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Effect of Armolipid on Lipid Profile in Children With Hypercholesterolemia

Primary Purpose

Dyslipidemias, Children, Only

Status
Completed
Phase
Not Applicable
Locations
Greece
Study Type
Interventional
Intervention
Effect of Armolipid on Lipid Profile in Children With Hypercholesterolemia
Sponsored by
Athens General Children's Hospital "Pan. & Aglaia Kyriakou"
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dyslipidemias

Eligibility Criteria

7 Years - 16 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria: LDL-C >150 mg/dl in more than two measurements, after therapeutic lifestyle changes for at least 6 months. Exclusion Criteria: Secondary hypercholesterolemia Presence of any chronic disease or growth and developmental disorders Abnormal liver, kidney or thyroid function Prior use of hypolipidemic or other medication, at least 6 months before participation in the study.

Sites / Locations

  • Lipid Outpatient Unit, 2nd Department of Pediatrics, Medical School, National and Kapodistrian University of Athens (NKUA), "P. & A. Kyriakou" Children's Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Armolipid

Arm Description

One tablet of Armolipid (Rottapharm S.p.A., Monza, Italia), containing 200 mg red yeast rice, 10 mg policosanols, 0.2 mg folic acid, 2.0 mg coenzyme Q10 and 0.5 mg astaxanthin was administered once-daily with lunch. Clinical and laboratory evaluation took place before and 6 (IQR: 5-8) and 16 (IQR: 11-19.7) months after treatment.

Outcomes

Primary Outcome Measures

Levels of LDL-C serum levels
LDL-C levels were evaluated in serum, after an overnight fast.

Secondary Outcome Measures

Improvement of other than LDL-C parameters of lipid profile, as well as the evaluation of hepatic and muscle enzymes elevation.
A lipid profile including TC, high density lipoprotein - cholesterol (HDL-C), non-high density lipoprotein - cholesterol (non-HDL-C), triglycerides (TGs), apolipoprotein A1 (Apo-A1), apolipoprotein B (Apo-B), and lipoprotein (a) [Lp(a)] levels was evaluated in serum, after an overnight fast. Serum creatinine, aspartate and alanine aminotransferases (AST and ALT) and creatine kinase (CK) were also assessed.

Full Information

First Posted
August 29, 2023
Last Updated
September 17, 2023
Sponsor
Athens General Children's Hospital "Pan. & Aglaia Kyriakou"
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1. Study Identification

Unique Protocol Identification Number
NCT06045377
Brief Title
Effect of Armolipid on Lipid Profile in Children With Hypercholesterolemia
Official Title
Effect of a Nutraceutical, Containing Red Yeast Rice and Polycosanols (Armolipid), on Lipid Profile in Children With Moderate and Severe Hypercholesterolemia.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
January 20, 2020 (Actual)
Primary Completion Date
June 25, 2022 (Actual)
Study Completion Date
September 5, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Athens General Children's Hospital "Pan. & Aglaia Kyriakou"

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Data concerning the effectiveness od nutraceuticals in children with dyslipidemia are lacking. The aim of the present study was to evaluate the efficacy and safety of the long-term use of a dietary supplement containing red yeast rice (RYR), combined with other natural compounds, in children and adolescents with hypercholesterolemia. A nutraceutical, containing RYR, polycosanols, coenzyme Q10, astaxanthin and folic acid (commercial name: Armolipid), was administered once-daily in 84 children/adolescents with moderate or severe hypercholesterolemia.
Detailed Description
This is a prospective single center cohort study conducted at Outpatient Lipid Unit of 2nd Department of Pediatrics of the National and Kapodistrian University of Athens at the "Panagiotis & Aglaia Kyriakou" Children's Hospital in Greece. The study complies with the Declaration of Helsinki and the protocol was reviewed and approved by the appropriate ethical committee. Parental informed written consent was obtained prior to enrollment. Study population: Ninety children and adolescents, aged 7 to 16 years, with primary dyslipidemia. All participants had a positive family history for hypercholesterolemia (LDL > 95th percentile) and most of them had a positive family history for premature CVD (<55 years for males and <60 years for females) in first or/and second-degree relatives. Eleven of them had a genetically confirmed diagnosis of HeFH, while the rest had a probable or positive HeFH according to the Dutch Lipid Clinic Network criteria. None of them had moderate or significant hypertriglyceridemia, even those with increased body mass index (BMI). All children followed a low saturated fat and low cholesterol diet by a trained dietician and had moderate or intense physical activity, for at least 6 months before the participation in the study. In addition, during the last 6 months, 19 of them consumed 1.5 - 2.5g of plant sterols daily in the form of a yogurt drink or spread. Lifestyle and eating habits were maintained throughout the study. A nutraceutical containing five natural substances formulated as a tablet with the commercial name Armolipid (Rottapharm S.p.A., Monza, Italia), was recommended in all participants. Every tablet contained 200 mg red yeast rice (RYR) extract equivalent to 3 mg of monacolin K, 10 mg policosanols, 0.2 mg folic acid, 2.0 mg coenzyme Q10 and 0.5 mg astaxanthin, and was citrinin-free. It was administered once-daily with lunch. All participants as well as their parents were interviewed using a data collection form, created specifically for this research. Details concerning compliance to supplement intake, as well as possible adverse effects were recorded and analysed. Six out of 90 children were excluded from the study because they did not comply with the recommendation for taking the supplement (compliance rate 93.3%). All the rest 84 children had one and 64 of them had two evaluations under Armolipid treatment. Clinical and Labolatory evaluation: A clinical and laboratory evaluation of all participants took place right before (Time 0, T0) and once (n=84, Time 1, T1) or twice (n=64, T1 and Time 2, T2) after the start of nutraceutical supplementation. The body weight (BW) in kg, the height (H) in cm were measured to the nearest 0.1 kg and 0.5 cm, respectively (TANITA, Corporation Tokyo), with children barefoot and lightly dressed. BMI was calculated as BW in kg per H in m2. The standard deviation scores (z-scores) of BW, H and BMI were also calculated according to a standardized age- and sex- specific calculator. Waist circumference (WC) in cm was measured and the ratio of WC/Height was calculated. Systolic (SBP) and diastolic blood pressure (DBP) in mmHg were measured three consecutive times using an automated oscillometric device (Dinamap V100, GE Medical Systems Information Technologies) and the average value of the three measurements was used in the statistical analysis. The stage of puberty was recorded according to Tanner stages (I-V) for boys and girls. A full lipid profile including TC, LDL-C, high density lipoprotein - cholesterol (HDL-C), non-high density lipoprotein - cholesterol (non-HDL-C), triglycerides (TGs), apolipoprotein A1 (Apo-A1), apolipoprotein B (Apo-B), and lipoprotein (a) [Lp(a)] levels was evaluated in serum, after an overnight fast. Serum creatinine, glucose, aspartate and alanine aminotransferases (AST and ALT), creatine kinase (CK), and thyroid-stimulating hormone (TSH) were also assessed. A full blood count was performed in all participants. TC, HDL-C, LDL-C, TGs, glucose, ALT, AST, CK and creatinine were measured using an enzymatic method (Roche Diagnostics) on an automatic analyzer (Cobass Integra 800), and Apo-A1, Apo-B, and Lp(a) by an immunonephelometric assay (Siemens BNII Nephelometer Analyzer), with an intra-assay and inter-assay variation <5% for all tests. Non-HDL-C was measured as TC minus HDL-C. All lipid values are expressed in mg/dL. Haematological parameters (full blood count) were analyzed using the SysmexXE-2100 automated haematology analyzer (Roche Diagnostics). All tests were performed according to the manufacturers' instructions. At the time of the examination, all children were healthy and none of them had a febrile or afebrile infection in the two weeks preceding the check-up.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dyslipidemias, Children, Only

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
90 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Armolipid
Arm Type
Experimental
Arm Description
One tablet of Armolipid (Rottapharm S.p.A., Monza, Italia), containing 200 mg red yeast rice, 10 mg policosanols, 0.2 mg folic acid, 2.0 mg coenzyme Q10 and 0.5 mg astaxanthin was administered once-daily with lunch. Clinical and laboratory evaluation took place before and 6 (IQR: 5-8) and 16 (IQR: 11-19.7) months after treatment.
Intervention Type
Dietary Supplement
Intervention Name(s)
Effect of Armolipid on Lipid Profile in Children With Hypercholesterolemia
Intervention Description
A prospective single center cohort study
Primary Outcome Measure Information:
Title
Levels of LDL-C serum levels
Description
LDL-C levels were evaluated in serum, after an overnight fast.
Time Frame
Laboratory evaluation before and 6 and 16 months after treatment
Secondary Outcome Measure Information:
Title
Improvement of other than LDL-C parameters of lipid profile, as well as the evaluation of hepatic and muscle enzymes elevation.
Description
A lipid profile including TC, high density lipoprotein - cholesterol (HDL-C), non-high density lipoprotein - cholesterol (non-HDL-C), triglycerides (TGs), apolipoprotein A1 (Apo-A1), apolipoprotein B (Apo-B), and lipoprotein (a) [Lp(a)] levels was evaluated in serum, after an overnight fast. Serum creatinine, aspartate and alanine aminotransferases (AST and ALT) and creatine kinase (CK) were also assessed.
Time Frame
Laboratory evaluation before and 6 and 16 months after treatment
Other Pre-specified Outcome Measures:
Title
Waist Circumference (WC) and the ratio of WC/Height
Description
WC in cm was measured and the ratio of WC/Height was calculated.
Time Frame
Clinical evaluation before and 6 and 16 months after treatment
Title
Systolic (SBP) and diastolic blood pressure (DBP)
Description
SBP and DBP in mmHg were measured three consecutive times using an automated oscillometric device (Dinamap V100, GE Medical Systems Information Technologies).
Time Frame
Clinical evaluation before and 6 and 16 months after treatment
Title
Body weight in kg
Description
The body weight (BW) in kg, measured to the nearest 0.1 kg (TANITA, Corporation Tokyo), with children barefoot and lightly dressed.
Time Frame
Clinical evaluation before and 6 and 16 months after treatment
Title
Body height in cm
Description
The body height (H) in cm, measured to the nearest 0.5 cm, (TANITA, Corporation Tokyo), with children barefoot.
Time Frame
Clinical evaluation before and 6 and 16 months after treatment
Title
BMI (calculated as body weight in kg per height in m2)
Description
BMI was calculated as BW in kg per H in m2. The standard deviation scores (z-scores) of BW, H and BMI were also calculated according to a standardized age- and sex- specific calculator.
Time Frame
Clinical evaluation before and 6 and 16 months after treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: LDL-C >150 mg/dl in more than two measurements, after therapeutic lifestyle changes for at least 6 months. Exclusion Criteria: Secondary hypercholesterolemia Presence of any chronic disease or growth and developmental disorders Abnormal liver, kidney or thyroid function Prior use of hypolipidemic or other medication, at least 6 months before participation in the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Achilleas Attilakos, Assoc.Prof
Organizational Affiliation
Athens Children's Hospital Pan. and Aglaia Kyriakou
Official's Role
Principal Investigator
Facility Information:
Facility Name
Lipid Outpatient Unit, 2nd Department of Pediatrics, Medical School, National and Kapodistrian University of Athens (NKUA), "P. & A. Kyriakou" Children's Hospital
City
Athens
Country
Greece

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
37322181
Citation
Watts GF, Gidding SS, Hegele RA, Raal FJ, Sturm AC, Jones LK, Sarkies MN, Al-Rasadi K, Blom DJ, Daccord M, de Ferranti SD, Folco E, Libby P, Mata P, Nawawi HM, Ramaswami U, Ray KK, Stefanutti C, Yamashita S, Pang J, Thompson GR, Santos RD. International Atherosclerosis Society guidance for implementing best practice in the care of familial hypercholesterolaemia. Nat Rev Cardiol. 2023 Jun 15. doi: 10.1038/s41569-023-00892-0. Online ahead of print.
Results Reference
background
PubMed Identifier
27685833
Citation
Santini A, Novellino E. Nutraceuticals in hypercholesterolaemia: an overview. Br J Pharmacol. 2017 Jun;174(11):1450-1463. doi: 10.1111/bph.13636. Epub 2016 Oct 29.
Results Reference
background
PubMed Identifier
34345932
Citation
Cicero AFG, Fogacci F, Stoian AP, Vrablik M, Al Rasadi K, Banach M, Toth PP, Rizzo M. Nutraceuticals in the Management of Dyslipidemia: Which, When, and for Whom? Could Nutraceuticals Help Low-Risk Individuals with Non-optimal Lipid Levels? Curr Atheroscler Rep. 2021 Aug 4;23(10):57. doi: 10.1007/s11883-021-00955-y.
Results Reference
background
PubMed Identifier
33669333
Citation
Cicero AFG, Kennedy C, Knezevic T, Bove M, Georges CMG, Satrauskiene A, Toth PP, Fogacci F. Efficacy and Safety of Armolipid Plus(R): An Updated PRISMA Compliant Systematic Review and Meta-Analysis of Randomized Controlled Clinical Trials. Nutrients. 2021 Feb 16;13(2):638. doi: 10.3390/nu13020638.
Results Reference
background
PubMed Identifier
20153154
Citation
Guardamagna O, Abello F, Baracco V, Stasiowska B, Martino F. The treatment of hypercholesterolemic children: efficacy and safety of a combination of red yeast rice extract and policosanols. Nutr Metab Cardiovasc Dis. 2011 Jun;21(6):424-9. doi: 10.1016/j.numecd.2009.10.015. Epub 2010 Feb 12.
Results Reference
background

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Effect of Armolipid on Lipid Profile in Children With Hypercholesterolemia

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