Summary of Study ST002704

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 PR001675. The data can be accessed directly via it's Project DOI: 10.21228/M8671J 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 IDST002704
Study TitleThe ECHO Cohort Exposome: First Steps using HHEAR Analysis – An Opportunity for ALL ECHO Cohorts to Contribute Type A Samples – Untargeted Analysis (UCP Cohort)
Study TypeProspective Cohort Study
Study SummaryThe Utah Children's Project is a prospetive cohort study of children and parents recruited from population-based and community-based samples. The purpose of the study is to study the influence of genetics and environment on child health and development. Eligibility required prior participation in a preconception or prenatal cohort study based at the University of Utah and/or Utah State University, with data and biospecimens available to carry forward into the Utah Children's project. The index child enrolled was a result of the pregnancy in the prior study, and up to one sibling was also eligible to enroll. At least one biologic parent enrolled, and both biologic parents were invited to enroll. For further information, contact ucp@hsc.utah.edu, or 801-587-7400. This research was supported by the Environmental influences on Child Health Outcomes (ECHO) Program, Office of The Director, National Institutes of Health. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. UCP is an ECHO cohort which is supported by the following ECHO Program Collaborators: ECHO Coordinating Center: Duke Clinical Research Institute, Durham, North Carolina: Smith PB, Newby KL, Benjamin DK; U2C OD023375 ECHO Data Analysis Center: Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland: Jacobson LP; Research Triangle Institute, Durham, North Carolina: Catellier D; U24 OD023382 North Carolina Human Health Exposure Analysis Resource Hub: Research Triangle Institute: Fennell T, University of North Carolina at Chapel Hill: Sumner S, University of North Carolina at Charlotte: Du X; U2C ES030857 Human Health Exposure Analysis Resource Coordinating Center: Westat, Inc., Rockville, Maryland: O’Brien B; U24 ES026539
Institute
University of Utah
DepartmentSchool of Medicine
Last NameStanford
First NameJoseph
AddressDFPM UU, 375 Chipeta Way #A, Salt Lake City, UT 84108
Emailjoseph.stanford@utah.edu
Phone(801) 587-3331
Submit Date2023-05-04
Total Subjects610
Study CommentsHHEAR Project EM20-0011, ECHO Project EC0376
Raw Data AvailableYes
Raw Data File Type(s)raw(Thermo)
Chear StudyYes
Analysis Type DetailLC-MS
Release Date2024-05-04
Release Version1
Joseph Stanford Joseph Stanford
https://dx.doi.org/10.21228/M8671J
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR001675
Project DOI:doi: 10.21228/M8671J
Project Title:The ECHO Cohort Exposome: First Steps using HHEAR Analysis – An Opportunity for ALL ECHO Cohorts to Contribute Type A Samples – Untargeted Analysis (UCP Cohort)
Project Type:C18 Reversed-Phase Broad Spectrum Metabolomics
Project Summary:This project was funded by the NIH Environmental influences on Child Health Outcomes (ECHO) Program. Untargeted metabolomics profiling data was acquired from urine samples provided by 14 ECHO cohorts.
Institute:NC HHEAR Hub
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) 282-9838
Funding Source:This research was supported by the Environmental influences on Child Health Outcomes (ECHO) Program, Office of The Director, National Institutes of Health. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. The UCP ECHO Cohort is supported by the following ECHO Program Collaborators: ECHO Coordinating Center: Duke Clinical Research Institute, Durham, North Carolina: Smith PB, Newby KL, Benjamin DK; U2C OD023375; ECHO Data Analysis Center: Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland: Jacobson LP; Research Triangle Institute, Durham, North Carolina: Catellier D; U24 OD023382; North Carolina Human Health Exposure Analysis Resource Hub: Research Triangle Institute: Fennell T, University of North Carolina at Chapel Hill: Sumner S, University of North Carolina at Charlotte: Du X; U2C ES030857; Human Health Exposure Analysis Resource Coordinating Center: Westat, Inc., Rockville, Maryland: O’Brien B; U24 ES026539

Subject:

Subject ID:SU002809
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606
Species Group:Mammals

Factors:

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

mb_sample_id local_sample_id Sample Type Batch
SA271418UCP_B_3blank 1
SA271419UCP_B_4blank 1
SA271420UCP_B_2blank 1
SA271421UCP_B_6blank 1
SA271422UCP_B_1blank 1
SA271423UCP_B_8blank 1
SA271424UCP_B_5blank 1
SA271425UCP_B_7blank 1
SA271426UCP_B_13blank 2
SA271427UCP_B_14blank 2
SA271428UCP_B_12blank 2
SA271429UCP_B_11blank 2
SA271430UCP_B_9blank 2
SA271431UCP_B_10blank 2
SA271432UCP_B_16blank 2
SA271433UCP_B_15blank 2
SA271434UCP_B_23blank 3
SA271435UCP_B_18blank 3
SA271436UCP_B_19blank 3
SA271437UCP_B_22blank 3
SA271438UCP_B_24blank 3
SA271439UCP_B_17blank 3
SA271440UCP_B_20blank 3
SA271441UCP_B_21blank 3
SA271442UCP_B_29blank 4
SA271443UCP_B_28blank 4
SA271444UCP_B_26blank 4
SA271445UCP_B_25blank 4
SA271446UCP_B_27blank 4
SA271447UCP_B_31blank 4
SA271448UCP_B_30blank 4
SA271449UCP_B_32blank 4
SA271450UCP_B_38blank 5
SA271451UCP_B_39blank 5
SA271452UCP_B_37blank 5
SA271453UCP_B_35blank 5
SA271454UCP_B_33blank 5
SA271455UCP_B_34blank 5
SA271456UCP_B_36blank 5
SA271457UCP_B_43blank 6
SA271458UCP_B_46blank 6
SA271459UCP_B_42blank 6
SA271460UCP_B_47blank 6
SA271461UCP_B_45blank 6
SA271462UCP_B_48blank 6
SA271463UCP_B_41blank 6
SA271464UCP_B_53blank 7
SA271465UCP_B_54blank 7
SA271466UCP_B_61blank 7
SA271467UCP_B_49blank 7
SA271468UCP_B_58blank 7
SA271469UCP_B_51blank 7
SA271470UCP_B_50blank 7
SA271471UCP_B_52blank 7
SA271472UCP_B_60blank 7
SA271473UCP_B_59blank 7
SA271474UCP_B_62blank 7
SA271475UCP_B_57blank 7
SA271476UCP_B_55blank 7
SA271303UCP_CHEAR_U_2CHEAR 1
SA271304UCP_CHEAR_U_1CHEAR 1
SA271305UCP_CHEAR_U_4CHEAR 1
SA271306UCP_CHEAR_U_3CHEAR 1
SA271307UCP_CHEAR_U_8CHEAR 2
SA271308UCP_CHEAR_U_5CHEAR 2
SA271309UCP_CHEAR_U_7CHEAR 2
SA271310UCP_CHEAR_U_6CHEAR 2
SA271311UCP_CHEAR_U_9CHEAR 3
SA271312UCP_CHEAR_U_12CHEAR 3
SA271313UCP_CHEAR_U_10CHEAR 3
SA271314UCP_CHEAR_U_11CHEAR 3
SA271315UCP_CHEAR_U_14CHEAR 4
SA271316UCP_CHEAR_U_13CHEAR 4
SA271317UCP_CHEAR_U_15CHEAR 4
SA271318UCP_CHEAR_U_16CHEAR 4
SA271319UCP_CHEAR_U_20CHEAR 5
SA271320UCP_CHEAR_U_17CHEAR 5
SA271321UCP_CHEAR_U_19CHEAR 5
SA271322UCP_CHEAR_U_18CHEAR 5
SA271323UCP_CHEAR_U_24CHEAR 6
SA271324UCP_CHEAR_U_22CHEAR 6
SA271325UCP_CHEAR_U_23CHEAR 6
SA271326UCP_CHEAR_U_21CHEAR 6
SA271327UCP_CHEAR_U_28CHEAR 7
SA271328UCP_CHEAR_U_26CHEAR 7
SA271329UCP_CHEAR_U_25CHEAR 7
SA271330UCP_CHEAR_U_29CHEAR 7
SA271331UCP_CHEAR_U_27CHEAR 7
SA271332UCP_CHEAR_U_31CHEAR 7
SA271333UCP_CHEAR_U_30CHEAR 7
SA271334UCP_HHEAR_U1_4HHEAR U1 1
SA271335UCP_HHEAR_U1_1HHEAR U1 1
SA271336UCP_HHEAR_U1_2HHEAR U1 1
SA271337UCP_HHEAR_U1_3HHEAR U1 1
SA271338UCP_HHEAR_U1_6HHEAR U1 2
SA271339UCP_HHEAR_U1_7HHEAR U1 2
SA271340UCP_HHEAR_U1_8HHEAR U1 2
SA271341UCP_HHEAR_U1_5HHEAR U1 2
SA271342UCP_HHEAR_U1_10HHEAR U1 3
SA271343UCP_HHEAR_U1_9HHEAR U1 3
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Collection:

Collection ID:CO002802
Collection Summary:N/A
Sample Type:Urine
Storage Conditions:-80℃

Treatment:

Treatment ID:TR002818
Treatment Summary:N/A

Sample Preparation:

Sampleprep ID:SP002815
Sampleprep Summary:Study samples were shipped from the University of Utah to the NC HHEAR Hub on dry ice. The NC HHEAR Hub 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 (QC study pools) 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. HHEAR Urine Pool 1 (50 µL each), HHEAR Urine Pool 2 (50 µL each), CHEAR reference urine (50 µL each) and NIST urine (SRM 3672) reference material (50 µL each) were provided by the NC HHEAR Hub. 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, study pool samples, HHEAR reference urine, CHEAR reference urine, NIST reference urine, 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

Combined analysis:

Analysis ID AN004384
Analysis type MS
Chromatography type Reversed phase
Chromatography system Thermo Vanquish
Column Waters ACQUITY UPLC HSS T3 (100 x 2.1mm,1.8um)
MS Type ESI
MS instrument type Orbitrap
MS instrument name Thermo Q Exactive HF-X Orbitrap
Ion Mode POSITIVE
Units Normalized intensity

Chromatography:

Chromatography ID:CH003289
Chromatography Summary:-
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

MS:

MS ID:MS004133
Analysis ID:AN004384
Instrument Name:Thermo Q Exactive HF-X Orbitrap
Instrument Type:Orbitrap
MS Type:ESI
MS Comments:Instrument: Thermo Q Exactive HFx Software: Xcalibur 4.1.31.9 for data acquisition; Progenesis QI 2.4 for data preprocessing
Ion Mode:POSITIVE
Capillary Temperature:320 °C
Capillary Voltage:3.5 KV
Collision Energy:20-45, ramp
Collision Gas:N2
Fragmentation Method:CID
Ion Spray Voltage:3.5kV
Ionization:ES+
Mass Accuracy:5 ppm
Desolvation Gas Flow:55
Desolvation Temperature:400 ℃
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