Summary of Study ST003104

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 PR001927. The data can be accessed directly via it's Project DOI: 10.21228/M8N42X This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST003104
Study TitleMetabolomics studies on human cardiac samples
Study SummaryTargeted metabolomics was performed to measure polar metabolites in both positive and negative ionization mode on left ventricular tissue acquired from pre-mortem healthy donor hearts as classified by formal pathological examination and stored at the Sydney Heart Bank. The minimum number of observations for young (age ≤ 25 years) and old (age ≥ 50 years) cohorts using liquid chromatography-tandem mass spectrometry (LC-MS/MS).
Institute
University of Sydney
DepartmentMedicine and Health
Last NameKoay
First NameYen Chin
AddressCharles Perkin Centre
Emailyen.koay@sydney.edu.au
Phone+61486275851
Submit Date2023-09-10
Num Groups2
Total Subjects25
Num Males15
Num Females10
Raw Data AvailableYes
Raw Data File Type(s)mzML
Analysis Type DetailAPI
Release Date2024-03-11
Release Version1
Yen Chin Koay Yen Chin Koay
https://dx.doi.org/10.21228/M8N42X
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR001927
Project DOI:doi: 10.21228/M8N42X
Project Title:The Human Cardiac “Age-OME”: Age-specific changes in myocardial molecular expression
Project Type:MS analysis
Project Summary:A substantial proportion of the World’s population is ageing. One of the most significant risk factors for heart disease is ageing. However, we do not understand how the human heart changes with age. Taking advantage of a unique set of pre-mortem, cryopreserved, non-diseased human hearts, we performed multi-omic analyses (transcriptomics, proteomics, metabolomics and lipidomics), coupled with biological computational modelling in younger (<25 years old) and older hearts (>50years old) to describe the molecular landscape of human cardiac ageing. In older hearts, we observed a downregulation of proteins involved in calcium signalling and of the contractile apparatus itself. In addition, we found a potential counteractive upregulation of central carbon generation of fuel, upregulation of glycolysis and increases in long-chain fatty acids. This is the first molecular data set of normal human cardiac ageing, which may have important implications for the development of age-related heart disease.
Institute:University of Sydney
Department:School of Medical Sciences
Laboratory:Cardiometabolic Medicine
Last Name:Koay
First Name:Yen Chin
Address:The Hub, Charles Perkins Centre, D17, The University of Sydney, NSW, 2006
Email:yen.koay@sydney.edu.au
Phone:+61486275851
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