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10th
South
China
International
Congress
of
CardiologyACE
trialsymposiumPrognostic
and
potential
therapeuticimplications
of
the
European
and
ChinaHeart
surveysLars
RydénKarolinska
InstitutetStockholm,
SwedenImplications
of
the
European
and
China
Heart
SurveysEuropean
Guidelines
on
Diabetes,
prediabetes
and
Cardiovascular
Diseasemay
be
downloadedfrom
Implications
of
the
European
and
China
Heart
SurveysDiabetes
and
prediabetes
is
more
common
amongpatients
with
coronary
artery
disease
than
imaginedGAMI1n=16434%NormoglycaemiaPrediabetesType
2
diabetes35%31%(1.
Norhammar
et
al.
Lancet.
2002;359:2140–4)(2.
Bartnik
et
al.
Eur
Heart
J.
2004;25:1880–90)(3.
Hu
et
al.
Eur
Heart
J.2006;27:2573–9)Dysglycemia
and
coronary
artery
diseaseGlucometabolic
category
by
OGTT
in
patients
without
known
perturbationsEHS2n=1,920CHS3n=2,26336%37%27%45%37%18%DMIGTIFGNormalOGTTOGTTFPGWHOFPGADA020406080100%WHO
1999
criterion(FPG
<
6.1mmol/l)ADA
2003
criterion(FPG
<
5.6mmol/l)5%21%27%5%8%8%%
of
all
with
OGTT(Bartnik,
Rydén
et
al
Heart
2007;
93:72)Dysglycemia
and
coronary
artery
diseaseClassification
according
to
FPG
or
OGTTMortality
in
CVDRelation
to
fasting
and
postprandial
glycemia
in
patients
without
diabetesAdjusted
for
age,
gender
andarea00.5<6.1 6.1-
6.9 7.0-
7.7
>7.8Fasting
glucose
(mmol/L)(The
DECODE
study
group
Lancet
1999;
354:617)<7.8>11.17.8-11.0
OGTTRelative
risk2.521.51(mmol/L)Guideline
recommendationsRecommendationClassLevelEarly
stages
of
hyperglycemia
and
asymptomatictype
2
DM
best
diagnosed
by
an
OGTT
that
givesfasting
and
2-hour
post-load
glucosevaluesIBOGTT
at
discharge(n=
168)DM33%NGT33%IGT34%Abnormal
67%Follow-uptime
(months)NormalAbnormalProbability
of
event
free
survivaltwo-sided
p
=
0.0020
10
20
30
4050Time
to
Major
Cardiovascular
Event0.80.70.01.00.9GAMI
-
major
cardiovascular
events(Bartnik
et
al
Europ
Heart
J
2004;
25:1990)GlucometabolicstateEuro
Heart
Survey
diabetes
and
the
heartSurvival
in
relation
to
glucometabolic
stateKnownDMNew
DM1.000.960.980100
200400300Follow
up
time
(days)(Lentzen
et
al
Europ
Heart
J
2006;
27:2969)0.92NormalIGT0.94Log
rank
test
p
<0.001Survival
probabilityGlucometabolic
stateGuideline
recommendationsRecommendationClassLevelThe
definition
and
diagnostic
classification
of
DMandprestates
should
be
based
on
the
level
of
subsequentrisk
for
cardiovascular
complicationsInformation
on
post-load
glucose
provides
betterinformation
about
future
risk
for
CV
disease
thanfasting
glucose,
and
elevated
post-load
glucosealso
predicts
increased
CV
risk
in
subjectswithnormal
fasting
glucoseIIBAProject
team
every
3
monthsStrict
therapeutic
targetsBehavioural
modificationfat
<30%
(satur
<10%)exercise
30
min
x3-5/weeksmoking
cess
coursesVitamin
supplementationStepwise
introduced
drugsHypoglycemic
regimenaccording
to
strict
rulesBy
their
GPGuidelines
byDanish
Med
Ass
1998&
2000Referral
if
neededn
=
53
(average
3
times/pat)Intensive
treatmentConventional
treatmentMultifactorial
intervention
in
type
2
diabetes(Gaede
et
al
New
Engl
Med
2003;348:383)The
Steno
2
study
–
8
year
follow
upManagement
principlesMultifactorial
intervention
in
type
2
diabetesThe
Steno
2
study
–
8
years
of
follow
upComposite
endpointCV-death,
MI
or
stroke,
CABG
or
PCI,
limb
amputation
or
vascularsurgeryImpact
of
intensive
therapyonCardiovascular
diseaseOR0.470.3995%
CI0.24-0.730.17-0.87NephropathyRetinopathy0.420.21-0.86Autonomic
neuropathy0.370.18-0.79(Gaede
et
al
New
Engl
Med
2003;348:383)MicrovascularMortality4
years13yearsn=80n=80n=160MicrovascularMortality4
years13yearsMacrovascular8
yearsMacrovascular8
yearsPrimaryendpoint1993199720012006Multifactorial
intervention
in
type
2
diabetes(Gaede
et
al
New
Engl
J
Med
2008;
358:
580
)The
Steno
2
study
–
13
years
follow
upExtendend
study
protocolConventionalIntensiveImpact
of
intensive
therapyonOR95%
CIARRp-valueAll-cause
mortality0.540.32-0.8920%0.015Cardiovascular
mortality0.430.19-0.9413%0.036Major
cardiovascular
events0.410.25-0.6329%<0.001Multifactorial
intervention
in
type
2
diabetesThe
Steno
2
study
13
year
follow
upNumber
of
patients
needed
to
treat
for13
years
to
aviodone...Death5Cardiovascular
death8Major
cardiovascular
event3Progression
tonephropathy5(Gaede
et
al
New
Engl
J
Med
2008;
358:
580
)p<0.00104000,910,920,940,930,960,950,970,981,000,99No
DM
EBM
+No
DM
EBM
-DM
EBM
+DM
EBM
-100
200
300Time
of
follow
up
(days)Euro
Heart
Survey
diabetes
and
the
heartImpact
of
Evidence
Based
Medicine
(EBM)
on1-yearmortality(Anselmino
et
al
Europ
J
Cardiovasc
Prev
Rehab
2008;
In
press)Cumulative
survivalEuro
Heart
Survey
diabetes
and
the
heartImpact
of
Evidence
Based
Medicine
(EBM)
on1-year
CVE0,820,860,900,941,000,98p<0.0010300400No
DM
EBM
+No
DM
EBM
-DM
EBM
+DM
EBM
-(Anselmino
et
al
Europ
J
Cardiovasc
Prev
Rehab
2008;
In
press)100
200Time
of
follow
up
(days)Cumulative
survivalp<0.00101004000,910,920,940,930,950,960,970,981,000,99DM
RV
+DM
RV
-No
DM
RV
+No
DM
RV
-Euro
Heart
Survey
diabetes
and
the
heartImpact
of
Revascularisation
on
1-year
mortality(Anselmino
et
al
Europ
J
Cardiovasc
Prev
Rehab
2008;
In
press)Cumulative
event
free
rate200
300Time
of
follow
up
(days)p<0.0010,800,820,840,860,880,900,920,940100200
300Time
of
follow
up
(days)400No
DM
RV
+No
DM
RV
-DM
RV
+DM
RV
-1,000,96Euro
Heart
Survey
diabetes
and
the
heartImpact
of
Revascularisation
on
1-year
cardiovascular
events(Anselmino
et
al
Europ
J
Cardiovasc
Prev
Rehab
2008;
In
press)Cumulative
event
free
rateEuro
Heart
Survey
diabetes
and
the
heartNumber
needed
to
treat
(NNT)
with
EBM
and
RevascularisationTreatment
typeDiabetesNNT
to
avoid
one
eventFatalCardiovascularEvidenceBasedNo1826141MedicineYes2432RevascularisationNo10541Yes3414Evidence
Based
MedicineRevascularization(Anselmino
et
al
Europ
J
Cardiovasc
Prev
Rehab
2008;
In
press)Guideline
recommendationsLifestyle
modificationSmokingcessationBPHbA1c (DCCT
standard)Venous
plasma
glucoseCholesterolLDLHDLTriglyceridesStructured
educationObligatory<130
/
80
mm
HgRenal
dysf
<125/75≤6.5%mmol/l<6.0mg/dl108<4.5175<1.870male
>1.0;
female>1.240;
76<1.7150VariableTargetImplications
of
the
European
and
China
Heart
SurveysDiabetes
and
prediabetes
is
more
common
amongpatients
with
coronary
artery
disease
than
imaginedNewly
detecteddysglycemia
relatesto
impairedprognosisA
multifactorial
riskfactor
management
importantGlucose
controlIn
patients
with
established
diabetesIn
patients
with
newly
detected
glycemic
perturbationswiwitthh
CCAADD(Stettler
C
et
al.
Am
Heart
J
2006;
152:
27)PeripheralCardiacCerebrovascularAny
macrovascularIncidence
Rate
Ratio●●●●●●●●Glycemic
controlEvidence
for
impact
on
cardiovasculareventsGlycemic
controlEvidence
for
impact
on
cardiovasculareventsThe
STOP
NIDDM
trial,
testing
the
possibility
to
preventprogression
from
impaired
glucose
tolerance
to
diabeteswith
acarbose….demonstrated
a
49%
relative
risk
reduction
of
the
three-year
risk
for
CVE
compared
to
placebo(Chiasson,
J.L.
et
al.
JAMA
2003;
290:486)Glycemic
controlIncidence
of
composite
cardiovascular
events
in
the
STOP-NIDDM
trial2
3
4
5Follow
up
time
(years)Cumulative
incidence
(%)01AcarbosePlacebo5(Chiasson,
J.L.
et
al.
JAMA
2003;
290:486)43210Log
rank
testp=0.04Cox
proportional
model
p=0.03496146763940EnrolledLostto
follow-upStudy
populationGlucometabolicstate
availableGlucometabolic
state
unknown285*736*1819OGTT 696FPG947Normal
glucoseregulation1116Impairedglucoseregulation1425Knowndiabetes452Newly
detecteddiabetes452Newly
detecteddiabetesGlycemic
controlExperiences
from
the
Euro
Heart
SurveyStudy
population(Lentzen
et
al
Europ
Heart
J
2006;
27:2969)Prescribedglucoselowering
drugs77(17%)1%16%<1%83%InsulinOraldrugsCombinationsNoprescriptionNewly
detecteddiabetesn
=
452Not
prescribedglucoselowering
drugs375
(83%)Glycemic
control(Anselmino
et
al;
Europ
Heart
J
2008;
29:177)Experiences
from
the
Euro
Heart
SurveyGlucose
lowering
drugs
at
follow
up
in
patients
with
newly
detected
diabetes0,900,940,920,960,981,00Log
rank
testp=0.047YesNo0100
200300400Cumulative
event
free
rateTime
of
follow
up
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