Summary of Study ST003110

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 PR001932. The data can be accessed directly via it's Project DOI: 10.21228/M80B0B 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 IDST003110
Study TitleInfluence of Lifestyle Factors on Epigenetic and Proteomic Biomarkers: A Cross-Sectional Comparison
Study TypeCross-sectional Study
Study SummaryThis cross-sectional study investigated differences in the plasma metabolome in two groups of adults that were of similar age but varied markedly in body composition and dietary and physical activity patterns. Study participants included 52 adults in the lifestyle group (LIFE) (28 males, 24 females) and 52 in the control group (CON) (27 males, 25 females). The results using an extensive untargeted UPLC-HRMS analysis with 10,535 metabolite peaks identified 83 metabolites and 16 metabolic pathways that differentiated LIFE and CON groups. A novel metabolite signature of positive lifestyle habits emerged from this analysis highlighted by lower plasma levels of numerous bile acids, an amino acid profile characterized by higher histidine and lower glutamic acid, glutamine, β-alanine, phenylalanine, tyrosine, and proline, an elevated vitamin D status, higher levels of beneficial fatty acids and gut microbiome catabolism metabolites from plant substrates, and reduced levels of N-glycan degradation metabolites and environmental contaminants. This study established that the plasma metabolome is strongly associated with body composition and lifestyle habits. The robust lifestyle metabolite signature identified in this study is consistent with an improved life expectancy and a reduced risk for chronic disease.
Institute
Appalachian State University
DepartmentDepartment of Biology
LaboratoryHuman Performance Laboratory
Last NameNieman
First NameDavid
AddressNorth Carolina Research Campus, 600 Laureate Way, Kannapolis, NC 28081
Emailniemandc@appstate.edu
Phone(828) 773-0056
Submit Date2024-02-16
Total Subjects104
Raw Data AvailableYes
Raw Data File Type(s)mzML, raw(Thermo)
Analysis Type DetailLC-MS
Release Date2025-02-28
Release Version1
David Nieman David Nieman
https://dx.doi.org/10.21228/M80B0B
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Project:

Project ID:PR001932
Project DOI:doi: 10.21228/M80B0B
Project Title:Untargeted Metabolomics Reveals Signatures of a Healthy Lifestyle
Project Type:C18 Reversed-Phase Broad Spectrum Metabolomics
Project Summary:This cross-sectional study investigated differences in the plasma metabolome in two groups of adults that were of similar age but varied markedly in body composition and dietary and physical activity patterns. Study participants included 52 adults in the lifestyle group (LIFE) (28 males, 24 females) and 52 in the control group (CON) (27 males, 25 females). The results using an extensive untargeted UPLC-HRMS analysis with 10,535 metabolite peaks identified 83 metabolites and 16 metabolic pathways that differentiated LIFE and CON groups. A novel metabolite signature of positive lifestyle habits emerged from this analysis highlighted by lower plasma levels of numerous bile acids, an amino acid profile characterized by higher histidine and lower glutamic acid, glutamine, β-alanine, phenylalanine, tyrosine, and proline, an elevated vitamin D status, higher levels of beneficial fatty acids and gut microbiome catabolism metabolites from plant substrates, and reduced levels of N-glycan degradation metabolites and environmental contaminants. This study established that the plasma metabolome is strongly associated with body composition and lifestyle habits. The robust lifestyle metabolite signature identified in this study is consistent with an improved life expectancy and a reduced risk for chronic disease.
Institute:Metabolomics and Exposome Laboratory at UNC Nutrition Research Institute
Department:Untargeted Analysis
Laboratory:Sumner Lab
Last Name:Rushing
First Name:Blake
Address:Nutrition Research Institute , University of North Carolina at Chapel Hill, 500 Laureate Way Kannapolis, NC 28081
Email:blake_rushing@unc.edu
Phone:(704) 250-5000

Subject:

Subject ID:SU003225
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606
Gender:Male and female
Species Group:Mammals

Factors:

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

mb_sample_id local_sample_id Sample source Phenotype Sample type
SA337144S_60Blood Control Study sample
SA337145S_58Blood Control Study sample
SA337146S_56Blood Control Study sample
SA337147S_63Blood Control Study sample
SA337148S_69Blood Control Study sample
SA337149S_76Blood Control Study sample
SA337150S_73Blood Control Study sample
SA337151S_54Blood Control Study sample
SA337152S_65Blood Control Study sample
SA337153S_52Blood Control Study sample
SA337154S_40Blood Control Study sample
SA337155S_37Blood Control Study sample
SA337156S_35Blood Control Study sample
SA337157S_43Blood Control Study sample
SA337158S_47Blood Control Study sample
SA337159S_50Blood Control Study sample
SA337160S_49Blood Control Study sample
SA337161S_77Blood Control Study sample
SA337162S_79Blood Control Study sample
SA337163S_97Blood Control Study sample
SA337164S_94Blood Control Study sample
SA337165S_93Blood Control Study sample
SA337166S_100Blood Control Study sample
SA337167S_101Blood Control Study sample
SA337168S_108Blood Control Study sample
SA337169S_107Blood Control Study sample
SA337170S_102Blood Control Study sample
SA337171S_90Blood Control Study sample
SA337172S_89Blood Control Study sample
SA337173S_81Blood Control Study sample
SA337174S_80Blood Control Study sample
SA337175S_33Blood Control Study sample
SA337176S_82Blood Control Study sample
SA337177S_84Blood Control Study sample
SA337178S_87Blood Control Study sample
SA337179S_86Blood Control Study sample
SA337180S_78Blood Control Study sample
SA337181S_64Blood Control Study sample
SA337182S_32Blood Control Study sample
SA337183S_22Blood Control Study sample
SA337184S_2Blood Control Study sample
SA337185S_1Blood Control Study sample
SA337186S_19Blood Control Study sample
SA337187S_18Blood Control Study sample
SA337188S_15Blood Control Study sample
SA337189S_11Blood Control Study sample
SA337190S_17Blood Control Study sample
SA337191S_10Blood Control Study sample
SA337192S_27Blood Control Study sample
SA337193S_3Blood Control Study sample
SA337194S_30Blood Control Study sample
SA337195S_28Blood Control Study sample
SA337196S_106Blood Life Study sample
SA337197S_8Blood Life Study sample
SA337198S_105Blood Life Study sample
SA337199S_109Blood Life Study sample
SA337200S_9Blood Life Study sample
SA337201S_12Blood Life Study sample
SA337202S_74Blood Life Study sample
SA337203S_75Blood Life Study sample
SA337204S_110Blood Life Study sample
SA337205S_13Blood Life Study sample
SA337206S_104Blood Life Study sample
SA337207S_7Blood Life Study sample
SA337208S_88Blood Life Study sample
SA337209S_98Blood Life Study sample
SA337210S_91Blood Life Study sample
SA337211S_95Blood Life Study sample
SA337212S_14Blood Life Study sample
SA337213S_5Blood Life Study sample
SA337214S_103Blood Life Study sample
SA337215S_99Blood Life Study sample
SA337216S_6Blood Life Study sample
SA337217S_85Blood Life Study sample
SA337218S_92Blood Life Study sample
SA337219S_83Blood Life Study sample
SA337220S_44Blood Life Study sample
SA337221S_42Blood Life Study sample
SA337222S_46Blood Life Study sample
SA337223S_48Blood Life Study sample
SA337224S_25Blood Life Study sample
SA337225S_26Blood Life Study sample
SA337226S_41Blood Life Study sample
SA337227S_72Blood Life Study sample
SA337228S_31Blood Life Study sample
SA337229S_34Blood Life Study sample
SA337230S_36Blood Life Study sample
SA337231S_38Blood Life Study sample
SA337232S_39Blood Life Study sample
SA337233S_51Blood Life Study sample
SA337234S_29Blood Life Study sample
SA337235S_61Blood Life Study sample
SA337236S_70Blood Life Study sample
SA337237S_62Blood Life Study sample
SA337238S_68Blood Life Study sample
SA337239S_67Blood Life Study sample
SA337240S_66Blood Life Study sample
SA337241S_59Blood Life Study sample
SA337242S_23Blood Life Study sample
SA337243S_53Blood Life Study sample
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Collection:

Collection ID:CO003218
Collection Summary:N/A
Sample Type:Blood (plasma)
Storage Conditions:-80℃

Treatment:

Treatment ID:TR003234
Treatment Summary:N/A

Sample Preparation:

Sampleprep ID:SP003231
Sampleprep Summary:Study samples were shipped from Human Performance Laboratory (Nieman Laboratory) at Appalachan State University to the UNC NRI Metabolomics and Exposome Laboratory (MEL) on dry ice. The MEL thawed and transferred 50 µL of the study samples to a new set of tubes and used them for the analysis. An additional 10 µL was taken from the original study sample and transferred to another tube to make the total study pool for this project, and then distributed with 50 µL per aliquot, used as quality control study pools (QCSP) throughout the whole analysis. All sample aliquots (50 µL each) and QC study pools (50 µL each) were stored at -80° C until the day of sample preparation. NIST plasma (SRM 1950) reference material (50 µL each) were provided by the MEL. LC-MS grade water (50 µL) was used as blanks. All samples were thawed at 4°C overnight before the preparation. Samples, including study samples, QCSP samples, NIST reference plasma, and blanks were mixed with 400 µL methanol containing 500 ng/mL tryptophan-d5 as internal standard and vortexed by a multiple tube vortex mixer for 2 min at 5000 rpm at room temperature. All samples were centrifuged at 16,000 rcf for 10 min at 4°C. The supernatant (350 µL) was transferred into a pre-labeled 2.0 mL Lo-bind Eppendorf tube, dried by a SpeedVac overnight, and stored at -80° C. For immediate analysis, 100 µL of water-methanol solution (95:5, v/v) was used to reconstitute the dried extracts. Samples were thoroughly mixed on a multiple tube vortex mixer for 10 min at 5000 rpm at room temperature and then centrifuged at 4°C for 10 min at 16,000 rcf. The supernatant was transferred to pre-labeled autosampler vials for data acquisition by LC-MS.
Processing Storage Conditions:4℃
Extraction Method:Vortex with methanol containing 500ng/ml tryptophan-d5 as internal standard
Extract Storage:-80℃
Sample Resuspension:Water-Methanol (95:5, v/v)
Sample Spiking:Tryptophan-d5 stock solution at 500 ng/mL

Chromatography:

Chromatography ID:CH003849
Chromatography Summary:Reversed phase
Instrument Name:Thermo Vanquish
Column Name:Waters ACQUITY UPLC HSS T3 (100 x 2.1mm,1.8um)
Column Pressure:6000-10000 psi
Column Temperature:50 ℃
Flow Gradient:Time(min) Flow Rate %A %B Curve 1. 0 0.4 99.0 1.0 5 2. 1.00 0.4 99.0 1.0 5 3. 16.00 0.4 1.0 99.0 5 4. 19.00 0.4 1.0 99.0 5 5. 19.50 0.4 99.0 1.0 5 6. 22.00 0.4 99.0 1.0 5
Flow Rate:0.4 mL/min
Injection Temperature:8 ℃
Internal Standard:Tryptophan-d5
Solvent A:100% water; 0.1% formic acid
Solvent B:100% methanol; 0.1% formic acid
Analytical Time:22 min
Weak Wash Solvent Name:10% methanol/90% water; 0.1% formic acid
Strong Wash Solvent Name:75% 2-Propanol/25% Water; 0.1% formic acid
Chromatography Type:Reversed phase

Analysis:

Analysis ID:AN005093
Analysis Type:MS
Acquisition Date:11/09/2211/11/2022
Software Version:Xcalibur 4.1.31.9
Detector Type:Orbitrap
Data Format:Profile
Chromatography ID:CH003849
Has Mz:1
Has Rt:1
Rt Units:Minutes
Results File:ST003110_AN005093_Results.txt
Units:Normalized Intensity
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