Interactions between genetics and the environment can explain variability seen in common neuropsychiatric disorders
While some diseases and disorders can be easily attributed to specific genetic mutations, for many diseases — especially neuropsychiatric ones — the causes are much more complicated, influenced by both genetic and environmental factors. A new study at the University of Chicago examined data from over 400,000 individuals to better understand how those two factors play into the variations seen in a number of neuropsychiatric disorders, with the hope of eventually identifying ways that individuals who are at risk can modify their environments to protect their mental health. The research was published on September 6 in Cell Reports Medicine.
“We’ve known for a long time that environmental factors have a great impact on neuropsychiatric diseases, so we wanted to look at how environmental factors interact with genetic ones,” said Hanxin Zhang, PhD, first author on the study and a research assistant at UChicago. “Our lab has access to the data for millions of people and their family relationships, which helps us to model shared genetic factors between family members, as well as shared environmental factors.”
The researchers used a database with health information from over 100,000 U.S. families to model those genetic factors, and linked it together with environmental data from the EPA through the ZIP codes and counties that the individuals and families had lived in.
According to their models, gene-environment interactions account for only a small portion of the variations seen in the rates of some psychiatric disorders, such as depression and substance abuse. Other disorders, however, showed that gene-environment interactions accounted for a much larger proportion, including attention-deficit/hyperactivity disorder (ADHD), anxiety/phobic disorders, recurrent headaches, sleep disorders and post-traumatic stress disorder (PTSD).
These results demonstrate the importance of considering not just an individual’s genetic background, but also their environmental exposure history.
“Genetics is viewed by many people as something like a verdict — you can’t change it,” said Andrey Rzhetsky, PhD, Edna K. Papazian Professor of Medicine and Human Genetics and senior author on the study. “Finding these gene-environment interactions give us hope that we can find some genetic variance that interactions with the environment so that, ideally, you could change your environment and escape the disease.”
For example, if a patient were to have a gene that put them at increased risk of migraines when exposed to hot climates, a physician might suggest they ensure that they have air conditioning in their home and avoid the head.
These kinds of studies are typically challenged by a lack of sufficient data, particularly when it comes to environmental data. “Environment is not well defined,” said Atif Khan, PhD, a staff scientist at UChicago. “And it’s massive. You could potentially measure billions of different environmental details to determine what’s important.”
The researchers also pointed out that environment can include more than simply the molecules measured by the EPA in the air, water and soil. “In this study, we’re looking specifically at living environments and environmental exposures, but an individual’s personal experience is also a kind of exposure,” said Zhang. “Especially when you are considering psychiatric diseases. For example, understanding the interactions children have in school would be very important, but it’s very, very difficult to collect this data on a large scale.”
In future research, the team hopes to examine some of these interactions more directly. “In this study, we just modeled a general interaction between genes and environment,” said Zhang. “Next, we could see if we can identify specific pairs of genes and environmental factors that play a role in the development of disease.”
Long term, and with enough data, the researchers believe they could even develop lifestyle plans based on an individual’s genetic makeup. “If we were able to identify a catalog of genetic variants interacting with specific environmental stimulation, we could design personalized environmental plans for patients at risk,” said Rzhetsky.
The study, “Gene-Environment Interactions Explain a Substantial Portion of Variability of Common Neuropsychiatric Disorders,” was supported by the DARPA Big Mechanism program under ARO contract W911NF1410333, by National Institutes of Health grants R01HL122712, 1P50MH094267, and U01HL108634-01, and by a gift from Liz and Kent Dauten.
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The University of Chicago Medicine, with a history dating back to 1927, is one of the nation’s leading academic health systems. It unites the missions of the University of Chicago Medical Center, Pritzker School of Medicine and the Biological Sciences Division. Twelve Nobel Prize winners in physiology or medicine have been affiliated with the University of Chicago Medicine. Its main Hyde Park campus is home to the Center for Care and Discovery, Bernard Mitchell Hospital, Comer Children’s Hospital and the Duchossois Center for Advanced Medicine. It also has ambulatory facilities in Orland Park, South Loop, Homewood and River East as well as affiliations and partnerships that create a regional network of care. UChicago Medicine offers a full range of specialty-care services for adults and children through more than 40 institutes and centers including an NCI-designated Comprehensive Cancer Center. Together with Harvey-based Ingalls Memorial, UChicago Medicine has 1,296 licensed beds, nearly 1,300 attending physicians, over 2,800 nurses and about 970 residents and fellows.
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JOURNAL
Cell Reports Medicine
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