Project Details
Description
Project Summary/Abstract
Human gut microbiota, with its massive catalytical capacity and functional potential, may act as an “endocrine
organ” and significantly contribute to metabolic health. Indeed, basic microbiological research and culture-
based human studies have elucidated multiple pathways through which human gut microbiota may modulate
the risk of developing metabolic diseases, such as type 2 diabetes (T2D). Existing human studies also
demonstrated promising evidence supporting a link between microbiome and prevalent diabetes, although few
longitudinal studies have been conducted to establish a prospective relationship between microbiome and the
risk of developing T2D. This proposal represents major research efforts to significantly accelerate the
advances in the research of microbiome and T2D risk by examining prospective relationships between gut
microbial composition, functional potential, and fecal metabolome that operate in candidate pathways and T2D
risk. We will also use network analysis and other advanced methods to interrogate the overall metagenomic,
metatranscriptomic, and metabolomic profiles in fecal samples for the identification of novel microbial features
(i.e., microbes, their functional potential, gene transcription levels, and microbiota metabolites) and pathways
that might be involved in the development of T2D. As a secondary aim, we will evaluate the interplay between
diet and microbiome on fecal metabolome and T2D risk. Furthermore, these complementary, inter-connected
study aims will be realized by an experienced investigator team consisting of researchers with expertise in
microbiome, metabolomics, biomarker research, diabetes epidemiology, biostatistics, and bioinformatics. To
facilitate better generalizability and internal validity of research findings, we will examine these novel
associations in two US cohorts with complementary ethnic and socioeconomic profiles: Nurses’ Health Study II
and Hispanic Community Health Study / Study of Latinos. Rich resources of these two cohorts, including fecal
samples, repeated assessments of diet, lifestyle, medical history, and use of medications, longitudinal follow-
up on diabetes status, and infrastructure for sample preparation/storage and computing, will empower the
investigators to accomplish the proposed aims cost-effectively. To strengthen between-institution collaboration
and ensure a successful implementation of the proposed research, Drs. Qi Sun (at Harvard T.H. Chan School
of Public Health) and Qibin Qi (at Albert Einstein College of Medicine) will share the responsibility of
overseeing the overall conduct of research through the Multiple PI mechanism. In summary, this project will
elucidate prospective associations of gut microbiome and fecal metabolome with T2D risk and facilitate
discoveries of novel microbial features relevant to T2D risk. As such, the proposed research has a great
potential to identify novel microbiota-related risk or beneficial factors for developing more targeted and
individualized strategies for the prevention and management of diabetes.
Status | Active |
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Effective start/end date | 1/19/21 → 12/31/23 |
Funding
- National Institute of Diabetes and Digestive and Kidney Diseases: $669,600.00
- National Institute of Diabetes and Digestive and Kidney Diseases: $547,270.00
- National Institute of Diabetes and Digestive and Kidney Diseases: $547,270.00
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