). Likewise, the content of linoleic acid in adipose tissue was neither substantially nor statistically significantly correlated with 5-lipoxygenase expression in plaque (r = −0.06, 95% CI: -0.35; 0.24, p = 0.70), LTB4 in plaques (r = −0.09, 95% CI: -0.37; 0.21, p = 0.55), cysteinyl leukotrienes in plaques (r = 0.09, 95% CI: -0.21; 0.37, p = 0.57), or urine LTE4 levels (r = −0.05, 95% CI: -0.34; 0.25, p = 0.73).
Correlations between the content of EPA and ARA in adipose tissue, plasma, and atherosclerotic plaques
In this study, we analyzed the content of EPA and ARA in adipose tissue biopsies from subjects with peripheral artery disease and evaluated whether these fatty acids were associated with the expression of 5-lipoxygenase as well as the formation of LTB4 and cysteinyl leukotrienes in femoral plaques. Furthermore, we measured the content of ARA and EPA in both plasma and plaques in order to establish a possible biological pathway in which the content of ARA and EPA in adipose tissue could affect the 5-lipoxygenase pathway in the arterial wall.
Our major finding, was a statistically significant association between the content of ARA in adipose tissue and the expression of 5-lipoxygenase in atherosclerotic plaques, which persisted after adjustment for age, sex, and BMI. We also observed a weak positive correlation between adipose tissue ARA contents and LTB4 formation in plaques which, however, did not reach statistical significance (p = 0.14). Other investigators have previously assessed the expression of 5-lipoxygenase in atherosclerotic plaques [12–16] although none of them assessed femoral artery plaques. Two recent studies [13, 15] have linked both 5-lipoxygenase expression and LTB4 formation to carotid plaque instability by reporting higher levels in unstable compared to stable plaques, as assessed by the presence of recent neurological symptoms. Other results supporting these findings were reported by Zhou et al.  who found that 5-lipoxygenase expression and LTB4 formation in carotid plaques were higher in diabetic compared to non-diabetic patients and by Spanbroek et al.  who found that 5-lipoxygenase expression was higher in more advanced atherosclerotic lesions. Although associations between the content of ARA and EPA in adipose tissue and 5-lipoxygenase pathway constituents in plaques have not been assessed previously, some indirect evidence for such an association has been derived from genetic studies. Dwyer et al.  thus reported that homozygous carriers of a short tandem repeat polymorphism in the promoter region of the gene encoding 5-lipoxygenase were significantly associated with a higher carotid intima-media thickness. This association was stronger for individuals with high dietary ARA intakes and attenuated for individuals with high dietary intake of marine omega-3 polyunsaturated fatty acids. In another genetic association study, Allayee et al.  was, however, unable to demonstrate an association between the same promoter polymorphism and the risk of myocardial infarction. However, subjects with high intakes of ARA had a significantly higher risk (OR = 1.32) of myocardial infarction compared to subjects with low ARA intakes (OR = 0.80). No gene-diet interaction was found for omega-3 fatty acids. In the present study, the finding of a positive association between the content of ARA in adipose tissue and the expression of 5-lipoxygenase in plaques is in line with the results of these nutrigenomic studies and thus provides further evidence for the importance of this fatty acid on the 5-lipoxygenase pathway. All together, these findings strengthen the hypothesis that the positive association between adipose tissue ARA and the risk of myocardial infarction [2–4] reported in epidemiological studies could be causal, at least partly, through higher expression of 5-lipoxygenase in the arterial wall.
Adipose tissue ARA was not correlated with either cysteinyl leukotriene formation in plaque or total body cysteinyl leukotriene formation, of which the latter can be estimated from urinary LTE4 levels . While evidence for a link between LTB4 and plaque instability is supported by quite concordant results from several studies, the role of cysteinyl leukotrienes in plaque biology is more ambiguous. Qiu et al.  found a positive correlation between plaque instability and mRNA levels of the enzymes used for LTB4 synthesis (5-lipoxygenase, 5-lipoxygenase activating protein, LTA4 hydrolase) but not for cysteinyl leukotriene synthesis (LTC4 synthase). On the other hand, urinary LTE4 levels have been reported to be significantly higher in patients suffering from acute coronary syndrome compared to controls , and cysteinyl leukotrienes have been shown to be capable of inducing coronary spasm in ex vivo atherosclerotic coronary arteries but not in normal arteries . Based on the results from the present study one could speculate that advanced femoral atherosclerotic plaques have a low expression of LTC4 synthase since 5-lipoxygenase expression was not significantly correlated to cysteinyl leukotriene levels in stimulated plaques.
We expected the content of EPA in adipose tissue to be associated with lower levels of leukotriene formation and 5-lipoxygenase expression in plaques, since dietary supplementation with fish oil (EPA + DHA) has been associated with increased stability of carotid plaques . Furthermore, the content of EPA in plaques was associated with more stable and less inflammatory plaques . Despite high correlations between EPA levels in adipose tissue, plasma phospholipids, and atherosclerotic plaques, suggesting a high degree of incorporation of dietary EPA into all these compartments, we actually found positive correlations between the content of EPA in adipose tissue and 5-lipoxygenase expression as well as LTB4 and cysteinyl leukotriene formation in plaques. These correlations were, however, non-significant, and hence no “harmful” association was detected per se, but surely, this study does not suggest any clinically beneficial association between EPA and the formation of 5-lipoxygenase products in femoral plaques. In a supplementary exploratory analysis, we determined correlation between the content of linoleic acid and docosahexaenoic acid in adipose tissue and 5-lipoxygenase expression and leukotriene formation in plaques, since these PUFA could potentially affect leukotriene formation in plaques. However, no significant correlations were observed.
Several weaknesses of this study should be acknowledged. The selection of study tissue is open for discussion. We looked at femoral artery plaques which were in a chronic stage of fibrosis, calcification, and most often without any lipid core which is in contrast to carotid plaques . The grade of inflammation in femoral plaques was lower than expected, making it harder to detect correlations between adipose tissue fatty acids and leukotriene formation/5-lipoxygenase expression in plaques. Furthermore, the extensive calcification in these plaques sometimes made them fall apart when they were dissected prior to stimulation. Only, coherent plaque tissue was weighed and stimulated (since calcium crystals would be inactive tissue), which could have introduced imprecision in the assessment of leukotriene formation from stimulated plaques, since they were expressed as ng leukotriene/g plaque. Furthermore, the formation of leukotrienes in plaques was measured after in vitro stimulation of plaques, which makes clinical interpretation of results more complex. Residual confounding cannot be excluded, since the size of the study only allowed us to include three potential confounders (age, sex, and BMI) in the multiple linear regression analyses. The main strength of the study is the accurate and reproducible assessment of the exposures of interest (adipose tissue ARA and EPA) and of 5-lipoxygenase expression in plaques.
We found a positive association between the content of ARA in adipose tissue and the expression of 5-lipoxygenase in femoral atherosclerotic plaques, but no significant correlation with leukotriene formation was seen. The content of EPA in adipose was not significantly correlated with any of the 5-lipoxygenase pathway constituents. Both the ARA and the EPA content in adipose tissue was significantly positively correlated with their respective PUFA in plasma phospholipids, which again was correlated with the respective PUFA in plaques. This study provides evidence for a possible biological link between the content of ARA in adipose tissue and coronary heart disease. However, confirmatory studies assessing the association between the content of ARA in adipose tissue and the expression of 5-lipoxygenase pathway constituents in more inflammatory plaques (i.e. carotid artery) should be undertaken in order to explore this hypothesis further.
Subjects and design
In a cross sectional design, we included fifty consecutive subjects scheduled for femoral artery thrombendarterectomy due to symptomatic peripheral artery disease. The inclusion criteria were: age > 18 years and a diagnosis of peripheral artery disease with planned femoral thrombendarterectomy. Exclusion criteria were any one of the following: allergic asthma or rhinitis, any chronic inflammatory disease, systemic steroid treatment, cancer, acute coronary syndrome within the last 30 days, and inability to give informed consent. Patient history, medication, vital parameters, and food frequency questionnaires were recorded at admission, while blood and urine samples were obtained in the fasting state on the day of surgery. Atherosclerotic femoral artery plaques as well as adipose tissue biopsies from the subcutis of the thigh were collected during surgery. Approval of the study was obtained from the regional research ethics committee (N-20100047), and all patients gave informed consent.
Analysis of atherosclerotic plaques
During femoral artery thrombendarterectomy, plaques were removed and placed in isotonic saline and immediately brought to the research laboratory together with the adipose tissue biopsy. Two small pieces of the plaque were cut off. The first piece was used for the analysis of leukotriene formation, while the other piece was used for analysing the content of ARA and EPA. The remaining part of the plaque was fixed in formalin followed by decalcification in formic acid.
Cross-sectioning of the plaque was performed at 3 mm intervals, and the resulting blocks were embedded in paraffin. From each block one 3 μm section was cut and stained with hematoxylin and eosin. An experienced consultant pathologist (MV) identified the histological section with the largest plaque area (culprit lesion) and did a descriptive histological evaluation of the atherosclerotic lesion in this section. Then, new 3 μm sections from this block and the two neighboring blocks were cut. We chose this area of the plaque since this is anticipated to contain the most inflammation [26, 27]. All three sections were immunostained for 5-lipoxygenase, using anti-5-lipoxygenase monoclonal rabbit antibody clone C49G1 (Cell Signaling Technology, Inc. USA). An irrelevant monoclonal rabbit antibody in the same concentration as the 5-lipoxygenase antibody was applied as negative control on representative slides and showed no staining reaction. For image acquisition (Figure 3), the immunostained slides were scanned on a nanozoomer HT 1.0 (Hamamatsu, Japan) with the 40× source lens setting and then loaded into image analysis application software developed for 5-lipoxygenase staining (Visiopharm, Denmark). The percentage of the plaque area occupied by 5-lipoxygenase for each section was then calculated automatically by the computer software and the average staining fraction from the three sections was used as the primary outcome. The intra-observer CV was 0% based on a re-evaluation of ten sections after 3 months.
The piece of plaque used for leukotriene analysis was cut into smaller pieces and put into stimulation vials. After stimulation with calcium ionophore A23187 the levels of LTB4 (R&D Systems, Minneapolis, USA) and cysteinyl leukotrienes (Enzo Life Sciences Inc, New York, USA) were quantified using solid phase immunoassay ELISA kits with a competitive technique. To adjust for inter-individual differences in the amount of plaque tissue, the levels of leukotrienes were expressed as ng/g plaque tissue. The intraserial CV was 5% for LTB4 and 4% for cysteinyl leukotriene measurements.
Lipids of the plaque were extracted according to Folch et al.  and the fatty acid composition was analyzed by gas chromatography as earlier described . The content of ARA and EPA was expressed as percent of total fatty acids and the intraserial CV was 26% for both fatty acids.
Analysis of the content of PUFA in adipose tissue
Adipose tissue biopsies from the subcutis of the thigh were obtained during surgery and placed in dry vials. Approximately 2–4 mg was analyzed for the content of individual PUFA using gas chromatography and the intraserial CV was 4% for ARA and 8% for EPA.
Analysis of the content of PUFA in plasma phospholipids
Fasting blood samples were collected from all patients on the day of surgery. In the assessment of the individual fatty acid contents in plasma phospholipids, total lipids were extracted from plasma according to Folch et al. . Separation of fatty acids from plasma phospholipids was done according to Burdge et al. . The fatty acid composition was analysed by gas chromatography and the intraserial CV was 1% for ARA and 2% for EPA.
Leukotriene E4 in urine
Quantification of urine LTE4 levels was done using a solid phase immunoassay ELISA kit (USCN life science Inc, Wuhan, China) and the intraserial CV was 17%.
We used Pearson’s product–moment coefficient of correlation model to explore associations between our exposures (adipose tissue EPA and ARA) and the primary outcomes (5-lipoxygenase, LTB4, cysteinyl leukotrienes in plaques) and secondary outcomes (urinary LTE4 levels, EPA and ARA in plasma phospholipids, EPA and ARA in plaques). We further explored associations with our primary outcomes using multivariable linear regression models, in which we included the following a priori selected potential confounders: Age (continuous), sex (dichotomous), and BMI (continuous). In exploratory analyses, we also evaluated adipose tissue linoleic acid and docosahexaenoic acid as exposure variables. The distributions of most of the variables were positively skewed, and logarithmic transformation was therefore applied when appropriate. Assumptions of normality, linear relationship, and equal variances were found to be satisfactory when assessed by relevant graphical plots. Statistical tests were two-tailed, and P < 0.05 was considered significant. The STATA 11 software package (Stata Corp., College Station, TX, US) was used for all analyses.
Coefficient of variation
Polyunsaturated fatty acid.
This work was kindly supported by grants from the Obelske Family Foundation and Dr. Heinrich Kopps Foundation.
- Perk J, De Backer G, Gohlke H, Graham I, Reiner Z, Verschuren WM, Albus C, Benlian P, Boysen G, Cifkova R, Deaton C, Ebrahim S, Fisher M, Germano G, Hobbs R, Hoes A, Karadeniz S, Mezzani A, Prescott E, Ryden L, Scherer M, Syvanne M, Scholte Op Reimer WJ, Vrints C, Wood D, Zamorano JL, Zannad F: European Guidelines on cardiovascular disease prevention in clinical practice (version 2012): The Fifth Joint Task Force of the European Society of Cardiology and Other Societies on Cardiovascular Disease Prevention in Clinical Practice (constituted by representatives of nine societies and by invited experts). Atherosclerosis. 2012, 223: 1-68. 10.1016/j.atherosclerosis.2012.05.007View ArticlePubMedGoogle Scholar
- Baylin A, Campos H: Arachidonic acid in adipose tissue is associated with nonfatal acute myocardial infarction in the central valley of Costa Rica. J Nutr. 2004, 134: 3095-3099.PubMedGoogle Scholar
- Kark JD, Kaufmann NA, Binka F, Goldberger N, Berry EM: Adipose tissue n-6 fatty acids and acute myocardial infarction in a population consuming a diet high in polyunsaturated fatty acids. Am J Clin Nutr. 2003, 77: 796-802.PubMedGoogle Scholar
- Nielsen M, Schmidt E, Stegger J, Gorst-Rasmussen A, Tjonneland A, Overvad K: Adipose tissue arachidonic acid content is associated with the risk of myocardial infarction: A Danish case-cohort study. Atherosclerosis. 2013,http://dx.doi.org/10.1016/j.atherosclerosis.2012.12.035Google Scholar
- Back M: Leukotriene signaling in atherosclerosis and ischemia. Cardiovasc Drugs Ther. 2009, 23: 41-48. 10.1007/s10557-008-6140-9PubMed CentralView ArticlePubMedGoogle Scholar
- Terano T, Salmon JA, Moncada S: Biosynthesis and biological activity of leukotriene B5. Prostaglandins. 1984, 27: 217-232.View ArticlePubMedGoogle Scholar
- Lee TH, Mencia-Huerta JM, Shih C, Corey EJ, Lewis RA, Austen KF: Effects of exogenous arachidonic, eicosapentaenoic, and docosahexaenoic acids on the generation of 5-lipoxygenase pathway products by ionophore-activated human neutrophils. J Clin Invest. 1984, 74: 1922-1933. 10.1172/JCI111612PubMed CentralView ArticlePubMedGoogle Scholar
- Dahlen SE, Hedqvist P, Hammarstrom S: Contractile activities of several cysteine-containing leukotrienes in the guinea-pig lung strip. Eur J Pharmacol. 1982, 86: 207-215. 10.1016/0014-2999(82)90318-1View ArticlePubMedGoogle Scholar
- Hodson L, Skeaff CM, Fielding BA: Fatty acid composition of adipose tissue and blood in humans and its use as a biomarker of dietary intake. Prog Lipid Res. 2008, 47: 348-380. 10.1016/j.plipres.2008.03.003View ArticlePubMedGoogle Scholar
- Pedersen JI, Ringstad J, Almendingen K, Haugen TS, Stensvold I, Thelle DS: Adipose tissue fatty acids and risk of myocardial infarction–a case–control study. Eur J Clin Nutr. 2000, 54: 618-625. 10.1038/sj.ejcn.1601064View ArticlePubMedGoogle Scholar
- Joensen AM, Overvad K, Dethlefsen C, Johnsen SP, Tjonneland A, Rasmussen LH, Schmidt EB: Marine n-3 polyunsaturated fatty acids in adipose tissue and the risk of acute coronary syndrome. Circulation. 2011, 124: 1232-1238. 10.1161/CIRCULATIONAHA.110.987057View ArticlePubMedGoogle Scholar
- Zhou YJ, Wang JH, Li L, Yang HW, de Wen L, He QC: Expanding expression of the 5-lipoxygenase/leukotriene B4 pathway in atherosclerotic lesions of diabetic patients promotes plaque instability. Biochem Biophys Res Commun. 2007, 363: 30-36. 10.1016/j.bbrc.2007.08.134View ArticlePubMedGoogle Scholar
- Cipollone F, Mezzetti A, Fazia ML, Cuccurullo C, Iezzi A, Ucchino S, Spigonardo F, Bucci M, Cuccurullo F, Prescott SM, Stafforini DM: Association between 5-lipoxygenase expression and plaque instability in humans. Arterioscler Thromb Vasc Biol. 2005, 25: 1665-1670. 10.1161/01.ATV.0000172632.96987.2dView ArticlePubMedGoogle Scholar
- Spanbroek R, Grabner R, Lotzer K, Hildner M, Urbach A, Ruhling K, Moos MP, Kaiser B, Cohnert TU, Wahlers T, Zieske A, Plenz G, Robenek H, Salbach P, Kuhn H, Radmark O, Samuelsson B, Habenicht AJ: Expanding expression of the 5-lipoxygenase pathway within the arterial wall during human atherogenesis. Proc Natl Acad Sci U S A. 2003, 100: 1238-1243. 10.1073/pnas.242716099PubMed CentralView ArticlePubMedGoogle Scholar
- Qiu H, Gabrielsen A, Agardh HE, Wan M, Wetterholm A, Wong CH, Hedin U, Swedenborg J, Hansson GK, Samuelsson B, Paulsson-Berne G, Haeggstrom JZ: Expression of 5-lipoxygenase and leukotriene A4 hydrolase in human atherosclerotic lesions correlates with symptoms of plaque instability. Proc Natl Acad Sci U S A. 2006, 103: 8161-8166. 10.1073/pnas.0602414103PubMed CentralView ArticlePubMedGoogle Scholar
- Allen S, Dashwood M, Morrison K, Yacoub M: Differential leukotriene constrictor responses in human atherosclerotic coronary arteries. Circulation. 1998, 97: 2406-2413. 10.1161/01.CIR.97.24.2406View ArticlePubMedGoogle Scholar
- Dwyer JH, Allayee H, Dwyer KM, Fan J, Wu H, Mar R, Lusis AJ, Mehrabian M: Arachidonate 5-lipoxygenase promoter genotype, dietary arachidonic acid, and atherosclerosis. N Engl J Med. 2004, 350: 29-37. 10.1056/NEJMoa025079View ArticlePubMedGoogle Scholar
- Allayee H, Baylin A, Hartiala J, Wijesuriya H, Mehrabian M, Lusis AJ, Campos H: Nutrigenetic association of the 5-lipoxygenase gene with myocardial infarction. Am J Clin Nutr. 2008, 88: 934-940.PubMed CentralPubMedGoogle Scholar
- Dal Negro RW, Visconti M, Micheletto C, Tognella S, Guerriero M: Reference urinary LTE4 levels in normal individuals: a pilot study. Eur Ann Allergy Clin Immunol. 2011, 43: 22-28.PubMedGoogle Scholar
- De Caterina R, Giannessi D, Lazzerini G, Bernini W, Sicari R, Cupelli F, Lenzi S, Rugolotto MM, Madonna R, Maclouf J: Sulfido-peptide leukotrienes in coronary heart disease - relationship with disease instability and myocardial ischaemia. Eur J Clin Invest. 2010, 40: 258-272. 10.1111/j.1365-2362.2010.02261.xView ArticlePubMedGoogle Scholar
- Thies F, Garry JM, Yaqoob P, Rerkasem K, Williams J, Shearman CP, Gallagher PJ, Calder PC, Grimble RF: Association of n-3 polyunsaturated fatty acids with stability of atherosclerotic plaques: a randomised controlled trial. Lancet. 2003, 361: 477-485. 10.1016/S0140-6736(03)12468-3View ArticlePubMedGoogle Scholar
- Cawood AL, Ding R, Napper FL, Young RH, Williams JA, Ward MJ, Gudmundsen O, Vige R, Payne SP, Ye S, Shearman CP, Gallagher PJ, Grimble RF, Calder PC: Eicosapentaenoic acid (EPA) from highly concentrated n-3 fatty acid ethyl esters is incorporated into advanced atherosclerotic plaques and higher plaque EPA is associated with decreased plaque inflammation and increased stability. Atherosclerosis. 2010, 212: 252-259. 10.1016/j.atherosclerosis.2010.05.022View ArticlePubMedGoogle Scholar
- Conner WE, Lin DS, Colvis C: Differential mobilization of fatty acids from adipose tissue. J Lipid Res. 1996, 37: 290-298.PubMedGoogle Scholar
- Conquer JA, Cheryk LA, Chan E, Gentry PA, Holub BJ: Effect of supplementation with dietary seal oil on selected cardiovascular risk factors and hemostatic variables in healthy male subjects. Thromb Res. 1999, 96: 239-250. 10.1016/S0049-3848(99)00106-1View ArticlePubMedGoogle Scholar
- Dalager S, Paaske WP, Kristensen IB, Laurberg JM, Falk E: Artery-related differences in atherosclerosis expression: implications for atherogenesis and dynamics in intima-media thickness. Stroke. 2007, 38: 2698-2705. 10.1161/STROKEAHA.107.486480View ArticlePubMedGoogle Scholar
- Dirksen MT, van der Wal AC, van den Berg FM, van der Loos CM, Becker AE: Distribution of inflammatory cells in atherosclerotic plaques relates to the direction of flow. Circulation. 1998, 98: 2000-2003. 10.1161/01.CIR.98.19.2000View ArticlePubMedGoogle Scholar
- Pasterkamp G, Schoneveld AH, van der Wal AC, Haudenschild CC, Clarijs RJ, Becker AE, Hillen B, Borst C: Relation of arterial geometry to luminal narrowing and histologic markers for plaque vulnerability: the remodeling paradox. J Am Coll Cardiol. 1998, 32: 655-662. 10.1016/S0735-1097(98)00304-0View ArticlePubMedGoogle Scholar
- Folch J, Lees M, Sloane Stanley GH: A simple method for the isolation and purification of total lipides from animal tissues. J Biol Chem. 1957, 226: 497-509.PubMedGoogle Scholar
- Burdge GC, Wright P, Jones AE, Wootton SA: A method for separation of phosphatidylcholine, triacylglycerol, non-esterified fatty acids and cholesterol esters from plasma by solid-phase extraction. Br J Nutr. 2000, 84: 781-787.PubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.