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MB Sample ID: SA274932

Local Sample ID:P_118
Subject ID:SU002838
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606

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Subject:

Subject ID:SU002838
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606

Factors:

Local Sample IDMB Sample IDFactor Level IDLevel ValueFactor Name
P_118SA274932FL035587NullGroup

Collection:

Collection ID:CO002831
Collection Summary:Patients included in this study (211 female subjects with median age of 43.5 years [range 19-78 years]) were followed at the French National Reference Center for SLE (Pitié-Salpêtrière Hospital, Paris, France) between January 2014 and December 2017. SLE was defined according to international guidelines (ACR) 19. Antiphospholipid syndrome (APS) was defined according to the revised Sapporo criteria 20. Each patient underwent a multi-detector CT scan (Siemens syngo.CT CaScoring) and CAC was quantified by means of the previously described Agatston scoring method 21. Duration of the disease, clinical involvements (skin, seritis, hematology, joints and nervous system), treatment regimens (steroids, methotrexate and hydroxychloroquine) and SLE variables (C3, anti-dsDNA, anti-nuclear and antiphospholipid (aPL) antibodies) are presented in Table 1. Disease activity was estimated by the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) score. The presence of cardiovascular risk factors, including hypertension, hypercholesterolemia, diabetes, obesity, smoking status, family or previous personal history of cardiovascular events and inflammation (US-CRP) was determined for all patients (Table 1). Patients were classified into 3 groups of coronary heart disease (CHD) risk according to the calcium score as defined by the Multi-Ethnic Study of Atherosclerosis (MESA) study 22 (low, CAC=0; moderate, 0 < CAC < 100, and high, CAC > 100).
Sample Type:Blood (plasma)

Treatment:

Treatment ID:TR002847
Treatment Summary:A blood sample was collected at the day of the CT scan for each patient by venipuncture from the antecubital vein into sterile BD Vacutainer tubes containing clot activator. Serum was separated immediately by low-speed centrifugation at 2500 rpm for 20 min at 4°C and was stored at -80°C until use.

Sample Preparation:

Sampleprep ID:SP002844
Sampleprep Summary:Serum lipids were extracted using a modified Folch method 26. Briefly, 10 µl serum supplemented with a mixture of internal standards were extracted using 1600 μl of acidified methanol:0.05N HCl (1:1 v/v) and 800 μl chloroform in the presence of an antioxidant, butylated hydroxytoluene. The lower organic phase was dried and lipids were reconstituted into 40µl of LC-MS compatible solvent and were quantified by LC-MS/MS.

Combined analysis:

Analysis ID AN004429 AN004430
Analysis type MS MS
Chromatography type HILIC HILIC
Chromatography system Shimadzu 20AD Shimadzu 20AD
Column Phenomenex Kinetex HILIC (150 x 3mm,2.6um) Phenomenex Kinetex HILIC (150 x 3mm,2.6um)
MS Type ESI ESI
MS instrument type QTRAP QTRAP
MS instrument name ABI Sciex 4000 QTrap ABI Sciex 4000 QTrap
Ion Mode POSITIVE POSITIVE
Units relative difference relative difference

Chromatography:

Chromatography ID:CH003328
Instrument Name:Shimadzu 20AD
Column Name:Phenomenex Kinetex HILIC (150 x 3mm,2.6um)
Column Temperature:45
Flow Gradient:-
Flow Rate:300ul/min
Solvent A:100% water; 0.2% acetic acid; 30mM ammonium acetate
Solvent B:100% acetonitrile; 0.2% acetic acid
Chromatography Type:HILIC

MS:

MS ID:MS004176
Analysis ID:AN004429
Instrument Name:ABI Sciex 4000 QTrap
Instrument Type:QTRAP
MS Type:ESI
MS Comments:MRM acquisition of low abundant phospho- and sphingolipid classes: PS, PA, LPC, LPE, cer, PG, PI, PE, PE-P this acquisition is called "short"
Ion Mode:POSITIVE
  
MS ID:MS004177
Analysis ID:AN004430
Instrument Name:ABI Sciex 4000 QTrap
Instrument Type:QTRAP
MS Type:ESI
MS Comments:MRM acquisition of abundant lipids following 100fold dilution for PC and SM analysis. This acquisition is called "short10x"
Ion Mode:POSITIVE
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