Genetics researchers close in on schizophrenia. Fifty new gene regions that increase the risk of developing schizophrenia have been identified. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
Never known before, fifty new gene regions that increase the risk of developing schizophrenia have been identified by recent research at the MRC Centre for Neuropsychiatric Genetics and Genomics at Cardiff University. The research team also accurately identified biological pathways that lead to the development of this disorder.
‘This study identifies fifty gene regions that contribute to the development of schizophrenia. It also finds that genes linked to schizophrenia risk are mostly crucial to normal development and therefore typically do not contain harmful mutations.’
The largest of its kind, the study examined genetic data in 100,000 individuals including 40,000 people with a diagnosis of schizophrenia and also found that some of the genes identified as increasing risk for schizophrenia have previously been associated with other neurodevelopmental disorders, including intellectual disability and autism spectrum disorders.Professor Sir Mike Owen, who leads the MRC Centre at Cardiff University, said: "These findings are another important step on the long road to new treatments for schizophrenia and will be crucial for identifying potential new drugs, which will become an increasing focus of our work in the coming years."
Another significant and unexpected finding was that the genes linked to schizophrenia risk are mostly crucial to normal development and therefore typically do not contain harmful mutations. This discovery will help researchers narrow down their search for the mechanisms of the disorder as these genes, commonly called 'loss-of-function intolerant', only account for around 15 percent of all the genes in the human genome.
Dr Antonio Pardinas, first author of the study, said: "We show for the first time that genetic variants that do not severely impact gene function, but presumably have a more subtle impact on these critical genes, increase the risk for developing schizophrenia."
The findings also explain a mystery that has puzzled psychiatrists and evolutionary geneticists alike: if people with schizophrenia have, on average, fewer children than people without the disorder, why does schizophrenia still affect so many people?
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"Many theories have emerged to explain this. One of these is that genetic risk for schizophrenia must have, or have had in the past, a positive effect to balance against the negative ones. We did not find any evidence for a so-called 'positive selection' but instead found that many gene variants linked to schizophrenia reside in regions of the genome in which natural selection is not very effective in the first place. Also, most of them do not have individually serious effects, and this makes them less likely to be selected, either for or against."
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Dr Rachael Panizzo, Programme Manager for Mental Health and Addiction at the Medical Research Council, added: "This large study provides further evidence of the complex genetics underlying schizophrenia. Advances in our understanding of the biological pathways and mechanisms involved will help uncover new targets for treatment, which could one day translate into better, more personalized care for people living with schizophrenia."
The complete research is published in the journal Nature Genetics.
Source-Eurekalert