A health-promoting diet rich in fiber, vitamins, minerals, phytochemicals, and healthy fats – combined with regular exercise – is the cornerstone of cardiovascular health. Foods such as green and leafy vegetables, soybeans and other beans, berries, nuts, garlic, and onions provide a powerful foundation by naturally reducing cholesterol production and/or absorption, improving vascular function and blood pressure, enhancing antioxidant defenses, and reducing inflammation.
However, carefully selected botanical supplements supplying cardioprotective phytochemicals can serve as a strategic accessory, amplifying the cardiovascular benefits of a Nutritarian diet.
Importantly, the same biological pathways that drive heart disease also underlie many other age-related chronic conditions, meaning that the phytochemicals that support cardiovascular health often confer broader benefits for brain and immune function, while helping protect against cancer, diabetes, and dementia.
Plant sterols
Plant sterols inhibit intestinal cholesterol absorption, leading to reductions in circulating total and LDL cholesterol, and ApoB.
Recommended daily dose for cardiovascular protection: 500 mg–2 g.
Plant sterols, found in the cell membranes of plants, are one of the many components of a healthful diet based on whole plant foods that keeps cholesterol levels in the favorable range. Plant sterols (also known as phytosterols):
Are naturally present in plant foods
Are structurally similar to cholesterol
Have similar functions in plant cell membranes to those of cholesterol in animal cell membranes
Naturally occur in whole plant foods, especially soybeans, peas, and nuts.1
When we consume plant sterols, they interfere with the absorption (and re-absorption) of cholesterol in the small intestine, which facilitates cholesterol excretion and reduces circulating cholesterol levels. Some evidence also suggests plant sterol supplementation could reduce very low-density lipoprotein (VLDL) production by the liver.2
Plant sterol supplements dose-dependently reduce LDL cholesterol by up to 12% for doses up to 2 grams daily.3 According to a 2024 meta-analysis of 26 randomized controlled trials, plant sterol supplements also reduce apolipoprotein B (ApoB), in addition to total and LDL cholesterol.4
The European Society of Cardiology has recommended plant sterol supplements alongside a healthful diet to decrease cholesterol levels, and the United States FDA has stated that plant sterols help to reduce total and LDL cholesterol.5,6 For people on cholesterol-lowering drugs, plant sterols can be taken alongside statins, leading to additional cholesterol reduction compared to statins alone.7
Plant sterols’ benefits extend beyond the cardiovascular system
Observational studies have shown that higher plant sterol intake is associated with a lower risk of cancers including lung, colorectal, breast, esophageal, and gastric cancers. 8 How plant sterol intake could affect cancer risk is still being investigated. But studies in cultured cells and animals suggest that plant sterols inhibit tumor cell proliferation and tumor growth, promote cell death in abnormal cells, reduce angiogenesis and tumor cell migration, and suppress the activity of oncogenes.9,10 From this research, dietary intakes of 200-500 mg/day plant sterols were estimated to be protective against cancer.8,9
Additionally, plant sterols are reported to play a protective therapeutic role in benign prostatic hypertrophy (BPH or enlarged prostate), a common medical condition in older men.11 Symptoms of BPH have been improved by supplementation of small doses (up to 130 mg) of plant sterols compared to placebo.12-14
Amla has cardioprotective effects through polyphenol-mediated reductions in oxidative stress and inflammation, improved endothelial function, and reduced cholesterol and blood glucose.
Recommended daily dose for cardiovascular protection: 500-1000 mg amla powder or extract
Amla fruit is also known as Indian gooseberry (Latin name Phyllanthus emblica or Emblica officinalis) but is not botanically related to the European gooseberry. Amla is a small, round, yellow-green fruit that grows on a tree native to South Asia and grown in several tropical areas. Amla fruit can be found in India, Nepal, Sri Lanka, Malaysia, China, and Thailand. The fruit is typically harvested in autumn and has a fibrous texture and sour flavor. It is usually not eaten raw.
Instead, it is pickled, made into chutneys and other condiments, or cooked into entrees or desserts. Amla is also used as an herbal remedy in traditional Ayurvedic formulas.
In addition to fiber and vitamin C, amla is a source of phytochemicals including :
Ellagic acid
Pectin
Tannins, such as emblicanins
Flavonoids including quercetin, apigenin, luteolin, myricetin, kampferol, naringenin, and rutin
Lab studies have linked these phytochemicals in amla to antibacterial, glucose-lowering, cholesterol-lowering, antioxidant, and anti-cancer effects.15,16
Many randomized controlled trials have evaluated amla’s effects on blood lipids, finding reductions in total, LDL and VLDL cholesterol, and triglycerides. On average, in these studies, amla supplementation resulted in a 15 mg/dl reduction in seven studies measuring LDL, 5.4 mg /dl in three studies measuring VLDL, and 22 mg/dl in six studies measuring triglycerides.15
Amla’s benefits are not limited to circulating lipid levels
In clinical studies, supplementation with amla fruit powder or extract improved antioxidant status, blood vessel function, and inflammatory markers. After 8 and 12 weeks of supplementation in 59 participants with metabolic syndrome taking 250 or 500 mg amla extract twice daily, the ability of the vessels to dilate, a measure of endothelial function, improved compared to placebo. Improvements in several oxidative stress biomarkers, such as nitric oxide, glutathione, and malondialdehyde, as well as the inflammatory marker C-reactive protein were also observed.17
Amla may also have beneficial effects on glycemic control. Although there were only two randomized controlled trials, a meta-analysis pooling their data found that amla supplementation ranging from 500 to 3000 mg/day reduced fasting blood glucose (on average by about 12.7 mg/dl).18
Pomegranate polyphenols, such as ellagic acid, support cardiovascular health by reducing inflammation and oxidation of LDL cholesterol.
Different studies have used a variety of doses and forms of these fruits, such as powders, juice, and extracts. Recommended daily dose for cardiovascular protection: approximately 200-500 mg pomegranate extract), 200-500 mg chokeberry powder or extract.
Pomegranate is rich in ellagic acid, punicalagins, and flavonoids with antioxidant and anti-inflammatory properties.19 In randomized controlled trials, pomegranate supplementation showed reduced:
Blood pressure
Cholesterol
Fasting blood glucose
Inflammation
Oxidative stress markers20-22
In a three-year study on patients with heart disease, daily supplementation with pomegranate juice resulted in regression of atherosclerotic plaque, whereas the control group experienced an increase in plaque thickness. The pomegranate group also showed a reduction in oxidized LDL and an improvement in total antioxidant status.23
The polyphenols in pomegranate modulate signaling pathways involved in cell proliferation, programmed cell death, inflammation, angiogenesis, adhesion, and metastasis, and regulation of gene expression.24 A few trials in patients with prostate cancer have shown an increase in PSA doubling time – slowing the rise in PSA levels.25 Pomegranate phytochemicals also have anti-estrogen effects – inhibition of the aromatase enzyme – that could help prevent breast cancer.26
Chokeberry (Aronia melanocarpa) is another antioxidant-rich fruit not typically found in our diets that promotes cardiovascular health. A meta-analysis of seven studies on chokeberry supplementation found reductions in systolic blood pressure and total cholesterol.27
LDL Biotect is a research-backed, plant-based supplement designed to work alongside a Nutritarian diet to optimize heart health, supplying plant sterols, amla fruit, pomegranate extract, and chokeberry.
Green tea
Green tea catechins, especially epigallocatechin gallate (EGCG), reduce oxidative stress, and drinking green tea is linked to lower cardiovascular disease and cancer risk across many studies.
Recommended daily dose for cardiovascular protection: 200-300 mg total green tea extract (limit to no more than 300 mg EGCG)
Green tea is rich in flavonoid antioxidants known as catechins, and drinking green tea regularly is associated with better cardiovascular health and a lower risk of several cancers.28-32 Green tea supplementation studies have found improvements in cholesterol and blood glucose levels, as well as oxidative stress markers.33-35
The anti-cancer effects of green tea extracts include:
Promoting immune function
Inhibiting inflammation and angiogenesis
Reducing tumor cell growth and proliferation.36
Clinical trials in patients with prostate cancer have shown reduced PSA and other cancer-related biomarkers.37,38 Supplementation with green tea extract or EGCG also reduced cancer-related biomarkers or tumor cell proliferation in clinical trials in women with breast cancer.39,40
Curcumin, the major bioactive compound in turmeric, targets inflammatory signaling pathways, leading to lower levels of inflammation and oxidative damage, while reducing cholesterol levels.
Recommended daily dose for cardiovascular protection: 100-400 mg/day; be cautious of high doses (1000 mg or more per day) when combined with absorption enhancers, because of reports of liver injury.
Turmeric phytochemicals, including curcuminoids and others, such as turmerones, have shown a variety of anti-cancer effects, especially through reducing inflammation, but also by affecting tumor cell survival, proliferation, and adhesion.41,42 Turmeric’s anti-inflammatory effects have been confirmed in randomized controlled trials,43 and turmeric or curcumin supplements also reduced total and LDL cholesterol.44 A few clinical trials have been conducted in patients with cancers, and have found improvements in cancer-related biomarkers, or have suggested that curcumin could be a helpful adjunct to other cancer treatments.45
Grape seeds are rich in antioxidant proanthocyanidins, with blood pressure-lowering properties.
Recommended daily dose for cardiovascular protection: 150-300 mg/day.
Grapes are common in typical diets, but the seeds, which are highest in antioxidants, in particular proanthocyanidins, are rarely eaten.46,47 Several studies have found reductions in blood pressure, cholesterol, or oxidative stress markers in response to grape seed extract supplementation.48-50 Studies also suggest grape seed proanthocyanidins have anti-cancer effects.51,52
Ultra Cell Biotect combines powerful superfoods including green tea extract, turmeric, and grape seed extract that enhance the body’s natural antioxidant defenses to protect cardiovascular health and promote healthy aging.
Coenzyme Q10
Coenzyme Q10 is a natural antioxidant that’s also crucial for producing cellular energy in heart muscle cells. Levels decline with age.
Recommended daily dose for cardiovascular protection: 100-200 mg/day.
CoQ10 is an antioxidant produced naturally in the mitochondria of our cells, where it scavenges free radicals and helps generate energy in the form of ATP. The antioxidant actions of CoQ10 protect cells in the heart and blood vessels from oxidative damage and maintain healthy blood pressure levels. CoQ10 also promotes the production of other natural antioxidants in the body. CoQ10 is present in high concentrations in heart muscle, and CoQ10levels decline with age.53-55 Randomized controlled trials have found that CoQ10 supplementation:
Reduced oxidative stress markers
Improved endothelial function
Reduced blood pressure and blood glucose.55-58
CoQ10 supplementation may be especially helpful for people who take cholesterol-lowering statin drugs, which may decrease the production of CoQ10.53,54 Studies have found CoQ10 supplementation increases CoQ10 levels in people taking statins, and improved statin-associated muscle symptoms.59-62
Dr. Fuhrman’s CoQ10 protects cardiac muscle from oxidative damage and supports healthy blood vessel function and cellular energy production.
References
Linus Pauling Institute Micronutrient Information Center, Oregon State University. Phytosterols [https://lpi.oregonstate.edu/mic/dietary-factors/phytochemicals/phytosterols]
Li X, Xin Y, Mo Y, et al. The Bioavailability and Biological Activities of Phytosterols as Modulators of Cholesterol Metabolism.Molecules 2022, 27.
Chen Y, She Y, Kaur R, et al. Is Plant Sterols a Good Strategy to Lower Cholesterol?J Oleo Sci 2019, 68:811-816.
Zhang YF, Qiao W, Feng H, et al. Effects of phytosterol supplementation on lipid profiles and apolipoproteins: A meta-analysis of randomized controlled trials.Medicine (Baltimore) 2024, 103:e40020.
Mach F, Baigent C, Catapano AL, et al. 2019 ESC/EAS Guidelines for the management of dyslipidaemias: lipid modification to reduce cardiovascular risk: The Task Force for the management of dyslipidaemias of the European Society of Cardiology (ESC) and European Atherosclerosis Society (EAS).European Heart Journal 2019, 41:111-188.
Food Labeling: Health Claims; Plant Sterol/Stanol Esters and Coronary Heart Disease. (Food and Drug Administration ed., vol. 21 CFR 101. pp. 54686-547392000:54686-54739.
Han S, Jiao J, Xu J, et al. Effects of plant stanol or sterol-enriched diets on lipid profiles in patients treated with statins: systematic review and meta-analysis.Sci Rep 2016, 6:31337.
Jiang L, Zhao X, Xu J, et al. The Protective Effect of Dietary Phytosterols on Cancer Risk: A Systematic Meta-Analysis.Journal of Oncology 2019, 2019:7479518.
Cioccoloni G, Soteriou C, Websdale A, et al. Phytosterols and phytostanols and the hallmarks of cancer in model organisms: A systematic review and meta-analysis.Critical Reviews in Food Science and Nutrition 2022, 62:1145-1165.
Bao X, Zhang Y, Zhang H, Xia L. Molecular Mechanism of β-Sitosterol and its Derivatives in Tumor Progression.Frontiers in Oncology 2022, Volume 12 - 2022.
Macoska JA. The use of beta-sitosterol for the treatment of prostate cancer and benign prostatic hyperplasia.Am J Clin Exp Urol 2023, 11:467-480.
Klippel KF, Hiltl DM, Schipp B. A multicentric, placebo-controlled, double-blind clinical trial of beta-sitosterol (phytosterol) for the treatment of benign prostatic hyperplasia. German BPH-Phyto Study group.Br J Urol 1997, 80:427-432.
Berges RR, Kassen A, Senge T. Treatment of symptomatic benign prostatic hyperplasia with beta-sitosterol: an 18-month follow-up.BJU Int 2000, 85:842-846.
Sudeep HV, Thomas JV, Shyamprasad K. A double blind, placebo-controlled randomized comparative study on the efficacy of phytosterol-enriched and conventional saw palmetto oil in mitigating benign prostate hyperplasia and androgen deficiency.BMC Urology 2020, 20:86.
Brown PDS, Ketter N, Vis-Dunbar M, Sakakibara BM. Clinical effects of Emblica officinalis fruit consumption on cardiovascular disease risk factors: a systematic review and meta-analysis.BMC Complement Med Ther 2023, 23:190.
Gul M, Liu ZW, Iahtisham Ul H, et al. Functional and Nutraceutical Significance of Amla (Phyllanthus emblica L.): A Review.Antioxidants (Basel) 2022, 11.
Usharani P, Merugu PL, Nutalapati C. Evaluation of the effects of a standardized aqueous extract of Phyllanthus emblica fruits on endothelial dysfunction, oxidative stress, systemic inflammation and lipid profile in subjects with metabolic syndrome: a randomised, double blind, placebo controlled clinical study.BMC Complementary and Alternative Medicine 2019, 19:97.
Setayesh L, Haghighat N, Rasaei N, et al. The impact of Emblica Officinalis (Amla) on lipid profile, glucose, and C-reactive protein: A systematic review and meta-analysis of randomized controlled trials.Diabetes Metab Syndr 2023, 17:102729.
Wang D, Ozen C, Abu-Reidah IM, et al. Vasculoprotective Effects of Pomegranate (Punica granatum L.).Front Pharmacol 2018, 9:544.
Lorzadeh E, Heidary Z, Mohammadi M, et al. Does pomegranate consumption improve oxidative stress? A systematic review and meta-analysis of randomized controlled clinical trials.Clin Nutr ESPEN 2022, 47:117-127.
Mohammadi S, Heshmati J, Baziar N, et al. Impacts of supplementation with pomegranate on cardiometabolic risk factors: A systematic review and dose-response meta-analysis.Nutrition, Metabolism and Cardiovascular Diseases 2025, 35.
Bahari H, Rafiei H, Goudarzi K, et al. The effects of pomegranate consumption on inflammatory and oxidative stress biomarkers in adults: a systematic review and meta-analysis.Inflammopharmacology 2023, 31:2283-2301.
Aviram M, Rosenblat M, Gaitini D, et al. Pomegranate juice consumption for 3 years by patients with carotid artery stenosis reduces common carotid intima-media thickness, blood pressure and LDL oxidation.Clinical Nutrition 2004, 23:423-433.
Rauf A, Olatunde A, Akram Z, et al. The Role of Pomegranate (Punica granatum) in Cancer Prevention and Treatment: Modulating Signaling Pathways From Inflammation to Metastasis.Food Science & Nutrition 2025, 13:e4674.
Paller CJ, Pantuck A, Carducci MA. A review of pomegranate in prostate cancer.Prostate Cancer Prostatic Dis 2017, 20:265-270.
Jang JY, Kim D, Im E, Kim ND. Therapeutic Potential of Pomegranate Extract for Women's Reproductive Health and Breast Cancer.Life (Basel) 2024, 14.
Hawkins J, Hires C, Baker C, et al. Daily supplementation with aronia melanocarpa (chokeberry) reduces blood pressure and cholesterol: a meta analysis of controlled clinical trials.J Diet Suppl 2021, 18:517-530.
Pang J, Zhang Z, Zheng TZ, et al. Green tea consumption and risk of cardiovascular and ischemic related diseases: A meta-analysis.Int J Cardiol 2016, 202:967-974.
Tran HH, Mansoor M, Butt SRR, et al. Impact of Green Tea Consumption on the Prevalence of Cardiovascular Outcomes: A Systematic Review.Cureus 2023, 15:e49775.
Tang N, Wu Y, Zhou B, et al. Green tea, black tea consumption and risk of lung cancer: a meta-analysis.Lung Cancer 2009, 65:274-283.
Ogunleye AA, Xue F, Michels KB. Green tea consumption and breast cancer risk or recurrence: a meta-analysis.Breast Cancer Res Treat 2010, 119:477-484.
Zheng J, Yang B, Huang T, et al. Green Tea and Black Tea Consumption and Prostate Cancer Risk: An Exploratory Meta-Analysis of Observational Studies.Nutrition and Cancer 2011:1-10.
Dehzad MJ, Ghalandari H, Nouri M, et al. Effects of green tea supplementation on antioxidant status and inflammatory markers in adults: a grade-assessed systematic review and dose-response meta-analysis of randomised controlled trials.J Nutr Sci 2025, 14:e25.
Jia MJ, Liu XN, Liang YC, et al. The effect of green tea on patients with type 2 diabetes mellitus: A meta-analysis.Medicine (Baltimore) 2024, 103:e39702.
Neyestani TR, Nikooyeh B. A comprehensive overview on the effects of green tea on anthropometric measures, blood pressure, glycemic and lipidemic status: An umbrella review and meta meta-analysis study.Nutr Metab Cardiovasc Dis 2022, 32:2026-2040.
Shirakami Y, Shimizu M. Possible Mechanisms of Green Tea and Its Constituents against Cancer.Molecules 2018, 23.
McLarty J, Bigelow RL, Smith M, et al. Tea polyphenols decrease serum levels of prostate-specific antigen, hepatocyte growth factor, and vascular endothelial growth factor in prostate cancer patients and inhibit production of hepatocyte growth factor and vascular endothelial growth factor in vitro.Cancer Prev Res (Phila) 2009, 2:673-682.
Henning SM, Wang P, Said JW, et al. Randomized clinical trial of brewed green and black tea in men with prostate cancer prior to prostatectomy.Prostate 2015, 75:550-559.
Zhang G, Wang Y, Zhang Y, et al. Anti-cancer activities of tea epigallocatechin-3-gallate in breast cancer patients under radiotherapy.Curr Mol Med 2012, 12:163-176.
Lazzeroni M, Guerrieri-Gonzaga A, Gandini S, et al. A Presurgical Study of Lecithin Formulation of Green Tea Extract in Women with Early Breast Cancer.Cancer Prev Res (Phila) 2017, 10:363-370.
Aggarwal BB, Yuan W, Li S, Gupta SC. Curcumin-free turmeric exhibits anti-inflammatory and anticancer activities: Identification of novel components of turmeric.Mol Nutr Food Res 2013, 57:1529-1542.
Akter K, Gul K, Mumtaz S. Revisiting Curcumin in Cancer Therapy: Recent Insights into Molecular Mechanisms, Nanoformulations, and Synergistic Combinations.Curr Issues Mol Biol 2025, 47.
Dehzad MJ, Ghalandari H, Nouri M, Askarpour M. Antioxidant and anti-inflammatory effects of curcumin/turmeric supplementation in adults: A GRADE-assessed systematic review and dose–response meta-analysis of randomized controlled trials.Cytokine 2023, 164:156144.
Dehzad MJ, Ghalandari H, Amini MR, Askarpour M. Effects of curcumin/turmeric supplementation on lipid profile: A GRADE-assessed systematic review and dose–response meta-analysis of randomized controlled trials.Complementary Therapies in Medicine 2023, 75:102955.
Curcumin (Curcuma, Turmeric) and Cancer (PDQ(R)): Health Professional Version. In PDQ Cancer Information Summaries. Bethesda (MD)2025
Gu L, Kelm MA, Hammerstone JF, et al. Concentrations of proanthocyanidins in common foods and estimations of normal consumption.J Nutr 2004, 134:613-617.
Xia EQ, Deng GF, Guo YJ, Li HB. Biological activities of polyphenols from grapes.Int J Mol Sci 2010, 11:622-646.
Foshati S, Rouhani MH, Amani R. The effect of grape seed extract supplementation on oxidative stress and inflammation: A systematic review and meta-analysis of controlled trials.Int J Clin Pract 2021, 75:e14469.
Zhang H, Liu S, Li L, et al. The impact of grape seed extract treatment on blood pressure changes: A meta-analysis of 16 randomized controlled trials.Medicine (Baltimore) 2016, 95:e4247.
Asbaghi O, Nazarian B, Reiner Ž, et al. The effects of grape seed extract on glycemic control, serum lipoproteins, inflammation, and body weight: A systematic review and meta-analysis of randomized controlled trials.Phytotherapy Research 2020, 34:239-253.
Mao JT, Lu QY, Xue B, et al. A Pilot Study of a Grape Seed Procyanidin Extract for Lung Cancer Chemoprevention.Cancer Prev Res (Phila) 2019, 12:557-566.
Katiyar SK, Athar M. Grape seeds: ripe for cancer chemoprevention.Cancer Prev Res (Phila) 2013, 6:617-621.
Zozina VI, Covantev S, Goroshko OA, et al. Coenzyme Q10 in Cardiovascular and Metabolic Diseases: Current State of the Problem.Curr Cardiol Rev 2018, 14:164-174.
Sood B, Keenaghan M: Coenzyme Q10. In StatPearls. Treasure Island (FL) ineligible companies. Disclosure: Michael Keenaghan declares no relevant financial relationships with ineligible companies.2023
Samimi F, Namiranian N, Sharifi-Rigi A, et al. Coenzyme Q10: A Key Antioxidant in the Management of Diabetes-Induced Cardiovascular Complications—An Overview of Mechanisms and Clinical Evidence.International Journal of Endocrinology 2024, 2024:2247748.
Daei S, Ildarabadi A, Goodarzi S, Mohamadi-Sartang M. Effect of Coenzyme Q10 Supplementation on Vascular Endothelial Function: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.High Blood Pressure & Cardiovascular Prevention 2024, 31:113-126.
Dabbaghi Varnousfaderani S, Musazadeh V, Ghalichi F, et al. Alleviating effects of coenzyme Q10 supplements on biomarkers of inflammation and oxidative stress: results from an umbrella meta-analysis.Frontiers in Pharmacology 2023, Volume 14 - 2023.
Karimi M, Pirzad S, Hooshmand F, et al. Effects of coenzyme Q10 administration on blood pressure and heart rate in adults: A systematic review and meta-analysis of randomized controlled trials.Int J Cardiol Cardiovasc Risk Prev 2025, 26:200424.
Bargossi AM, Grossi G, Fiorella PL, et al. Exogenous CoQ10 supplementation prevents plasma ubiquinone reduction induced by HMG-CoA reductase inhibitors.Molecular Aspects of Medicine 1994, 15:s187-s193.
Mabuchi H, Nohara A, Kobayashi J, et al. Effects of CoQ10 supplementation on plasma lipoprotein lipid, CoQ10 and liver and muscle enzyme levels in hypercholesterolemic patients treated with atorvastatin: a randomized double-blind study.Atherosclerosis 2007, 195:e182-189.
Kovacic S, Habicht SD, Eckert GP. Effects of coenzyme Q10 supplementation on myopathy in statin-treated patients: a systematic review and meta-analysis.J Nutr Sci 2025, 14:e72.
Ahmad K, Manongi NJ, Rajapandian R, et al. Effectiveness of Coenzyme Q10 Supplementation in Statin-Induced Myopathy: A Systematic Review.Cureus 2024, 16:e68316.
Joel Fuhrman, M.D. is a board-certified family physician, seven-time New York Times bestselling author and internationally recognized expert on nutrition and natural healing, who specializes in preventing and reversing disease through nutritional methods. Dr. Fuhrman coined the term “Nutritarian” to describe his longevity-promoting, nutrient dense, plant-rich eating style.
For over 30 years, Dr. Fuhrman has shown that it is possible to achieve sustainable weight loss and reverse heart disease, diabetes and many other illnesses using smart nutrition. In his medical practice, and through his books and PBS television specials, he continues to bring this life-saving message to hundreds of thousands of people around the world.
Plant-derived supplements for cardiovascular protection and whole-body health
January 27, 2026 by Joel Fuhrman, MD
A health-promoting diet rich in fiber, vitamins, minerals, phytochemicals, and healthy fats – combined with regular exercise – is the cornerstone of cardiovascular health. Foods such as green and leafy vegetables, soybeans and other beans, berries, nuts, garlic, and onions provide a powerful foundation by naturally reducing cholesterol production and/or absorption, improving vascular function and blood pressure, enhancing antioxidant defenses, and reducing inflammation.
However, carefully selected botanical supplements supplying cardioprotective phytochemicals can serve as a strategic accessory, amplifying the cardiovascular benefits of a Nutritarian diet.
Importantly, the same biological pathways that drive heart disease also underlie many other age-related chronic conditions, meaning that the phytochemicals that support cardiovascular health often confer broader benefits for brain and immune function, while helping protect against cancer, diabetes, and dementia.
Plant sterols
Plant sterols inhibit intestinal cholesterol absorption, leading to reductions in circulating total and LDL cholesterol, and ApoB.
Recommended daily dose for cardiovascular protection: 500 mg–2 g.
Plant sterols, found in the cell membranes of plants, are one of the many components of a healthful diet based on whole plant foods that keeps cholesterol levels in the favorable range. Plant sterols (also known as phytosterols):
When we consume plant sterols, they interfere with the absorption (and re-absorption) of cholesterol in the small intestine, which facilitates cholesterol excretion and reduces circulating cholesterol levels. Some evidence also suggests plant sterol supplementation could reduce very low-density lipoprotein (VLDL) production by the liver.2
Plant sterol supplements dose-dependently reduce LDL cholesterol by up to 12% for doses up to 2 grams daily.3 According to a 2024 meta-analysis of 26 randomized controlled trials, plant sterol supplements also reduce apolipoprotein B (ApoB), in addition to total and LDL cholesterol.4
The European Society of Cardiology has recommended plant sterol supplements alongside a healthful diet to decrease cholesterol levels, and the United States FDA has stated that plant sterols help to reduce total and LDL cholesterol.5,6 For people on cholesterol-lowering drugs, plant sterols can be taken alongside statins, leading to additional cholesterol reduction compared to statins alone.7
Sources:
The Bioavailability and Biological Activities of Phytosterols as Modulators of Cholesterol Metabolism
Effects of phytosterol supplementation on lipid profiles and apolipoproteins: A meta-analysis of randomized controlled trials
Effects of plant stanol or sterol-enriched diets on lipid profiles in patients treated with statins: systematic review and meta-analysis
Plant sterols’ benefits extend beyond the cardiovascular system
Observational studies have shown that higher plant sterol intake is associated with a lower risk of cancers including lung, colorectal, breast, esophageal, and gastric cancers. 8 How plant sterol intake could affect cancer risk is still being investigated. But studies in cultured cells and animals suggest that plant sterols inhibit tumor cell proliferation and tumor growth, promote cell death in abnormal cells, reduce angiogenesis and tumor cell migration, and suppress the activity of oncogenes.9,10 From this research, dietary intakes of 200-500 mg/day plant sterols were estimated to be protective against cancer.8,9
Additionally, plant sterols are reported to play a protective therapeutic role in benign prostatic hypertrophy (BPH or enlarged prostate), a common medical condition in older men.11 Symptoms of BPH have been improved by supplementation of small doses (up to 130 mg) of plant sterols compared to placebo.12-14
Sources:
The Protective Effect of Dietary Phytosterols on Cancer Risk: A Systematic Meta-Analysis
Molecular Mechanism of β-Sitosterol and its Derivatives in Tumor Progression
The use of beta-sitosterol for the treatment of prostate cancer and benign prostatic hyperplasia
Amla fruit
Amla has cardioprotective effects through polyphenol-mediated reductions in oxidative stress and inflammation, improved endothelial function, and reduced cholesterol and blood glucose.
Recommended daily dose for cardiovascular protection: 500-1000 mg amla powder or extract
Amla fruit is also known as Indian gooseberry (Latin name Phyllanthus emblica or Emblica officinalis) but is not botanically related to the European gooseberry. Amla is a small, round, yellow-green fruit that grows on a tree native to South Asia and grown in several tropical areas. Amla fruit can be found in India, Nepal, Sri Lanka, Malaysia, China, and Thailand. The fruit is typically harvested in autumn and has a fibrous texture and sour flavor. It is usually not eaten raw.
Instead, it is pickled, made into chutneys and other condiments, or cooked into entrees or desserts. Amla is also used as an herbal remedy in traditional Ayurvedic formulas.
In addition to fiber and vitamin C, amla is a source of phytochemicals including :
Lab studies have linked these phytochemicals in amla to antibacterial, glucose-lowering, cholesterol-lowering, antioxidant, and anti-cancer effects.15,16
Many randomized controlled trials have evaluated amla’s effects on blood lipids, finding reductions in total, LDL and VLDL cholesterol, and triglycerides. On average, in these studies, amla supplementation resulted in a 15 mg/dl reduction in seven studies measuring LDL, 5.4 mg /dl in three studies measuring VLDL, and 22 mg/dl in six studies measuring triglycerides.15
Sources:
Clinical effects of Emblica officinalis fruit consumption on cardiovascular disease risk factors: a systematic review and meta-analysis
Functional and Nutraceutical Significance of Amla (Phyllanthus emblica L.): A Review
Amla’s benefits are not limited to circulating lipid levels
In clinical studies, supplementation with amla fruit powder or extract improved antioxidant status, blood vessel function, and inflammatory markers. After 8 and 12 weeks of supplementation in 59 participants with metabolic syndrome taking 250 or 500 mg amla extract twice daily, the ability of the vessels to dilate, a measure of endothelial function, improved compared to placebo. Improvements in several oxidative stress biomarkers, such as nitric oxide, glutathione, and malondialdehyde, as well as the inflammatory marker C-reactive protein were also observed.17
Amla may also have beneficial effects on glycemic control. Although there were only two randomized controlled trials, a meta-analysis pooling their data found that amla supplementation ranging from 500 to 3000 mg/day reduced fasting blood glucose (on average by about 12.7 mg/dl).18
Sources:
Evaluation of the effects of a standardized aqueous extract of Phyllanthus emblica fruits on endothelial dysfunction, oxidative stress, systemic inflammation and lipid profile in subjects with metabolic syndrome: a randomised, double blind, placebo controlled clinical study
The impact of Emblica Officinalis (Amla) on lipid profile, glucose, and C-reactive protein: A systematic review and meta-analysis of randomized controlled trials
Pomegranate and chokeberry (aronia)
Pomegranate polyphenols, such as ellagic acid, support cardiovascular health by reducing inflammation and oxidation of LDL cholesterol.
Different studies have used a variety of doses and forms of these fruits, such as powders, juice, and extracts. Recommended daily dose for cardiovascular protection: approximately 200-500 mg pomegranate extract), 200-500 mg chokeberry powder or extract.
Pomegranate is rich in ellagic acid, punicalagins, and flavonoids with antioxidant and anti-inflammatory properties.19 In randomized controlled trials, pomegranate supplementation showed reduced:
In a three-year study on patients with heart disease, daily supplementation with pomegranate juice resulted in regression of atherosclerotic plaque, whereas the control group experienced an increase in plaque thickness. The pomegranate group also showed a reduction in oxidized LDL and an improvement in total antioxidant status.23
Sources:
Impacts of supplementation with pomegranate on cardiometabolic risk factors: A systematic review and dose-response meta-analysis
The effects of pomegranate consumption on inflammatory and oxidative stress biomarkers in adults: a systematic review and meta-analysis
Pomegranate juice consumption for 3 years by patients with carotid artery stenosis reduces common carotid intima-media thickness, blood pressure and LDL oxidation
Pomegranate’s anti-cancer effects
The polyphenols in pomegranate modulate signaling pathways involved in cell proliferation, programmed cell death, inflammation, angiogenesis, adhesion, and metastasis, and regulation of gene expression.24 A few trials in patients with prostate cancer have shown an increase in PSA doubling time – slowing the rise in PSA levels.25 Pomegranate phytochemicals also have anti-estrogen effects – inhibition of the aromatase enzyme – that could help prevent breast cancer.26
Chokeberry (Aronia melanocarpa) is another antioxidant-rich fruit not typically found in our diets that promotes cardiovascular health. A meta-analysis of seven studies on chokeberry supplementation found reductions in systolic blood pressure and total cholesterol.27
Sources:
The Role of Pomegranate (Punica granatum) in Cancer Prevention and Treatment: Modulating Signaling Pathways From Inflammation to Metastasis
Daily supplementation with aronia melanocarpa (chokeberry) reduces blood pressure and cholesterol: a meta analysis of controlled clinical trials
LDL Biotect is a research-backed, plant-based supplement designed to work alongside a Nutritarian diet to optimize heart health, supplying plant sterols, amla fruit, pomegranate extract, and chokeberry.
Green tea
Green tea catechins, especially epigallocatechin gallate (EGCG), reduce oxidative stress, and drinking green tea is linked to lower cardiovascular disease and cancer risk across many studies.
Recommended daily dose for cardiovascular protection: 200-300 mg total green tea extract (limit to no more than 300 mg EGCG)
Green tea is rich in flavonoid antioxidants known as catechins, and drinking green tea regularly is associated with better cardiovascular health and a lower risk of several cancers.28-32 Green tea supplementation studies have found improvements in cholesterol and blood glucose levels, as well as oxidative stress markers.33-35
The anti-cancer effects of green tea extracts include:
Clinical trials in patients with prostate cancer have shown reduced PSA and other cancer-related biomarkers.37,38 Supplementation with green tea extract or EGCG also reduced cancer-related biomarkers or tumor cell proliferation in clinical trials in women with breast cancer.39,40
Sources:
Impact of Green Tea Consumption on the Prevalence of Cardiovascular Outcomes: A Systematic Review
Effects of green tea supplementation on antioxidant status and inflammatory markers in adults: a grade-assessed systematic review and dose-response meta-analysis of randomised controlled trials
A comprehensive overview on the effects of green tea on anthropometric measures, blood pressure, glycemic and lipidemic status: An umbrella review and meta meta-analysis study
Possible Mechanisms of Green Tea and Its Constituents against Cancer
Randomized clinical trial of brewed green and black tea in men with prostate cancer prior to prostatectomy
A Presurgical Study of Lecithin Formulation of Green Tea Extract in Women with Early Breast Cancer
Turmeric
Curcumin, the major bioactive compound in turmeric, targets inflammatory signaling pathways, leading to lower levels of inflammation and oxidative damage, while reducing cholesterol levels.
Recommended daily dose for cardiovascular protection: 100-400 mg/day; be cautious of high doses (1000 mg or more per day) when combined with absorption enhancers, because of reports of liver injury.
Turmeric phytochemicals, including curcuminoids and others, such as turmerones, have shown a variety of anti-cancer effects, especially through reducing inflammation, but also by affecting tumor cell survival, proliferation, and adhesion.41,42 Turmeric’s anti-inflammatory effects have been confirmed in randomized controlled trials,43 and turmeric or curcumin supplements also reduced total and LDL cholesterol.44 A few clinical trials have been conducted in patients with cancers, and have found improvements in cancer-related biomarkers, or have suggested that curcumin could be a helpful adjunct to other cancer treatments.45
Sources:
Curcumin-free turmeric exhibits anti-inflammatory and anticancer activities: Identification of novel components of turmeric
Antioxidant and anti-inflammatory effects of curcumin/turmeric supplementation in adults: A GRADE-assessed systematic review and dose–response meta-analysis of randomized controlled trials
Effects of curcumin/turmeric supplementation on lipid profile: A GRADE-assessed systematic review and dose–response meta-analysis of randomized controlled trials
Curcumin (Curcuma, Turmeric) and Cancer (PDQ(R)): Health Professional Version
Grape seed
Grape seeds are rich in antioxidant proanthocyanidins, with blood pressure-lowering properties.
Recommended daily dose for cardiovascular protection: 150-300 mg/day.
Grapes are common in typical diets, but the seeds, which are highest in antioxidants, in particular proanthocyanidins, are rarely eaten.46,47 Several studies have found reductions in blood pressure, cholesterol, or oxidative stress markers in response to grape seed extract supplementation.48-50 Studies also suggest grape seed proanthocyanidins have anti-cancer effects.51,52
Sources:
Biological activities of polyphenols from grapes
The effect of grape seed extract supplementation on oxidative stress and inflammation: A systematic review and meta-analysis of controlled trials
The impact of grape seed extract treatment on blood pressure changes: A meta-analysis of 16 randomized controlled trials
The effects of grape seed extract on glycemic control, serum lipoproteins, inflammation, and body weight: A systematic review and meta-analysis of randomized controlled trials
A Pilot Study of a Grape Seed Procyanidin Extract for Lung Cancer Chemoprevention
Ultra Cell Biotect combines powerful superfoods including green tea extract, turmeric, and grape seed extract that enhance the body’s natural antioxidant defenses to protect cardiovascular health and promote healthy aging.
Coenzyme Q10
Coenzyme Q10 is a natural antioxidant that’s also crucial for producing cellular energy in heart muscle cells. Levels decline with age.
Recommended daily dose for cardiovascular protection: 100-200 mg/day.
CoQ10 is an antioxidant produced naturally in the mitochondria of our cells, where it scavenges free radicals and helps generate energy in the form of ATP. The antioxidant actions of CoQ10 protect cells in the heart and blood vessels from oxidative damage and maintain healthy blood pressure levels. CoQ10 also promotes the production of other natural antioxidants in the body. CoQ10 is present in high concentrations in heart muscle, and CoQ10levels decline with age.53-55 Randomized controlled trials have found that CoQ10 supplementation:
CoQ10 supplementation may be especially helpful for people who take cholesterol-lowering statin drugs, which may decrease the production of CoQ10.53,54 Studies have found CoQ10 supplementation increases CoQ10 levels in people taking statins, and improved statin-associated muscle symptoms.59-62
Sources:
Effect of Coenzyme Q10 Supplementation on Vascular Endothelial Function: A Systematic Review and Meta-Analysis of Randomized Controlled Trials
Effects of coenzyme Q10 administration on blood pressure and heart rate in adults: A systematic review and meta-analysis of randomized controlled trials
Exogenous CoQ10 supplementation prevents plasma ubiquinone reduction induced by HMG-CoA reductase inhibitors
Effects of coenzyme Q10 supplementation on myopathy in statin-treated patients: a systematic review and meta-analysis
Dr. Fuhrman’s CoQ10 protects cardiac muscle from oxidative damage and supports healthy blood vessel function and cellular energy production.
Joel Fuhrman, M.D. is a board-certified family physician, seven-time New York Times bestselling author and internationally recognized expert on nutrition and natural healing, who specializes in preventing and reversing disease through nutritional methods. Dr. Fuhrman coined the term “Nutritarian” to describe his longevity-promoting, nutrient dense, plant-rich eating style.
For over 30 years, Dr. Fuhrman has shown that it is possible to achieve sustainable weight loss and reverse heart disease, diabetes and many other illnesses using smart nutrition. In his medical practice, and through his books and PBS television specials, he continues to bring this life-saving message to hundreds of thousands of people around the world.