Summary of Study ST000285
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 PR000227. The data can be accessed directly via it's Project DOI: 10.21228/M89P43 This work is supported by NIH grant, U2C- DK119886.
See: https://www.metabolomicsworkbench.org/about/howtocite.php
Study ID | ST000285 |
Study Title | NMR-based Metabolomics for CRC Diagnosis |
Study Type | Disease Diagnosis |
Study Summary | Despite the fact that colorectal cancer (CRC) is one of the most prevalent and deadly cancers in the world, the development of improved and robust biomarkers to enable screening, surveillance, and therapy monitoring of CRC continues to be evasive. In particular, patients with colon polyps are at higher risk of developing colon cancer; however, noninvasive methods to identify these patients suffer from poor performance. In consideration of the challenges involved in identifying metabolite biomarkers in individuals with high risk for colon cancer, we have investigated NMR-based metabolite profiling in combination with numerous demographic parameters to investigate the ability of serum metabolites to differentiate polyp/CRC patients from healthy subjects. We also investigated the effect of disease risk on different groups of biologically related metabolites. Our study may explain some of the challenges and promise a novel avenue for future metabolite profiling methodologies. |
Institute | University of Washington |
Department | Anesthesiology and Pain Medicine |
Laboratory | Northwest Metabolomics Research Center |
Last Name | Gu |
First Name | Haiwei |
Address | 850 Republican St., Seattle WA 98109 |
draftery@uw.edu | |
Phone | 206-543-9709 |
Submit Date | 2016-12-17 |
Num Groups | 3 |
Total Subjects | 233 |
Analysis Type Detail | NMR |
Release Date | 2015-12-21 |
Release Version | 1 |
Select appropriate tab below to view additional metadata details:
Project:
Project ID: | PR000227 |
Project DOI: | doi: 10.21228/M89P43 |
Project Title: | NMR-based Metabolomics for CRC Diagnosis |
Project Type: | NMR study |
Project Summary: | Despite the fact that colorectal cancer (CRC) is one of the most prevalent and deadly cancers in the world, the development of improved and robust biomarkers to enable screening, surveillance, and therapy monitoring of CRC continues to be evasive. In particular, patients with colon polyps are at higher risk of developing colon cancer; however, noninvasive methods to identify these patients suffer from poor performance. In consideration of the challenges involved in identifying metabolite biomarkers in individuals with high risk for colon cancer, we have investigated NMR-based metabolite profiling in combination with numerous demographic parameters to investigate the ability of serum metabolites to differentiate polyp/CRC patients from healthy subjects. We also investigated the effect of disease risk on different groups of biologically related metabolites. Our study may explain some of the challenges and promise a novel avenue for future metabolite profiling methodologies. |
Institute: | University of Washington |
Department: | Anesthesiology and Pain Medicine |
Laboratory: | Northwest Metabolomics Research Center |
Last Name: | Raftery |
First Name: | Daniel |
Address: | 850 Republican St., Seattle WA 98109 |
Email: | draftery@uw.edu |
Phone: | 206-543-9709 |
Subject:
Subject ID: | SU000305 |
Subject Type: | Human |
Subject Species: | Homo sapiens |
Taxonomy ID: | 9606 |
Age Or Age Range: | 21-86 |
Weight Or Weight Range: | 45-172 kg |
Height Or Height Range: | 137-200 cm |
Gender: | 64 M and 63 F |
Human Ethnicity: | Indicated in the Study Design |
Human Smoking Status: | Indicated in the Study Design |
Human Alcohol Drug Use: | Indicated in the Study Design |
Species Group: | Human |
Factors:
Subject type: Human; Subject species: Homo sapiens (Factor headings shown in green)
mb_sample_id | local_sample_id | Disease type |
---|---|---|
SA012561 | 416 | Colorectal Cancer |
SA012562 | 411 | Colorectal Cancer |
SA012563 | 410 | Colorectal Cancer |
SA012564 | 417 | Colorectal Cancer |
SA012565 | 421 | Colorectal Cancer |
SA012566 | 425 | Colorectal Cancer |
SA012567 | 422 | Colorectal Cancer |
SA012568 | 152 | Colorectal Cancer |
SA012569 | 419 | Colorectal Cancer |
SA012570 | 154 | Colorectal Cancer |
SA012571 | 403 | Colorectal Cancer |
SA012572 | 168 | Colorectal Cancer |
SA012573 | 389 | Colorectal Cancer |
SA012574 | 162 | Colorectal Cancer |
SA012575 | 157 | Colorectal Cancer |
SA012576 | 408 | Colorectal Cancer |
SA012577 | 156 | Colorectal Cancer |
SA012578 | 427 | Colorectal Cancer |
SA012579 | 431 | Colorectal Cancer |
SA012580 | 115 | Colorectal Cancer |
SA012581 | 448 | Colorectal Cancer |
SA012582 | 447 | Colorectal Cancer |
SA012583 | 452 | Colorectal Cancer |
SA012584 | 454 | Colorectal Cancer |
SA012585 | 457 | Colorectal Cancer |
SA012586 | 109 | Colorectal Cancer |
SA012587 | 455 | Colorectal Cancer |
SA012588 | 444 | Colorectal Cancer |
SA012589 | 122 | Colorectal Cancer |
SA012590 | 133 | Colorectal Cancer |
SA012591 | 434 | Colorectal Cancer |
SA012592 | 173 | Colorectal Cancer |
SA012593 | 132 | Colorectal Cancer |
SA012594 | 435 | Colorectal Cancer |
SA012595 | 440 | Colorectal Cancer |
SA012596 | 125 | Colorectal Cancer |
SA012597 | 429 | Colorectal Cancer |
SA012598 | 388 | Colorectal Cancer |
SA012599 | 285 | Colorectal Cancer |
SA012600 | 253 | Colorectal Cancer |
SA012601 | 284 | Colorectal Cancer |
SA012602 | 250 | Colorectal Cancer |
SA012603 | 289 | Colorectal Cancer |
SA012604 | 295 | Colorectal Cancer |
SA012605 | 292 | Colorectal Cancer |
SA012606 | 291 | Colorectal Cancer |
SA012607 | 283 | Colorectal Cancer |
SA012608 | 257 | Colorectal Cancer |
SA012609 | 263 | Colorectal Cancer |
SA012610 | 277 | Colorectal Cancer |
SA012611 | 276 | Colorectal Cancer |
SA012612 | 278 | Colorectal Cancer |
SA012613 | 279 | Colorectal Cancer |
SA012614 | 282 | Colorectal Cancer |
SA012615 | 281 | Colorectal Cancer |
SA012616 | 300 | Colorectal Cancer |
SA012617 | 304 | Colorectal Cancer |
SA012618 | 355 | Colorectal Cancer |
SA012619 | 200 | Colorectal Cancer |
SA012620 | 354 | Colorectal Cancer |
SA012621 | 357 | Colorectal Cancer |
SA012622 | 193 | Colorectal Cancer |
SA012623 | 177 | Colorectal Cancer |
SA012624 | 187 | Colorectal Cancer |
SA012625 | 202 | Colorectal Cancer |
SA012626 | 343 | Colorectal Cancer |
SA012627 | 320 | Colorectal Cancer |
SA012628 | 312 | Colorectal Cancer |
SA012629 | 310 | Colorectal Cancer |
SA012630 | 322 | Colorectal Cancer |
SA012631 | 325 | Colorectal Cancer |
SA012632 | 214 | Colorectal Cancer |
SA012633 | 332 | Colorectal Cancer |
SA012634 | 469 | Colorectal Cancer |
SA012635 | 139 | Colorectal Cancer |
SA012636 | 514 | Colorectal Cancer |
SA012637 | 512 | Colorectal Cancer |
SA012638 | 515 | Colorectal Cancer |
SA012639 | 516 | Colorectal Cancer |
SA012640 | 517 | Colorectal Cancer |
SA012641 | 26 | Colorectal Cancer |
SA012642 | 511 | Colorectal Cancer |
SA012643 | 24 | Colorectal Cancer |
SA012644 | 508 | Colorectal Cancer |
SA012645 | 509 | Colorectal Cancer |
SA012646 | 510 | Colorectal Cancer |
SA012647 | 518 | Colorectal Cancer |
SA012648 | 519 | Colorectal Cancer |
SA012649 | 555 | Colorectal Cancer |
SA012650 | 561 | Colorectal Cancer |
SA012651 | 562 | Colorectal Cancer |
SA012652 | 575 | Colorectal Cancer |
SA012653 | 34 | Colorectal Cancer |
SA012654 | 49 | Colorectal Cancer |
SA012655 | 520 | Colorectal Cancer |
SA012656 | 521 | Colorectal Cancer |
SA012657 | 53 | Colorectal Cancer |
SA012658 | 28 | Colorectal Cancer |
SA012659 | 77 | Colorectal Cancer |
SA012660 | 513 | Colorectal Cancer |
Collection:
Collection ID: | CO000299 |
Collection Summary: | Serum samples from patients with CRC, polyps, and matched healthy controls were obtained from the Indiana University School of Medicine. Following the IRB protocol approved by both Indiana and Purdue Universities, patients undergoing colonoscopy for CRC screening were evaluated and blood from the consented patients was obtained after overnight fasting and bowel preparation but prior to colonoscopy. Blood samples were allowed to clot at room temperature for 45 min and then centrifuged at 2000 rpm for 10 min. The sera were collected, and aliquoted into separate vials, then transported to Purdue University over dry ice and stored at -80°C until used for analysis. |
Sample Type: | Blood |
Blood Serum Or Plasma: | Serum |
Treatment:
Treatment ID: | TR000319 |
Treatment Summary: | No treatment |
Human Fasting: | Overnight |
Sample Preparation:
Sampleprep ID: | SP000313 |
Sampleprep Summary: | Each frozen serum sample was thawed and vortexed; 530 µL aliquots were mixed with 5 µL sodium azide solution (5% in H2O). The resulting solution was centrifuged, and 530 µL was transferred to a 5 mm NMR tube. A coaxial capillary containing 60 µL TSP (20.9 nmol) in D2O was placed into the NMR tube to serve as a chemical shift and quantitative reference. The samples were randomized before performing the NMR experiments. |
Analysis:
Analysis ID: | AN000453 |
Analysis Type: | NMR |
Num Factors: | 3 |
NMR:
NMR ID: | NM000059 |
Analysis ID: | AN000453 |
Instrument Name: | Bruker Avance III |
Instrument Type: | FT-NMR |
NMR Experiment Type: | 1D 1H |
Spectrometer Frequency: | 500 MHz |
NMR Probe: | HCN cryogenic probe |
NMR Solvent: | D2O |
NMR Tube Size: | 5 mm |
Pulse Sequence: | CPMG, NOESY |
Chemical Shift Ref Cpd: | TSP |
Temperature: | 25C |
Number Of Scans: | 128 |
Spectral Width: | 6000 Hz |
Num Data Points Acquired: | 16K |
Line Broadening: | 0.5 Hz |
Binned Increment: | 0.00587 |