Dyslexia is known to run in families – partly because of genetic factors – but until now little was known about the specific genes that relate to the risk of it developing.
Identifying specific genetic variants that may play a role has proved challenging. Now researchers say they have identified about 170 genes and 42 specific genetic variants significantly associated with dyslexia in the largest such study to date.
While 15 of these variants have previously been linked to cognitive ability and educational attainment, the remaining 27 are newly identified – meaning they have not previously been linked to traits associated with dyslexia. Ad
The research, led by Edinburgh University and published in 2022, is the largest genetic study of dyslexia to date. It involves more than 50,000 adults who have been diagnosed with dyslexia, and for a control group, more than one million adults who have not.
Researchers tested the connection between millions of genes with dyslexia and found 42 significant ones. Some of these are associated with other conditions, such as language delay, and with thinking skills and academic achievement. Many, however, are new and could represent genes more specifically associated with mental processes essential for learning to read.
Many of the genes linked to dyslexia are also linked to attention deficit hyperactivity disorder (ADHD).
Researchers say they were able to predict how well children and adults from four other research studies could read and spell using the genetic information from the study, but it was not accurate enough for a diagnosis.
Lead researcher Michelle Luciano, of the University of Edinburgh’s School of Philosophy, Psychology and Language Sciences, said the study sheds light on many unanswered questions around dyslexia.
She said: “Our findings show that common genetic differences have very similar effects in boys and girls, and that there is a genetic link between dyslexia and ambidexterity.