Study sheds light on the causes of cerebral palsy
Cerebral palsy (CP) is the most common cause of physical disability in children. Every year 140 children are diagnosed with cerebral palsy in Quebec.
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 成人VR视频 Health Centre (RI-MUHC) has uncovered strong evidence for genetic causes of cerebral palsy that turns experts鈥� understanding of the condition on its head.
The study, published online聽in Nature Communications could have major implications on the future of counselling, prevention and treatment of children with cerebral palsy.
鈥淥ur research suggests that there is a much stronger genetic component to cerebral palsy than previously suspected,鈥� says the lead study author Dr. Maryam Oskoui, Paediatric neurologist at The Montreal Children鈥檚 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 成人VR视频. 鈥淗ow 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.鈥�
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.
鈥淲hen I showed the results to our clinical geneticists, initially they were floored,鈥� says Dr. Stephen Scherer, Principal Investigator of the study and Director of The Centre for Applied Genomics (TCAG) at SickKids. 鈥淚n light of the findings, we suggest that genomic analyses be integrated into the standard of practice for diagnostic assessment of cerebral palsy.鈥�
The study also demonstrates that there are many different genes involved in cerebral palsy. 鈥淚t鈥檚 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,鈥� says Scherer, who is also Director of the University of Toronto McLaughlin Centre. 鈥淚nterestingly, 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鈥檝e opened many doors for new research into cerebral palsy.鈥澛犅�
鈥淔inding an underlying cause for a child鈥檚 disability is an important undertaking in management,鈥� says Dr. Michael Shevell, co-director of the Canadian Cerebral Palsy Registry and Chair of the Department of Paediatrics at the MCH-MUHC. 鈥淧arents 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.鈥�
Clinically relevant copy number variations detected in cerebral palsy, in Nature Communications
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 R茅seau de recherche sur le d茅veloppement, la sant茅 et le bien-锚tre de l'enfant (RSDE) des Fonds de Recherche en Sant茅 du Qu茅bec (FRSQ) and NeuroDevNet. Dr. Maryam Oskoui is a FRQS Chercheur-Boursier Clinicien Junior 1.
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