Summary of Study ST002418

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 PR001556. The data can be accessed directly via it's Project DOI: 10.21228/M8K429 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 IDST002418
Study TitleSerum metabolomics and lipidomics profiling in iliac arteriovenous fistula creation in clinical patients: part 2
Study TypeStudy of the serum metabolome in patients with end stage kidney disease before and 6-weeks after iliac arteriovenous fistula creation via 1H NMR
Study SummaryThis project is focused on a longitudinal analysis of the small molecules metabolomes in end stage renal disease patients undergoing iliac arteriovenous fistula creation using solution state NMR spectroscopy. It was hypothesized that after 6-weeks of AVF creation, these patients would present with altered serum metabolite features.
Institute
University of Florida
DepartmentApplied Physiology and Kinesiology
LaboratoryRm 42 and Rm 43
Last NameKhattri
First NameRam
Address1864 Stadium RD, Gainesville, FL, 32611, USA
Emailrbk11@ufl.edu
Phone3307856045
Submit Date2022-12-22
Num Groups2
Total Subjects45 subjects, 2 samples per subject, total of 90 samples
Num Males36
Num Females9
Study CommentsStudy of the serum metabolome in patients with end stage kidney disease before and 6-weeks after iliac arteriovenous fistula creation via 1H NMR
Raw Data AvailableYes
Raw Data File Type(s)fid
Analysis Type DetailNMR
Release Date2023-12-22
Release Version1
Ram Khattri Ram Khattri
https://dx.doi.org/10.21228/M8K429
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Sample Preparation:

Sampleprep ID:SP002513
Sampleprep Summary:Serum samples are associated with binding of residual proteins with DSS signal, resulting broaden DSS peak. The presence of the residual proteins, even after performing modified FOLCH extraction, was observed for serum samples, making it un-reliable for quantitative purpose. In this study, we coupled two extraction protocols to extract metabolites from the serum samples. Modified FOLCH extraction was performed as a first step to separate out water-soluble and lipid-soluble metabolites/compounds. Furthermore, acetonitrile:isopropanol:water (3:3:2 vol/vol/vol) extraction was performed on aqueous phase samples that we obtained from modified FOLCH extraction.
Sampleprep Protocol Filename:AVF-NMR_Lipid_Phase_Procedures.docx
Processing Method:Lyophilization and Homogenization
Processing Storage Conditions:-80℃
Extraction Method:Modified FOLCH extraction for lipid phase samples
Extract Storage:-80℃
Sample Resuspension:In 700 microliter of CDCl3 with 10 mM of pyrazine as internal standard for lipid phase samples
Sample Spiking:10 mM of TSP for urine samples
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