Twenty-five-point drop in IQ caused by lack of gene copy

Public Release: 27-Jan-2016


‘To understand mental disorders, we must quantify the specific effect of each contributing gene mutation.’ — Dr. Sébastien Jacquemont, geneticist

University of Montreal

No autism is alike. This is also true of most mental disorders. “We now understand that each gene mutation has a specific effect, which adds to other effects to draw a unique picture of the disease in each patient,” said Dr. Sébastien Jacquemont, a geneticist who sees on a daily basis children who are referred to him for a potential genetic diagnosis of mental disorder such as autism. To understand this additive effect, a precise quantification of the effect each identified mutation has in these patients is necessary. “We have just discovered, for example, that a missing copy of a region in chromosome 16 results in a 25-point intelligence quotient (IQ) drop in carriers. Addition of a copy in the same genomic region results in an approximate 16-point drop. Strangely enough, even if carriers show much differentiated sets of symptoms – and sometimes no symptoms at all – the specific effect of these two mutations seems to remain the same,” said Jacquemont, who is a clinical researcher at CHU Sainte-Justine, the mother-child hospital affiliated to University of Montreal, where he is also professor. Together with international collaborators, the scientist authored an article in the renowned scientific journal JAMA Psychiatry.

To reach these conclusions, the researchers measured the intelligence of 700 family members who had at least one relative carrying the same genetic mutation on chromosome 16, which is known to predispose to autistic spectrum disorders. Even in study participants whose IQ was considered to be normal, the researchers found a substantial 25 points IQ drop induced by 16p11.2 gene deletions. Indeed, it is quite common for mutation carriers to show no mental health problems.

“Intellectual faculties are the sum of many factors, the majority of which are genetic and inherited from parents. Each first-degree relative – parents and offspring, siblings – has 50% of their genetic code in common and therefore 50% of the genetic factors that partially determine cognition,” said Dr. Jacquemont. Studying families thus enabled the researchers to measure the factors that combine with the mutations which effects they wanted to quantify. “For example, depending on the additional factors involved, a 25-point IQ drop can determine whether or not a person has crossed the threshold of ‘intellectual disability.”

Further studies are needed to quantify the effect of all mutations associated with autism and characterize the additive effects that lead to this psychiatric disorder. “No single mutation can cause the whole set of clinical signs shown by these patients,” concludes the scientist.


About the study

The article “Defining the effect of the 16p11.2 duplication on cognition, behavior, and medical comorbidities” was published online on December 2, 2015 in JAMA Psychiatry. Dr. Sébastien Jacquemont is a clinician-geneticist at CHU Sainte-Justine and associate professor in the Department of Pediatrics at the University of Montreal. His work is financially supported through a career award from the Swiss National Science Foundation.

Categories: . Epigenetic effect

Leave a Reply

Fill in your details below or click an icon to log in: Logo

You are commenting using your account. Log Out /  Change )

Google photo

You are commenting using your Google account. Log Out /  Change )

Twitter picture

You are commenting using your Twitter account. Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. Log Out /  Change )

Connecting to %s

%d bloggers like this: