Summary of Study ST001845
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 PR000667. The data can be accessed directly via it's Project DOI: 10.21228/M8FX07 This work is supported by NIH grant, U2C- DK119886.
See: https://www.metabolomicsworkbench.org/about/howtocite.php
Study ID | ST001845 |
Study Title | Identification of unique metabolite networks between Latino and Caucasian patients with nonalcoholic fatty liver disease (NAFLD) (part V) |
Study Summary | Nonalcoholic fatty liver disease (NAFLD) is a spectrum of liver pathology ranging from simple steatosis to nonalcoholic steatohepatitis (NASH); the latter is characterized by inflammation and fibrosis. Risk factors for NALFD include obesity, diabetes, hyperlipidemia, and hypertension—all of which are features of metabolic syndrome. NAFLD is a very heterogeneous disease, as it presents in different patterns in males and females and in patients from different ethnicities, with unclear predictors for development and severity of disease. Previous studies have shown that NAFLD is 1.4 times more frequent in Hispanics than in Caucasians. One of the major challenges in NAFLD is the lack of accurate, noninvasive biomarkers for the detection of the most aggressive presentation, NASH. The gold standard for the diagnosis is liver biopsy, which is an invasive procedure associated with possible complications. Noninvasive diagnosis of NASH is a major unmet medical need and there are no ethnicity-specific biomarkers that can diagnose this condition and predict its progression. Therefore, the main gap in knowledge that this proposal and line of research will address is the characterizing the different plasma and liver metabolomics profile of patients with fatty liver from two ethnicities (Latinos vs. Caucasians) and of both sexes. The overall hypothesis of the present study is that the higher incidence of nonalcoholic fatty liver (NAFL) in Latino patients is reflected in a different plasma and liver metabolomics profile compared to Caucasian patients with further sex-related differences. Characterization of metabolite networks can aid in identifying the mechanistic underpinnings of sex and ethnic driven differences in NAFL which could help diagnose and establish a prognosis of this condition, especially in the critical transition from NAFL to the more aggressive nonalcoholic steatohepatitis (NASH).To address this hypothesis, plasma metabolomics profile of samples from male and female Latino and Caucasian bariatric surgery patients with NAFL and from healthy subjects will be compared. Metabolomics findings will be related with liver pathology and liver transcriptome profiles from intraoperatively obtained liver biopsies using correlation, network, and pathway analysis. |
Institute | University of California, Davis |
Department | Department of Internal Medicine, Division of Gastroenterology and Hepatology |
Laboratory | Medici Lab |
Last Name | Medici |
First Name | Valentina |
Address | 4150 V Street - PSSB Suite 3500 - 95817 Sacramento CA |
vmedici@ucdavis.edu | |
Phone | (916) 734 3751 |
Submit Date | 2021-06-21 |
Raw Data Available | Yes |
Raw Data File Type(s) | wiff |
Analysis Type Detail | GC-MS |
Release Date | 2021-07-05 |
Release Version | 1 |
Select appropriate tab below to view additional metadata details:
Project:
Project ID: | PR000667 |
Project DOI: | doi: 10.21228/M8FX07 |
Project Title: | Identification of unique metabolite networks between Latino and Caucasian patients with nonalcoholic fatty liver disease (NAFLD) |
Project Summary: | Nonalcoholic fatty liver disease (NAFLD) is a spectrum of liver pathology ranging from simple steatosis to nonalcoholic steatohepatitis (NASH); the latter is characterized by inflammation and fibrosis. Risk factors for NALFD include obesity, diabetes, hyperlipidemia, and hypertension—all of which are features of metabolic syndrome. NAFLD is a very heterogeneous disease, as it presents in different patterns in males and females and in patients from different ethnicities, with unclear predictors for development and severity of disease. Previous studies have shown that NAFLD is 1.4 times more frequent in Hispanics than in Caucasians. One of the major challenges in NAFLD is the lack of accurate, noninvasive biomarkers for the detection of the most aggressive presentation, NASH. The gold standard for the diagnosis is liver biopsy, which is an invasive procedure associated with possible complications. Noninvasive diagnosis of NASH is a major unmet medical need and there are no ethnicity-specific biomarkers that can diagnose this condition and predict its progression. Therefore, the main gap in knowledge that this proposal and line of research will address is the characterizing the different plasma and liver metabolomics profile of patients with fatty liver from two ethnicities (Latinos vs. Caucasians) and of both sexes. The overall hypothesis of the present study is that the higher incidence of nonalcoholic fatty liver (NAFL) in Latino patients is reflected in a different plasma and liver metabolomics profile compared to Caucasian patients with further sex-related differences. Characterization of metabolite networks can aid in identifying the mechanistic underpinnings of sex and ethnic driven differences in NAFL which could help diagnose and establish a prognosis of this condition, especially in the critical transition from NAFL to the more aggressive nonalcoholic steatohepatitis (NASH).To address this hypothesis, plasma metabolomics profile of samples from male and female Latino and Caucasian bariatric surgery patients with NAFL and from healthy subjects will be compared. Metabolomics findings will be related with liver pathology and liver transcriptome profiles from intraoperatively obtained liver biopsies using correlation, network, and pathway analysis. |
Institute: | University of California, Davis |
Department: | Department of Internal Medicine, Division of Gastroenterology and Hepatology |
Laboratory: | Medici Lab |
Last Name: | Medici |
First Name: | Valentina |
Address: | GI and Hepatology Division Academic Office - 4150 V Street - PSSB Suite 3500 - 95817 Sacramento CA |
Email: | vmedici@ucdavis.edu |
Phone: | (916) 734 3751 |
Subject:
Subject ID: | SU001922 |
Subject Type: | Human |
Subject Species: | Homo sapiens |
Taxonomy ID: | 9606 |
Age Or Age Range: | 23-73 |
Gender: | Male and female |
Human Race: | Hispanic and Caucasian |
Factors:
Subject type: Human; Subject species: Homo sapiens (Factor headings shown in green)
mb_sample_id | local_sample_id | factor |
---|---|---|
SA171645 | 840422-28_021 | N / A |
SA171646 | 840422-20_014 | NAFLD-CAU |
SA171647 | 840422-19_013 | NAFLD-CAU |
SA171648 | 840422-24_016 | NAFLD-CAU |
SA171649 | 840422-27_018 | NAFLD-CAU |
SA171650 | 840422-30_019 | NAFLD-CAU |
SA171651 | 840422-01_001 | NAFLD-CAU |
SA171652 | 840422-25_017 | NAFLD-CAU |
SA171653 | 840422-17_011 | NAFLD-CAU |
SA171654 | 840422-16_010 | NAFLD-CAU |
SA171655 | 840422-08_006 | NAFLD-CAU |
SA171656 | 840422-04_003 | NAFLD-CAU |
SA171657 | 840422-13_008 | NAFLD-CAU |
SA171658 | 840422-03_002 | NAFLD-CAU |
SA171659 | 840422-14_009 | NAFLD-CAU |
SA171660 | 840422-05_004 | NAFLD-CAU |
SA171661 | 840422-44_020 | NAFLD-HIS |
SA171662 | 840422-10_007 | NAFLD-HIS |
SA171663 | 840422-18_012 | NAFLD-HIS |
SA171664 | 840422-21_015 | NAFLD-HIS |
SA171665 | 840422-07_005 | NAFLD-HIS |
Showing results 1 to 21 of 21 |
Collection:
Collection ID: | CO001915 |
Collection Summary: | Blood was collected as a part of a routine/pre-operation check up, not more than 2 weeks prior to operation day (bariatric surgery) for the NAFLD group and among normal BMI healthy volunteers for the control group. All volunteers were fasted 10-12 hours before collection. Liver obtained during surgery (no preservatives, flash-frozen) |
Sample Type: | Blood |
Treatment:
Treatment ID: | TR001934 |
Treatment Summary: | Subjects were divided into two groups either: Healthy control or Nonalcoholic fatty liver disease (NAFLD) |
Sample Preparation:
Sampleprep ID: | SP001928 |
Sampleprep Summary: | 1 Thaw plasma samples on ice 2 Vortex plasma sample and pipette 50µl in polypropylene Eppendorf tube/Plate 3 Add Surrogate Standards of the 3 lipid classes (as needed) and other reagents as in the following table: Plasma Sample 10x Oxylipid Surrogate STDs CUDA + PHAU Anti-oxidant ACN/MeOH SUM 4 Vortex for 30sec 5 Centrifuge at 6°C for 5 min at 15,000 g (or 1,800 g for plates) 6 Take the supernatant (~240µl) into new Eppendorf tube/filter plate 7 Spin Filter (0.1 um) or plate filter (0.2um) for 5 min @ 12,000 g (1,800g for plate) 8 place aliquotes of samples into vials, or plate, and cap vials or seal plates 9 Store in -20°C until analysis |
Combined analysis:
Analysis ID | AN002988 |
---|---|
Analysis type | MS |
Chromatography type | HILIC |
Chromatography system | Thermo Vanquish |
Column | Waters Acquity BEH Amide (150 x 2.1mm,1.7um) |
MS Type | ESI |
MS instrument type | Triple quadrupole |
MS instrument name | ABI Sciex 4000 QTrap |
Ion Mode | UNSPECIFIED |
Units | nM |
Chromatography:
Chromatography ID: | CH002217 |
Chromatography Summary: | Targeted oxylipin analysis |
Instrument Name: | Thermo Vanquish |
Column Name: | Waters Acquity BEH Amide (150 x 2.1mm,1.7um) |
Chromatography Type: | HILIC |
MS:
MS ID: | MS002778 |
Analysis ID: | AN002988 |
Instrument Name: | ABI Sciex 4000 QTrap |
Instrument Type: | Triple quadrupole |
MS Type: | ESI |
MS Comments: | analyzed by a Waters UPLC with a 2.1×150 mm, 1.7 µm Acquity BEH column, ESI (+) and (-) switching and detection by multi-reaction monitoring on an Sciex 6500+ QTRAP mass spectrometer. We validated this method for linearity, limit of detection, limit of quantitation, inter- and intra-day reproducibility, and recovery for all targets, yielding better than 15% relative standard deviation and (spiked) recoveries of greater than 80%. |
Ion Mode: | UNSPECIFIED |