Return to study ST001929 main page

MB Sample ID: SA178532

Local Sample ID:180731bJWsa03_2
Subject ID:SU002007
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606
Gender:Female

Select appropriate tab below to view additional metadata details:


Subject:

Subject ID:SU002007
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606
Gender:Female

Factors:

Local Sample IDMB Sample IDFactor Level IDLevel ValueFactor Name
180731bJWsa03_2SA178532FL022254B393u8.2_040Subject
180731bJWsa03_2SA178532FL022254C1treatment

Collection:

Collection ID:CO002000
Collection Summary:Urine biospecimens were collected during cross-over trial among premenopausal women conducted from 2007-2010, and details about the study design and population are published elsewhere (Morimoto et al 2014; Maskarinec et al 2011; Maskarinec et al 2012). The BEAN2 trial was a cross-over study with six months on a high- and a low-soy diet, each separated by a 1-month washout period. The objective of the study was to evaluate soy intake and nipple aspirate fluid, a possible indicator of breast cancer risk. Eligibility criteria for the parent study included a normal mammogram, no oral contraceptives, not pregnant, no previous cancer diagnosis or breast surgery, regular menstrual periods, low soy intake, and the ability to produce nipple aspirate fluid. There were 84 women from the original trial who had eight stored urine samples over the cross-over intervention, from which 60 samples were selected for metabolomics analysis.
Sample Type:Urine

Treatment:

Treatment ID:TR002019
Treatment Summary:As part of the parent study, daidzein, equol, and ODMA concentrations were analyzed by liquid chromatography tandem mass spectrometry (LC-MS/MS) as detailed elsewhere (Franke et al 2009). These previously measured concentrations were used to classify metabotypes. Each urine sample was identified as being ODMA producer/non-producer and equol producer/non-producer based on a cut-off of equol/ODMA:daidzein ratio of 0.018 (36). All samples, except two samples, which were excluded from selection, had daidzein concentrations >2 nmol/mg creatinine, indicating sufficient presence of the precursor metabolite for metabolite detection.

Sample Preparation:

Sampleprep ID:SP002013
Sampleprep Summary:Urine samples were stored at -80C.

Combined analysis:

Analysis ID AN003137
Analysis type MS
Chromatography type GC
Chromatography system Leco Pegasus IV GC
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

Chromatography:

Chromatography ID:CH002319
Chromatography Summary:Urine samples were analyzed by the National Institutes of Health (NIH) West Coast Metabolomics Center in the Fiehn laboratory, using established protocols and more detail on these protocols are available elsewhere (Fiehn et al 2008). To consider broad aspects of metabolism relevant to diet, primary metabolism and biogenic amines platforms were evaluated. In brief, primary metabolism metabolites were assayed using automated liner exchange-cold injection system, gas chromatography-time of flight mass spectrometry (ALEX-CIS GCTOF).
Instrument Name:Leco Pegasus IV GC
Column Name:Restek Rtx-5Sil (30m x 0.25mm,0.25um)
Chromatography Type:GC

MS:

MS ID:MS002917
Analysis ID:AN003137
Instrument Name:Leco Pegasus IV TOF
Instrument Type:GC-TOF
MS Type:EI
MS Comments:fter hard ionization by electron ionization, one electron gets abstracted from the intact molecules which hence become positively charged. The standardized -70 eV ionization voltage is so high that molecules fragment into multiple product ions, which may also form rearrangements among each other. Fragments are then analyzed by time of flight mass spectrometry which is made here by the vendor Leco corporation not to obtain accurate mass information at high resolution but instead to obtain mass spectra at very high sensitivity and speed. Mass spectrometry parameters are used as follows: a Leco Pegasus IV mass spectrometer is used with unit mass resolution at 17 spectra s-1 from 80-500 Da at -70 eV ionization energy and 1800 V detector voltage with a 230°C transfer line and a 250°C ion source.
Ion Mode:POSITIVE
  logo