Innovative Strategies For Risk Reduction Following CABG

NCT ID: NCT00462436

Last Updated: 2010-07-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

35 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-02-28

Study Completion Date

2010-05-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Background: Treatment targets for cardiac risk factor reduction are not being met. Therefore, there is a need for new strategies to assist patients in meeting these goals.

Objective: To determine the amount of any additional benefit on risk factor reduction associated with the consumption of the "dietary portfolio" (a low fat diet with soy, nuts and viscous fibres), above that achieved with medical management in diabetic patients following cardiac surgery.

Description: 35 cardiac surgery patients with diabetes will be instructed on how to incorporate the dietary portfolio foods into their diet for four weeks. Changes in blood cholesterol, markers of inflammation, blood sugar control and modifiable risk factors will be assessed after 2 and 4 weeks of therapy.

Relevance: Maximizing cardiac risk factor reduction through a combined approach (dietary plus medication) should improve outcomes, reduce rates of re-hospitalization and improve quality of life in diabetic patients after heart surgery.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Introduction: The consumption of a dietary portfolio has been found to successfully reduce LDL cholesterol by 30% in hyperlipidemic, non-diabetic patients under highly controlled conditions. Given the burden of cardiovascular disease in the diabetic population, it is now important that we evaluate whether consumption of the dietary portfolio can reduce modifiable risk factors and improve diabetic control above that associated with medical therapy alone in this population. The reduction of modifiable risk factors, particularly in the diabetic patient with coronary artery disease, should not only improve long-term outcomes thereby reducing re-admissions and subsequently the burden of the diabetic patient on the health care system, but also improve quality of life for these patients. This pilot project will determine the efficacy, feasibility and tolerability of an aggressive dietary strategy, the dietary portfolio of functional foods to reduce cardiovascular risk factors in diabetic patients following CABG.

Study Objectives: This study will determine to what extent the self selected "modified" dietary portfolio (without sterols) together with statin therapy will:

* reduce total and LDL cholesterol
* increase endothelial cell number and function and reduce CRP levels.
* reduce markers of inflammation and insulin resistance
* the study will also determine the tolerability of and compliance with the portfolio diet

Primary Hypothesis: The consumption of the modified dietary portfolio will have a pleiotropic effect with current statin therapy resulting in an additional reduction in LDL cholesterol of 25% after four weeks of treatment.

Secondary Hypotheses: The addition of the dietary portfolio together with statin therapy will:

* significantly increase measures of endothelial function and endothelial progenitor cell counts
* significantly reduce CRP levels
* be feasible and well tolerated by most bypass patients
* result in a compliance rate of 70% with the main components of the diet
* significantly improve the plasma total-C:HDL-C ratio, and total-C, HDL-C, apolipoproteins A-I and B levels after both two and four weeks of treatment
* significantly reduce markers of inflammation at four weeks (CRP, IL-6 and TNF)
* improve indices of glycemic control (HOMA), oxidized LDL and LDL particle size

Trial Design:

Subject Selection: Participants will be screened from those patients returning for their routine six week follow-up visit following their coronary artery bypass graft surgery. Eligible patients will be invited to participate in this secondary prevention trial by their surgeon. The six week time point for recruitment not only allows direct patient interaction but also ensures that sufficient time has passed for normalization of the lipid profile post CABG (20). Finally, at this time, most patients have also seen their cardiologist and have had their medication regimen adjusted following surgery, which should allow for a window of stable medical care over the course of the study.

Patients with type II diabetes are selected for this study as 1) this group of patients is at a higher risk of developing post-operative complications and therefore are most likely to receive the maximal benefit from risk factor modification, and 2) this group has increased cardiovascular risk and therefore should benefit on multiple levels by the addition of the portfolio diet including, but not limited to reduced LDL cholesterol, blood pressure, CRP and inflammatory response but also in improved insulin sensitivity and endothelial function. Finally since estrogen levels influence endothelial function, pre-menopausal women will be excluded from this pilot study.

Study Design: This is non-randomized pilot study investigating the magnitude of cardiovascular risk reduction achieved by the addition of a "modified portfolio diet" (DPF)(without plant sterols) consumed for one month under real life conditions in diabetic patients on statin therapy who have known cardiovascular disease. The four week intervention period has previously been found to be sufficient for significant changes in the primary outcome variable (LDL cholesterol) to occur but will be short enough to minimize the confounding effects of changes in medication and physical activity in hypercholesterolemic subjects not on statin therapy(21).

The study will involve one baseline and two follow-up visits (Figure 1). At baseline, demographic, anthropometric (weight, height, body mass index (BMI), waist/hip ratio) and medical/cardiac history will be obtained including a detailed list of current medications. Resting blood pressure will be measured (see analytic methods). Information regarding exercise and smoking habits will also be obtained at this time. Participants will receive comprehensive dietary advice by a trained registered dietitian at the Risk Factor Modification Centre. The DPF group will conform to current therapeutic diets appropriate for hypercholesterolemic subjects (\<7% of energy saturated fat, \<200 mg/d cholesterol) with the addition of a combination of viscous fibers, soy protein and almonds. Participants will be instructed on how to select and follow this diet and will be provided with samples of appropriate foods to assist in the initial selection of and compliance with the DPF. All participants will receive a weekly allowance for the purchase of appropriate foods. The portfolio diet plan will include foods which contribute 8 g/1000 kcal viscous fiber as β-glucan (oats, barley, oat bran breads and soups) and psyllium (cereal), 17 g soy protein/1000 kcal (soy burgers, hot dogs, links, other meat analogues, milks, yogurts and cheese) and 22 g nuts (almonds)/1000 kcal. Participants at the Risk Factor Modification Centre have been maintained on this level of fiber intake for 4-month periods (22). Moderate weight loss (0.5kg/week) for those with a BMI \>25 and routine physical activity using the guidelines from the Guide to Cardiac surgery will be encouraged as part of this secondary prevention strategy. During the baseline visit, the coordinator (MSc student) will complete a 24 hour dietary recall to obtain an idea of estimated dietary intake. This recall together with calculated energy requirements using established equations will be used to assess individual energy intake. Using this estimate, the coordinator will advise the participant on how to incorporate the DPF into their eating patterns. The coordinator will instruct patients on detailed diet history recording, and each participant will be provided printed booklets in which to record the food items and their approximate size. Since determining compliance is an important end-point, self-taring scales will be provided to assist with accuracy. Subjects will be asked to complete daily a checklist of their consumption of the three key foods or food components of the portfolio diet (23,24). Assessment of the checklists for the three key dietary components will provide not only an estimate of compliance but will also assist patients in monitoring on a daily basis how many foods from the portfolio they have consumed. The coordinator will complete 4 random 24 hour recalls with each study subject, using standardized techniques, throughout the study period in order to validate the compliance checklist data. Recall data will be analyzed using a program based on USDA data (25) with additional data on foods analyzed in the laboratory for protein, total fat, and dietary fiber using the methods of the Association of Official Analytical Chemists (AOAC) (26) as well as the tables of Anderson and Bridges (27).

Since the DPF is part of a comprehensive secondary prevention strategy, all participants will be encouraged to follow the guidelines for physical activity (30 minutes, 3-5 times per week) outlined in the Guide for Cardiac Surgery Outpatient Handbook. The amount of physical activity will be recorded using a pedometer and will be recorded at the bottom of their food checklist. Fasting blood samples will be collected for primary and secondary markers of cardiovascular risk, insulin resistance and endothelial function. Brachial artery vasoreactivity will be completed at the same time of day with each participant under fasting conditions. Medications will be held the morning of the test.

Significance of Proposal: This study will determine the magnitude of any additional cardiovascular risk reduction associated with the consumption of the "modified dietary portfolio" in diabetic patients with coronary artery disease on statin therapy. Furthermore, since the dietary portfolio is an aggressive strategy, this study will also determine the feasibility and tolerability of this type of intervention in patients living in the community. Finally, this study may justify a larger secondary prevention trial looking at the effect of this intervention on cardiac outcomes and rates of re-hospitalization following bypass grafting. Aggressive, innovative, patient driven dietary strategies may complement medical management improving the ability of patients to meet treatment targets ultimately resulting in improved patient outcomes and quality of life following bypass graft surgery.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Coronary Artery Disease Type II Diabetes Mellitus

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Consumption of Dietary Portfolio

The study involves following an aggressive low fat diet that is high in viscous fiber, nuts and soy protein. The diet is individually tailored to meet individual participants needs.

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

1. Patients with type II diabetes mellitus
2. Recently (\<5 months) undergone coronary artery bypass graft surgery
3. Taking cholesterol lowering medication

Exclusion Criteria

1. Can not speak English and have no available interpreter
2. Refuse Informed Consent
3. Had "off pump" CABG
4. Are intolerant of statins
5. Are pre-menopausal (women) or are on HRT
6. Have serious concomitant disease
7. Take insulin
8. Are \<18 years of age
9. receive incomplete revascularization
10. documented history of drug or alcohol abuse
11. Intend to become pregnant during study period
12. Have an unreliable psychological condition that makes them unlikely to comply
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Canadian Diabetes Association

OTHER

Sponsor Role collaborator

Unity Health Toronto

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

St. Michael's Hospital

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Mary Keith, PhD, RD

Role: PRINCIPAL_INVESTIGATOR

Unity Health Toronto

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

St. Michael's Hospital

Toronto, Ontario, Canada

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Canada

References

Explore related publications, articles, or registry entries linked to this study.

Herlitz J, Wognsen GB, Emanuelsson H, Haglid M, Karlson BW, Karlsson T, Albertsson P, Westberg S. Mortality and morbidity in diabetic and nondiabetic patients during a 2-year period after coronary artery bypass grafting. Diabetes Care. 1996 Jul;19(7):698-703. doi: 10.2337/diacare.19.7.698.

Reference Type BACKGROUND
PMID: 8799622 (View on PubMed)

Morricone L, Ranucci M, Denti S, Cazzaniga A, Isgro G, Enrini R, Caviezel F. Diabetes and complications after cardiac surgery: comparison with a non-diabetic population. Acta Diabetol. 1999 Jun;36(1-2):77-84. doi: 10.1007/s005920050149.

Reference Type BACKGROUND
PMID: 10436257 (View on PubMed)

Carson JL, Scholz PM, Chen AY, Peterson ED, Gold J, Schneider SH. Diabetes mellitus increases short-term mortality and morbidity in patients undergoing coronary artery bypass graft surgery. J Am Coll Cardiol. 2002 Aug 7;40(3):418-23. doi: 10.1016/s0735-1097(02)01969-1.

Reference Type BACKGROUND
PMID: 12142105 (View on PubMed)

Schwartz L, Kip KE, Frye RL, Alderman EL, Schaff HV, Detre KM; Bypass Angioplasty Revascularization Investigation. Coronary bypass graft patency in patients with diabetes in the Bypass Angioplasty Revascularization Investigation (BARI). Circulation. 2002 Nov 19;106(21):2652-8. doi: 10.1161/01.cir.0000038885.94771.43.

Reference Type BACKGROUND
PMID: 12438289 (View on PubMed)

Post Coronary Artery Bypass Graft Trial Investigators. The effect of aggressive lowering of low-density lipoprotein cholesterol levels and low-dose anticoagulation on obstructive changes in saphenous-vein coronary-artery bypass grafts. N Engl J Med. 1997 Jan 16;336(3):153-62. doi: 10.1056/NEJM199701163360301.

Reference Type BACKGROUND
PMID: 8992351 (View on PubMed)

Pearson TA, Peters TD. The treatment gap in coronary artery disease and heart failure: community standards and the post-discharge patient. Am J Cardiol. 1997 Oct 30;80(8B):45H-52H. doi: 10.1016/s0002-9149(97)00820-5.

Reference Type BACKGROUND
PMID: 9372998 (View on PubMed)

EUROASPIRE I and II Group; European Action on Secondary Prevention by Intervention to Reduce Events. Clinical reality of coronary prevention guidelines: a comparison of EUROASPIRE I and II in nine countries. EUROASPIRE I and II Group. European Action on Secondary Prevention by Intervention to Reduce Events. Lancet. 2001 Mar 31;357(9261):995-1001. doi: 10.1016/s0140-6736(00)04235-5.

Reference Type BACKGROUND
PMID: 11293642 (View on PubMed)

Grundy SM, Balady GJ, Criqui MH, Fletcher G, Greenland P, Hiratzka LF, Houston-Miller N, Kris-Etherton P, Krumholz HM, LaRosa J, Ockene IS, Pearson TA, Reed J, Washington R, Smith SC Jr. Primary prevention of coronary heart disease: guidance from Framingham: a statement for healthcare professionals from the AHA Task Force on Risk Reduction. American Heart Association. Circulation. 1998 May 12;97(18):1876-87. doi: 10.1161/01.cir.97.18.1876. No abstract available.

Reference Type BACKGROUND
PMID: 9603549 (View on PubMed)

McFarlane SI, Jacober SJ, Winer N, Kaur J, Castro JP, Wui MA, Gliwa A, Von Gizycki H, Sowers JR. Control of cardiovascular risk factors in patients with diabetes and hypertension at urban academic medical centers. Diabetes Care. 2002 Apr;25(4):718-23. doi: 10.2337/diacare.25.4.718.

Reference Type BACKGROUND
PMID: 11919131 (View on PubMed)

George PB, Tobin KJ, Corpus RA, Devlin WH, O'Neill WW. Treatment of cardiac risk factors in diabetic patients: How well do we follow the guidelines? Am Heart J. 2001 Nov;142(5):857-63. doi: 10.1067/mhj.2001.119132.

Reference Type BACKGROUND
PMID: 11685175 (View on PubMed)

Hiss RG, Anderson RM, Hess GE, Stepien CJ, Davis WK. Community diabetes care. A 10-year perspective. Diabetes Care. 1994 Oct;17(10):1124-34. doi: 10.2337/diacare.17.10.1124.

Reference Type BACKGROUND
PMID: 7821131 (View on PubMed)

Grundy SM, Cleeman JI, Merz CN, Brewer HB Jr, Clark LT, Hunninghake DB, Pasternak RC, Smith SC Jr, Stone NJ; National Heart, Lung, and Blood Institute; American College of Cardiology Foundation; American Heart Association. Implications of recent clinical trials for the National Cholesterol Education Program Adult Treatment Panel III guidelines. Circulation. 2004 Jul 13;110(2):227-39. doi: 10.1161/01.CIR.0000133317.49796.0E.

Reference Type BACKGROUND
PMID: 15249516 (View on PubMed)

Ridker PM. Clinical application of C-reactive protein for cardiovascular disease detection and prevention. Circulation. 2003 Jan 28;107(3):363-9. doi: 10.1161/01.cir.0000053730.47739.3c. No abstract available.

Reference Type BACKGROUND
PMID: 12551853 (View on PubMed)

Ooi M, Cooper A, Lloyd G, Jackson G. A study of lipid profile before and after coronary artery bypass grafting. Br J Clin Pract. 1996 Dec;50(8):433-5.

Reference Type BACKGROUND
PMID: 9039713 (View on PubMed)

Jenkins DJ, Kendall CW, Marchie A, Faulkner DA, Wong JM, de Souza R, Emam A, Parker TL, Vidgen E, Lapsley KG, Trautwein EA, Josse RG, Leiter LA, Connelly PW. Effects of a dietary portfolio of cholesterol-lowering foods vs lovastatin on serum lipids and C-reactive protein. JAMA. 2003 Jul 23;290(4):502-10. doi: 10.1001/jama.290.4.502.

Reference Type BACKGROUND
PMID: 12876093 (View on PubMed)

Jenkins DJ, Wolever TM, Rao AV, Hegele RA, Mitchell SJ, Ransom TP, Boctor DL, Spadafora PJ, Jenkins AL, Mehling C, et al. Effect on blood lipids of very high intakes of fiber in diets low in saturated fat and cholesterol. N Engl J Med. 1993 Jul 1;329(1):21-6. doi: 10.1056/NEJM199307013290104.

Reference Type BACKGROUND
PMID: 8389421 (View on PubMed)

Bingham SA, Gill C, Welch A, Day K, Cassidy A, Khaw KT, Sneyd MJ, Key TJ, Roe L, Day NE. Comparison of dietary assessment methods in nutritional epidemiology: weighed records v. 24 h recalls, food-frequency questionnaires and estimated-diet records. Br J Nutr. 1994 Oct;72(4):619-43. doi: 10.1079/bjn19940064.

Reference Type BACKGROUND
PMID: 7986792 (View on PubMed)

Goldberg GR, Black AE, Jebb SA, Cole TJ, Murgatroyd PR, Coward WA, Prentice AM. Critical evaluation of energy intake data using fundamental principles of energy physiology: 1. Derivation of cut-off limits to identify under-recording. Eur J Clin Nutr. 1991 Dec;45(12):569-81.

Reference Type BACKGROUND
PMID: 1810719 (View on PubMed)

25. The Agricultural Research Service. Composition of Foods, Agriculture Handbook No 8. Washington, DC, US Department of Agriculture, 1992.

Reference Type BACKGROUND

26. Association of Official Analytical Chemists. AOAC Official Methods of Analysis. Washington, DC, Association of Official Analytical Chemists, 1980.

Reference Type BACKGROUND

Anderson JW, Bridges SR. Dietary fiber content of selected foods. Am J Clin Nutr. 1988 Mar;47(3):440-7. doi: 10.1093/ajcn/47.3.440.

Reference Type BACKGROUND
PMID: 2831703 (View on PubMed)

Fagerberg B, Hulthe J, Bokemark L, Wikstrand J. Low-density lipoprotein particle size, insulin resistance, and proinsulin in a population sample of 58-year-old men. Metabolism. 2001 Jan;50(1):120-4. doi: 10.1053/meta.2001.18570.

Reference Type BACKGROUND
PMID: 11172485 (View on PubMed)

Garvey WT, Kwon S, Zheng D, Shaughnessy S, Wallace P, Hutto A, Pugh K, Jenkins AJ, Klein RL, Liao Y. Effects of insulin resistance and type 2 diabetes on lipoprotein subclass particle size and concentration determined by nuclear magnetic resonance. Diabetes. 2003 Feb;52(2):453-62. doi: 10.2337/diabetes.52.2.453.

Reference Type BACKGROUND
PMID: 12540621 (View on PubMed)

Lamarche B, St-Pierre AC, Ruel IL, Cantin B, Dagenais GR, Despres JP. A prospective, population-based study of low density lipoprotein particle size as a risk factor for ischemic heart disease in men. Can J Cardiol. 2001 Aug;17(8):859-65.

Reference Type BACKGROUND
PMID: 11521128 (View on PubMed)

St-Pierre AC, Ruel IL, Cantin B, Dagenais GR, Bernard PM, Despres JP, Lamarche B. Comparison of various electrophoretic characteristics of LDL particles and their relationship to the risk of ischemic heart disease. Circulation. 2001 Nov 6;104(19):2295-9. doi: 10.1161/hc4401.098490.

Reference Type BACKGROUND
PMID: 11696468 (View on PubMed)

Krauss RM. Dense low density lipoproteins and coronary artery disease. Am J Cardiol. 1995 Feb 23;75(6):53B-57B. doi: 10.1016/0002-9149(95)80012-h.

Reference Type BACKGROUND
PMID: 7863975 (View on PubMed)

Williams PT, Haskell WL, Vranizan KM, Krauss RM. The associations of high-density lipoprotein subclasses with insulin and glucose levels, physical activity, resting heart rate, and regional adiposity in men with coronary artery disease: the Stanford Coronary Risk Intervention Project baseline survey. Metabolism. 1995 Jan;44(1):106-14. doi: 10.1016/0026-0495(95)90296-1.

Reference Type BACKGROUND
PMID: 7854154 (View on PubMed)

Berneis KK, Krauss RM. Metabolic origins and clinical significance of LDL heterogeneity. J Lipid Res. 2002 Sep;43(9):1363-79. doi: 10.1194/jlr.r200004-jlr200.

Reference Type BACKGROUND
PMID: 12235168 (View on PubMed)

Asahara T, Murohara T, Sullivan A, Silver M, van der Zee R, Li T, Witzenbichler B, Schatteman G, Isner JM. Isolation of putative progenitor endothelial cells for angiogenesis. Science. 1997 Feb 14;275(5302):964-7. doi: 10.1126/science.275.5302.964.

Reference Type BACKGROUND
PMID: 9020076 (View on PubMed)

Asahara T, Masuda H, Takahashi T, Kalka C, Pastore C, Silver M, Kearne M, Magner M, Isner JM. Bone marrow origin of endothelial progenitor cells responsible for postnatal vasculogenesis in physiological and pathological neovascularization. Circ Res. 1999 Aug 6;85(3):221-8. doi: 10.1161/01.res.85.3.221.

Reference Type BACKGROUND
PMID: 10436164 (View on PubMed)

Takahashi T, Kalka C, Masuda H, Chen D, Silver M, Kearney M, Magner M, Isner JM, Asahara T. Ischemia- and cytokine-induced mobilization of bone marrow-derived endothelial progenitor cells for neovascularization. Nat Med. 1999 Apr;5(4):434-8. doi: 10.1038/7434.

Reference Type BACKGROUND
PMID: 10202935 (View on PubMed)

Vasa M, Fichtlscherer S, Aicher A, Adler K, Urbich C, Martin H, Zeiher AM, Dimmeler S. Number and migratory activity of circulating endothelial progenitor cells inversely correlate with risk factors for coronary artery disease. Circ Res. 2001 Jul 6;89(1):E1-7. doi: 10.1161/hh1301.093953.

Reference Type BACKGROUND
PMID: 11440984 (View on PubMed)

Tepper OM, Galiano RD, Capla JM, Kalka C, Gagne PJ, Jacobowitz GR, Levine JP, Gurtner GC. Human endothelial progenitor cells from type II diabetics exhibit impaired proliferation, adhesion, and incorporation into vascular structures. Circulation. 2002 Nov 26;106(22):2781-6. doi: 10.1161/01.cir.0000039526.42991.93.

Reference Type BACKGROUND
PMID: 12451003 (View on PubMed)

Schachinger V, Britten MB, Zeiher AM. Prognostic impact of coronary vasodilator dysfunction on adverse long-term outcome of coronary heart disease. Circulation. 2000 Apr 25;101(16):1899-906. doi: 10.1161/01.cir.101.16.1899.

Reference Type BACKGROUND
PMID: 10779454 (View on PubMed)

Anderson TJ, Uehata A, Gerhard MD, Meredith IT, Knab S, Delagrange D, Lieberman EH, Ganz P, Creager MA, Yeung AC, et al. Close relation of endothelial function in the human coronary and peripheral circulations. J Am Coll Cardiol. 1995 Nov 1;26(5):1235-41. doi: 10.1016/0735-1097(95)00327-4.

Reference Type BACKGROUND
PMID: 7594037 (View on PubMed)

Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Treacher DF, Turner RC. Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia. 1985 Jul;28(7):412-9. doi: 10.1007/BF00280883.

Reference Type BACKGROUND
PMID: 3899825 (View on PubMed)

Verma S, Kuliszewski MA, Li SH, Szmitko PE, Zucco L, Wang CH, Badiwala MV, Mickle DA, Weisel RD, Fedak PW, Stewart DJ, Kutryk MJ. C-reactive protein attenuates endothelial progenitor cell survival, differentiation, and function: further evidence of a mechanistic link between C-reactive protein and cardiovascular disease. Circulation. 2004 May 4;109(17):2058-67. doi: 10.1161/01.CIR.0000127577.63323.24. Epub 2004 Apr 12.

Reference Type BACKGROUND
PMID: 15078802 (View on PubMed)

Lieberman EH, Gerhard MD, Uehata A, Selwyn AP, Ganz P, Yeung AC, Creager MA. Flow-induced vasodilation of the human brachial artery is impaired in patients <40 years of age with coronary artery disease. Am J Cardiol. 1996 Dec 1;78(11):1210-4. doi: 10.1016/s0002-9149(96)00597-8.

Reference Type BACKGROUND
PMID: 8960576 (View on PubMed)

Jenkins DJ, Kendall CW, Marchie A, Parker TL, Connelly PW, Qian W, Haight JS, Faulkner D, Vidgen E, Lapsley KG, Spiller GA. Dose response of almonds on coronary heart disease risk factors: blood lipids, oxidized low-density lipoproteins, lipoprotein(a), homocysteine, and pulmonary nitric oxide: a randomized, controlled, crossover trial. Circulation. 2002 Sep 10;106(11):1327-32. doi: 10.1161/01.cir.0000028421.91733.20.

Reference Type BACKGROUND
PMID: 12221048 (View on PubMed)

Jenkins DJ, Kendall CW, Jackson CJ, Connelly PW, Parker T, Faulkner D, Vidgen E, Cunnane SC, Leiter LA, Josse RG. Effects of high- and low-isoflavone soyfoods on blood lipids, oxidized LDL, homocysteine, and blood pressure in hyperlipidemic men and women. Am J Clin Nutr. 2002 Aug;76(2):365-72. doi: 10.1093/ajcn/76.2.365.

Reference Type BACKGROUND
PMID: 12145008 (View on PubMed)

Jenkins DJ, Kendall CW, Augustin LS, Martini MC, Axelsen M, Faulkner D, Vidgen E, Parker T, Lau H, Connelly PW, Teitel J, Singer W, Vandenbroucke AC, Leiter LA, Josse RG. Effect of wheat bran on glycemic control and risk factors for cardiovascular disease in type 2 diabetes. Diabetes Care. 2002 Sep;25(9):1522-8. doi: 10.2337/diacare.25.9.1522.

Reference Type BACKGROUND
PMID: 12196421 (View on PubMed)

Keith M, Kuliszewski MA, Liao C, Peeva V, Ahmed M, Tran S, Sorokin K, Jenkins DJ, Errett L, Leong-Poi H. A modified portfolio diet complements medical management to reduce cardiovascular risk factors in diabetic patients with coronary artery disease. Clin Nutr. 2015 Jun;34(3):541-8. doi: 10.1016/j.clnu.2014.06.010. Epub 2014 Jun 28.

Reference Type DERIVED
PMID: 25023926 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

REB06-179C

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.