the hematocrit effect in dried micro sampling...different strategies for coping with the hematocrit...
TRANSCRIPT
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Different strategies for copingDifferent strategies for coping with the hematocrit effect in dried
blood micro‐sampling
Sara Capiau, Pieter M.M. De Kesel and Christophe P. StoveChristophe Stove@UGent [email protected]
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What can be analyzed with DBS?
(Almost) everything:
DNA/mRNAproteins
(trace) elements(trace) elementssmall molecules
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General pros and cons of DBS sampling
• Ease of sampling/home sampling • Correct sampling• Minimally invasive• Small blood volumes
• Contamination risk• Sensitive analysis required
• Representative matrix (blood)• Stabilizing effect
• Extensive validation required‐ Site of punchingg
• Reduced biohazard • Convenient & cost‐effective
‐ Blood volume spotted‐ Hematocrit effectConvenient & cost effective
transport and storage• Straightforward sample
• Correlation between venous and capillary blood levels
Straightforward sample processing and analysis
• AutomatableAutomatable• # Animals ↓
De Kesel et al., Bioanalysis, 2013
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General pros and cons of DBS sampling
• Ease of sampling/home sampling • Correct sampling• Minimally invasive• Small blood volumes
• Contamination risk• Sensitive analysis required
• Representative matrix (blood)• Stabilizing effect
• Extensive validation required‐ Site of punchingg
• Reduced biohazard • Convenient & cost‐effective
‐ Blood volume spotted‐ Hematocrit effectConvenient & cost effective
transport and storage• Straightforward sample
• Correlation between venous and capillary blood levels
Straightforward sample processing and analysis
• AutomatableAutomatable• # Animals ↓
De Kesel et al., Bioanalysis, 2014
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The Hct effect in practice
0 180.18
2014
0 35Swart, 2
0.35
urger &
m, d
en B
0 50: Wilh
elm
0.50
Source:
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The Hct effect: a two‐fold problem
The impact of blood hematocrit can be divided into two aspects:
ANALYTICAL IMPACT
• Viscosity of the blood (differential spreading of blood with high and low Hct)low Hct)
• Extraction efficiency of the compounds (i.e. recovery)
• Matrix effects
PHYSIOLOGICAL IMPACT
• Blood‐to‐plasma ratio of compounds( f i bl d l [ ])(cfr. comparison blood‐plasma [ ])
*Hemato‐critical issues in quantitative analysis of dried blood spot: challenges and solutions. De Kesel et al. Bioanalysis, 2014
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Whole DBS analysis
Pre‐cut Dried Blood SpotsPre cut Dried Blood SpotsYouhnovski et al., Rapid Comm. Mass Spectrom., 2011
f d d l dPerforated Dried Blood SpotsLi et al., Bioanalysis, 2011
Dried Matrix On Paper DisksMeesters et al., Bioanalysis, 2012
All require volumetric application of DBS!
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DBS: Direct application vs. volumetric application
Volumetric application Non‐volumetric applicationVolumetric application Non‐volumetric application
vs.
Lab or Hospital Sampling @ home
Partial punch analysis Whole DBS analysis
Lab or Hospital Sampling @ home
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Microfluidic‐based volumetric sampling (1)
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Microfluidic‐based volumetric sampling (1)
http://dbs‐system.ch/technology/
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Microfluidic‐based volumetric sampling (2)
G. Lenk, Karolinska Inst, SWEDEN
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Microfluidic‐based volumetric sampling (3)
HemaPENTM (Trajan Scientific and Medical)
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Volumetric Absorptive Microsampling
VAMS (Mitra®,VAMS (Mitra , Phenomenex) Volumetric sampling (10.2 ul), irrespective of hematocrit
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Volumetric Absorptive Microsampling
Study Set‐up:
U l f EDTA i l d bl d• Use left‐over EDTA‐anticoagulated bloodfrom patients ( hospital departments)
• Compare liquid blood – VAMS – DBS
• Analytes: caffeine & paraxanthine
De Kesel et al., Analytica Chimica Acta, 2015
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Volumetric Absorptive Microsampling
4550 [Caffeine]
2530354045
510152025
e (%
)
15‐10‐505
ffere
nce
35‐30‐25‐20‐15
Dif
‐50‐45‐40‐35
0.15 0.2 0.25 0.3 0.35 0.4 0.45 0.5 0.550.15 0.2 0.25 0.3 0.35 0.4 0.45 0.5 0.55
Hematocrit0.15 0.20 0.25 0.30 0.35 0.40 0.45 0.50 0.55
De Kesel et al., Analytica Chimica Acta, 2015
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Volumetric Absorptive Microsampling
4550 [Caffeine]
2530354045
510152025
e (%
)
15‐10‐505
ffere
nce
35‐30‐25‐20‐15
Dif
‐50‐45‐40‐35
0.15 0.20 0.25 0.30 0.35 0.40 0.45 0.50 0.550.15 0.20 0.25 0.30 0.35 0.40 0.45 0.50 0.55
Hematocrit0.15 0.20 0.25 0.30 0.35 0.40 0.45 0.50 0.55
De Kesel et al., Analytica Chimica Acta, 2015
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Volumetric Absorptive Microsampling
4550 [Caffeine]
2530354045
510152025
e (%
)
15‐10‐505
ffere
nce
35‐30‐25‐20‐15
Dif
‐50‐45‐40‐35
0.15 0.20 0.25 0.30 0.35 0.40 0.45 0.50 0.550.15 0.20 0.25 0.30 0.35 0.40 0.45 0.50 0.55
Hematocrit0.15 0.20 0.25 0.30 0.35 0.40 0.45 0.50 0.55
De Kesel et al., Analytica Chimica Acta, 2015
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Volumetric Absorptive Microsampling
4550 [Caffeine]
2530354045
510152025
e (%
)
15‐10‐505
ffere
nce
35‐30‐25‐20‐15
Dif
‐50‐45‐40‐35
0.15 0.20 0.25 0.30 0.35 0.40 0.45 0.50 0.550.15 0.20 0.25 0.30 0.35 0.40 0.45 0.50 0.55
Hematocrit0.15 0.20 0.25 0.30 0.35 0.40 0.45 0.50 0.55
De Kesel et al., Analytica Chimica Acta, 2015
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Volumetric Absorptive MicrosamplingEvaluation of impact of hematocrit on recovery:
• VAMS: Similar extraction procedure as for DBSp
• recovery at higher hematocrits
The calibration line had been set up at a relative high Ht; because of the impact of the Ht recovery of the vast majority because of the impact of the Ht, recovery of the vast majority
of the samples will be slightly higher than that of the calib.’sDe Kesel et al., Analytica Chimica Acta, 2015
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Volumetric Absorptive Microsampling
Evaluation of impact of hematocrit on recovery:
→ extraction at 60 °C
Hct Caffeine Paraxanthine
Low QC High QC Low QC High QCLow QC High QC Low QC High QC
0.21 101.21 ± 3.40 98.45 ± 1.37 102.39 ± 2.76 98.26 ± 1.56
Absolute recovery
(mean ± SD, %)
0.42 101.46 ± 0.70 100.14 ± 2.76 99.20 ± 2.60 102.84 ± 1.66
0.48 106.77 ± 3.11 100.51 ± 2.64 100.62 ± 0.90 103.35 ± 1.58(mean SD, %) 0.48 106.77 3.11 100.51 2.64 100.62 0.90 103.35 1.58
0.62 104.68 ± 3.77 100.70 ± 2.05 103.80 ± 5.66 97.85 ± 4.31
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The Hct effect: a two‐fold problem
The impact of blood hematocrit can be divided into two aspects:
ANALYTICAL IMPACT
• Viscosity of the blood (differential spreading of blood with high and low Hct)low Hct)
• Extraction efficiency of the compounds (i.e. recovery)
• Matrix effects
PHYSIOLOGICAL IMPACT Also to be
• Blood‐to‐plasma ratio of compounds( f i bl d l [ ])
Also to beevaluated in volumetric
(cfr. comparison blood‐plasma [ ]) DBS applications
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Hct effect on extraction recovery
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New materials
Qyntest® (Qynion):
Non cellulose multilayered material that would allow even spreading ofNon‐cellulose multilayered material that would allow even spreading of blood, irrespective of hematocrit
Mengerink et al, Bioanalysis, 2015
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New Formats
HemaspotTM (Spot‐On‐Sciences) :
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Minimizing the Hct effect
Prepare calibrators in blood with an appropriate Hct
s, 2013
., Bioanalysi
Capiau
et a
l.Sado
nes & C
De Kesel, S
=> Define target population
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The hematocrit issue: a chicken‐and‐egg‐situation
Perform DBS analysis in a validated Hct interval
11;
u et al., 201
3
Only samples
oanalysis, 201
nes & Capiau
within this Hctrange yield valid
l
gels et al., Bio
Kesel, Sado
n results
Ing
De
However, how does one know ifthe Hct of a given DBS lies withinthi i t l?this interval?
Need for Hct prediction Need for Hct prediction
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Estimating the Hct of DBS: K+
• [K+] intracellularly >> [K+] plasma and > 99% of cells are RBCs[K+] ti htl t ll d l i t i di id l i bilit• [K+] are tightly controlled no large interindividual variability
• K+ is universal• K+ proved to be stable in DBSK proved to be stable in DBS• K+ easily measurable in DBS
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Estimating the Hct of DBS: K+
Bring a 3‐mm DBS punch in a small tube
Extract 2X with 50 µl 2.5 mM KCl in ultrapure H2Op 2
Measure [K+] in 90 µl via indirect potentiometry using the ISE (Ion Selective Electrode) module of theSelective Electrode) module of the Cobas 8000 Clinical Chemistry
Analyzer
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Estimating the Hct of DBS: Application
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K+‐based algorithm to correct for Hct effect
healthy volunteers (n = 61)&&
hospital patients (n = 117)
venous whole blood venous DBS
To determine[caffeine] [caffeine] To determineHct‐effect
T di t
[caffeine][paraxanthine]
[caffeine][paraxanthine]
To predictHct
[K+]
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K+‐based algorithm to correct for Hct effect[caffeine] > LLOQ
n = 100 Hct range 0 18 – 0 47 Hct range 0.18 0.47
Reference set (n = 50)
• [Caffeine]DBS – [Caffeine]Blood303540
Corrected [DBS]
DEDUCE NEW CORRECTION ALGORITHM:051015202530
nce (%
)
Corrected [DBS]=
[DBS]*((‐0.4141*[K+]) + 1.5052) ‐30‐25‐20‐15‐10‐50
Differen
‐40‐35‐30
0.4 0.6 0.8 1.0 1.2 1.4 1.6[K+]
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K+‐based algorithm to correct for Hct effect[caffeine] > LLOQ
n = 100 Hct range 0 18 – 0 47 Hct range 0.18 0.47
Test set (n = 50)
• [Caffeine]DBS – [Caffeine]Blood303540
Corrected [DBS]
APPLY NEW CORRECTION ALGORITHM:
051015202530
nce (%
)
[ ]=
[DBS]*((‐0.4141*[K+]) + 1.5052) ‐30‐25‐20‐15‐10‐50
Differen
‐40‐35‐30
0.4 0.6 0.8 1.0 1.2 1.4 1.6[K+]
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K+‐based algorithm to correct for Hct effect[caffeine] > LLOQ
n = 100 Hct range 0 18 – 0 47 Hct range 0.18 0.47
Test set (n = 50)
• [Caffeine]DBS – [Caffeine]Blood303540
303540
• [Caffeine]corrected – [Caffeine]Blood
051015202530
nce (%
)
051015202530
nce (%
)
‐30‐25‐20‐15‐10‐50
Differen
‐30‐25‐20‐15‐10‐50
Differen
‐40‐35‐30
0.4 0.6 0.8 1.0 1.2 1.4 1.6[K+]
‐40‐35‐30
0.4 0.6 0.8 1.0 1.2 1.4 1.6[K+]
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K+‐based algorithm to correct for Hct effect[paraxanthine] > LLOQ
n = 103 Hct range 0 17 – 0 47 Hct range 0.17 0.47
Test set (n = 103)
303540 • [PRX]DBS – [PRX]Blood
Corrected [DBS]
APPLY NEW CORRECTION ALGORITHM:
051015202530
nce (%
)
Corrected [DBS]=
[DBS]*((‐0.4141*[K+]) + 1.5052) ‐30‐25‐20‐15‐10‐50
Differen
‐40‐35‐30
0.4 0.6 0.8 1.0 1.2 1.4 1.6[K+]
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K+‐based algorithm to correct for Hct effect[paraxanthine] > LLOQ
n = 103 Hct range 0 17 – 0 47 Hct range 0.17 0.47
Test set (n = 103)
303540 • [PRX]DBS – [PRX]Blood
303540
• [PRX]corrected – [PRX]Blood
051015202530
nce (%
)
051015202530
nce (%
)
‐30‐25‐20‐15‐10‐50
Differen
‐30‐25‐20‐15‐10‐50
Differen
‐40‐35‐30
0.4 0.6 0.8 1.0 1.2 1.4 1.6[K+]
‐40‐35‐30
0.4 0.6 0.8 1.0 1.2 1.4 1.6[K+]
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Estimating the Hct of DBS: K+
• Straightforward sample prep • Requires sample prep• Straightforward sample prep.• Routine analyzer• Cheap
• Requires sample prep.• Destructive• Time consuming• Cheap
• Stable3 h
• Time‐consuming
• 3‐mm punch
• Adopted by other groups
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Estimating the Hct of DBS: Hemoglobin
Optimization of extraction solventOptimization of extraction solvent
3h‐old DBS
3d‐old DBS Cobas 8000
Hb is apparently not stableStability of Hb in DBS vs. time
b(%
)
Total [Hb] vs. time
L)
Hb is apparently not stable
onof to
talH
b
MetHb↑
HbO ↓ al [H
b] (g
/dCo‐oximeter
Time (days)
Fractio HbO2 ↓
Tota
Time (days) Time (days)
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Estimating the Hct of DBS: Hemoglobin
• Additional Hb derivatives formed upon drying!
• Different Hb derivatives not all detected using routine measurements
HYPOTHESIS: Sum HbO2, metHb and HC = constant = measure for Hct?
*Age estimation of blood stains by hemoglobin derivative determination using reflectance spectroscopy. Bremmer et al. Forensic Sci Int. 2011
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Estimating the Hct of DBS: Hemoglobin
• Bremmer et al.:
Method that estimates the age of bloodspatters on crime scenes using the relative abundance of these Hb‐derivativesg
Non‐contact diffuse reflectance spectroscopy
Could we use this technique to measure the different Hb derivatives in DBS (and hence the Hb sum)?
YES! => non‐contact Hct estimation before DBS analysis
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Estimating the Hct of DBS: Hemoglobin
Method completely validated (Hct estimation independent of age DBS!)
i l ( 288)EDTA patient samples (n = 288)• Whole blood: ‘true’ Hct using Sysmex XE‐5000• Venous DBS: calculated HCT using non‐contact method
=> 234 out of 288 samples within 15% of true Hct> 234 out of 288 samples within 15% of true Hct=> 270 out of 288 samples within 20% of true Hct
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Estimating the Hct of DBS: Hemoglobin
Use of Hct prediction for Hct correction• Caffeine reference set: correlation between estimated Hct andCaffeine reference set: correlation between estimated Hct and
extent of Hct effect• Set up of Hct correction algorithmp g• Application to test set
30%
40%
and DBS
Caffeine test set (n = 48)
0%
10%
20%
en who
le blood
a
‐20%
‐10%
0%0.100 0.200 0.300 0.400 0.500 0.600
fferen
ce betwee
‐40%
‐30%% dif
Estimated Hct
![Page 42: the hematocrit effect in dried micro sampling...Different strategies for coping with the hematocrit effect in dried blood micro‐sampling Sara Capiau, Pieter M.M. De Kesel and Christophe](https://reader034.vdocument.in/reader034/viewer/2022042211/5eb07d0f08e386402c0a6037/html5/thumbnails/42.jpg)
Estimating the Hct of DBS: Hemoglobin
Use of Hct prediction for Hct correction• Caffeine reference set: correlation between estimated Hct andCaffeine reference set: correlation between estimated Hct and
extent of Hct effect• Set up of Hct correction algorithmp g• Application to test set
30%
40%
and DBS
Caffeine test set (n = 48)
0%
10%
20%
en who
le blood
a
‐20%
‐10%
0%0.100 0.200 0.300 0.400 0.500 0.600
fferen
ce betwee
‐40%
‐30%% dif
Estimated Hct
![Page 43: the hematocrit effect in dried micro sampling...Different strategies for coping with the hematocrit effect in dried blood micro‐sampling Sara Capiau, Pieter M.M. De Kesel and Christophe](https://reader034.vdocument.in/reader034/viewer/2022042211/5eb07d0f08e386402c0a6037/html5/thumbnails/43.jpg)
Estimating the Hct of DBS: Hemoglobin
Hemoglobin‐based hematocrit prediction: Non‐destructiveNon destructive No punching No sample prep No sample prep. Very fast Does not interrupt workflow drastically Does not interrupt workflow drastically Cheap Hi hl d ibl Highly reproducible Applicable for hematocrit correction
MERE SCANNING SUFFICES TO KNOW THE HCT OF A DBS!
![Page 44: the hematocrit effect in dried micro sampling...Different strategies for coping with the hematocrit effect in dried blood micro‐sampling Sara Capiau, Pieter M.M. De Kesel and Christophe](https://reader034.vdocument.in/reader034/viewer/2022042211/5eb07d0f08e386402c0a6037/html5/thumbnails/44.jpg)
Dried Plasma Spots
![Page 45: the hematocrit effect in dried micro sampling...Different strategies for coping with the hematocrit effect in dried blood micro‐sampling Sara Capiau, Pieter M.M. De Kesel and Christophe](https://reader034.vdocument.in/reader034/viewer/2022042211/5eb07d0f08e386402c0a6037/html5/thumbnails/45.jpg)
Dried Plasma Spots
2015
nalysis,,
rm, B
ioa
Stur
![Page 46: the hematocrit effect in dried micro sampling...Different strategies for coping with the hematocrit effect in dried blood micro‐sampling Sara Capiau, Pieter M.M. De Kesel and Christophe](https://reader034.vdocument.in/reader034/viewer/2022042211/5eb07d0f08e386402c0a6037/html5/thumbnails/46.jpg)
Dried Plasma Spots
![Page 47: the hematocrit effect in dried micro sampling...Different strategies for coping with the hematocrit effect in dried blood micro‐sampling Sara Capiau, Pieter M.M. De Kesel and Christophe](https://reader034.vdocument.in/reader034/viewer/2022042211/5eb07d0f08e386402c0a6037/html5/thumbnails/47.jpg)
Dried Plasma Spots
Hemaspot SETM (Spot‐On‐Sciences):
![Page 48: the hematocrit effect in dried micro sampling...Different strategies for coping with the hematocrit effect in dried blood micro‐sampling Sara Capiau, Pieter M.M. De Kesel and Christophe](https://reader034.vdocument.in/reader034/viewer/2022042211/5eb07d0f08e386402c0a6037/html5/thumbnails/48.jpg)
Conclusion
![Page 49: the hematocrit effect in dried micro sampling...Different strategies for coping with the hematocrit effect in dried blood micro‐sampling Sara Capiau, Pieter M.M. De Kesel and Christophe](https://reader034.vdocument.in/reader034/viewer/2022042211/5eb07d0f08e386402c0a6037/html5/thumbnails/49.jpg)
Thank You!