Summary of Study ST001826

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 PR001153. The data can be accessed directly via it's Project DOI: 10.21228/M8P10F 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 IDST001826
Study TitleMetabolomic and lipidomic profiles of CKD in obese patients in serum and urine (part 3 of 3)
Study TypeHuman nephropathy in CKD obese patients
Study SummaryObesity is a global pandemic with an increase prevalence over the years. This condition elevates the risk of developing cardiovascular diseases, hypertension and renal pathologies, like chronic kidney disease (CKD). In the present study, the metabolomic and the lipidomic profiles of CKD obese patients were analyzed comparing with obese subjects without CKD. Subsequently, CKD obese patients underwent bariatric surgery and the effect of surgery in the CKD progression of these subjects was evaluated. Serum and urine were measured by LC-MS and GC-HRAM equipment.
Institute
University Rey Juan Carlos
DepartmentBasics Science of Health
Last NameLanzon
First NameBorja
AddressAvenida de Atenas S/N, Alcorcón, Madrid, 28922, Spain
Emailborja.lanzon@urjc.es
Phone663692554
Submit Date2021-04-02
Num Groups2
Total Subjects16
Raw Data AvailableYes
Raw Data File Type(s)mzML
Analysis Type DetailGC-MS
Release Date2021-06-14
Release Version1
Borja Lanzon Borja Lanzon
https://dx.doi.org/10.21228/M8P10F
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Project:

Project ID:PR001153
Project DOI:doi: 10.21228/M8P10F
Project Title:Metabolomic and lipidomic profiles of CKD in obese patients in serum and urine (part 1 of 3)
Project Type:Human nephropathy in CKD obese patients
Project Summary:Obesity is a global pandemic with an increase prevalence over the years. This condition elevates the risk of developing cardiovascular diseases, hypertension and renal pathologies, like chronic kidney disease (CKD). In the present study, the metabolomic and the lipidomic profiles of CKD obese patients were analyzed comparing with obese subjects without CKD. Subsequently, CKD obese patients underwent bariatric surgery and the effect of surgery in the CKD progression of these subjects was evaluated. Serum and urine were measured by LC-MS and GC-HRAM equipment.
Institute:University Rey Juan Carlos
Department:Basics Science of Health
Last Name:Lanzon
First Name:Borja
Address:Avenida de Atenas S/N
Email:borja.lanzon@urjc.es
Phone:663692554

Subject:

Subject ID:SU001903
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606
Age Or Age Range:53 ± 15
Weight Or Weight Range:116 ± 25
Gender:Male and female

Factors:

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

mb_sample_id local_sample_id Genotype
SA169349OD8OD
SA169350OD1OD
SA169351OD7OD
SA169352OD6OD
SA169353OD2OD
SA169354OD4OD
SA169355OD3OD
SA169356OD5OD
SA169357ODBS7ODBS
SA169358ODBS8ODBS
SA169359ODBS6ODBS
SA169360ODBS4ODBS
SA169361ODBS5ODBS
SA169362ODBS1ODBS
SA169363ODBS2ODBS
SA169364ODBS3ODBS
SA169365QC6QC
SA169366QC5QC
SA169367QC2QC
SA169368QC1QC
SA169369QC3QC
SA169370QC4QC
Showing results 1 to 22 of 22

Collection:

Collection ID:CO001896
Collection Summary:Urine, first void in the morning, were collected, aliquoted and stored at -80 °C until extraction.
Sample Type:Urine
Collection Frequency:First void
Storage Conditions:-80℃

Treatment:

Treatment ID:TR001916
Treatment Summary:150 µl of urine of each sample were randomized and vortex-mixed with 400 µl of MeOH at -20 °C containing 1 ppm of a mix of internal standards. Samples were oximated and silylated. Samples were analyzed in a Orbitrap system.

Sample Preparation:

Sampleprep ID:SP001909
Sampleprep Summary:30 µl of serum of each sample were randomized and vortex-mixed with 400 µl of MeOH at -20 °C containing 1 ppm of the following internal standards: heptadecanoic acid, valine-d8, succinic acid-d4 and glutamic acid-d5 (Sigma-Aldrich). Samples were incubated on ice for 30 min and centrifuged (9600 rpm, 3 min). After that, 350 µl (400 µl for urine) of the supernatant of each serum sample were transferred to a V-shaped GC-vial. Stability and reproducibility of the system were checked with pooled samples prepared colleting from all the extracts the same quantity of the remained supernatant. Afterwards, pooled samples were vortex-mixed, centrifuged and 350 µl (400 µl for urine) of the supernatant of each aliquot were transferred to a V-shaped GC-vial. Derivatization. Supernatants were evaporate to dryness in a nitrogen flow. Then, samples were converted to trimethylsilyl (TMS) and methoxime (MEOX) derivate(s). Consequently, 25 µl of MOX reagent in pyridine (20 mg/ml) were added, samples were vortex-mixed and incubated for 60 min at 45 °C. After oximation, silylation was performed adding 25 µl of MSTFA, samples were vortex-mixed and incubated for 60 min at 45 °C.

Combined analysis:

Analysis ID AN002962
Analysis type MS
Chromatography type Normal phase
Chromatography system Q Exactive GC orbitrap
Column Agilent Technologies (30 m x 0.25mm, 0.25um)
MS Type EI
MS instrument type Triple quadrupole
MS instrument name Thermo Q Exactive Orbitrap
Ion Mode POSITIVE
Units Area

Chromatography:

Chromatography ID:CH002195
Chromatography Summary:GC-HRAM analysis were performed in a Q Exative GC Orbitrap system (Thermo Scientific), mounted with a Rxi Guard column purchased at Restek (10 m X 0.37 mm, 0.25 µm i.d.) and a capillary column provided by Agilent Technologies (30 m, 0.25 mm, 0.25 µm i.d.). Injection (1µ) was done in splitless mode with a TriPlus RSH autosampler system provided by Thermo. Oven temperature was keep at 70 °C for the first 5 minutes. Then, temperature was increased to 260 °C (10 °C/min) to reach in the final step 300 °C (40 °C/min) for 5 min. The carrier gas used was Helium with a flow of 2.0 ml/min. Scan range and resolution were adjusted to 50 – 500 m/z and 60,000 respectively. MS Detector was operated in EI positive mode.
Instrument Name:Q Exactive GC orbitrap
Column Name:Agilent Technologies (30 m x 0.25mm, 0.25um)
Chromatography Type:Normal phase

MS:

MS ID:MS002752
Analysis ID:AN002962
Instrument Name:Thermo Q Exactive Orbitrap
Instrument Type:Triple quadrupole
MS Type:EI
MS Comments:GC-HRAM analysis were performed in a Q Exactive GC Orbitrap system (Thermo Scientific), mounted with a Rxi Guard column purchased at Restek (10 m X 0.37 mm, 0.25 µm i.d.) and a capillary column provided by Agilent Technologies (30 m, 0.25 mm, 0.25 µm i.d.). Injection (1µ) was done in splitless mode with a TriPlus RSH autosampler system provided by Thermo. Oven temperature was keep at 70 °C for the first 5 minutes. Then, temperature was increased to 260 °C (10 °C/min) to reach in the final step 300 °C (40 °C/min) for 5 min. The carrier gas used was Helium with a flow of 2.0 ml/min. Scan range and resolution were adjusted to 50 – 500 m/z and 60,000 respectively. MS Detector was operated in EI positive mode. The ion source and the transfer line were kept at 280 °C.
Ion Mode:POSITIVE
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