NGFN PLUS TP13: Endophenotyping With Functional Magnetic Resonance Imaging (fMRI)

Sponsor
Charite University, Berlin, Germany (Other)
Overall Status
Completed
CT.gov ID
NCT01503931
Collaborator
Central Institute of Mental Health, Mannheim (Other), University Hospital, Bonn (Other)
480
1
60
8

Study Details

Study Description

Brief Summary

The mesolimbic dopaminergic reward system is a key structure underlying addictive behaviour in alcohol addiction and is under control of prefrontal glutamatergic neurotransmission. The aim of the present multicenter-study in Berlin, Bonn and Mannheim is to use functional magnetic resonance imaging (fMRI) in alcohol addiction for endophenotyping in order to study the relevance of genetic variation, in particular in dopaminergic and glutamatergic genes, for addiction. The investigators will use a temporal discounting and a cue reactivity paradigm in alcoholics and healthy controls in order to 1) test the impact of genetic variation on activation of the mesolimbic system in these populations and to 2) to test their predictive effects for treatment outcome in alcoholics. The subproject will thus bridge animal research on genetically determined cue reactivity and human studies in alcoholics. Furthermore, the investigators will link these results to the measurement of glutamate and glutamine with magnetic resonance spectroscopy (MRS) in subproject SP14.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Alcohol addiction is one of the most common neuropsychiatric diseases in today's society. Chronic misuse of alcohol not only causes significant physical and psychological damage in afflicted individuals, it also represents a serious social and economic problem. Despite the availability of a range of psychological and medical therapies, the risk of relapse for dependent individuals remains high even after years of abstinence. New, more effective therapies are urgently needed. Approximately 50% of the predisposition to develop an alcohol addiction is genetically inherited. In order to create improved treatment approaches and novel diagnostic tools, an enhanced knowledge of the genetic basis and biology of alcohol addiction is a prerequisite.

    The aim of this multi-centre study is to investigate how and which genetic variations increase the risk for developing an alcohol-addiction. To achieve this, scientists in Berlin, Bonn and Mannheim will examine specific brain mechanisms that play important roles in alcohol dependence. Functional Magnetic Resonance Imaging (fMRI), a technique that makes it possible to observe the brain 'at work', will be used to reveal brain mechanisms affected by alcohol addiction such as the processing of reward and punishment, behaviour control and memory. It will then be investigated which genes or gene-gene interactions underlie these neuronal mechanisms. This powerful approach has the potential to uncover 'addiction-pathways' through which genes affect personality, drinking behaviours and success in staying abstinent via their influences on neuronal mechanisms.

    A special emphasis of this project lies upon the so-called 'reward system', which processes naturally rewarding stimuli (e.g. food, sex) and which, in alcohol-dependent individuals, changes perceptions and behaviours in such a way that they become progressively more focused on alcohol. Two major neurotransmitters are involved in the workings of the reward system: 'dopamine' and more indirectly 'glutamate'. The project will investigate how dopaminergic and glutamatergic genes influence the neural mechanisms of reward processing, other neural mechanisms, personality, drinking behaviours and therapy success. In the long run, this knowledge might lead to more effective therapies such as the development of new medications.

    This large-scale study will be conducted with several hundreds of alcohol-dependent patients and non-dependent individuals over a period of five years.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    480 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Endophenotyping With fMRI: Genetic Modulation and Treatment Response
    Study Start Date :
    Jun 1, 2008
    Actual Primary Completion Date :
    Feb 1, 2013
    Actual Study Completion Date :
    Jun 1, 2013

    Arms and Interventions

    Arm Intervention/Treatment
    Alcohol-dependent patients

    men and women, aged 18 to 75 legally effective, written informed consent for participation within the study right handedness no other psychiatric disorder according to ICD 10 no psychotropic substances within the last 7 days

    Healthy control subjects

    men and women, aged 18 to 75 legally effective, written informed consent for participation within the study right handedness no psychiatric disorder according to ICD 10 no psychotropic substances within the last 7 days

    Outcome Measures

    Primary Outcome Measures

    1. blood oxygenation level dependent (BOLD) response [first assessment timepoint (alc.dep. patients: up to 21 days after detoxification)]

      investigation of neuronal activation of the mesolimbic system in alcohol-dependent patients and healthy controls using 3 tesla magnetic resonance imaging

    2. Genetic endophenotypes [second assessment timepoint: 3 days after first assessment time point]

      study the relevance of genetic variation, in particular in dopaminergic and glutamatergic genes, for addiction

    Secondary Outcome Measures

    1. Treatment response [6 month follow up period beginning after second assessment timepoint]

      test the predictive effects of endophenotypes (genetic and imaging factors) for treatment outcome (relapse vs. abstinence) in alcohol-dependent patients

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 75 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:

    Healthy Controls

    • men and women, aged 18 to 75

    • legally effective, written informed consent for participation within the study

    • right handedness

    • no psychiatric disorder according to ICD 10

    • no psychotropic substances within the last 7 days Alcohol-dependent patients

    • men and women, aged 18 to 75

    • legally effective, written informed consent for participation within the study

    • right handedness

    • no other psychiatric disorder according to ICD 10

    • no psychotropic substances within the last 7 days

    Exclusion Criteria:
    • physical disorders, which might interfere with the planned examination (e.g. cerebral or organic disorder)

    • MR-contraindication (z.B. pace maker, metalic or electronic implants, metal splinters, operation clips)

    • anamnestic manifest psychiatric axis I disorder and/or axis II according to ICD-10 except alcohol dependence for patients

    • medication or drug dependence

    • medication or drug abuse (randomized urin testing)

    • insufficient knowledge of German language

    • claustrophobia

    • for women: pregnancy (exclusion via pregnancy test)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Dept. of Psychiatry and Psychotherapy, Charité - Universitätsmedizin Berlin Berlin Germany 10117

    Sponsors and Collaborators

    • Charite University, Berlin, Germany
    • Central Institute of Mental Health, Mannheim
    • University Hospital, Bonn

    Investigators

    • Principal Investigator: Andreas Heinz, MD, Charite University, Berlin, Germany

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    Andreas Heinz, Prof. Dr. med., Charite University, Berlin, Germany
    ClinicalTrials.gov Identifier:
    NCT01503931
    Other Study ID Numbers:
    • 01GS08159
    First Posted:
    Jan 4, 2012
    Last Update Posted:
    Jan 28, 2016
    Last Verified:
    Jan 1, 2016
    Keywords provided by Andreas Heinz, Prof. Dr. med., Charite University, Berlin, Germany
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 28, 2016