Gene-environment Interactions and Brain Functional Connectivity in Attention Deficit Hyperactivity Disorder
Primary Purpose
Attention Deficit Hyperactivity Disorder
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Methylphenidate
Sponsored by
About this trial
This is an interventional basic science trial for Attention Deficit Hyperactivity Disorder focused on measuring ADHD, ADRA2A, Methylphenidate, Response
Eligibility Criteria
Inclusion Criteria:
- Clinical diagnosis of Attention-deficit Hyperactivity Disorder
- 6-18 years old
Exclusion Criteria:
- History of neurological diseases, including convulsive disorders or brain damage
- IQ below 70
- Pervasive developmental disorder (autism)
- Language difficulties or learning disorders (reading disorders, mathematics disorders and disorders of written expression).
- Tourette's syndrome
- Bipolar disorder
- Psychosis
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Methylphenidate
Arm Description
Participants were treated with methylphenidate (ranging from to 63mg) for 8 weeks. Doses of methylphenidate were titrated depending on symptoms and adverse eff ects at the 2nd and 4th weeks of treatment.
Outcomes
Primary Outcome Measures
Change From Baseline ADHD Rating Scale-IV Scores at 8 Weeks
Attendtion-deficit hyperactivity disorder (ADHD) Rating Scale-IV is the sum of 18 questions, ranging from 0 (no symptoms) to 54 (worst possible symptoms).
Change from baseline ADHD Rating Scale-IV scores at 8 weeks was calculated as baseline minus 8 weeks.
Secondary Outcome Measures
Clinical Global Impression-Improvement Scale at 8 Weeks
Clinical Global Impression-Improvement (CGI-I) scale is a one-item measure evaluating the change from the initiation of treatment on a seven-point scale: "Compared to the patient's condition at baseline [prior to medication initiation], this patient's condition is: 1=very much improved since the initiation of treatment; 2=much improved; 3=minimally improved; 4=no change from baseline (the initiation of treatment); 5=minimally worse; 6= much worse; 7=very much worse since the initiation of treatment.
Clinical Global Impression-Improvement was measured at 8 weeks.
Full Information
NCT ID
NCT01912352
First Posted
July 16, 2013
Last Updated
November 26, 2014
Sponsor
Seoul National University
Collaborators
Korea Research Foundation
1. Study Identification
Unique Protocol Identification Number
NCT01912352
Brief Title
Gene-environment Interactions and Brain Functional Connectivity in Attention Deficit Hyperactivity Disorder
Official Title
Gene-environment Interactions and Brain Functional Connectivity Associated With Norepinephrine System Genes in Attention Deficit Hyperactivity Disorder
Study Type
Interventional
2. Study Status
Record Verification Date
November 2014
Overall Recruitment Status
Completed
Study Start Date
May 2010 (undefined)
Primary Completion Date
April 2013 (Actual)
Study Completion Date
April 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Seoul National University
Collaborators
Korea Research Foundation
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The aims of the current study are to examine gene-environment interactions associated with norepinephrine (NE) system genes (ADRA2A, SLC6A2) in ADHD, and to evaluate whether genetic changes in norepinephrine pathway are associated with differences in functional connectivity of white matter fiber tracts, as measured by diffusion tensor imaging (DTI). Furthermore, this study aims to examine neurobiological markers, such as intermediate neuroimaging phenotypes or neuropsychological endophenotypes associated with the pathophysiology of ADHD. Through evaluating drug responses and side effects with the associated measures of clinical, neuropsychological and neuroimaging characteristics, investigators would like to investigate predictors of treatment response associated with NE system genes in ADHD.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Attention Deficit Hyperactivity Disorder
Keywords
ADHD, ADRA2A, Methylphenidate, Response
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
83 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Methylphenidate
Arm Type
Experimental
Arm Description
Participants were treated with methylphenidate (ranging from to 63mg) for 8 weeks. Doses of methylphenidate were titrated depending on symptoms and adverse eff ects at the 2nd and 4th weeks of treatment.
Intervention Type
Drug
Intervention Name(s)
Methylphenidate
Primary Outcome Measure Information:
Title
Change From Baseline ADHD Rating Scale-IV Scores at 8 Weeks
Description
Attendtion-deficit hyperactivity disorder (ADHD) Rating Scale-IV is the sum of 18 questions, ranging from 0 (no symptoms) to 54 (worst possible symptoms).
Change from baseline ADHD Rating Scale-IV scores at 8 weeks was calculated as baseline minus 8 weeks.
Time Frame
baseline and 8 weeks
Secondary Outcome Measure Information:
Title
Clinical Global Impression-Improvement Scale at 8 Weeks
Description
Clinical Global Impression-Improvement (CGI-I) scale is a one-item measure evaluating the change from the initiation of treatment on a seven-point scale: "Compared to the patient's condition at baseline [prior to medication initiation], this patient's condition is: 1=very much improved since the initiation of treatment; 2=much improved; 3=minimally improved; 4=no change from baseline (the initiation of treatment); 5=minimally worse; 6= much worse; 7=very much worse since the initiation of treatment.
Clinical Global Impression-Improvement was measured at 8 weeks.
Time Frame
baseline and 8 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Clinical diagnosis of Attention-deficit Hyperactivity Disorder
6-18 years old
Exclusion Criteria:
History of neurological diseases, including convulsive disorders or brain damage
IQ below 70
Pervasive developmental disorder (autism)
Language difficulties or learning disorders (reading disorders, mathematics disorders and disorders of written expression).
Tourette's syndrome
Bipolar disorder
Psychosis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jae-Won Kim, MD., PhD.
Organizational Affiliation
Seoul National University and Seoul National University Hospital
Official's Role
Principal Investigator
12. IPD Sharing Statement
Citations:
PubMed Identifier
29905488
Citation
Kim JI, Kim JW, Shin I, Kim BN. Effects of Interaction Between DRD4 Methylation and Prenatal Maternal Stress on Methylphenidate-Induced Changes in Continuous Performance Test Performance in Youth with Attention-Deficit/Hyperactivity Disorder. J Child Adolesc Psychopharmacol. 2018 Oct;28(8):562-570. doi: 10.1089/cap.2018.0054. Epub 2018 Jun 15.
Results Reference
derived
PubMed Identifier
25964505
Citation
Kim JW, Sharma V, Ryan ND. Predicting Methylphenidate Response in ADHD Using Machine Learning Approaches. Int J Neuropsychopharmacol. 2015 May 10;18(11):pyv052. doi: 10.1093/ijnp/pyv052.
Results Reference
derived
PubMed Identifier
25201318
Citation
Hong SB, Zalesky A, Park S, Yang YH, Park MH, Kim B, Song IC, Sohn CH, Shin MS, Kim BN, Cho SC, Kim JW. COMT genotype affects brain white matter pathways in attention-deficit/hyperactivity disorder. Hum Brain Mapp. 2015 Jan;36(1):367-77. doi: 10.1002/hbm.22634. Epub 2014 Sep 9.
Results Reference
derived
Learn more about this trial
Gene-environment Interactions and Brain Functional Connectivity in Attention Deficit Hyperactivity Disorder
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