Nutraceutical pill containing berberine versus ezetimibe on plasma lipid pattern in hypercholesterolemic subjects and its additive effect in patients with familial hypercholesterolemia on stable cholesterol-lowering treatment
Open accessAbstract
Background: Although statins (STs) are drugs of first choice in hypercholesterolemic patients, especially in those at high cardiovascular risk, some of them are intolerant to STs or refuse treatment with these drugs. In view of this, we have evaluated the lipid-lowering effect of a nutraceutical pill containing berberine (BBR) and of ezetimibe, as alternative treatments, in monotherapy or in combination, in 228 subjects with primary hypercholesterolemia (HCH), with history of STs intolerance or refusing STs treatment. In addition, since PCSK9 was found up-regulated by STs dampening their effect through an LDL receptors (LDLRs) degradation, and BBR suppressed PCSK9 expression in cellular studies, we supplemented the stable lipid-lowering therapy of 30 genotype-confirmed Familial Hypercholesterolemia heterozygotes (HeFH) with BBR, searching for a further plasma cholesterol reduction. Plasma lipid pattern was evaluated at baseline and during treatments. Results: In HCH subjects the nutraceutical pill resulted more effective than EZE in lowering LDL cholesterol (−31.7% vs −25.4%, P < 0.001) and better tolerated. On treatment, LDL-C level below 3.36 mmol/L (≤130 mg/dl) was observed in 28.9% of subjects treated with the nutraceutical pill and 11.8% of those treated with EZE (P <0.007). In the group treated with EZE the subjects carrying the G allele of the g.1679 C > G silent polymorphism of NPC1L1 gene showed a higher response to EZE than homozygous for the common allele (GG + CG: LDL-C −29.4±5.0%, CC −23.6±6.5%, P <0.001). Combined treatment with these drugs was as effective as STs in moderate doses (LDL cholesterol −37%, triglycerides −23%). In HeFH patients the addition of BBR resulted in LDL cholesterol reductions inversely related to those induced by the stable therapy (r = −0.617, P <0.0001), with mean 10.5% further decrease. Conclusions: The alternative treatments tested in our HCH subjects were rather effective and safe. The findings in HeFH patients suggest that BBR might act in vivo increasing expression and stability of LDLRs and/or suppressing PCSK9 expression.
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Ezetimibe efficacy has been improved by the association with RYR, policosanol, and berberine.
“Ezetimibe efficacy has been improved by the association with RYR, policosanol, and berberine [108, 109]”
From Nutraceuticals in the Management of Dyslipidemia: Which, When, and for Whom? Could Nutraceuticals Help Low-Risk Individuals with Non-optimal Lipid Levels? (2021) · cites this paper as [109]
Combined treatment with these drugs was as effective as moderate-dose statins, lowering LDL-C by 37% and TC by 23%.
“Combined treatment with these drugs was as effective as statins in moderate doses (LDL-C À37%, TC À23%) (147).”
From The Role of Nutraceuticals in Statin Intolerant Patients (2018) · cites this paper as [147]
In 228 hypercholesterolemic subjects with statin intolerance or refusal, a nutraceutical pill (berberine 500 mg, policosanol 10 mg, RYR 200 mg) reduced LDL-C more than ezetimibe (-31.7% vs -25.4%) and was better tolerated; LDL-C <3.36 mmol/l occurred in 28.9% vs 11.8%.
“In hypercholesterolemic subjects, the nutraceutical pill compared with ezetimibe resulted in more effective reduction of LDL-C (À31.7 vs. À25.4%;p < 0.001) and was better tolerated; LDL-C levels below 3.36 mmol/l (#130 mg/dl) were observed in 28.9% of subjects treated with the nutraceutical pill and 11.8% of those treated with ezetimibe (p < 0.007) (147).”
From The Role of Nutraceuticals in Statin Intolerant Patients (2018) · cites this paper as [147]
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References 50 · Cited by 79
- Authors
- Pisciotta, L., Bellocchio, A., & Bertolini, S.
- Affiliations
- University of Genoa (IT)
- Corresponding author
- Bertolini, Stefano
- Venue
- Lipids in Health and Disease
- Published
- 2012-09-22
- Volume
- 11
- Issue
- 1
- Pages
- 123-123
- ISSN
- 1476-511X (ISSN-L)
- PMC
- PMC3477057
- OpenAlex
- W2168287213
- Cited by
- 79
- References
- 50
- Citations by year
- 2025: 2 · 2024: 3 · 2023: 7 · 2022: 2 · 2021: 4 · 2020: 5 · 2019: 8 · 2018: 8 · 2017: 10 · 2016: 11 · 2015: 8 · 2014: 7 · 2013: 4
- FWCI
- 6.16
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Lipids in Health and Disease (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- CINECA IRIS Institutial Research Information System (University of Genoa) (submittedVersion)
- Topics
- Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
- Health Sciences › Medicine › Pharmacology › Berberine and alkaloids research
- Health Sciences › Medicine › Surgery › Natural Products and Biological Research
- Keywords
- berberine, ezetimibe, nutraceuticals, hypercholesterolemia, familial hypercholesterolemia, LDL cholesterol lowering, statin intolerance, PCSK9, plasma lipids, triglycerides, combination therapy, LDL receptor degradation, cardiovascular risk reduction, treatment tolerability, statin-sparing therapy
- MeSH terms
- Ezetimibe, Aged, Anticholesteremic Agents, Azetidines, Berberine, Biological Products, Drug Combinations, Drug Therapy, Combination, Fatty Alcohols, Female, Humans, Hypercholesterolemia, Lipids, Cholesterol, LDL, Male, Middle Aged, Mutation, Receptors, LDL, Triglycerides, Statistics, Nonparametric, Dietary Supplements
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