pre-ide slides v6 - critical care canada forum...title pre-ide slides v6 author oanh dang created...
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![Page 1: pre-IDE Slides v6 - Critical Care Canada Forum...Title pre-IDE Slides v6 Author Oanh Dang Created Date 11/3/2015 1:42:54 PM](https://reader034.vdocument.in/reader034/viewer/2022051823/5fed84e4cfe25070af696c50/html5/thumbnails/1.jpg)
Genotype to Target Therapy
Keith R. Walley, MD
St. Paul’s Hospital
University of British Columbia
Conflict: Cyon Therapeutics.
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Hypothesis
• Polymorphisms in genes relevant to
therapy alter response to therapy – and
could be used to target therapy.
• How do we get there?
1. Response to vasopressin
2. 2- adrenergic receptor
3. Activated Protein C
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Vasopressin and Septic Shock Trial (VASST)
N Engl J Med. 358:877-887, 2008
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Choose a Therapy to Almost WorksAll patients
Log-rank statistic
p = 0.27 day 28
p = 0.10 day 90
VasopressinNorepinephrine
0 10 30 50 70 90
00.2
0.4
0.6
0.8
1
Days since initiation of study drug
Pro
babili
ty o
f surv
ival
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Low severity of shock stratum5 g/min < NE < 15 g/min
VasopressinNorepinephrine
0 10 30 50 70 90
00.2
0.4
0.6
0.8
1
Days since initiation of study drug
Pro
babili
ty o
f surv
ival
Log-rank statistic
p = 0.05 day 28
p = 0.03 day 90
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Does genotype play a role?Vasopressin V1a receptor genetic variation in voles
“In addition, males overexpressing the V1aR in the ventral pallidal
region, but not control males, formed strong partner preferences
after an overnight cohabitation, without mating, with a female.”
Pitkow LJ et al. J Neurosci. 2001 Sep 15;21(18):7392-6
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Also in Humans?
Genetic variation in the vasopressin receptor 1a gene
(AVPR1A) associates with pair-bonding behavior in humans.
Walum H et al. PNAS. 105:14153-6, 2008
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Candidate Genes and SNPsSPH Severe Sepsis Cohort: Vasopressinase
rs18059
p < 0.09
0
10
20
30
40
50
TT/CT CC
28
-day m
ort
ality
(%
)
285 81
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Identification of 230 SNPs in a huge haplotype
block (160 kb) covering the LNPEP region and
genotypingLinkage disequilibrium plot (HapMap
European ancestry)
LNPEPLRAP
50
kb
halpotype block
Identification of 230
SNPs by re-sequencing
Genotyping 230 SNPs
in the derivation cohort
Screening 230 SNPs
on 28-day mortality
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uncorrected P values, Armitage’s test for trend
rs4869317
Major allele model(TT vs. AT+AA)
rs4869317
P = 4.4 x 10-4
LNPEP – Vasopressinase SNPs
SPH Derivation cohort (n=589)
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P=0.0013 P=0.026
LNPEP – Vasopressinase SNP
rs4869317 in Septic Shock
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Constant infusion for 72 hours
One-compartment model (CP = R (1-e-kt) / VD)
P=0.028
(VASST, Vasopressin patients, n=45)
Circulating Vasopressin Levels Vasopressin Clearance
n=21 n=24
Mechanism: Vasopressinase SNP
alters vasopressin clearance
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Biological Plausibility: Vasopressinase SNP
and serum sodium post cardiac surgery
(Cardiac surgical ICU, n=977)
P=0.045Locus specific
heritability *
Genetic Variance
Total Variance= 0.800
LNPEP rs4869317
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0
20
40
60
TT/CT CC
Mort
ality
(%
)
LNPEP genotype
NE n = 139
AVP n = 140
Treatment effect: replication
SPH VASST
0
20
40
60
80
TT/CT CC
Mort
ality
(%
)
LNPEP genotype
NE n = 81
AVP n = 73
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Vasopressinase (LNPEP)
• rs4869317 TT patients have high mortality
in septic shock.
• How? rs4869317 TT patients have
increased vasopressin clearance.
– Decreased vasopressin levels in septic shock
– Increased [Na+] before cardiac surgery
(decreased ADH)
– Functional SNP(s) not identified yet
– Best SNP for response to vasopressin?
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Vasopressinase (LNPEP)
• rs4869317 TT patients have high mortality
in septic shock.
• Precision strategy: Vasopressin for T
allelle carriers. Not for others.
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2- Adrenergic
Receptor
Asthma
Cys/Gly/Gln homozygotes
are hypo-responders to
salbutamol
Cys/Gly/Gln marked by A
allele of ADRB2 rs1042717
G/A polymorphism
p=0.0022
p=0.0006
Nakada TA, Russell JA, Boyd JH, Aguirre-Hernandez R, Thain KR, Thair SA, Nakada E, McConechy M, Walley KR. β2-Adrenergic receptor
gene polymorphism is associated with mortality in septic shock. Am J Respir Crit Care Med. 181(2):143-149, 2010.
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Good response to steroidsS
urv
iva
l
1.0
0.8
0.6
0.4
0
0.2
Days0 7 14 21 28
No Acute Steroids
SPH AA
AG or GG
Acute Steroids
SPH
Days0 7 14 21 28
AA
AG or GG1.0
0.8
0.6
0.4
0
0.2
Days0 7 14 21 28
VASSTAA
AG or GG1.0
0.8
0.6
0.4
0
0.2
Days0 7 14 21 28
1.0
0.8
0.6
0.4
0
0.2
AA
AG or GG
Su
rviv
al
VASST
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2- Adrenergic receptor genotype
• Cys/Gly/Gln homozygotes (rs1042717 AA)
adversely respond to adrenergic agonists,
including increased mortality.
• Precision strategy: Non-adrenergic
vasopressors for AA homozygotes.
Steroids may help.
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Protein C / PAI-1 combination genotypeAbsolute Risk Reduction in 28-day mortality due to rhAPC
-20
0
20
40
AR
R (
%)
+/+
+/-
-/- -20
0
20
40
AR
R (
%)
+/+
+/-
-/-
-20
0
20
40
AR
R (
%)
+/+
+/-
-/-
SPH PROWESS VASSTSurvival ~ Age + APACHEII +Caucasian + rhAPC + genotype
Meta-analysis p<0.0001
p=0.062 p<0.0002 p=0.040
SPH PROWESS VASST
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Protein C / PAI-1 genotype
• Response to rhAPC depends on Protein C
and PAI-1 genotype.
• Precision strategy: Treat severe sepsis
patients who have a +/+ Protein C and
PAI-1 combination genotype with rhAPC.
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Summary
• Genotype could be used to guide sepsis
therapy (following confirmatory large
prospective studies).
1. Vasopressin
2. 2-adrenergic receptor
3. Activated Protein C
• Therapies that don’t work for all might work
for some.
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Co-investigator
Jim Russell
Databases
VASST Investigators
PROWESS Investigators
Funding
Heart & Stroke Foundation
CIHR
Michael Smith Foundation
Sirius Genomics Inc.
People
Cheryl Holmes
Lauralynn MacIntyre
Ainsley Sutherland
Dave Shaw
Sanjay Manocha
Horatio Groshaus
Anan Wattanathum
Tony Gordon
Hugh Wellman
Taka Nakada
Emily Nakada
Katherine Thain
Simone Thair
Melissa McConechy
Lynda Lazosky
John Boyd
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Cancer 1.2
Cardiovascular Disease 4.5
Infectious Disease 5.8
1. Sorensen TI et al. NEJM 1988; 318: 727
Parents
(Death of a biological parent <50 years)
Relative Risk of
Adoptee Adults
Role of Heredity in Sepsis(1)
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Single Nucleotide Polymorphisms
• Most common genetic variant
• Common SNPs (minor allele frequency > 5%)
occur every ~500 base pairs