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Efficacy and Safety of Armolipid Plus(®): An Updated PRISMA Compliant Systematic Review and Meta-Analysis of Randomized Controlled Clinical Trials

Armolipid Plus(®) is a multi-constituent nutraceutical that claims to improve lipid profiles. The aim of this PRISMA compliant systematic review and meta-analysis was to globally evaluate the efficacy and safety of Armolipid Plus(®) on the basis of the available randomized, blinded, controlled clini...

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Autores principales: Cicero, Arrigo F. G., Kennedy, Cormac, Knežević, Tamara, Bove, Marilisa, Georges, Coralie M. G., Šatrauskienė, Agnė, Toth, Peter P., Fogacci, Federica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7920267/
https://www.ncbi.nlm.nih.gov/pubmed/33669333
http://dx.doi.org/10.3390/nu13020638
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author Cicero, Arrigo F. G.
Kennedy, Cormac
Knežević, Tamara
Bove, Marilisa
Georges, Coralie M. G.
Šatrauskienė, Agnė
Toth, Peter P.
Fogacci, Federica
author_facet Cicero, Arrigo F. G.
Kennedy, Cormac
Knežević, Tamara
Bove, Marilisa
Georges, Coralie M. G.
Šatrauskienė, Agnė
Toth, Peter P.
Fogacci, Federica
author_sort Cicero, Arrigo F. G.
collection PubMed
description Armolipid Plus(®) is a multi-constituent nutraceutical that claims to improve lipid profiles. The aim of this PRISMA compliant systematic review and meta-analysis was to globally evaluate the efficacy and safety of Armolipid Plus(®) on the basis of the available randomized, blinded, controlled clinical trials (RCTs). A systematic literature search in several databases was conducted in order to identify RCTs assessing the efficacy and safety of dietary supplementation with Armolipid Plus(®). Two review authors independently identified 12 eligible studies (1050 included subjects overall) and extracted data on study characteristics, methods, and outcomes. Meta-analysis of the data suggested that dietary supplementation with Armolipid Plus(®) exerted a significant effect on body mass index (mean difference (MD) = −0.25 kg/m(2), p = 0.008) and serum levels of total cholesterol (MD = −25.07 mg/dL, p < 0.001), triglycerides (MD = −11.47 mg/dL, p < 0.001), high-density lipoprotein cholesterol (MD = 1.84 mg/dL, p < 0.001), low-density lipoprotein cholesterol (MD = −26.67 mg/dL, p < 0.001), high sensitivity C reactive protein (hs-CRP, MD = −0.61 mg/L, p = 0.022), and fasting glucose (MD = −3.52 mg/dL, p < 0.001). Armolipid Plus(®) was well tolerated. This meta-analysis demonstrates that dietary supplementation with Armolipid Plus(®) is associated with clinically meaningful improvements in serum lipids, glucose, and hs-CRP. These changes are consistent with improved cardiometabolic health.
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spelling pubmed-79202672021-03-02 Efficacy and Safety of Armolipid Plus(®): An Updated PRISMA Compliant Systematic Review and Meta-Analysis of Randomized Controlled Clinical Trials Cicero, Arrigo F. G. Kennedy, Cormac Knežević, Tamara Bove, Marilisa Georges, Coralie M. G. Šatrauskienė, Agnė Toth, Peter P. Fogacci, Federica Nutrients Article Armolipid Plus(®) is a multi-constituent nutraceutical that claims to improve lipid profiles. The aim of this PRISMA compliant systematic review and meta-analysis was to globally evaluate the efficacy and safety of Armolipid Plus(®) on the basis of the available randomized, blinded, controlled clinical trials (RCTs). A systematic literature search in several databases was conducted in order to identify RCTs assessing the efficacy and safety of dietary supplementation with Armolipid Plus(®). Two review authors independently identified 12 eligible studies (1050 included subjects overall) and extracted data on study characteristics, methods, and outcomes. Meta-analysis of the data suggested that dietary supplementation with Armolipid Plus(®) exerted a significant effect on body mass index (mean difference (MD) = −0.25 kg/m(2), p = 0.008) and serum levels of total cholesterol (MD = −25.07 mg/dL, p < 0.001), triglycerides (MD = −11.47 mg/dL, p < 0.001), high-density lipoprotein cholesterol (MD = 1.84 mg/dL, p < 0.001), low-density lipoprotein cholesterol (MD = −26.67 mg/dL, p < 0.001), high sensitivity C reactive protein (hs-CRP, MD = −0.61 mg/L, p = 0.022), and fasting glucose (MD = −3.52 mg/dL, p < 0.001). Armolipid Plus(®) was well tolerated. This meta-analysis demonstrates that dietary supplementation with Armolipid Plus(®) is associated with clinically meaningful improvements in serum lipids, glucose, and hs-CRP. These changes are consistent with improved cardiometabolic health. MDPI 2021-02-16 /pmc/articles/PMC7920267/ /pubmed/33669333 http://dx.doi.org/10.3390/nu13020638 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cicero, Arrigo F. G.
Kennedy, Cormac
Knežević, Tamara
Bove, Marilisa
Georges, Coralie M. G.
Šatrauskienė, Agnė
Toth, Peter P.
Fogacci, Federica
Efficacy and Safety of Armolipid Plus(®): An Updated PRISMA Compliant Systematic Review and Meta-Analysis of Randomized Controlled Clinical Trials
title Efficacy and Safety of Armolipid Plus(®): An Updated PRISMA Compliant Systematic Review and Meta-Analysis of Randomized Controlled Clinical Trials
title_full Efficacy and Safety of Armolipid Plus(®): An Updated PRISMA Compliant Systematic Review and Meta-Analysis of Randomized Controlled Clinical Trials
title_fullStr Efficacy and Safety of Armolipid Plus(®): An Updated PRISMA Compliant Systematic Review and Meta-Analysis of Randomized Controlled Clinical Trials
title_full_unstemmed Efficacy and Safety of Armolipid Plus(®): An Updated PRISMA Compliant Systematic Review and Meta-Analysis of Randomized Controlled Clinical Trials
title_short Efficacy and Safety of Armolipid Plus(®): An Updated PRISMA Compliant Systematic Review and Meta-Analysis of Randomized Controlled Clinical Trials
title_sort efficacy and safety of armolipid plus(®): an updated prisma compliant systematic review and meta-analysis of randomized controlled clinical trials
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7920267/
https://www.ncbi.nlm.nih.gov/pubmed/33669333
http://dx.doi.org/10.3390/nu13020638
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