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Moderate Alcohol Consumption, Risk of Cardiovascular Disease and Type 2 Diabetes: Influence of Alcohol Oxidation

Primary Purpose

Cardiovascular Disease, Type 2 Diabetes

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Alcohol: 25 gday (white wine)
Sponsored by
TNO
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cardiovascular Disease focused on measuring Moderate alcohol consumption, Alcohol dehydrogenase 1c polymorphism, PPAR-gamma activated gene expression

Eligibility Criteria

40 Years - 65 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria: Healthy women aged 40 to 65 years Absence of menstrual period for at least 2 years Homozygotes for the ADH1C*1 or ADH1C*2 allele of ADH1C I349V polymorphism Alcohol consumption ≥ 5 and ≤ 21 units/week Exclusion Criteria: Smoking Family history of alcoholism History of medical or surgical events that may significantly affect the study outcome, particularly metabolic or endocrine disorders and gastrointestinal disorders Recent blood donation

Sites / Locations

    Outcomes

    Primary Outcome Measures

    PPAR-gamma activated gene expression

    Secondary Outcome Measures

    Risk factors of cardiovascular disease and type 2 diabetes
    Postprandial changes of HPA-axis activity

    Full Information

    First Posted
    January 31, 2006
    Last Updated
    August 15, 2006
    Sponsor
    TNO
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00285909
    Brief Title
    Moderate Alcohol Consumption, Risk of Cardiovascular Disease and Type 2 Diabetes: Influence of Alcohol Oxidation
    Official Title
    Effect of Moderate Alcohol Consumption on PPAR-γ Activity and Risk Markers of Metabolic Disease: Influence of Genetic Variation in Alcohol Oxidation
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2006
    Overall Recruitment Status
    Completed
    Study Start Date
    March 2006 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    June 2006 (undefined)

    3. Sponsor/Collaborators

    Name of the Sponsor
    TNO

    4. Oversight

    5. Study Description

    Brief Summary
    Moderate alcohol consumption is associated with a decreased risk of cardiovascular disease and type 2 diabetes. The association of alcohol consumption with cardiovascular disease is mediated by a functional polymorphism of alcohol dehydrogenase 1c, but the effect of this polymorphism on alcohol metabolism is only investigated in vitro. The risk reduction of moderate alcohol consumption for cardiovascular disease is explained largely by an increase of HDL cholesterol, but an increase of adiponectin concentrations after moderate alcohol consumption may also be involved. It seems likely that adiponectin is a mediator for the association of moderate alcohol consumption with type 2 diabetes. The mechanism by which moderate alcohol consumption increases adiponectin concentrations is unknown, but ppar-gamma activation may be involved. effects of this polymorphism on mediators of this relation are not known. This study therefore investigates the effect of moderate alcohol consumption and the influence of alcohol dehydrogenase 1c polymorphism on ppar-gamma activated gene expression and risk factors of cardiovascular disease and type 2 diabetes.
    Detailed Description
    Objectives : To investigate the effect of moderate alcohol consumption and influence of genetic variation of ethanol oxidation on: PPAR-γ activated gene expression Markers of coronary heart disease or type 2 diabetes Postprandial changes of HPA-axis activity among 36 postmenopausal women with ADH1C genotype associated with slow or fast alcohol metabolism. Design : Randomized, controlled, not blinded crossover trial with 1 week wash-out preceding each treatment period Participants Description : Apparently healthy postmenopausal women Number : 36 Study substances Test substance : White wine (ca. 25 g alcohol/day) Reference substance : White grape juice Study treatments Treatment A: 250 ml white wine daily (ca. 25 g alcohol/day) Treatment B: 250 ml white grape juice daily Study period - Duration : two periods of 6 weeks preceded by 1 week wash-out period Test parameters: Adiponectin mRNA expression Expression of PPAR-gamma activated genes: CD36, lipoprotein lipase, AP2 Markers of cardiovascular disease (blood lipid profile, Lp-PLA2 activity, hs-CRP, fibrinogen) Markers of type 2 diabetes (adiponectin, adiponectin oligomers, insulin sensitivity) Parameters of alcohol oxidation (postprandial: blood alcohol and acetate, acetaldehyde) HPA-axis activity (postprandial & fasting: cortisol, ACTH, testosterone)

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Cardiovascular Disease, Type 2 Diabetes
    Keywords
    Moderate alcohol consumption, Alcohol dehydrogenase 1c polymorphism, PPAR-gamma activated gene expression

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Crossover Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    36 (false)

    8. Arms, Groups, and Interventions

    Intervention Type
    Behavioral
    Intervention Name(s)
    Alcohol: 25 gday (white wine)
    Primary Outcome Measure Information:
    Title
    PPAR-gamma activated gene expression
    Secondary Outcome Measure Information:
    Title
    Risk factors of cardiovascular disease and type 2 diabetes
    Title
    Postprandial changes of HPA-axis activity

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    40 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Healthy women aged 40 to 65 years Absence of menstrual period for at least 2 years Homozygotes for the ADH1C*1 or ADH1C*2 allele of ADH1C I349V polymorphism Alcohol consumption ≥ 5 and ≤ 21 units/week Exclusion Criteria: Smoking Family history of alcoholism History of medical or surgical events that may significantly affect the study outcome, particularly metabolic or endocrine disorders and gastrointestinal disorders Recent blood donation
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Henk FJ Hendriks, PhD.
    Organizational Affiliation
    TNO
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    24548643
    Citation
    Joosten MM, Schrieks IC, Hendriks HF. Effect of moderate alcohol consumption on fetuin-A levels in men and women: post-hoc analyses of three open-label randomized crossover trials. Diabetol Metab Syndr. 2014 Feb 18;6(1):24. doi: 10.1186/1758-5996-6-24.
    Results Reference
    derived
    PubMed Identifier
    18504547
    Citation
    Joosten MM, Beulens JW, Kersten S, Hendriks HF. Moderate alcohol consumption increases insulin sensitivity and ADIPOQ expression in postmenopausal women: a randomised, crossover trial. Diabetologia. 2008 Aug;51(8):1375-81. doi: 10.1007/s00125-008-1031-y. Epub 2008 May 27.
    Results Reference
    derived

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    Moderate Alcohol Consumption, Risk of Cardiovascular Disease and Type 2 Diabetes: Influence of Alcohol Oxidation

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