Official Title
Personalized Environment and Genes Study
Brief Title
Personalized Environment and Genes Study
Protocol ID
NCT00341237
Lead Sponsor
National Institute of Environmental Health Sciences (NIEHS)
Brief Summary
Despite the overwhelming focus on genetic and genomic causes of human disease over the
past two decades, it has been estimated that genetics is currently known to explain only
20% and 40% of the etiology of common disease. Thus, it is becoming increasingly apparent
that human disease is a consequence of both genetic susceptibility and environmental
exposures. Importantly, while individuals cannot change their genetic composition, we do
have the ability both personally and as a society, to influence our environment,
promoting health and decreasing the risk of disease. The Personalized Environment and
Genes Study (PEGS) aims to determine how the environment and gene-environment
interactions can inform our understanding of human health and disease. As science has
evolved, so too has the science of this project. This evolution was reflected in a change
in the title of this project from the Environmental Polymorphisms Registry (EPR) to the
Personalized Environment and Genes Study (PEGS) to more accurately reflect the science
that can be conducted. PEGS is a unique resource because of the depth of environmental
phenotyping which includes extensive information from exposome surveys, as well as whole
genome sequencing on a significant number of participants in the cohort. While it is
small relative to genomic cohorts, none of these have the extensive environmental data
that is present in PEGS. In addition, other cohorts with deep environmental data lack the
depth of genomic data that is present in PEGS. Importantly, PEGS has already provided
important analytic advances that are of great interest to and can be confirmed in larger
cohorts such as All of Us.
The Personalized Environment and Genes Study (PEGS) aims to provide a resource for
environmental health translational research by examining gene-environment interactions in
health and disease. PEGS is an extension of two previous efforts where it began as a
pilot study, the Environmental Polymorphisms Study (EPS; IRB# 02E9004) and was approved
subsequently as a full protocol titled the Environmental Polymorphisms Registry (EPR)
(IRB #04-E-N0053 and transitioned to its current ID# 04-E-0053). The EPR was envisioned
as a phenotype-by-genotype registry of participants who had donated DNA samples, and who
had agreed to be contacted for follow-up clinical translational studies based on their
DNA genotypes. At the time, the only information available was a participant s age, sex,
race, and ethnicity. Further phenotyping of a participant and/or any biospecimens
obtained were investigated during a follow-up translational clinical study on
participants recruited based on their genotype (hence phenotype-by-genotype) and the PEGS
was the first recruit-by- genotype study at the NIH. Following a period focused on
recruiting approximately 15,000 participants to enable genotyping of rare (approximately
1% minor allele frequency) single nucleotide polymorphisms (SNPs), the PEGS Consortium
Project was undertaken in 2010- 2011 to examine, using the DNA of nearly 4,000
participants, approximately 700 SNPs in approximately 80 environmental response genes
that work in concert with environmental exposures to elicit a phenotype. Several clinical
follow-up studies, genotype-phenotype association studies, and publications have resulted
from the PEGS Consortium Project.
To expand phenotype information available to researchers, the Health and Exposure
Questionnaire was administered between 2013-2014. In 2017, a more detailed Exposome
Questionnaire which includes questions relating to the external and internal exposome was
administered. This was an important resource through which to integrate exposures with
genotype-phenotype association studies.
Whole genome sequencing has now been performed on approximately 4700 participants who
were reconsented for this purpose, as indicated above. Questionnaire data was fully
adjudicated and combined in a robust and searchable database. With the increased power of
the data available, the project was renamed as the Personalized Environment and Genes
Study (PEGS) and rolled out in Sept. 2021.
...
Detailed Description
Study Description: The Personalized Environment and Genes Study (PEGS) integrates genetic
and environmental data to understand disease etiology, identify disease risk factors, and
improve disease prevention.
Objectives: The objective of PEGS is to provide a resource for environmental health
translational research by examining environment and gene-environment interactions in
health and disease. PEGS will incorporate exposure and health information with or without
genomic information to address the following objectives.
- Primary Objective: To uncover novel environmental risk factors for the most
prevalent health conditions and diseases.
- Secondary Objective: To use an environmental precision medicine framework to uncover
genetic susceptibilities to specific environmental exposures that can ultimately be
used to provide a fuller understanding of individual risks for diseases.
Endpoints:
Primary Endpoints:
1. Dichotomous phenotype (multiple analyses; each analysis is focused on a single
dichotomous phenotype of clinical interest,
or a group of mechanistically related dichotomous phenotypes) Example: asthma;
2. Continuous phenotype (multiple analyses; each analysis is focused on a clinically
relevant continuous phenotype). Example: FEV1, an indicator of asthma severity.
Secondary Endpoints:
1. Phenome (simultaneous assessment of all clinically relevant phenotypes);
2. Exposome.
Study Period
Enrollment Count
25,000 participants
Eligibility Criteria
- INCLUSION CRITERIA
In order to be eligible for participation in this study, an individual must meet all of
the following criteria:
- Adults greater than or equal to 18 years of age
- If female, must not be (self-reported as) pregnant. At the time of enrollment, a
pregnancy test will only be done at the PI s discretion.
- Able to understand and provide written informed consent
- Able to come to the NIEHS Clinical Research Unit (CRU) for enrollment and
study-related visits/procedures.
EXCLUSION CRITERIA
An individual who does not meet the inclusion criteria listed above is excluded from
participation in this study.
Filters
Diabetes
Heart Disease
Asthma
RECRUITING
ADULT
OLDER_ADULT