Summary of Study ST001949
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 PR001236. The data can be accessed directly via it's Project DOI: 10.21228/M8Z10X 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.
Study ID | ST001949 |
Study Title | Plasma Metabolome Normalization in Rheumatoid Arthritis following initiation of Methotrexate and the Identification of Metabolic Biomarkers of Efficacy |
Study Type | Clinical |
Study Summary | Methotrexate (MTX) efficacy in the treatment of rheumatoid arthritis (RA) is variable and unpredictable, resulting in a need to identify biomarkers to guide drug therapy. This study evaluates changes in the plasma metabolome associated with response to MTX in RA with the goal of understanding the metabolic basis for MTX efficacy towards the identification of potential metabolic biomarkers of MTX response. |
Institute | University of Kansas |
Department | Pharmacy Practice |
Laboratory | Funk |
Last Name | Medcalf |
First Name | Matthew |
Address | 2106 Olathe Boulevard |
mmedcalf@ku.edu | |
Phone | 13147880236 |
Submit Date | 2021-10-20 |
Num Groups | 3 |
Total Subjects | 40 |
Num Males | 9 |
Num Females | 31 |
Raw Data Available | Yes |
Analysis Type Detail | GC-MS |
Release Date | 2022-11-07 |
Release Version | 1 |
Select appropriate tab below to view additional metadata details:
Project:
Project ID: | PR001236 |
Project DOI: | doi: 10.21228/M8Z10X |
Project Title: | Plasma Metabolome Normalization in Rheumatoid Arthritis following initiation of Methotrexate and the Identification of Metabolic Biomarkers of Efficacy |
Project Type: | Clinical |
Project Summary: | Methotrexate (MTX) efficacy in the treatment of rheumatoid arthritis (RA) is variable and unpredictable, resulting in a need to identify biomarkers to guide drug therapy. This study evaluates changes in the plasma metabolome associated with response to MTX in RA with the goal of understanding the metabolic basis for MTX efficacy towards the identification of potential metabolic biomarkers of MTX response. |
Institute: | University of Kansas |
Department: | Pharmacy Practice |
Laboratory: | Funk |
Last Name: | Medcalf |
First Name: | Matthew |
Address: | 2106 Olathe Boulevard |
Email: | mmedcalf@ku.edu |
Phone: | 13147880236 |
Funding Source: | KL2TR002367 |
Subject:
Subject ID: | SU002027 |
Subject Type: | Human |
Subject Species: | Homo sapiens |
Taxonomy ID: | 9606 |
Age Or Age Range: | 21 - 84 |
Gender: | Male and female |
Factors:
Subject type: Human; Subject species: Homo sapiens (Factor headings shown in green)
mb_sample_id | local_sample_id | Condition |
---|---|---|
SA183864 | 15_015 | Control |
SA183865 | 14_014 | Control |
SA183866 | 16_016 | Control |
SA183867 | 13_013 | Control |
SA183868 | 19_019 | Control |
SA183869 | 1_001 | Control |
SA183870 | 20_020 | Control |
SA183871 | 12_012 | Control |
SA183872 | 18_018 | Control |
SA183873 | 17_017 | Control |
SA183874 | 4_004 | Control |
SA183875 | 3_003 | Control |
SA183876 | 11_011 | Control |
SA183877 | 2_002 | Control |
SA183878 | 6_006 | Control |
SA183879 | 5_005 | Control |
SA183880 | 9_009 | Control |
SA183881 | 8_008 | Control |
SA183882 | 7_007 | Control |
SA183883 | 10_010 | Control |
SA183884 | 45_045 | RA |
SA183885 | 43_043 | RA |
SA183886 | 39_039 | RA |
SA183887 | 47_047 | RA |
SA183888 | 37_037 | RA |
SA183889 | 41_041 | RA |
SA183890 | 57_057 | RA |
SA183891 | 59_059 | RA |
SA183892 | 35_035 | RA |
SA183893 | 55_055 | RA |
SA183894 | 53_053 | RA |
SA183895 | 51_051 | RA |
SA183896 | 49_049 | RA |
SA183897 | 31_031 | RA |
SA183898 | 25_025 | RA |
SA183899 | 27_027 | RA |
SA183900 | 29_029 | RA |
SA183901 | 23_023 | RA |
SA183902 | 33_033 | RA |
SA183903 | 21_021 | RA |
SA183904 | 54_054 | RA+MTX |
SA183905 | 52_052 | RA+MTX |
SA183906 | 60_060 | RA+MTX |
SA183907 | 24_024 | RA+MTX |
SA183908 | 58_058 | RA+MTX |
SA183909 | 26_026 | RA+MTX |
SA183910 | 56_056 | RA+MTX |
SA183911 | 22_022 | RA+MTX |
SA183912 | 48_048 | RA+MTX |
SA183913 | 32_032 | RA+MTX |
SA183914 | 40_040 | RA+MTX |
SA183915 | 38_038 | RA+MTX |
SA183916 | 34_034 | RA+MTX |
SA183917 | 42_042 | RA+MTX |
SA183918 | 30_030 | RA+MTX |
SA183919 | 36_036 | RA+MTX |
SA183920 | 28_028 | RA+MTX |
SA183921 | 46_046 | RA+MTX |
SA183922 | 44_044 | RA+MTX |
SA183923 | 50_050 | RA+MTX |
Showing results 1 to 60 of 60 |
Collection:
Collection ID: | CO002020 |
Collection Summary: | Venous blood samples were collected in 8.5 mL ACD Solution A BD Vacutainer tubes for the healthy control, and RA patients prior to initiation of MTX and at a 16 week follow up visit. Venous blood samples were collected and separated into plasma and cellular fractions by centrifugation at 3,000 RPM in a Thermo Scientific Sorvall Legend XTR centrifuge for 10 minutes. The resulting plasma supernatant was separated into aliquots and stored at -80 ⁰C prior to analysis. |
Sample Type: | Blood (plasma) |
Storage Conditions: | -80℃ |
Additives: | ACD |
Treatment:
Treatment ID: | TR002039 |
Treatment Summary: | Biobanked plasma samples were acquired from a subset of RA patients (n=20) that participated in a 16-week multicenter open-label study that sought to evaluated predictors of MTX response in RA (ClinicalTrials.gov NCT03414502) (PMID: 32911284). The study included sites within the Rheumatology Arthritis Investigational Network (RAIN). For each patient, plasma samples at baseline and 16-weeks were provided for analysis. All patients received 15 mg/week of MTX and 1 mg/day of folic acid upon enrollment. The MTX does was escalated to 20 mg/week in patients that did not achieve clinical remission by 8 weeks, as tolerated. |
Treatment Compound: | Methotrexate |
Treatment Route: | Subcutaneous or Oral |
Treatment Dose: | 15-20 mg/week |
Treatment Doseduration: | 16 weeks |
Sample Preparation:
Sampleprep ID: | SP002033 |
Sampleprep Summary: | Plasma samples were sent to the West Coast Metabolomics Center and were processed according to laboratory Standard Operating Procedures for samples preparations of blood plasma or serum samples for lipidomic, biogenic amine, and primary metabolomic analysis using a biphasic MeOH/MTBE/Water extraction procedure. The upper organic phase was used for lipidomics analysis and the aqueous phase was used for analysis of primary metabolism and biogenic amines. |
Sampleprep Protocol Filename: | Biogenic_Amines.Data Processing Lipidomics.Data Processing Primary_Metabolism.Data_Processing |
Combined analysis:
Analysis ID | AN003173 |
---|---|
Analysis type | MS |
Chromatography type | GC |
Chromatography system | Leco Pegasus IV |
Column | Restek Rtx-5Sil (30m x 0.25mm,0.25um) |
MS Type | EI |
MS instrument type | GC-TOF |
MS instrument name | Leco Pegasus IV TOF |
Ion Mode | POSITIVE |
Units | Peak Height Intensity |
Chromatography:
Chromatography ID: | CH002346 |
Instrument Name: | Leco Pegasus IV |
Column Name: | Restek Rtx-5Sil (30m x 0.25mm,0.25um) |
Chromatography Type: | GC |
MS:
MS ID: | MS002951 |
Analysis ID: | AN003173 |
Instrument Name: | Leco Pegasus IV TOF |
Instrument Type: | GC-TOF |
MS Type: | EI |
MS Comments: | MS acquisition, data processing, and feature assignments were conducted at the West Coast Metabolomics Center. Please reference the attached protocols. |
Ion Mode: | POSITIVE |