MassIVE MSV000098996

Partial Public

Metabolic adaptation during cardiac exercise rehabilitation in patients after a first myocardial infarction

Description

Cardiac rehabilitation (CR) is highly beneficial in post-myocardial infarction (MI) patients; however, its metabolic impact remains underexplored. This study investigated metabolic and lipidomic adaptations to an intensive CR program in 25 non-diabetic male patients (<75 years) following a first uncomplicated ST-elevation MI (STEMI). CR involved 24 +/- 3 sessions, with baseline and final clinical assessments and, in a subgroup of 17 patients, longitudinal dried blood spots (DBS) were collected and metabolomics/lipidomics analysis was also performed. CR significantly improved clinical outcomes, including the 6-minute walk test, B-type natriuretic peptide (BNP), left ventricular ejection fraction (LVEF%), C-reactive protein (CRP), and homocysteine levels. Metabolomic analysis showed long-term positive adaptations, notably increased N-acetyl-L-tyrosine (NAT), suggesting a mitohormesis response to exercise-induced mitochondrial stress. The third training session exhibited the highest metabolic adaptation, primarily in energy metabolism pathways like the TCA cycle, indicating enhanced oxidative energy generation and improved exercise performance. The lipidome displayed an acute response to the first training, with upregulation of phosphatidylserines (PS). Predicted increased activity of PSS1, enzymes vital for PS synthesis, underscores PS's protective role in myocardial damage and its contribution to muscle activity. These findings highlight CR's beneficial metabolic adaptations, potentially via mitohormesis, and suggest modulating NAT and PS levels could enhance patient recovery and cardiac function. [doi:10.25345/C52F7K441] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: Metabolomics ; Lipidomics ; Dried blood spots ; Acute myocardial infarction ; Cardiac rehabilitation ; Physical training ; DatasetType:Metabolomics

Contact

Principal Investigators:
(in alphabetical order)
Giuseppe Paglia, University of Milano-Bicocca, Italy
Submitting User: SimoneSerrao
Number of Files:
Total Size:
Spectra:
Subscribers:
 
Owner Reanalyses
Experimental Design
    Conditions:
    Biological Replicates:
    Technical Replicates:
 
Identification Results
    Proteins (Human, Remapped):
    Proteins (Reported):
    Peptides:
    Variant Peptides:
    PSMs:
 
Quantification Results
    Differential Proteins:
    Quantified Proteins:
 
Browse Dataset Files
 
FTP Download Link (click to copy):

- Dataset Reanalyses


+ Dataset History


Click here to queue conversion of this dataset's submitted spectrum files to open formats (e.g. mzML). This process may take some time.

When complete, the converted files will be available in the "ccms_peak" subdirectory of the dataset's FTP space (accessible via the "FTP Download" link to the right).
Number of distinct conditions across all analyses (original submission and reanalyses) associated with this dataset.

Distinct condition labels are counted across all files submitted in the "Metadata" category having a "Condition" column in this dataset.

"N/A" means no results of this type were submitted.
Number of distinct biological replicates across all analyses (original submission and reanalyses) associated with this dataset.

Distinct replicate labels are counted across all files submitted in the "Metadata" category having a "BioReplicate" or "Replicate" column in this dataset.

"N/A" means no results of this type were submitted.
Number of distinct technical replicates across all analyses (original submission and reanalyses) associated with this dataset.

The technical replicate count is defined as the maximum number of times any one distinct combination of condition and biological replicate was analyzed across all files submitted in the "Metadata" category. In the case of fractionated experiments, only the first fraction is considered.

"N/A" means no results of this type were submitted.
Originally identified proteins that were automatically remapped by MassIVE to proteins in the SwissProt human reference database.

"N/A" means no results of this type were submitted.
Number of distinct protein accessions reported across all analyses (original submission and reanalyses) associated with this dataset.

"N/A" means no results of this type were submitted.
Number of distinct unmodified peptide sequences reported across all analyses (original submission and reanalyses) associated with this dataset.

"N/A" means no results of this type were submitted.
Number of distinct peptide sequences (including modified variants or peptidoforms) reported across all analyses (original submission and reanalyses) associated with this dataset.

"N/A" means no results of this type were submitted.
Total number of peptide-spectrum matches (i.e. spectrum identifications) reported across all analyses (original submission and reanalyses) associated with this dataset.

"N/A" means no results of this type were submitted.
Number of distinct proteins quantified across all analyses (original submission and reanalyses) associated with this dataset.

Distinct protein accessions are counted across all files submitted in the "Statistical Analysis of Quantified Analytes" category having a "Protein" column in this dataset.

"N/A" means no results of this type were submitted.
Number of distinct proteins found to be differentially abundant in at least one comparison across all analyses (original submission and reanalyses) associated with this dataset.

A protein is differentially abundant if its change in abundance across conditions is found to be statistically significant with an adjusted p-value <= 0.05 and lists no issues associated with statistical tests for differential abundance.

Distinct protein accessions are counted across all files submitted in the "Statistical Analysis of Quantified Analytes" category having a "Protein" column in this dataset.

"N/A" means no results of this type were submitted.
This dataset may not contain all raw spectra data as originally deposited in PRIDE. It has been imported to MassIVE for reanalysis purposes, so its spectra data here may consist solely of processed peak lists suitable for reanalysis with most software.