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1.
Article in English | MEDLINE | ID: mdl-35240343

ABSTRACT

BACKGROUND: Attention-deficit/hyperactivity disorder is characterized by neurobiological heterogeneity, possibly explaining why not all patients benefit from a given treatment. As a means to select the right treatment (stratification), biomarkers may aid in personalizing treatment prescription, thereby increasing remission rates. METHODS: The biomarker in this study was developed in a heterogeneous clinical sample (N = 4249) and first applied to two large transfer datasets, a priori stratifying young males (<18 years) with a higher individual alpha peak frequency (iAPF) to methylphenidate (N = 336) and those with a lower iAPF to multimodal neurofeedback complemented with sleep coaching (N = 136). Blinded, out-of-sample validations were conducted in two independent samples. In addition, the association between iAPF and response to guanfacine and atomoxetine was explored. RESULTS: Retrospective stratification in the transfer datasets resulted in a predicted gain in normalized remission of 17% to 30%. Blinded out-of-sample validations for methylphenidate (n = 41) and multimodal neurofeedback (n = 71) corroborated these findings, yielding a predicted gain in stratified normalized remission of 36% and 29%, respectively. CONCLUSIONS: This study introduces a clinically interpretable and actionable biomarker based on the iAPF assessed during resting-state electroencephalography. Our findings suggest that acknowledging neurobiological heterogeneity can inform stratification of patients to their individual best treatment and enhance remission rates.


Subject(s)
Attention Deficit Disorder with Hyperactivity , Methylphenidate , Male , Humans , Attention Deficit Disorder with Hyperactivity/drug therapy , Retrospective Studies , Treatment Outcome , Methylphenidate/therapeutic use , Atomoxetine Hydrochloride/therapeutic use
2.
J Integr Neurosci ; 6(1): 175-90, 2007 Mar.
Article in English | MEDLINE | ID: mdl-17472228

ABSTRACT

AIMS: QEEG and neuropsychological tests were used to investigate the underlying neural processes in dyslexia. METHODS: A group of dyslexic children were compared with a matched control group from the Brain Resource International Database on measures of cognition and brain function (EEG and coherence). RESULTS: The dyslexic group showed increased slow activity (Delta and Theta) in the frontal and right temporal regions of the brain. Beta-1 was specifically increased at F7. EEG coherence was increased in the frontal, central and temporal regions for all frequency bands. There was a symmetric increase in coherence for the lower frequency bands (Delta and Theta) and a specific right-temporocentral increase in coherence for the higher frequency bands (Alpha and Beta). Significant correlations were observed between subtests such as Rapid Naming Letters, Articulation, Spelling and Phoneme Deletion and EEG coherence profiles. DISCUSSION: The results support the double-deficit theory of dyslexia and demonstrate that the differences between the dyslexia and control group might reflect compensatory mechanisms. INTEGRATIVE SIGNIFICANCE: These findings point to a potential compensatory mechanism of brain function in dyslexia and helps to separate real dysfunction in dyslexia from acquired compensatory mechanisms.


Subject(s)
Brain Mapping , Brain/pathology , Brain/physiopathology , Dyslexia/pathology , Dyslexia/physiopathology , Electroencephalography , Adolescent , Analysis of Variance , Child , Female , Humans , Male , Models, Biological , Neuropsychological Tests
3.
J Integr Neurosci ; 5(1): 49-74, 2006 Mar.
Article in English | MEDLINE | ID: mdl-16544366

ABSTRACT

New treatments for Alzheimer's disease require early detection of cognitive decline. Most studies seeking to identify markers of early cognitive decline have focused on a limited number of measures. We sought to establish the profile of brain function measures which best define early neuropsychological decline. We compared subjects with subjective memory complaints to normative controls on a wide range of EEG derived measures, including a new measure of event-related spatio-temporal waves and biophysical modeling, which derives anatomical and physiological parameters based on subject's EEG measurements. Measures that distinguished the groups were then related to cognitive performance on a variety of learning and executive function tasks. The EEG measures include standard power measures, peak alpha frequency, EEG desynchronization to eyes-opening, and global phase synchrony. The most prominent differences in subjective memory complaint subjects were elevated alpha power and an increased number of spatio-temporal wave events. Higher alpha power and changes in wave activity related most strongly to a decline in verbal memory performance in subjects with subjective memory complaints, and also declines in maze performance and working memory reaction time. Interestingly, higher alpha power and wave activity were correlated with improved performance in reverse digit span in the subjective memory complaint group. The modeling results suggest that differences in the subjective memory complaint subjects were due to a decrease in cortical and thalamic inhibitory gains and slowed dendritic time-constants. The complementary profile that emerges from the variety of measures and analyses points to a nonlinear progression in electrophysiological changes from early neuropsychological decline to late-stage dementia, and electrophysiological changes in subjective memory complaint that vary in their relationships to a range of memory-related tasks.


Subject(s)
Cognition Disorders/physiopathology , Cognition/physiology , Electroencephalography , Geriatric Assessment , Memory/physiology , Aged , Aged, 80 and over , Analysis of Variance , Biophysical Phenomena , Biophysics , Cognition Disorders/diagnosis , Female , Humans , Male , Middle Aged , Models, Statistical , Neural Networks, Computer , Neuropsychological Tests/statistics & numerical data , Predictive Value of Tests , Time Factors , Verbal Learning/physiology
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