The Effects of ProAlgaZyme on HDL Cholesterol in Individuals With Metabolic Syndrome

Health Enhancement Products

Status

Unknown

Conditions

Hyperlipidemia

Metabolic Syndrome

Treatments

Drug: ProAlgaZyme

Study type

Interventional

Funder types

Industry

Identifiers

NCT00518960

H-0003-02

MARC007-003

Details and patient eligibility

About

The purpose of this study is to determine the effectiveness of ProAlgaZyme in increasing levels of HDL 'good' cholesterol and decreasing total cholesterol and C-reactive protein in patients with Metabolic Syndrome.

Full description

Cardiovascular disease (CVD) is the most common cause of mortality in the United States. In 1988, Reaven, et al. published findings that indicate a majority of individuals who developed CVD had multiple concurrent risk factors including dyslipidemia, hypertension, and hyperglycemia. Reaven, et al., defined this cluster of risk factors as Syndrome X and hypothesized that insulin resistance was the underlying factor in its development. Over time, metabolic syndrome has been used as a more meaningful term and additional risk factors have been associated with its diagnosis (Grundy, et al. 2004). Metabolic syndrome is an increasingly prevalent problem in the United States and other westernized nations. It is estimated that approximately 50 million Americans have metabolic syndrome. The risk factors linked to metabolic syndrome include:

Abdominal obesity
Atherogenic dyslipidemia (high triglycerides, low HDL cholesterol and high LDL cholesterol)
Elevated blood pressure
Insulin resistance with or without glucose intolerance
Pro-thrombotic state (e.g., high fibrinogen or plasminogen activator inhibitor-1 in the blood)
Pro-inflammatory state [e.g. elevated C-reactive protein (CRP)in the blood]

The management goals for metabolic syndrome include reducing the risk for developing CVD and type 2 diabetes. Therefore, therapy is directed at reducing LDL cholesterol, blood pressure and glucose as well as increasing HDL cholesterol levels. Additional interventions to control blood pressure and lipids provide the next line of treatment for patients with metabolic syndrome.

ProAlgaZyme, a novel fermentation product of a freshwater algae ecosystem, will be evaluated in this trial for its effects on circulating lipids. According to the sponsor, ProAlgaZyme is expected to increase the circulating levels of HDL cholesterol while lowering total cholesterol and CRP. ProAlgaZyme was previously tested in a double blind, placebo controlled, pilot trial in 60 subjects with metabolic syndrome (30 subjects per arm), conducted at the University of Yaoundé, Cameroon. Statistically significant (p < 0.05 or better) improvements were seen in total cholesterol, HDL-C and C-reactive protein when compared to placebo. (In Press - Lipids in Health and Disease)

The present study will evaluate the effect of ProAlgaZyme versus placebo on blood lipids and hsCRP in subjects who meet the criteria for Metabolic Syndrome.

Enrollment

28 patients

Sex

All

Ages

40 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Body mass index 28-40
Subjects with at least 3 of the following parameters:
- Elevated waist circumference: Men - Equal to or greater than 40 in (102cm); Women - Equal to or greater than 35 in (88cm)
- Elevated triglycerides: Equal to or greater than 150 mg/dL
- Reduced HDL ("good") cholesterol: Men - Less than 40 mg/dL; Women - Less than 50 mg/dL
- Elevated blood pressure: Equal to or greater than 130/85 mmHg
- Elevated fasting glucose: Equal to or greater than 100 mg/dL
- Elevated CRP: Equal to or greater than 5 mg/L
Subjects with ability to comprehend and complete the questionnaires and forms
Subjects whose schedules permit 4 visits to the study center over the duration of the trial
Subjects who are likely to comply with study procedures and test article consumption
Subjects who are likely to abstain from taking unauthorized supplements/medications or participating in any other clinical trial or experimental treatment during this trial

Exclusion criteria

Subjects with uncontrolled hypertension as defined as greater than 180/95 mmHg (subjects may be re-screened after adequate blood pressure control has been maintained)
Women who are pregnant or lactating, or who are of child-bearing potential and not using an acceptable method of birth control
Subjects with a history of hepatic or renal disease, insulin dependent diabetes, active cancer, HIV infection or blood dyscrasias
Current use of lipid-lowering medications, anti-inflammatories such as low-dose aspirin, or herbal therapies known to affect inflammation or blood lipids 8 weeks prior to study entry
Current use of Metformin
More than moderate alcohol use (> 14 drinks per week)
Use of illicit drugs
Acute coronary syndrome, heart failure, CVA, or coronary intervention within 6 months prior to study
Serious or unstable medical or psychological conditions that, in the opinion of the investigator, would compromise the subject's safety or successful participation in the study