Summary of Study ST002736

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 PR001700. The data can be accessed directly via it's Project DOI: 10.21228/M8ZM7F 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 IDST002736
Study TitleAssessing mitochondrial bioenergetics in coronary artery disease: A translational multiomic tissue study in humans (The AMBITION study).
Study SummaryBackground: Severe or recurrent myocardial ischemia can lead to chronic left ventricular (LV) dysfunction and heart failure in patients with coronary artery disease (CAD). Objectives: To assess the multiomic profile of LV myocardium in patients with stable CAD. Methods: Patients undergoing coronary artery bypass grafting (CABG) had preoperative quantitative stress perfusion cardiovascular magnetic resonance. During surgery, paired transmural LV biopsies were acquired on the beating heart from a region of inducible ischemia, and a remote LV segment. LV samples from human organ donors were used as controls. Myocardial biopsies underwent high-energy phosphate quantification, liquid chromatography-mass spectrometry and single-nuclei ribonucleic acid sequencing. Results: From 33 patients, 63 LV biopsies were acquired on the beating heart during CABG (mean age 60±9 years, median LV ejection fraction 67% [IQR: 61-71%]). Analysis of LV samples from 11 essentially healthy donor hearts were included. The global myocardial ATP/ADP ratio was reduced in CAD patients as compared to donor LV tissue (median [IQR]: 2.2 [1.5-2.8] versus 7.4 [6.8-8.6], P=0.001), with increased expression of oxidative phosphorylation (OXPHOS) genes encoding the electron transport chain complexes across multiple cell types. Paired analyses of biopsies obtained during CABG from LV segments with or without inducible ischemia revealed no significant difference in the ATP/ADP ratio (P=0.36), broader metabolic profile or expression of ventricular cardiomyocyte genes implicated in OXPHOS. Conclusions: Our results suggest that viable human myocardium in patients with stable CAD has global alterations in bioenergetic and transcriptional profile without large regional differences between areas with or without inducible ischemia.
Institute
Imperial College London
Last NameJones
First NameRichard Elis
AddressRoyal Brompton Hospital
Emailrichard.jones34@nhs.net
Phone02073528121
Submit Date2023-05-29
Raw Data AvailableYes
Raw Data File Type(s)raw(Thermo)
Analysis Type DetailLC-MS
Release Date2023-07-06
Release Version1
Richard Elis Jones Richard Elis Jones
https://dx.doi.org/10.21228/M8ZM7F
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Factors:

Subject type: Human; Subject species: Homo sapiens (Factor headings shown in green)

mb_sample_id local_sample_id Treatment
SA288685RJ_3CC1Ischemic
SA288686RJ_4DD1Ischemic
SA288687RJ_10JJ1Ischemic
SA288688RJ_2BB1Ischemic
SA288689RJ_29CF2Ischemic
SA288690RJ_21DF1Ischemic
SA288691RJ_22EG1Ischemic
SA288692RJ_28BE1Ischemic
SA288693RJ_8HH1Ischemic
SA288694RJ_24IK2Ischemic
SA288695RJ_26KM1Ischemic
SA288696RJ_25JL1Ischemic
SA288697RJ_23FH1Ischemic
SA288698RJ_9II1Ischemic
SA288699RJ_30DG1Ischemic
SA288700RJ_27AD1Ischemic
SA288701RJ_6KK1Ischemic
SA288702RJ_20CE1Ischemic
SA288703RJ_16IJ1Ischemic
SA288704RJ_32FI1Ischemic
SA288705RJ_15GH1Ischemic
SA288706RJ_33GJ1Ischemic
SA288707RJ_14EF1Ischemic
SA288708RJ_13CD1Ischemic
SA288709RJ_34HK1Ischemic
SA288710RJ_17KL1Ischemic
SA288711RJ_19BD1Ischemic
SA288712RJ_11LL1Ischemic
SA288713RJ_18AC1Ischemic
SA288714RJ_12AB1Ischemic
SA288715RJ_31EH1Ischemic
SA288716RJ_26PN2Remote
SA288717RJ_33TQ1Remote
SA288718RJ_34SP1Remote
SA288719RJ_32UR1Remote
SA288720RJ_29XU1Remote
SA288721RJ_25SQ1Remote
SA288722RJ_31VS1Remote
SA288723RJ_28YV1Remote
SA288724RJ_30WT1Remote
SA288725RJ_27ZW1Remote
SA288726RJ_4WW1Remote
SA288727RJ_15TS1Remote
SA288728RJ_16RQ1Remote
SA288729RJ_17PO1Remote
SA288730RJ_14VU1Remote
SA288731RJ_13XW1Remote
SA288732RJ_10QQ1Remote
SA288733RJ_11OO1Remote
SA288734RJ_12ZY1Remote
SA288735RJ_18ZX1Remote
SA288736RJ_19YW1Remote
SA288737RJ_6PP1Remote
SA288738RJ_8SS1Remote
SA288739RJ_9RR1Remote
SA288740RJ_5VV1Remote
SA288741RJ_2YY1Remote
SA288742RJ_20XV1Remote
SA288743RJ_21WU1Remote
SA288744RJ_22VT1Remote
SA288745RJ_24TR2Remote
Showing results 1 to 61 of 61
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