Awardee OrganizationBETH ISRAEL DEACONESS MEDICAL CENTER
Description
Abstract Text
Project Summary
Thyroid hormone (TH) is a critical regulator of metabolism and body weight in humans. Indeed,
TH has been shown to regulate energy expenditure, lipid levels and insulin sensitivity to
improve metabolic outcome. Because of these beneficial effects, TH or one of its analogs are
potential therapeutics for a wide variety of metabolic disease. However, if excessively dosed
TH has significant side effects especially on the heart and bone. Remarkably, TH action in
humans is determined almost exclusively by the use of the thyrotropin (TSH) assay which
depends only upon TH action at the level of the hypothalamus and pituitary. Thus, there is a
critical need for improved biomarkers that would allow for tailoring of TH therapy to improve
metabolic health and allow for enhanced safety. To begin to accomplish this we have used
metabolomic profiling and mouse genetic models to began to characterize TH sensitive
pathways in vivo. Our preliminary work has identified unique metabolites that are regulated by
TH that serve both as biomarkers and also as mediators of thyroid hormone action. In this
proposal in the first aim we will extend our analysis of the regulation of metabolite profiles by
TH in a tissue-specific and TH receptor specific fashion and extend our analysis into humans
for the first time. In the second Aim we will determine the mechanism by which TH regulates
methionine metabolism which is likely critical to TH ability to control gene expression and
regulate programs such as fatty acid oxidation. In the third Aim we will use novel genetic
mouse models to determine how TH controls cholesterol metabolism gaining further insight
into a key pathway regulated by TH. Together, completion of these Aims will provide for a new
platform for both understanding and defining TH action in vivo.
Public Health Relevance Statement
Narrative
Thyroid hormone is major regulator of body weight and metabolic status in humans. Despite its
prominent role in normal human function and in replacement therapy our ability to determine its
beneficial effects are limited as our diagnostic tests have remained similar for 50 years. The
goal of this application is to use novel biochemical and genetic platforms to better understand
thyroid hormones beneficial effects on metabolism in order to better tailor replacement therapy
in patients and to aid in the development of novel therapies for metabolic disease.
National Institute of Diabetes and Digestive and Kidney Diseases
CFDA Code
847
DUNS Number
071723621
UEI
C1CPANL3EWK4
Project Start Date
16-September-2013
Project End Date
31-July-2018
Budget Start Date
16-September-2013
Budget End Date
31-July-2014
Project Funding Information for 2013
Total Funding
$533,374
Direct Costs
$368,674
Indirect Costs
$164,700
Year
Funding IC
FY Total Cost by IC
2013
National Institute of Diabetes and Digestive and Kidney Diseases
$533,374
Year
Funding IC
FY Total Cost by IC
Sub Projects
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