clinical reference materials at irmm - alzheimer's association...clinical reference materials...
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Serving society
Stimulating innovation
Supporting legislation
Joint Research Centre IRMM
Clinical reference materials at IRMM
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23 April 2012 2
Court of Auditors
The European Parliament
The Council of Ministers
Committee of the Regions
Court of Justice
The European Commission(the ‘College’ of Commissioners)
Economic and Social
Committee
SG RELEX ENTR ENV SANCO JRC...
IHCP
RTD
IRMMIPSC…..
IPTS
JRC Institutes:
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7 Institutes in 5 Member States
IRMM - Geel, Belgium
Institute for Reference Materials and Measurements
ITU - Karlsruhe, Germany
Institute for Transuranium Elements
IE - Petten, The Netherlands
Institute for Energy
IPSC - Ispra, Italy
Institute for the Protection and Security of the Citizen
IES - Ispra, Italy
Institute for Environment and Sustainability
IHCP - Ispra, Italy
Institute for Health and Consumer Protection
IPTS - Seville, Spain
Institute for Prospective Technological Studies
EC: Joint Research Centre
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23 April 2012 4
The mission of the IRMM is to promotea common and reliable
European measurement systemin support of EU policies.
Confidence in Measurements®
http://www.irmm.jrc.be
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Microbiol.CRMs
FoodCRMs
Soil/Sediment
CRMs WaterCRMs
TSEQCMs
ClinicalCRMs
GMOCRMs
Engin. Mat.CRMs
Microorganisms
Prions
PAHs
Mycotoxins PCBs
Dioxins
Vitamins Proximates
Elements
Proteins
Enzymes
Impact toughness
Size
Ions
Hormones
Veterinarydrugs
Metal species
Hydrocarbons
Isotopes
DNA
RM Programmes
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Collaborations forclinical RMs
IRMM
CliniciansIFCC
(International Federation for ClinicalChemistry and Laboratory Medicine)
IVD industry(Siemens, Roche, Abbott, Beckman
Coulter, …)
• Collaboration with IFCC working groups
• Production of reference materials• Development of international standards (ISO)• CCQM, JCTLM• Biomolecular research and method development (only for needs notaddressed elswhere than in IRMM)
JCTLM(Joint Committee for Traceability in
Laboratory Medicine)
CCQM(Comité Consultatif …)
ISO REMCOISO Guides 30-35
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Reference Materials
non-certified RMs Certified RMs
metrologically valid establish-ment of property value(s)
additional investigations
− homogeneous subsamples
− appropriate stability
− homogeneous subsamples
− appropriate stabilitymaterial
characteristics
• property value(s) traceable toadequate reference system
• stated meas. uncertainty
• stated homogeneity & stability
• intended use
• statements onhomogeneity& stability
accompanying information
� calibration
� trueness control
� full method validation
� all QA/QC measures
� performance controls(precision, consistency)of methods or labs(internal & external)
� method developments
main applications
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Reference Materials for Laboratory Medicine
Hormones in human serumCortisol (unspiked/spiked) ERM AD 192/193
Cortisol (reference serum panel) ERM AD 451
Progesterone (low/high) ERM DA 347/BCR-348R
Thyroxine (T4) IRMM-4683,3',5-triiodothyronine (T3) IRMM-469Estradiol-17 beta BCR 576/577/578(low/medium/high)
Electrolytes and trace elements in blood and serumHuman blood: BCR 634/635/636Cd, PbHuman serum: BCR 637/638/639Al, Se, Zn
Organic molecules in human serumCreatinine (low/medium/high) BCR 573/574/575Creatinine interfering substancesBCR 573i
Coagulation factorsBovine thromboplastin ERM AD 148Rabbit thromboplastin ERM AD 149
ProteinsApolipoprotein A I BCR 393Thyroglobulin (Tg) BCR 457Glycated heamoglobin IRMM/IFCC 466Non-glycated heamoglobin IRMM/IFCC 467Alphafoetoprotein BCR 486Prostate specific antigen (PSA) BCR 613
Proteins in human serum12 proteins ERM-DA470k/IFCC(A2M, AAG, AAT, ALB, C3c, C4, HPT, IgA, IgG, IgM, TSF, TTR)CRP ERM-DA474/IFCCCystatin C EMR-DA471/IFCC
EnzymesGamma-glutamyltransferase ERM AD 452Lactate dehydrogenase 1 ERM AD 453Alanine aminotransferase ERM AD 454Aspartate aminotransferase ERM-DA 457/IFCCCreatine kinase-2 (CK-MB) ERM AD 455Creatine kinase (CK-BB) BCR 299Pancreatic alpha-amylase IRMM/IFCC-456Prostatic acid phosphatase BCR 410Adenosine deaminase BCR 647Pancreatic lipase BCR 693Recombinant lipase BCR 694
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Traceability in clinical chemistry
Directive 98/79/EC on In Vitro Diagnostic Medical Devices requires
traceability of values assigned to calibrators and controls through
available reference measurement procedures and reference materials
of higher order
EC mandated standard related to the IVD directive: ISO 17511; In vitro
diagnostic medical devices - Metrological traceability of values
assigned to calibrators and control materials
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23 April 2012 10
Routine sample result
e.g. AAA, refractive index
“Pure” protein
CRM matrix material
Reference procedure, immunoassay ring trial
Value transfer 1: LC-MS, immunoassay
Value transfer 2: immunoassay
Immunoassay
Definition of the SI unit
Manufacturer’sworking calibrator
Manufacturer’sproduct calibrator
Traceability chain
Quality controlmaterial
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Traceability hGH
70-75 % 5-10 %
10 %
variable
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Routine sample result
e.g. LC-MS
Recombinant protein LC-MS
polyclonalimmunoassay
Immunoassay
Definition of the SI unit
Manufacturer’sworking calibrator
Manufacturer’sproduct calibrator
22 kDa
=
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Traceability and comparability via reference materials
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e.g. ERM-DA470k/IFCC
Certified for ALB, AAG,
AAT, A2M, C3c, C4, HPT,
IgA, IgG, IgM, TRF, TTR
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Standardisation for IgM achieved by:
- Collaboration between different partners (RM producer, IFCC, IVD manufacturers)
0.0
0.5
1.0
1.5
2.0
0.0 1.0 2.0 3.0 4.0
IgM2011
ERM-DA470 ERM-DA470k/IFCC
- Reference material that is fit for its purpose, and commutable (previous experience + 3 years of hard work by a large team)
- Development of value transfer protocols (Blirup-Jensen et al. 2001)
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Underlying assumption
Being traceable to a common standard or stated reference should ensure that
independently obtained measurement results will overlap within their stated
uncertainties and at a certain level of confidence with the true value
and consequently with each other
- provided measurement procedures applied in the traceability chain
determine the same measurand
- if the comparison measurements do not introduce unrecognised bias
(e.g. matrix effects, differential extraction etc.)
- if all relevant uncertainty components are included in the estimate
of the combined uncertainties
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Commutability
Wide spread belief:
Use of a common standard (eventually with an arbitrarily assigned unit)
to calibrate different methods will improve comparability of
measurement results
Only true under the condition that
- the methods to be compared measure the same analyte or different analytes but in a constant relationship in the samplesto be analysed
- the common standard is commutable, i.e. behaves in the same way as patient samples for the methods used
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0
100
200
300
400
500
600
700
0 50 100 150 200 250 300 350 400 450
ext.Limit
ext.Limit
CS
ERM-DA470
Ellipse
ERM-DA470k (vial 1)
Ellipse
ERM-DA472 (liq.)
(vial 1)
Ellipse
Method 1
Method 2
Example: Commutability of CRMs for CER
ERM-DA470 (freeze-dried)
ERM-DA470k (freeze-dried)
ERM-DA472 (liquid frozen)
Comparing the response of
(candidate) CRMs with the response of clinical samples
ERM-DA470 is not commutable for this combination of methods
CRM used to calibrate both methods
Method 1
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Requirements for a clinical CRM
Traceability of valuesTo ensure the continuity of measurement results from assays calibrated against successive reference materials
Commutability: resemble patient samples
HomogeneityThe difference between the vials must be sufficiently small
StabilityThe material must be stable over many years
Correct concentration range:The relevant decision interval should be covered, e.g. for CRP a reference material at 1 mg/L is not useful
Low turbidity (for turbidimetry, nephelometry)
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Planning beforeCRM production
• Evaluation of the comparability of measurementresults obtained with different methods
• Definition of the measurand (e.g. Tau phosphorylatedon position XXX)
• Concept for the traceability/ reference measurementsystem
• Reference method?
• Proposal for starting materials
• e.g. CSF spiked with recombinant protein
• Feasibility studies on processing, stabilisation of the material.
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CRM planning
PlanningMaterial selection
Homogeneitystudy
Storage ProcessingInterim transportand storage
Short-termstability study
Long-termstability study
Value assignment
Commutability study
Follow-up stabilitymonitoring of CRM
Assessmentby experts
Documentation
CRM Distribution and Sales
Materialcollection
Feasibility study
(collection, processing, characterisation, commutability)
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Parameters of interest
In cerebrospinal fluid:
• Amyloid β 42 (Aβ42) healthy > 500 ng/L
• Decrease in Alzheimer patients by about 50 %
• Total tau healthy < 300 ng/L
• Increased in Alzheimer Disease (AD), Creutzfeld-Jacob (CJD), stroke
by about 300 %
• Reflects the intensity of neuronal degeration
• 6 isoforms
• Phosphorylated tau (P-tau)
• Increased in AD, not CJD and stroke
• Many phosphorylation sites, Thr181 is main one
• Reflects neurofibrillary tangles
• α-synuclein
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Methods
All heterogenous immunoassaysInterlaboratory CVs 20-35 %
• Amyloid β 42 (Aβ42)• INNOTEST ELISA Novex• Luminex X-map with INNO-Bia AlsBio3• MesoScale Discovery (MSD), different antibodies
• Total tau • INNOTEST ELISA• Luminex X-map with INNO-Bia AlsBio3
• Phosphorylated tau (P-tau)• INNOTEST ELISA• Luminex X-map with INNO-Bia AlsBio3
• α-synuclein
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1 Comparability of measurement results
• Variation between laboratories: Aliquots of pooled CSF
(Mattsson et al. 2011)
• Innotest ELISA, Luminex xMAP, Mesoscale: between lab CV 13-36 %
• Difference in absolute values (Mattsson et al. 2011) :
• Factor 2-10 difference
• Correllation: 150 Individual clinical samples (Reijn et al. 2007)
• Innotest (ELISA), Luminex (xMAP): Between method CVs about 30 %
• Correllation between ELISA and xMAP:
� r = 0.87 Aββββ42 total group
� r = 0.93 t-tau total group
� r = 0.88 P-tau total group
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Feasibility studies
Pilot batches can be produced to:
• Test the stability of the material
• Verify the commutability of the material
• Compare different formats of the material (e.g. liquid frozen and lyophilised)
Decision of format of the material
• Perform a feasibility studies for the value assignmentwith all the laboratories involved
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Format of the material ?
Intended use: Quality control or calibration?
Target analytes:• Amyloid ββββ 42 (Aββββ42)• Total tau• Phosphorylated tau (P-tau)
Target concentration of analytes: For calibration the concentration should be at the high end of the measurement interval, e.g. 500 ng/L
Nature of the matrix: natural if commutable materialCSF collected from neurosurgery patients with ventricular drains or
hydrocephalus patients?
Nature of the protein: native, isoform mix or recombinant
Definitation of the measurand: e.g. Aββββ42 peptide sequence, either method defined or structurally defined
Intended traceability statement: traceable to the SI
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Certification measurements
• Homogeneity
• Stability
• Characterisation/ value assignment
uLTS = 0.73 %
4,50
4,75
5,00
5,25
5,50
5,75
6,00
6,25
6,50
0 1 2 3 4 5 6 7 8
Dataset number
Cys
C [
mg
/L]
4,50
4,75
5,00
5,25
5,50
5,75
6,00
6,25
6,50
0 1 2 3 4 5 6 7 8
Dataset number
Cys
C [
mg
/L]
Uchar, rel = 0.74 %
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Method performance
In house: Biochem/ Biotech laboratories
External: validated suppliers / collaborators
• Selection criteria (# for homogeneity/stability and characterisation)
• Organisation of feasibility studies, training
RSD = 55 % RSD = 11 %
PT study CRM characterisation
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value assignment
Different approaches possible:
• Arbitrary units (IU) – normally not our approach
• By reference method (not yet available for Alzheimers’proteins)
• By ring trial:
- At least 6 independent datasets
- Requires a valid calibrant: e.g. pure protein solution value assigned by amino acid analysis and dry mass determinationspiked into a backgound matrix.
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dispatch conditions
• stability during dispatch (up to 60 °C)• relevant temperatures tested (-20, +4, 18, 40, 60)
4 °C 60 °C
Time/weeks Time/weeks
• Significant slope?
• Uncertainty negligible?
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Shelf life
Results from a 12-month stability study →→→→ uLTS
uLTS = 0.73 %
Stability monitoring over entire shelflife of material (may be up to 20-30 years)
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Documentation
+
certificatematerial
+
Full report
Examples: http://irmm.jrc.ec.europa.eu/Pages/rmcatalogue.aspx
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Thanks!