* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download THE EFFECTS OF NEUROFEEDBACK TRAINING ON ADULT ADHD
Generalized anxiety disorder wikipedia , lookup
Dissociative identity disorder wikipedia , lookup
Treatments for combat-related PTSD wikipedia , lookup
Asperger syndrome wikipedia , lookup
Antisocial personality disorder wikipedia , lookup
Drug rehabilitation wikipedia , lookup
Conversion disorder wikipedia , lookup
Diagnosis of Asperger syndrome wikipedia , lookup
Diagnostic and Statistical Manual of Mental Disorders wikipedia , lookup
Conduct disorder wikipedia , lookup
Treatment of bipolar disorder wikipedia , lookup
Depression in childhood and adolescence wikipedia , lookup
Child psychopathology wikipedia , lookup
Executive dysfunction wikipedia , lookup
Parent management training wikipedia , lookup
Impulsivity wikipedia , lookup
Christopher Gillberg wikipedia , lookup
Externalizing disorders wikipedia , lookup
Sluggish cognitive tempo wikipedia , lookup
Attention deficit hyperactivity disorder wikipedia , lookup
Attention deficit hyperactivity disorder controversies wikipedia , lookup
Adult attention deficit hyperactivity disorder wikipedia , lookup
COST B27 ENOC Joint WGs Meeting Swansea UK, 16-18 September 2006 THE EFFECTS OF NEUROFEEDBACK TRAINING ON ADULT ADHD M.Numan Ermutlu M.D. Istanbul Science University, Faculty of Medicine, Department of Physiology Prof Dr Sacit Karamürsel Istanbul University, Istanbul Faculty of Medicine, Department of Physiology 1 Attention-deficit/hyperactivity disorder is a multifactorial disorder with complex etiology and strong genetic underpinnings (Faraone 2004) . The inattention component of ADHD is manifested as: daydreaming distractibility difficulty focusing on a single task for a prolonged period whereas the hyperactivity component is expressed as: fidgeting excessive talking restlessness. 2 The symptoms of ADHD predispose to accidents, create strain in interpersonal relationships, and disrupt the environment through interruptions and inappropriate behavior. 3 It is notable that the more overt symptoms of hyperactivity/impulsivity tend to wane early in life, whereas the more covert symptom of inattention tends to persist over time (Biederman et al 1996). 4 Adults with retrospectively defined childhood-onset and persistent ADHD show a pattern of psychological dysfunction, psychosocial disability, psychiatric comorbidity, and school failure that resembles the well-known features of childhood ADHD (Biederman et al 2004). 5 Follow-up studies have found that 5%–66% of children with ADHD persist with this disorder in adulthood (Biederman et al 1993). Current epidemiologic studies estimate the prevalence of adult ADHD to be between 3% and 5% (Faraone 2004; Kessler 2004). 6 The treatment of ADHD mainly consists of using stimulatory drugs. The stimulating drugs have cardiovascular risks especially for adults. Neurofeedback treatment (NF) had also been shown to be effective in ADHD and impulse control (Lubar and Shouse1976; Lubar 1989, Linden et al 1996; Othmer et al 1999; Fuchs et al 2003) . Neurofeedback treatment has no known cardiovascular or other morbidity and/or mortality increasing effects. 7 In this study the preliminary findings of six adult ADHD patients (age 22-32; 2F, 4M) were reported. The ADHD subjects (DSMIV TR) who had either diagnosed as ADHD in childhood or had fulfilled the scores for Wender-Utah Rating Scale for ADHD in Adults (Öncü et al, 2005-Turkish version) were enrolled for the study. 8 They were given Adult ADD/ADHD DSM IV- based Diagnostic, Screening and Rating Scale (Turgay) (Günay et al. 2004- Turkish version) and their ERP were recorded with passive and active oddball paradigm before and after training. 9 The training protocol was consisted of 40 sessions of beta (15-22 Hz) and SMR (12- 15 Hz) increase/theta (4-7 Hz) decrease. Each session was 3036 minutes long divided equally between beta and SMR. 10 Theta/beta ratios 3 2,5 2 before 1,5 after 1 0,5 0 1 2 3 4 5 6 Subjects 11 Theta/SMR ratios 3 2,5 2 before 1,5 after 1 0,5 0 1 2 3 4 5 6 Subjects 12 Amplitude (uV) P3b amplitudes before and after NF training 18 16 14 12 10 8 6 4 2 0 before after 1 2 3 4 5 6 Subjects 13 P3a amlitudes before and after NF training 12 Amplitude (uV) 10 8 before 6 after 4 2 0 1 2 3 4 5 6 Subjects 14 MMN latency before and after NF training Latency (ms) 250 202 200 150 133 175 158 195 175 155 153 148 140 138 125 before after 100 50 0 1 2 3 4 5 6 Subjects 15 MMN amplitudes before and after NF training Subjects Amplitude (uV) -5 -4 -3 before -2 after -1 0 1 2 3 4 5 6 16 Adult ADD/ADHD DSM IV- based Diagnostic, Screening and Rating Scale Scores 35 30 25 20 15 10 31 28 26 13 25 16 23 14 16 19 18 before after 9 5 0 1 2 3 4 5 6 17 Scores for Problems Related with ADD/ADHD 40 35 30 25 20 15 10 36 36 34 33 38 27 22 18 24 20 14 before after 13 5 0 1 2 3 4 5 6 18 After 40 treatment sessions Adult ADD/ADHD Diagnostic and Rating Inventory scores decreased more than 50% and P300 amplitudes increased between 50-100%. 19 A low P3 amplitude is present in various disinhibitory conditions such as substance abuse (Herning, 1996, Biggins et al., 1997, Brigham et al., 1997, Anokhin et al., 2000 and Iacono et al., 2004) antisocial personality (Hesselbrock et al., 1993, O'Connor et al., 1994 and Costa et al., 2000), conduct disorder (Iacono et al., 2002), attention-deficit hyperactivity disorder (Frank et al., 1998, Rubia et al., 1998, Pliszka et al., 2000; Branderies et al,2002; Klorman, 1991 and van der Stelt et al., 2001). 20 SMR and beta –1 training were shown to increase P3 amplitude in normals (Egner and Gruzelier, 2004). The increase in the amplitude of P3b can be the result of effective inhibitory control and increased arousal as a result of SMR and Beta-1 trainings respectively. 21 Our preliminary results suggest that neurofeedback training might be an effective treatment modality for adult ADHD. P3b amplitude and MMN latency can be a useful electrophysiological tool to follow up the progress of NF training. However, controlled trials comparing NT and drugs should be done in order to establish its efficiency. 22