TY - JOUR
T1 - Development of tract-specific white matter pathways during early reading development in at-risk children and typical controls
AU - Wang, Yingying
AU - Mauer, Meaghan V.
AU - Raney, Talia
AU - Peysakhovich, Barbara
AU - Becker, Bryce L.C.
AU - Sliva, Danielle D.
AU - Gaab, Nadine
N1 - Funding Information:
This study was supported by the Eunice Kennedy Shriver National Institute of Child Health and Human Development #R01HD65762-01/04 (awarded to N.G.), Charles H. Hood Foundation (awarded to N.G.), and Boston Children’s Hospital Pilot Grant (awarded to N.G.).
PY - 2017
Y1 - 2017
N2 - Developmental dyslexia is a neurodevelopmental disorder with a strong genetic basis. Previous studies observed white matter alterations in the left posterior brain regions in adults and school-age children with dyslexia. However, no study yet has examined the development of tract-specific white matter pathways from the pre-reading to the fluent reading stage in children at familial risk for dyslexia (FHD+) versus controls (FHD-). This studyexamined white matter integrityatpre-reading, beginning, and fluent reading stages cross-sectionally (n=78) and longitudinally (n =45) using an automated fiber-tract quantification method. Our findings depict white matter alterations and atypical lateralization of the arcuate fasciculus at the pre-reading stage in FHD+ versus FHD-children. Moreover, we demonstrate faster white matter development in subsequent good versus poor readers and a positive association between white matter maturation and reading development using a longitudinal design. Additionally, the combination of white matter maturation, familial risk, and psychometric measures best predicted later reading abilities. Furthermore, within FHD+ children, subsequent good readers exhibited faster white matter development in the right superior longitudinal fasciculus compared with subsequent poor readers, suggesting a compensatory mechanism. Overall, our findings highlight the importance of white matter pathway maturation in the development of typical and atypical reading skills.
AB - Developmental dyslexia is a neurodevelopmental disorder with a strong genetic basis. Previous studies observed white matter alterations in the left posterior brain regions in adults and school-age children with dyslexia. However, no study yet has examined the development of tract-specific white matter pathways from the pre-reading to the fluent reading stage in children at familial risk for dyslexia (FHD+) versus controls (FHD-). This studyexamined white matter integrityatpre-reading, beginning, and fluent reading stages cross-sectionally (n=78) and longitudinally (n =45) using an automated fiber-tract quantification method. Our findings depict white matter alterations and atypical lateralization of the arcuate fasciculus at the pre-reading stage in FHD+ versus FHD-children. Moreover, we demonstrate faster white matter development in subsequent good versus poor readers and a positive association between white matter maturation and reading development using a longitudinal design. Additionally, the combination of white matter maturation, familial risk, and psychometric measures best predicted later reading abilities. Furthermore, within FHD+ children, subsequent good readers exhibited faster white matter development in the right superior longitudinal fasciculus compared with subsequent poor readers, suggesting a compensatory mechanism. Overall, our findings highlight the importance of white matter pathway maturation in the development of typical and atypical reading skills.
KW - Developmental dyslexia
KW - Familial risk
KW - Longitudinal
KW - Tractography
KW - White matter development
UR - http://www.scopus.com/inward/record.url?scp=85021308767&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85021308767&partnerID=8YFLogxK
U2 - 10.1093/cercor/bhw095
DO - 10.1093/cercor/bhw095
M3 - Article
C2 - 27114172
AN - SCOPUS:85021308767
SN - 1047-3211
VL - 27
SP - 2469
EP - 2485
JO - Cerebral cortex (New York, N.Y. : 1991)
JF - Cerebral cortex (New York, N.Y. : 1991)
IS - 4
ER -