Summary: A recent review outlines the genetic complexity of schizophrenia, highlighting nearly 300 common genetic variants and over 20 rare variants linked to the disorder. Researchers emphasize that schizophrenia’s genetic basis is multifaceted, involving multiple genes rather than a single cause.
Environmental factors like lifestyle and stress also play crucial roles. This understanding underscores the need for comprehensive research to develop better interventions for schizophrenia.
Key Facts:
- Schizophrenia is linked to nearly 300 common and over 20 rare genetic variants.
- The disorder’s complexity involves multiple genes, not single-gene causation.
- Environmental factors like lifestyle and stress significantly impact schizophrenia risk.
Source: UNC
Patrick Sullivan, MD, FRANZCP, the Yeargan Distinguished Professor of Psychiatry and Genetics at the UNC School of Medicine, and researchers at the Karolinska Institutet in Stockholm, Sweden, have developed a comprehensive outline of the genetics of schizophrenia.
The review was published in Nature Reviews Neuroscience.
Schizophrenia is a neuropsychiatric disorder featuring recurrent episodes of psychosis – such as hallucinations, delusions, and disorganized thinking – with many patients developing apathy, social withdrawal, and poor emotional control as a result.
Because schizophrenia has been known to run in families for centuries, researchers have turned to genetic testing and analyses to identify risk factors for the condition. Recent genomic research on schizophrenia has identified nearly 300 common genetic variants and over 20 rare variants as significant risk factors for the disorder.
These discoveries have emerged from extensive genome-wide association studies, whole-exome sequencing, and other analyses. Simultaneously, studies of the functional organization of the brain have shed light on the intricate cellular composition and interconnections of the brain in both neurotypical individuals and those with schizophrenia.
These findings reveal a surprising complexity in the mechanisms underlying schizophrenia, emphasizing the role of multiple genes rather than single-gene causation.
This “polygenicity” highlights a mechanism that remains challenging to fully understand due to the lack of robust theoretical frameworks and experimental tools. Sullivan and colleagues reviewed these issues and provided ideas for a path forward in the Nature Reviews Neuroscience article.
However, Sullivan and colleagues stress that environmental factors (including lifestyle, drug use, poverty, stress, and complications at birth) are also relevant in addition to genomic risk.
Although these factors are more difficult to study compared to the genome, this genetic information is important for researchers to consider because some environmental factors are modifiable.
“The findings to date resoundingly indicate complexity,” wrote Sullivan, who is also director of the UNC Center for Psychiatric Genomics and the UNC Suicide Prevention Institute.
“Rather than being a deterrent to future research, this knowledge underscores the importance of accepting schizophrenia as a genetic and environmental enigma and scaling our research accordingly in our efforts improve the lives of those impacted by schizophrenia.”
About this schizophrenia and genetics research news
Author: Kendall Daniels
Source: UNC
Contact: Kendall Daniels – UNC
Image: The image is credited to Neuroscience News
Original Research: Closed access.
“Schizophrenia genomics: genetic complexity and functional insights” by Patrick Sullivan et al. Nature Reviews Neuroscience
Abstract
Schizophrenia genomics: genetic complexity and functional insights
Determining the causes of schizophrenia has been a notoriously intractable problem, resistant to a multitude of investigative approaches over centuries.
In recent decades, genomic studies have delivered hundreds of robust findings that implicate nearly 300 common genetic variants (via genome-wide association studies) and more than 20 rare variants (via whole-exome sequencing and copy number variant studies) as risk factors for schizophrenia.
In parallel, functional genomic and neurobiological studies have provided exceptionally detailed information about the cellular composition of the brain and its interconnections in neurotypical individuals and, increasingly, in those with schizophrenia.
Taken together, these results suggest unexpected complexity in the mechanisms that drive schizophrenia, pointing to the involvement of ensembles of genes (polygenicity) rather than single-gene causation.
In this Review, we describe what we now know about the genetics of schizophrenia and consider the neurobiological implications of this information.
