Ignite Creation Date:
2025-12-24 @ 9:24 PM
Ignite Modification Date:
2025-12-25 @ 7:10 PM
Study NCT ID:
NCT00143832
Status:
UNKNOWN
Last Update Posted:
2007-03-20
First Post:
2005-08-31
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
Genetic Risk for Attention Deficit Hyperactivity Disorder Expressed in Brain Functioning
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D001289', 'term': 'Attention Deficit Disorder with Hyperactivity'}], 'ancestors': [{'id': 'D019958', 'term': 'Attention Deficit and Disruptive Behavior Disorders'}, {'id': 'D065886', 'term': 'Neurodevelopmental Disorders'}, {'id': 'D001523', 'term': 'Mental Disorders'}]}}, 'protocolSection': {'designModule': {'studyType': 'OBSERVATIONAL', 'designInfo': {'timePerspective': 'OTHER', 'observationalModel': 'CASE_CONTROL'}, 'enrollmentInfo': {'count': 90}}, 'statusModule': {'overallStatus': 'UNKNOWN', 'lastKnownStatus': 'RECRUITING', 'startDateStruct': {'date': '2004-09'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2007-03', 'lastUpdateSubmitDate': '2007-03-18', 'studyFirstSubmitDate': '2005-08-31', 'studyFirstSubmitQcDate': '2005-08-31', 'lastUpdatePostDateStruct': {'date': '2007-03-20', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2005-09-02', 'type': 'ESTIMATED'}}, 'conditionsModule': {'keywords': ['fMRI'], 'conditions': ['Attention Deficit Hyperactivity Disorder']}, 'referencesModule': {'references': [{'pmid': '16712804', 'type': 'RESULT', 'citation': 'Durston S, Mulder M, Casey BJ, Ziermans T, van Engeland H. Activation in ventral prefrontal cortex is sensitive to genetic vulnerability for attention-deficit hyperactivity disorder. Biol Psychiatry. 2006 Nov 15;60(10):1062-70. doi: 10.1016/j.biopsych.2005.12.020. Epub 2006 May 19.'}, {'pmid': '18174826', 'type': 'DERIVED', 'citation': 'Durston S, Fossella JA, Mulder MJ, Casey BJ, Ziermans TB, Vessaz MN, VAN Engeland H. Dopamine transporter genotype conveys familial risk of attention-deficit/hyperactivity disorder through striatal activation. J Am Acad Child Adolesc Psychiatry. 2008 Jan;47(1):61-67. doi: 10.1097/chi.0b013e31815a5f17.'}], 'seeAlsoLinks': [{'url': 'http://www.niche-lab.nl', 'label': 'Lab homepage with info for subjects (in Dutch)'}]}, 'descriptionModule': {'briefSummary': 'Poor inhibitory control has been proposed to be central to the cognitive deficits and symptomatology associated with Attention Deficit Hyperactivity Disorder (ADHD). ADHD is a highly heritable disorder with an increased incidence among the siblings of affected individuals. In the current proposal we investigate the expression of genetic susceptibility for ADHD in brain functioning. We will study cognitive functioning in patients with ADHD, their unaffected siblings and healthy matched controls. Our aims are 1) to determine whether increased familial risk for ADHD is associated with differential patterns of brain activation compared to normally developing children, during the performance of tasks designed to probe cognitive functions that are compromised in ADHD and 2) to determine whether differential patterns of activation are similar for boys with ADHD and their unaffected siblings.', 'detailedDescription': 'Poor inhibitory control has been proposed to be central to the cognitive deficits and symptomatology associated with Attention Deficit Hyperactivity Disorder (ADHD). ADHD is a highly heritable disorder with an increased incidence among the siblings of affected individuals. Although studies investigating candidate genes are underway, as yet it remains unclear via which mechanisms the presence of risk genes leads to symptomatology. There is evidence to suggest that individuals at increased genetic risk display some of the cognitive deficits associated with the disorder. In particular poor inhibitory control has been put forward as a potential marker for familial ADHD. Neuroimaging techniques now make it possible to investigate the neural substrate of cognitive deficits associated with psychiatric disorders. Magnetic resonance imaging (MRI) has been used to demonstrate that the neural substrate of cognitive brain function is affected in ADHD. Using a task that taxes inhibitory systems at varying levels of task demands, we demonstrated that increased susceptibility to interference in children with ADHD is paralleled by differences in brain activation, with these children displaying a relative lack of fronto-striatal activation. In a recent study, we demonstrated that the unaffected siblings of patients with ADHD show cortical volumetric deficits, similar to patients themselves. This suggests that individuals at increased risk for ADHD share some of the neural basis of cognitive deficits associated with this disorder. In the current proposal we set out to investigate the expression of genetic susceptibility for ADHD in brain functioning. We will study cognitive functioning in patients with ADHD, their unaffected siblings and healthy matched controls focusing on cognitive control. Our aims are 1) to determine whether increased familial risk for ADHD is associated with differential patterns of brain activation compared to normally developing children, during the performance of tasks designed to probe cognitive functions that are compromised in ADHD and 2) to determine whether differential patterns of activation are similar for boys with ADHD and their unaffected siblings. We intend to include 30 boys with ADHD, 30 of their brothers without ADHD, and 30 matched normal controls in 3 studies focusing on cognitive control and similar cognitive functions that are compromised in ADHD. We will include 10 boys in each group for each study. The proposed studies will utilize variations of a parametric go nogo paradigm previously developed. All subjects will be asked to participate in a functional MR scanning session lasting up to an hour. The whole visit will last a maximum of two hours. There are no known risks associated with MR scanning, therefore this procedure is considered completely safe. By participating in a simulation prior to the scan, we will also minimize anxiety for the subjects. Furthermore, the study will immediately be terminated if a subject becomes anxious, or otherwise indicates that he no longer wishes to participate. All subjects will be offered a gift certificate as a token of appreciation for their effort. In addition, they will be reimbursed for travel expenses.'}, 'eligibilityModule': {'sex': 'MALE', 'stdAges': ['CHILD', 'ADULT'], 'maximumAge': '20 Years', 'minimumAge': '8 Years', 'healthyVolunteers': True, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Age 8 - 20 years\n* Male\n\nInclusion Criteria for Patients with ADHD:\n\n* DSM-IV (APA, 1994) diagnosis of ADHD, according to DISC interview\n* Scores in the clinical range on the Child Behavior Checklist (CBCL) and Teacher Rating Form(TRF)\n* One brother who meets the inclusion criteria for siblings\n\nInclusion Criteria for Unaffected Siblings:\n\n* No DSM-IV (APA, 1994) diagnosis according to DISC interview\n* No scores in the clinical range on the Child Behavior Checklist (CBCL) and Teacher Rating Form (TRF)\n\nInclusion Criteria for Controls:\n\n* No DSM-IV (APA, 1994) diagnosis, according to DISC interview\n* No scores in the clinical range on the Child Behavior Checklist (CBCL) and Teacher Rating Form (TRF)\n\nExclusion Criteria:\n\n* IQ \\< 70\n* Illness of the cardiovascular, the endocrine, the pulmonal or the gastrointestinal system\n* Presence of metal objects in or around the body (pacemaker, dental braces)\n* History of or present neurological disorder\n* For individuals over 12 years of age: legal incompetence, defined as the obvious inability to comprehend the information that is presented by the investigator and is outlined in the Information letter and on which the decision to participate in the study is to be based'}, 'identificationModule': {'nctId': 'NCT00143832', 'briefTitle': 'Genetic Risk for Attention Deficit Hyperactivity Disorder Expressed in Brain Functioning', 'organization': {'class': 'OTHER', 'fullName': 'UMC Utrecht'}, 'officialTitle': 'Genetic Risk for Attention Deficit Hyperactivity Disorder Expressed in Brain Functioning', 'orgStudyIdInfo': {'id': 'P03.0465C'}, 'secondaryIdInfos': [{'id': 'METC 04/124'}]}, 'contactsLocationsModule': {'locations': [{'city': 'Utrecht', 'status': 'RECRUITING', 'country': 'Netherlands', 'contacts': [{'name': 'Martijn Mulder, M.Sc.', 'role': 'CONTACT', 'email': 'M.Mulder-7@azu.nl', 'phone': '+31 30 250 8161'}, {'name': 'Janna van Belle, M.Sc.', 'role': 'CONTACT', 'email': 'J.vanBelle@umcutrecht.nl', 'phone': '+31 30 250 3275'}, {'name': 'Martijn Mulder, M.Sc.', 'role': 'PRINCIPAL_INVESTIGATOR'}], 'facility': 'Dept. of Child and Adolescent Psychiatry, UMC Utrecht', 'geoPoint': {'lat': 52.09083, 'lon': 5.12222}}], 'centralContacts': [{'name': 'Sarah Durston, Ph.D.', 'role': 'CONTACT', 'email': 'S.Durston@umcutrecht.nl', 'phone': '+31 30 250 8161'}], 'overallOfficials': [{'name': 'Sarah Durston, Ph.D.', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'RMI of Neuroscience, UMC Utrecht'}, {'name': 'Herman van Engeland, M.D. Ph.D.', 'role': 'STUDY_CHAIR', 'affiliation': 'RMI of Neuroscience, UMC Utrecht'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'UMC Utrecht', 'class': 'OTHER'}, 'collaborators': [{'name': 'Netherlands Organisation for Scientific Research', 'class': 'OTHER_GOV'}]}}}