Canadian study sheds surprising light on the causes of cerebral palsy
Wider use of genetic testing in children with CP should be considered.
Dr. Michael Shevell and Dr. Maryam Oskoui both study co-authors and researchers at the Research Institute of the MUHC from the Child Health and Human Development Program. McGill University Health Centre MUHC
The Hospital for Sick Children and McGill University Health Centre August 3, 2015
Cerebral palsy (CP) is the most common cause of physical disability in children. It has historically been considered to be caused by factors such as birth asphyxia, stroke and infections in the developing brain of babies. In a new game-changing Canadian study, a research team from The Hospital for Sick Children (SickKids) and the Research Institute of the McGill University Health Centre (RI-MUHC) has uncovered strong evidence for genetic causes of cerebral palsy that turns experts’ understanding of the condition on its head.
The study, published in Nature Communications, could have major implications on the future of counselling, prevention and treatment of children with cerebral palsy.
“Our research suggests that there is a much stronger genetic component to cerebral palsy than previously suspected,” says the lead study author Dr. Maryam Oskoui, Paediatric neurologist at The Montreal Children’s Hospital (MCH) of the MUHC, co-director of the Canadian Cerebral Palsy Registry and an Assistant Professor in the Department of Paediatrics and Department of Neurology and Neurosurgery at McGill University. “How these genetic factors interplay with other established risk factors remains to be fully understood. For example, two newborns exposed to the same environmental stressors will often have very different outcomes. Our research suggests that our genes impart resilience, or conversely a susceptibility to injury.”
Image 1: MRI of the brain of a healthy child: gray matter is pale gray and white matter is dark gray. Image 2: MRI of the brain of a child with cerebral palsy: red arrows show scarring over the central gray matter leading to stiffness and problems in the co-ordination of movements. McGill University Health Centre MUHC
Children with cerebral palsy have difficulties in their motor development early on, and often have epilepsy and learning, speech, hearing and visual impairments. Two out of every thousand births are affected by cerebral palsy with a very diverse profile; some children are mildly affected while others are unable to walk on their own or communicate. Genetic testing is not routinely done or recommended, and genetic causes are searched for only in rare occasions when other causes cannot be found.
The research team performed genetic testing on 115 children with cerebral palsy and their parents from the Canadian Cerebral Palsy Registry, many of which had other identified risk factors. They found that 10 per cent of these children have copy number variations (CNVs) affecting genes deemed clinically relevant. In the general population such CNVs are found in less than one per cent of people. CNVs are structural alterations to the DNA of a genome that can be present as deletions, additions, or as reorganized parts of the gene that can result in disease.
“When I showed the results to our clinical geneticists, initially they were floored,” says Dr. Stephen Scherer, Principal Investigator of the study and Director of The Centre for Applied Genomics (TCAG) at SickKids. “In light of the findings, we suggest that genomic analyses be integrated into the standard of practice for diagnostic assessment of cerebral palsy.”
The study also demonstrates that there are many different genes involved in cerebral palsy. “It’s a lot like autism, in that many different CNVs affecting different genes are involved which could possibly explain why the clinical presentations of both these conditions are so diverse,” says Scherer, who is also Director of the University of Toronto McLaughlin Centre. “Interestingly, the frequency of de novo, or new, CNVs identified in these patients with cerebral palsy is even more significant than some of the major CNV autism research from the last 10 years. We’ve opened many doors for new research into cerebral palsy.”
“Finding an underlying cause for a child’s disability is an important undertaking in management,” says Dr. Michael Shevell, co-director of the Canadian Cerebral Palsy Registry and Chair of the Department of Paediatrics at the MCH-MUHC. “Parents want to know why their child has particular challenges. Finding a precise reason opens up multiple vistas related to understanding, specific treatment, prevention and rehabilitation. This study will provide the impetus to make genetic testing a standard part of the comprehensive assessment of the child with cerebral palsy.”
| This study was supported by NeuroDevNet Networks Centre of Excellence, the Canadian Institutes of Health Research (CIHR), Genome Canada, the University of Toronto McLaughlin Centre, and SickKids Foundation. The Canadian Cerebral Palsy Registry has been funded by the Réseau de recherche sur le développement, la santé et le bien-être de l’enfant (RSDE) des Fonds de Recherche en Santé du Québec (FRSQ) and NeuroDevNet. Dr. Maryam Oskoui is a FRQS Chercheur-Boursier Clinicien Junior 1. |
| This paper is an example of how SickKids is contributing to making Ontario Healthier, Wealthier and Smarter. |
Source The Hospital for Sick Children and McGill University Health Centre
via EurekAlert! AAAS
| References |
Clinically relevant copy number variations detected in cerebral palsy, Oskoui M, Gazzellone MJ, Thiruvahindrapuram B, Zarrei M, Andersen J, Wei J, Wang Z, Wintle RF, Marshall CR, Cohn RD, Weksberg R, Stavropoulos DJ, Fehlings D, Shevell MI, Scherer SW. Nat Commun. 2015 Aug 3;6:7949. doi: 10.1038/ncomms8949. PDF
