Identification of genetic variants causing dyslexia increases the likelihood of earlier diagnosis and effective intervention

Updated on: Friday, June 14, 2013

Scientists have identified genetic variants that can predispose children to dyslexia and language impairment, a finding that increases the likelihood of earlier diagnosis and more effective interventions.

Researchers at Yale School of Medicine analysed data from more than 10,000 children born in 1991-1992 who were part of the Avon Longitudinal Study of Parents and Children (ALSPAC) conducted by investigators at the University of Bristol in UK.

Senior author Dr Jeffrey R Gruen, professor of pediatrics, genetics, and investigative medicine at Yale and his team used the ALSPAC data to unravel the genetic components of reading and verbal language.

In the process, they identified genetic variants that can predispose children to dyslexia and language impairment.

In previous studies, Gruen and his team found that dopamine-related genes ANKK1 and DRD2 are involved in language processing.

In further non-genetic studies, they found that prenatal exposure to nicotine has a strong negative affect on both reading and language processing. They had also previously found that a gene called DCDC2 was linked to dyslexia.

In this new study, Gruen and colleagues looked deeper within the DCDC2 gene to pinpoint the specific parts of the gene that are responsible for dyslexia and language impairment.

They found that some variants of a gene regulator called READ1 (regulatory element associated with dyslexia1) within the DCDC2 gene are associated with problems in reading performance while other variants are strongly associated with problems in verbal language performance.

Gruen said these variants interact with a second dyslexia risk gene called KIAA0319.

"When you have risk variants in both READ1 and KIAA0319, it can have a multiplier effect on measures of reading, language, and IQ," he said.

"People who have these variants have a substantially increased likelihood of developing dyslexia or language impairment," he added.

"These findings are helping us to identify the pathways for fluent reading, the components of those pathways; and howthey interact," said Gruen.

Identification of genetic variants causing dyslexia increases the likelihood of earlier diagnosis and effective intervention

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