Neural Changes following Remediation in Adult Developmental Dyslexia

Slides:



Advertisements
Similar presentations
Recent Findings in the Neurobiology & Neuropsychology of Reading Processes A. Maerlender, Ph.D. Clinical School Services & Learning Disorders.
Advertisements

Copyright © 2011 American Medical Association. All rights reserved.
Volume 63, Issue 3, Pages (August 2009)
Polymodal Motion Processing in Posterior Parietal and Premotor Cortex
Volume 56, Issue 6, Pages (December 2007)
Volume 20, Issue 5, Pages (May 1998)
Abnormal Visual Motion Processing Is Not a Cause of Dyslexia
Volume 47, Issue 6, Pages (September 2005)
Neurodegenerative Diseases Target Large-Scale Human Brain Networks
Avi Mendelsohn, Yossi Chalamish, Alexander Solomonovich, Yadin Dudai 
Communicative Signaling Activates ‘Broca's’ Homolog in Chimpanzees
A Common Network of Functional Areas for Attention and Eye Movements
The Human Hippocampus and Spatial and Episodic Memory
Volume 72, Issue 6, Pages (December 2011)
Volume 41, Issue 5, Pages (March 2004)
Neural Changes following Remediation in Adult Developmental Dyslexia
The Neural Basis of Body Form and Body Action Agnosia
Developmental dyslexia is characterized by the co-existence of visuospatial and phonological disorders in Chinese children  Wai Ting Siok, John A. Spinks,
Volume 92, Issue 5, Pages (December 2016)
Christian Grefkes, Peter H. Weiss, Karl Zilles, Gereon R. Fink  Neuron 
Disruption of Large-Scale Brain Systems in Advanced Aging
Rajeev D.S. Raizada, Russell A. Poldrack  Neuron 
Volume 55, Issue 3, Pages (August 2007)
Volume 63, Issue 3, Pages (August 2009)
Timothy J. Vickery, Marvin M. Chun, Daeyeol Lee  Neuron 
The Neural Basis of Hyperlexic Reading
Can We Share a Pain We Never Felt
Selective Entrainment of Theta Oscillations in the Dorsal Stream Causally Enhances Auditory Working Memory Performance  Philippe Albouy, Aurélien Weiss,
Neural Correlates of Visual Working Memory
Parallel Interdigitated Distributed Networks within the Individual Estimated by Intrinsic Functional Connectivity  Rodrigo M. Braga, Randy L. Buckner 
Talia Konkle, Aude Oliva  Neuron  Volume 74, Issue 6, Pages (June 2012)
Between Thoughts and Actions: Motivationally Salient Cues Invigorate Mental Action in the Human Brain  Avi Mendelsohn, Alex Pine, Daniela Schiller  Neuron 
Volume 25, Issue 11, Pages (June 2015)
Volume 45, Issue 4, Pages (February 2005)
Negative BOLD Differentiates Visual Imagery and Perception
Distributed Neural Systems for the Generation of Visual Images
Moral Judgments Recruit Domain-General Valuation Mechanisms to Integrate Representations of Probability and Magnitude  Amitai Shenhav, Joshua D. Greene 
The Functional Neuroanatomy of Object Agnosia: A Case Study
Volume 62, Issue 6, Pages (June 2009)
The Future of Memory: Remembering, Imagining, and the Brain
Know Your Place: Neural Processing of Social Hierarchy in Humans
A Higher Order Motion Region in Human Inferior Parietal Lobule
Volume 63, Issue 5, Pages (September 2009)
Uri Hasson, Orit Furman, Dav Clark, Yadin Dudai, Lila Davachi  Neuron 
Negative BOLD Differentiates Visual Imagery and Perception
Josef Parvizi, Anthony D. Wagner  Neuron 
Volume 92, Issue 5, Pages (December 2016)
Neural Primacy of the Salience Processing System in Schizophrenia
René Marois, Hoi-Chung Leung, John C. Gore  Neuron 
Hugo D Critchley, Christopher J Mathias, Raymond J Dolan  Neuron 
Volume 68, Issue 1, Pages (October 2010)
Cerebral Responses to Change in Spatial Location of Unattended Sounds
Volume 34, Issue 1, Pages (March 2002)
Orienting Attention Based on Long-Term Memory Experience
The Neural Correlates of Third-Party Punishment
Brain Mechanisms for Extracting Spatial Information from Smell
Predictive Neural Coding of Reward Preference Involves Dissociable Responses in Human Ventral Midbrain and Ventral Striatum  John P. O'Doherty, Tony W.
The Neural Bases of Cognitive Conflict and Control in Moral Judgment
Role of the Cerebellum in Adaptation to Delayed Action Effects
Christian J. Fiebach, Jesse Rissman, Mark D'Esposito  Neuron 
Sharon L. Thompson-Schill, Mark D'Esposito, Irene P. Kan  Neuron 
Volume 22, Issue 1, Pages (January 1999)
Under-Recruitment and Nonselective Recruitment
Cortical Mechanisms Specific to Explicit Visual Object Recognition
Volume 40, Issue 3, Pages (October 2003)
Common Prefrontal Regions Coactivate with Dissociable Posterior Regions during Controlled Semantic and Phonological Tasks  Brian T Gold, Randy L Buckner 
Human Posterior Parietal Cortex Flexibly Determines Reference Frames for Reaching Based on Sensory Context  Pierre-Michel Bernier, Scott T. Grafton  Neuron 
Volume 36, Issue 1, Pages (September 2002)
Dynamic Statistical Parametric Mapping
DMN changes in patients with HE
Presentation transcript:

Neural Changes following Remediation in Adult Developmental Dyslexia Guinevere F. Eden, Karen M. Jones, Katherine Cappell, Lynn Gareau, Frank B. Wood, Thomas A. Zeffiro, Nicole A.E. Dietz, John A. Agnew, D.Lynn Flowers  Neuron  Volume 44, Issue 3, Pages 411-422 (October 2004) DOI: 10.1016/j.neuron.2004.10.019

Figure 1 Functional Anatomy of Phonological Manipulation in Normal Readers, Dyslexic Readers, and Normal Readers Greater Than Dyslexic Readers Task-related signal change was derived by contrasting simple Word Repetition of an aurally presented word with repeating words after performing Sound Deletion on the first phoneme. Localization is based on stereotaxic coordinates in x (medial-lateral), y (antero-posterior), and z (superior-inferior) directions and refers to the location of maximal activation within a cluster (indicated by the highest Z score). Areas of significant activity within 15.0 mm of the cortical surface are projected to the surface of the brain (Z = 3.10; p < 0.001, uncorrected; limited to clusters >80 contiguous 2 mm cubic voxels). Brain activity attributed to phonological manipulation in normal readers (A) was observed in left occipitotemporal, inferior parietal, and inferior frontal cortex, consistent with previous studies. The thalamus and cerebellum were also bilaterally active (these deeper foci are not seen in the figure). In the right hemisphere, the following regions were identified: inferior and middle temporal cortex as well as middle frontal gyrus. The dyslexic group (B) showed activity related to phonological manipulation in bilateral inferior parietal, inferior frontal, middle temporal cortex, precuneus, and cerebellum. A between-group statistical comparison of the control and dyslexic groups (C) revealed less activity in the dyslexic group in left inferior parietal regions (supramarginal and angular gyri), superior parietal lobule, precuneus, and medial frontal gyrus. Dyslexic subjects also displayed less activation in several right hemisphere regions compared to controls: the occipitotemporal junction, as seen in the figure, and medial structures including precuneus, medial frontal, fusiform, and cingulate gyri (not seen in these lateral projections). Neuron 2004 44, 411-422DOI: (10.1016/j.neuron.2004.10.019)

Figure 2 Phonological Processing and Reading-Related Changes following Training in the Dyslexic Intervention and Nonintervention Groups Significant gains were observed in several measures, including (A) phonological processing in the aural and visual modality, (B) nonword decoding, phonemic transfer, reading accuracy, and (C) oral paragraph reading accuracy but not rate or comprehension. Percent changes are plotted so that tests with different scales can be more easily compared. (A) Phonological Processing: Test of Auditory Analysis Skills (TAAS) and Visual Symbol Imagery (SI). (B) Single-word Decoding Skills: Woodcock-Johnson-Revised Word Attack subtest (WJRWA), Decoding Skills Test (DST), and Wide Range Achievement Test (WRAT). (C) Secondary Reading Skills: Gray Oral Reading Test Third Edition (GORT), accuracy, rate, and comprehension. For the source of these measures, see Experimental Procedures. Neuron 2004 44, 411-422DOI: (10.1016/j.neuron.2004.10.019)

Figure 3 Functional Anatomy of Phonological Manipulation following Reading Remediation Task-related signal changes underlying phonological processing were computed by contrasting Word Repetition with Sound Deletion of aurally presented words for both dyslexic groups prior to and following the intervention and entered into an ANOVA. A Group × Session interaction revealed intervention-related increases during phonological manipulation in left parietal cortex and fusiform gyrus, indicative of functional increases in regions previously reported as activated by normal readers. This fusiform region extended into the left BA 37, but anterior and inferior to what is considered the “visual word form” area (Cohen et al., 2002). Right hemisphere increases included posterior superior temporal sulcus/gyrus and parietal cortex, thereby representing right hemisphere homologs of regions usually seen in the left hemisphere in good readers. Significantly activated areas are shown in bold in the accompanying table (Z = 3.10; p < 0.001, uncorrected and extended in clusters of at least 80 contiguous 2 mm cubic voxels; *p < 0.05, corrected for multiple comparisons). Left middle frontal cortex (BA 46) and right hemisphere frontal regions also increased, but fell short of the statistical threshold. Neuron 2004 44, 411-422DOI: (10.1016/j.neuron.2004.10.019)