Genome Environment Microbiome and Metabolome in Autism Study
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- STATUS
- Recruiting
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- End date
- Dec 29, 2025
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- participants needed
- 600
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- sponsor
- Massachusetts General Hospital
Summary
GEMMA is a multicenter longitudinal observational study that follows children who are
genetically at-risk of developing
Description
The GEMMA study will address genomic, environmental, microbiome, and metabolomic factors that
may affect the development of
Genome: The project will study children who have a first-degree relative (sibling) with ASD so that investigators can understand how their genes may contribute to whether they develop ASD or not. A number of genetic variants identified to date occur in genes encoding glycosylated extracellular proteins and in enzymes directly involved in glycosylation. Investigators will perform whole genome sequencing in the subgroup of children that will develop ASD in order to learn more about these specific genes and also to identify other genes that may be involved in ASD pathogenesis. The genetic variant landscape will be mapped and variants will be annotated and interpreted based on all contextual information available. This effort will enable the identification of patient- and cohort-specific variations that can then be further refined into biomarker signatures and optimized into predictive and diagnostic markers of ASD.
Environment: When infants enroll in the study, investigators will record information about
their environment including whether they were born vaginally or by
Microbiome: The human gut, compromised of the small and large intestine, is home to many
types of bacteria. These bacteria help to break down and digest food, provide the body with
energy, and make
Metabolome: The processes that occur in the gut, such as the digestion of foods and
production of
Details
Condition | Pervasive developmental disorder |
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Age | 1years or below |
Clinical Study Identifier | NCT04271774 |
Sponsor | Massachusetts General Hospital |
Last Modified on | 19 February 2024 |
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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