Summary of Study ST000464

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR000356. The data can be accessed directly via it's Project DOI: 10.21228/M81K5Z This work is supported by NIH grant, U2C- DK119886.

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Study IDST000464
Study TitleTranspulmonary metabolomics in pulmonary arterial hypertension
Study SummaryWe hypothesize that transpulmonary metabolomic profiling will demonstrate a PAH-specific metabolic signature. We will examine organ-specific metabolism by measuring blood flowing into (pulmonary artery) and out of (pulmonary artery wedge) the pulmonary circulation at the time of right heart catheterization (RHC). We will compare PAH to patients without PH and to a disease control cohort with PH due to left heart disease (pulmonary ventrical hypertension - PVH).
Institute
University of North Carolina
LaboratorySumner Lab
Last NameSumner
First NameSusan
AddressEastern Regional Comprehensive Metabolomics Resource Core, UNC Nutrition Research Institute, 500 Laureate Way, Kannapolis, NC, 28081
Emailsusan_sumner @unc.edu
Phone704-250-5066
Submit Date2016-09-07
Raw Data AvailableYes
Raw Data File Type(s)1r
Analysis Type DetailNMR
Release Date2018-10-10
Release Version1
Susan Sumner Susan Sumner
https://dx.doi.org/10.21228/M81K5Z
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR000356
Project DOI:doi: 10.21228/M81K5Z
Project Title:Transpulmonary metabolomics in pulmonary arterial hypertension
Project Summary:Pulmonary arterial hypertension (PAH) is a progressive and incurable disease characterized by obliteration of the pulmonary arterioles, elevated pulmonary vascular resistance (PVR), and eventual right heart failure and death. Current medical therapy for PAH is aimed at reducing PVR by targeting pathways involved in vasodilation. Pulmonary vasodilators improve functional capacity but do not target the underlying vascular obstruction. Despite multiple approved therapies, median survival after diagnosis is less than five years, indicating that additional therapeutic targets are needed.
Institute:Vanderbilt University
Last Name:Brittain
First Name:Evan
Address:2525 West End Ave, Suite 300, Nashville TN 37203
Email:evan.brittain@Vanderbilt.Edu
Phone:(615) 322-2318
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