Cardiovascular complications of thyroid dysfunction · Cardiovascular complications of thyroid...
Transcript of Cardiovascular complications of thyroid dysfunction · Cardiovascular complications of thyroid...
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CardiovascularCardiovascular complicationscomplications of of thyroidthyroid dysfunctiondysfunction
Brigitte VelkeniersDepartment of Internal Medicine-EndocrinologyUZ-Brussel Free University of Brussels (VUB)
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titel2 16-12-2007Klein I, Circulation, 2007
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titel3 16-12-2007
Direct effects of T3
on the heart
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titel4 16-12-2007
KleinN Engl J Med2001
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titel5 16-12-2007
T3 and contractile events:
inotropic effects (related to contraction)
lusitropic effects (related to relaxation)T3 markedly shortens diastolic relaxation .
The hyperthyroid heart relaxes with a higher speed, whereas diastole is prolonged in hypothyroid states(lusitropic activity)
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titel6 16-12-2007
Klein , N Engl J Med, 2001
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titel7 16-12-2007
Effects of treatment of hyperthyroidism on cardiovascular morbidity and mortality
Subclinical thyroid dysfunction and the cardiovascular system
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titel8 16-12-2007
Hyperthyroidism and the cardiovascular system
Cardiac arrhytmia and hyperthyroidism
Long term morbidity and mortality of treated
hyperthyroidism
Effects of subclinical hyperthyroidism on the
CV system (to treat or not to treat ?)
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titel9 16-12-2007
Hyperthyroidism and the heart
Parry 1786
“ There is one malady which I have in five cases seen, coincident with what appeared enlargement of the heart , and which, so far as I know has not been noticed in that connection, by medical writers. The malady to which I allude is enlargement of the thyroidgland “
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titel10 16-12-2007
Cardiac symptoms in hyperthyroid patients
chronotropic alterations: sinus tachycardiaatrial fibrillationshortened PR intervals
inotropic alterations: increased CIincreased stroke volumedecreased ejection perioddiastolic relaxation shortened
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titel11 16-12-2007
Main symptoms: palpitations
increase in heart rate
maintained circadian rhythm of heart rate
increased heart rate variability
increased incidence of atrial fibrillation (AF)
ventricular arrhytmia = rare in patients without
cardiac disease
24 h ECG recordings
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titel12 16-12-2007
Cellular mechanisms of AF and hyperthyroidism
Genomic and non genomic actions on atrialion channelsEnlargement of atrium as a result of the expanded blood volumeHigh prevalence of pulmonary hypertension ( no effect on pulmonary vasculature) and atrioventricular valve regurgitation(65 % of patients with Graves’ disease were found to have PAHT) Marvisi et al, Eur J Intern Med, 2006
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titel13 16-12-2007
Prevalence of AF
10-15 % of hyperthyroid patients develop AF , risk increases with age
Prevalence of hyperthyroidism in newly diagnosed AF:< 1 – 15 %
(Nakazawa et al, 2000; Forfar et al , 1979)
Screening for TSH:American College of Cardiology and American Heart Association(ACC – AHA)Task ForceN Engl J Med, Page RL 2004
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titel14 16-12-2007
Is the frequency of stroke and systemic embolismincreased in thyrotoxic AF? Very controversial
Thrombo-embolic risk in thyrotoxic AF increases with
age
men
o associated cardiomyopathy (ischemic or valvular disease,congestiveheart failure)
Danish National Registry
No controlled studies have evaluated the impact of anticoagulation onmorbidity and mortality
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titel15 16-12-2007
Only one study included treated patients with hyperthyroidismAFASAK study Peterson, lancet 1989Thromboembolic events :16 in warfarin arm (5%)12 in aspirin arm (4%)13 in placebo group ( 4%)Insufficient to draw conclusions
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titel16 16-12-2007
Antithrombotic therapy should be chosen based on associated risks and the risk of bleeding, as stated by international guidelines
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titel17 16-12-2007
Objectives of treatment
Rhythm control (β-blockade)
treatment of hyperthyroidism (anti-thyroid drugs, I131)
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titel18 16-12-2007
Shimizu et al, Thyroid, 2002
Timing of spontaneous restoration to sinus rhythmafter attainment of euthyroidism
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titel19 16-12-2007
Shimizu et al, Thyroid, 2002
Proportion of patients remaining in sinus rythm with timeafter cardioversion
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titel20 16-12-2007
Hyperthyroid-tachycardiomyopathyRate related left ventricular dysfunction and heart failure
Pre cardioversion Post cardioversion
With the courtesy of Prof Guy Van Camp
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titel21 16-12-2007
Hyperthyroidism and left ventricularhypertrophy and mortality
Left VH = risk factor for:
ischemic heart disease
CVA
heart failure
ventricular arrhytmia
sudden death
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Dorr et al., JCEM, 2005Association of hyperthyroidism and Left Ventricular HypertrophyCross sectional survey in West-Pomerania , Germany1510 participants
1.5% 0.5%13.3%
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titel23 16-12-2007
Dorr et al., JCEM, 2005Association of hyperthyroidism and Left Ventricular Hypertrophy OR and 95% CICross sectional survey in West-Pomerania , Germany1510 participants
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titel24 16-12-2007
Follow-up after treatment of hyperthyroidism: morbidity en mortality
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titel25 16-12-2007
Main studies on cardiovascular mortality in treated overt hyperthyroidism
Increase in all cause mortality (SMR, 1.3; 95% CI, 1.2-1.4), risk of fatal events due to circulatory system disease (SMR, 1.4; 95% CI, 1.3-1.6)
Mortality data and causes of death compared with data on age-specific mortality
1763 hyperthyroid subjects, treated with radioactive iodine
Retrospective cohort-studyPart of the Cooperative ThyrotoxicosisTherapy follow up Study17.2 years follow-up
Goldman et al 1988USA
Main outcomeMain measures
SubjectsDesignStudy
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titel26 16-12-2007
Increased risks of cardiovascular diseases in toxic goiter (RR, 1.50; 95% CI, 1.11-2.02) and Graves’ disease (1.42; 95% CI, 1.20-1.67) despite restoration of euthyroidism
Number of hospitalizations for cardio or cerebrovascular disease or death compared to matched control patients
2230 patients with toxic multinodulargoiter or Graves’disease
Retrospective (medical records), case-control study; 20-year follow-up
Nyirenda et al 2005Scotland
Increased risk of death from cardiovascular disease (SMR 1.65; 95% CI, 1.59-1.71)
Causes of death matched with a cause of death register (matched)
10000 hyperthyroid patients after radioiodine treatment
Case-control study; 15-year follow-up
Hall et al 1993Sweden
Main outcomeMain measuresSubjectsDesignStudy
Main studies on cardiovascular mortality in treated overt hyperthyroidism
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titel27 16-12-2007
Main studies on cardiovascular mortality in treated overt hyperthyroidism
Increase in all cause mortality (SMR, 1.1; 95% CI, 1.1-1.2), risk of fatal events due to cardiovascular disease (SMR, 1.2; 95% CI, 1.2-1.3), and cerebrovascular disease (SMR, 1.4; 95% CI, 1.2-1.5)
Mortality data and causes of death compared with data on sex –and age-specific mortality
7209 hyperthyroid subjects, treated with radioactive iodine
Retrospective Population-based cohort-study
At least 7 years and some patients 40 years105028 person years of follow-upMean follow-up 14.6 years
Franklyn et al 1998UK
Main outcomeMain measuresSubjectsDesignStudy
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titel28 16-12-2007
1. Increased all-cause (SMR, 1.14; 95 % CI, 1.04-1.24) and cardiovascular mortality (SMR 1.19; 95% DI 1.05-1.35) in hyperthyroid patients.
2. Decreased all-cause, mortality (HR, 0.65; 95% CI 0.54-0.79) and circulatory mortality (HR, 0.65; 95% CI, 0.48-0.87) during T4 therapy of post radioiodine hypothyroidism compared to periods without T4 substitution.
1. Causes of death compared with age- and period-specific mortality
2. Influence of T4 therapy and subclinical thyroid dysfunction on mortality
2668 individuals with overt hyperthyroidism, aged 40 years or older, treated with radioiodine
Population-based surveyUK
Mean follow-up 6 years
Franklyn et al 2005
UK
Main outcomeMain measuresSubjectsDesignStudy
Main studies on cardiovascular mortality in treated overt hyperthyroidism
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titel29 16-12-2007
No increase in all-cause mortality or cardiovascular mortality.Increased risk of arrhytmiaSIR: 2.71 (1.63-4.24)
All cause mortalityCardiovascular events compared with data on age-specific mortality and morbidity
3888 hyperthyroid patients
Population based cohort –study
Mean follow-up 5 years
Flynn et al2006
UK
Main outcomeMain measuresSubjectsDesignStudy
Main studies on cardiovascular mortality in treated overt hyperthyroidism
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titel30 16-12-2007
1. Increased all-cause mortality in treated hyperthyroid patients. RR 1.12 (CI 1.03-1.20) only in patients older 60 years., in patients with nodular thyroid disease but not in patients with Graves’disease
2. Increased CV mortality (RR1.19 (CI 1.07-1.32) cerebrovascular disease mortality (RR 1.40)
3. Decreased all-cause mortality with development of hypothyroidism that was treated
( RR 0.52)
1. Causes of death compared to controls
2. Mortality of patients with Graves’ disease compared to multinodulargoiter
2793 individuals with overt hyperthyroidism, treated with radioiodine compared to 2793 reference subjects
Prospective Case control study
Mean follow-up 9 years
Mesto et al 2007
Finland
Main outcomeMain measuresSubjectsDesignStudy
Main studies on cardiovascular mortality in treated overt hyperthyroidism
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titel31 16-12-2007
Overt hyperthyroidism Conclusions
Hyperthyroidism increases CV morbidity ( AF, Le VH) and mortality
In those who have been treated for hyperthyroidism the increasedrisk of arrhythmia persists with increased CV mortality (cerebrovascular and cardiovascular disease) in some (Franklyn, Metso) but not all studies (Flynn ).
The increased mortality is probably explained by hyperthyroidismResults based on 4 different populations (USA, Sweden, Finland, UK)
Most patients with increased CV risks had multinodular goiter and were treated with higher doses of radioiodine
Levothyroxine - treated hypothyroidism after radioiodine seems to protect against excess mortality (Franklyn, Metso)
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titel32 16-12-2007
A 67 year old woman presents with palpitations and is found to be in atrial fibrillation at a rate of 120 beats per minute. The only other finding on physical examinationis a goiter, which is known to be long-standing. Echocardiography shows neither valvular disease nor left ventricular systolic dysfunction. The serum TSH is less than 0.05 mU/l, and the serum fT3 and FT4 concentrations are in the normal range. Should the thyroid dysfunction be treated?
“clinical vignette”
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titel33 16-12-2007
SUBCLINICAL HYPERTHYROIDISM
Definition:TSH below normal range usually suppressed ,normal fT4 fT3
Etiology:Exogenous subclinical hyperthyroidismAsssociated with LT4 therapyEndogenous subclinical hyperthyroidismGraves’ diseaseMultinodular goitreAutonomously functioning noduleActivating mutations of TSH R Bieberman et al. 2001Transient:Thyroiditis de Quervain, silent, postpartumDrug induced amiodarone, interferon
dd low TSHNon thyroidal illness , dopamine , corticosteroids
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SUBCLINICAL HYPERTHYROIDISM
PrevalenceVaries according to iodine intake, age and functional sensitivity of TSH assay
Parle et al. 1991 6%Sawin et a. 1994 1.8Hollowel et al 2002 0.7%after exclusion of patients with thyroid disease
Approximately 25% of patients on LT4 have low TSH
PROGRESSION TO OVERT HYPERTHYROIDISMWiersinga et al.1995 5% per yearSanrock et al.1993 4% per yearSawin et al. 1991 3 % over 4 years
with autonomously functioning nodules
Persons with low but detectable TSH may recover spontaneously
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titel35 16-12-2007
Serum thyrotropin measurement in the communityMeyerovitch et al Arch Intern Med, 2007
422242 patients included
No history or treatment for thyoid disorders
95 % normal TSH( 0.35-5.5 mU/l), 1.2% decreased TSH (< 0.35 mU/l), 3 % were elevated (< 5.5-10 mU/L), 0.7 % were highly elevated (< 10 mu/l)
After 5 years of follow-up in the group with suppressed TSH 51.2% became normal
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titel36 16-12-2007Copyright restrictions may apply.Meyerovitch, J. et al. Arch Intern Med 2007;167:1533-1538.
Distribution of second thyrotropin (TSH) results compared with the category of the first TSH measurement in patients with no medical treatment between measurements
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titel37 16-12-2007
SUBCLINICAL HYPERTHYROIDISMAND CARDIOVASCULAR MORBIDITY AND MORTALITY
Rationale for therapy?
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titel38 16-12-2007
Subclinical Hyperthyroidism and hypertension Walsh et al, Clin Endocrinol, 2006
Cross-sectional study of 2033 participants in the Busselton Thyroid Study with no history of thyroid disease
SBP, DBP and prevalence of hypertension
The prevalence of hypertension was higher in a group of subjects with subclinical hyperthyroidism ( n= 35) than in euthyroid patients OR 2.8 ( CI 1.3-6.0)
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titel39 16-12-2007
CV Morbidity: Left ventricular hypertrophy in subclinical hyperthyroidism ?
Biondi et al MGullu et al Mercuro et al Cardiac mass increase- posterior wall thickening- interventricular wall thickening- left ventricular mass increased- decreased isovolumetric relaxation time- decreased exercise capacity
Dorr et al. Cross-sectional population based study, 2005Doppler echocardiography : no increased incidence in LVMI (left
ventricular mass index)
Iqbal et al., Cross-sectional population based study,2007Transthoracal echography : No change in LVMI Changes in myocardial velocities measured by PTWD pulsed waved
tissue doppler (= diastolic dysfunction)
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titel40 16-12-2007
AF and subclinical hyperthyroidism
Tenerz et al, J Int Med, 1990
Prevalence AF: 8/40 patients
follow-up 2 years: + 3 patients
= 11/40 = 28 % subclinical hyperthyroidism
10 % euthyroid patients
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titel41 16-12-2007
Sawin et al, N Engl J Med, 1994
2007 individuals of the Framingham Cohort
≥ 60 years, no AF at the start of the study
61 persons : TSH ≤ 0.1 mU/L
187 persons : TSH 0.1 – 0.4 mU/L
1576 persons: TSH 0.4 – 5 mU/L
183 persons: TSH ≥ 5 mU/L
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TSH < 0.1 mU/L 21 % 3 RR
TSH 0.1 – 0.4 mU/L 18 % 1.8
normal TSH 8 %
Sawin et al, N Engl J Med, 1994
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titel43 16-12-2007
Auer et al, Lancet, 2002
23 638 patients613 subclinical hyperthyroidism (TSH < 0.4 mU/L)
AF
513 with normal TSH: 2.3 % RR78 with TSH ≤ 0.4: 12.7 % 5.2 (2.1 – 8.7)
After correction for age, other risk factors(hypertension, LVH, cardiomyopathy)
3No follow-up of cardiovascular morbidity, mortality
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Gammage et al, Arch Intern Med 2007
5860 subjects 65 years and olderMain outcome measures: thyroid function ( fT4 and TSH) and the presence of AF on resting ECG126 (2.2%) had subclinical hyperthyroidismIncreased prevalence of AF in patients with subclinical hyperthyroidism, compared to euthyroid individuals ( 9.5 % vs 4.7%) OR 2.27 Logistic regression showed fT4 concentration to be independently associated with risk of AF (even in euthyroid patients with normal TSH)
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titel45 16-12-2007
Mortality: Parle et al, Lancet, 2001
1191 persons ≥ 60 years, without T4 treatment, noantithyroid drugsserum TSH measured“baseline” , follow-up: 10 years
Standardized mortality ratio (SMR)
2.1 (1 – 4.5) after 2 years
2.2 (1.2 – 4) after 3 years
1.9 4 years
2 5 years
↑ mortality= ↑ mortality of cardiac and cerebrovascularevents
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titel46 16-12-2007
SUBCLINICAL HYPERTHYROID.
EXCESS VASCULAR MORTALITYCommunity basedcohort study :1160 patients aged 60 years or over not receiving T4 therapy or antithyroidmedications withsubclinicalhyperthyroidismfollowed over 10 yearsParle et al. 2000
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An estimate of relative and absolute excess mortality from all causes based on data searches and time-to-event meta-analysis of cohort studies
Seven cohorts = 290 patients with subclinical hyperthyroidism
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290
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All Cause mortality and subclinical hyperthyroidism
Pooled HR 1.72 ( 1.35-2.19)
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Absolute excess mortality calculated for US women and menCalculated with pooled HR and standard life table methods applied to a US reference population
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titel54 16-12-2007
Subclinical hyperthyroidism and CV system
Subclinical hyperthyroidism increases CV morbidity(AF ) and overall mortality
All cause mortality was increased two –fold The absolute excess mortality largely depends on age of diagnosis.
In contrast to all cause mortality ,mortality of coronary artery disease was not increased .
No placebo controlled studies on mortality after the treatment of subclinical hyperthyroidism.
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titel55 16-12-2007
The patient of the “vignette”
Surks et al., JAMA, 2004
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titel56 16-12-2007
Hypothyroidism and the CV system
Subclinical hypothyroidism and the CV system
Effects of treatment of hypothyroidism on CV system
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titel57 16-12-2007
Hypothyroidism and the CV system
Sir Dr William Smith Greenfield 1878
“ There was edema of the skin - much serous effusion
in the pericardium…the heart was large…the arteries
were everywhere thickened , the larger one
atheromatous ”
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titel58 16-12-2007
Clinical Hypothyroidism
BradycardiaMild hypertensionNarrowed pulse pressureDecreased cardiac contractilityAccelerated atherosclerosisCoronary atherosclerosisProlongation of the QT interval with ventricular irritability (rarely torsade de pointes)
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titel59 16-12-2007
A 69-year old woman is found to have a serum TSH of 7.9 mU/l on routine screening. Her only symptomsare mild fatigue, which has been present for more than 10 years , and difficulty losing weight. The results of the physical examination are normal, exceptfor a small, firm thyroid with a slightly irregularsurface. The serum cholesterol level is 220 mg/ dl, the LDL-C is 140 mg/dl, and a test for antibodiesagainst thyroperoxydase is positive. Should treatment with thyroxine be initiated?
“clinical vignette”
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titel60 16-12-2007
Age-specific Distribution of Serum TSH and Thyroid antibodies in the United States Population ; Implications of subclinical hypothyroidism J CEM , 2007 Surks MI, Hollowell JG
“TSH distribution progressively shifts toward higher concentrations with age. The prevalence of subclinical hypothyroidism may be significantly overestimated unless an age-specific range for TSH is employed”
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titel61 16-12-2007
Hypothyroidism (clinical and subclinical) and CV morbidity and mortality
Experimental data suggest that hypothyroidism may prolong life span in different animal models (reduced metabolic rate)
Overt hypothyroidism is associated with major CV risk factors such as hypertension, dyslipidemia, systemic inflammation, and insulin resistance.
Similar effects on cardiometabolic risk factors have been reported for subclinical hypothyroidism
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titel62 16-12-2007
Lipids
Cross sectional data: conflicting results : total cholesterol values in patients with subclinical hypothyroidism are similar to those of normal subjects
Colorado survey: statistically higher total and LDL cholesterol in subjects withMild thyroid failure vs. Euthyroid subjects ( TC 224 mg/dl, vs.216mg/dl)
Dia JCEM Mc Dermott fig3
Canaris et al., 2000
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titel63 16-12-2007
Hak et al., Ann Intern Med, 2000
Association of aorta atherosclerosis and myocardial infarction is strongerin subclinical hypothyroidism and associated thyroid autoimmunity
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titel64 16-12-2007Hak at al. 2000
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titel65 16-12-2007
Subclinical hypothyroidism and the risk of coronary heart disease : A meta-analysis Rodondi et al, AJM, 2006
Systematic review of all available data till April 2005
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titel66 16-12-2007
Subclinical hypothyroidism and the risk of coronary heart disease : A meta-analysis Rodondi et al, AJM, 2006
Review indicates that subclinical hypothyroidism is
associated with an increased risk of CHD (summary
OR for coronary artery disease: 1.81 (1.38-2.39)
Did not include the Gussekloo paper and three newly
published articles ( Walsch, Rodondi, Cappola)
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titel67 16-12-2007
Impact of subclinical thyroid disorders on coronary heart disease, cardiovascular and all cause mortality Singh et al In J Cardiol, 2007
Prevalence at baseline
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titel68 16-12-2007
Impact of subclinical thyroid disorders on coronary heart disease, cardiovascular and all cause mortality Singh et al In J Cardiol, 2007
Risk of developing CHD
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titel69 16-12-2007
Impact of subclinical thyroid disorders on coronary heart disease, cardiovascular and all cause mortality Singh et al In J Cardiol, 2007
All cause mortality
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titel70 16-12-2007
The relation of thyroid dysfunction with all-cause and circulatory mortalityVolzke et al, J Clin Endocrinol Metab, 2007
Pooling of studies revealed a NS HR for circulatory disease HR 1.21 ( 0,86- 1.69)Pooling of studies revealed a S HR for all-cause mortality HR 1.25 ( 1.03- 1.53)
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An estimate of relative and absolute excess mortality from all causes based on data searches and time-to-event meta-analysis of cohort studies
Seven cohorts = 1580 patients with subclinical hypothyroidism
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1580
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All Cause mortality and subclinical hypothyroidism
HR 1.03 (CI 0.78-1.35)In cohorts from the communityHR 1.76 ( CI 1.36- 2.30)In cohorts with comorbidities
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titel75 16-12-2007
Discrepancies among meta-analyses
All analyses quoted heterogeneity
Different end point analysed ( CV mortality or all cause mortality)
Data analysis of different publications may give some clues (severity of subclinical dysfunction, age of the population, comorbidity…) to the detrimental effects of subclinical hypothyroidism
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titel76 16-12-2007
The Fremantle Diabetes studyAustraliaChubb et al,clin Endocrinol 2006
Subclinical hypothyroidism and mortality in women with type 2 diabetes
Mild thyroid dysfunction in cardiac patientsItalyIervasi et Arch Intern Med 2007
Subclinical hypothyroidism and mortality in patients with heart disease
Interaction of subclinical hypothyroidism with other CV risk factors on CV related- and total mortality
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titel77 16-12-2007
Gussekloo et al, JAMA, 2004
Prospective follow-up of 85 years old in Leiden
599 participants
Aims: to determine the impact of subclinical thyroid dysfunction
on performance and survival in old age
Prevalence of subclinical hypothyroidism: 12 %
After 4 years of follow-up:
Lower cardiovascular mortality + morbidity
subclinical hyperthyroidism: ↑ CV mortality
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titel78 16-12-2007
Gussekloo et al., JAMA, 2004
Fig 2 cumulative mortality of participants
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titel79 16-12-2007
Subclinical Thyroid dysfunction as a risk factor for cardiovascular disease Walsh et al, Arch Intern Med, 2005
2108 subjects measurement of TSH and fT4
Cross sectional analysis of coronary artery disease
Longitudinal follow-up of cardiovascular mortality and
coronary artery events after a mean follow-up of 20
years
119 subjects with subclinical hypothyroidism
Mean age 51,3 years
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titel80 16-12-2007
Prevalence Odds Ratios for Coronary Heart Disease in the Cross-sectional Analysis of All Subjects*
Subclinical Thyroid dysfunction as a risk factor for cardiovascular disease , according to category of TSH elevationWalsh et al, Arch Intern Med, 2005 Cross-sectional data
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titel81 16-12-2007
Hazard Ratios for Coronary Heart Disease Events (Fatal and Nonfatal) in the Longitudinal Analysis of Subjects Free of Coronary Heart Disease at Baseline*
Subclinical Thyroid dysfunction as a risk factor for cardiovascular disease ,according to category of TSH elevationWalsh et al, Arch Intern Med, 2005
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titel82 16-12-2007
Subclinical Thyroid dysfunction as a risk factor for cardiovascular disease Walsh et al, Arch Intern Med, 2005Conclusions
At entry the prevalence of CHD was significantly increased after adjustment for age and sex in severe subclinical hypothyroidism ( TSH > 10 mU/l), but not in patients with mild to moderate hypothyroidism ( TSH 4.1- 10 mU/l)During the 20 years of follow-up ; the incidence of CHD disease was significantly increased in patients with severe SH ,whereas the increase was of borderline significance in the group with mild SHNo increased incidence of mortality from CVD in patients with SH of any degree
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titel83 16-12-2007
Subclinical hypothyroidism and the risk of heart failure, other cardiovascular events and deathRodondi et al , Arch. Intern Med, 2005
2730 men and women aged 70 to 79 years of age
4 years of follow-up
End-points: congestive heart failure, coronary artery
disease, stroke, peripheral arterial disease
Cardio-vascular-related and total mortality
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titel84 16-12-2007
Cumulative congestive heart failure (CHF) events in older subjects according to thyrotropin (TSH) levels
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titel85 16-12-2007
Subclinical hypothyroidism and the risk of heart failure, other cardiovascular events and death, according to category of TSH elevation Rodondi et al , Arch. Intern Med, 2005
Subclinical Hypothyroidism and the Risk of Cardiovascular-Related and Total Mortality NS
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titel86 16-12-2007
Subclinical hypothyroidism and the risk of heart failure, other cardiovascular events and deathConclusions Rodondi et al , Arch. Intern Med, 2005
At entry, no association existed between SH and the prevalence of CVD including congestive heart failure (CHF)
The incidence of CHF during the 4 year follow-up period was significantly increased in patients with moderate (TSH: 7-9.9 ) and severe SH (TSH > 10 mU/L), but not in patients with mild SH (TSH ,4.5-6.9 mU/L)
No association with increased death from CVD or the risk of incident CHD
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titel87 16-12-2007
Interventional studies and effects on atherosclerosis
Angiographic studyPerk et al. Can J Card 1997greater progression of coronary atherosclerosis in subclinical hypothyroidism compared to patients withnormal TSH
One underpowered study did not show an increase in cardiovascular morbidity and mortality in patients treatedwith T4 (only 29 patients , follow-up :12 years)Peterson et al.,Arch Intern Med , 1990
No placebo controlled trial available
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titel88 16-12-2007
SUBCLINICAL HYPOTHYROIDISMConclusions
Taken together the studies suggest that the incidence of cardiovascular disorders may be increased in subclinical hypothyroidism, particularly those with a TSH > 10 mU/L
The data support the idea that patients under 80 yearswith TSH > 10 mU/ L may benefit from treatment, but this remains to be proved in prospective randomized trials
The studies also suggest that subjects with mild SH ( TSH < 10mU/L) and patients older than 80 years show no increased CVD risk and that treatment would probably not be beneficial in the prevention of CVD
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titel89 16-12-2007
Mortality and vascular outcomes in patients treated for thyroid dysfunctionFlynn et al., JCEM, 2006
15889 patients treated for hypothyroidism between 1993 and 2001. Incident cases : 7904 patients
Primary outcome :All cause mortality (SMR)Circulatory mortality and cancer mortality (SMR)
Secondary end points:Serious vascular events , circulatory disease and cerebrovascular disease ( SIR= standardized incidence ratio )
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titel90 16-12-2007
Mortality and vascular outcomes in patients treated for thyroid dysfunctionFlynn et al., JCEM, 2006
Prevalence of treated hypothyroidism: 3.4%8.4 % of these patients had diabetes ( three times increased risk)Over 8 years mortality : SMR 1.03 (CI 0.99-1.07) : ns excess of 73 deaths, but there was an increase in cardiovascular disease mortality : 1.11( CI 1.00-1.23)Over 8 years serious vascular events :SIR 1.10 (CI 1.06-1.15 ): s. excess of 181 cases, adjusted for age, sex and diabetesOver 8 years there was an increased morbidity related to ischemic heart disease, dysrhythmias and cerebrovascular disease
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titel91 16-12-2007
Mortality and vascular outcomes in patients treated for thyroid dysfunction . ConclusionsFlynn et al., JCEM, 2006
Despite treatment for primary hypothyroidism with T4 patients are at increased risk of morbidity associated with vascular disease.
This risk is ongoing beyond the initial years of treatment
Biological explanations:Primary hypothyroidism was diagnosed late.Treatment with T4 may not fully reverse the atherosclerosis process
Treatment with T4 was not optimal ( normal TSH)
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titel92 16-12-2007
Mortality and vascular outcomes in patients treated for thyroid dysfunction
Shortcomings of the studyFlynn et al., JCEM, 2006
Reliance on SMR record-linkage (general practitioners)No adjustments for concurrent medications , ie statins
Unadjusted confounders ie smoking
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titel93 16-12-2007
Subclinical hypothyroidism :To treat?
High risk of progression to clinical hypothyroidism
Data on cardiovascular morbidity and mortality are controversial
dyslipidemia, endothelial dysfunction, hypercoagulation,
↓ fibrinolysis = substrates for ↑ cardiovascular mortality
No placebo-controlled studies on hard clinical endpoints (CV mortality en morbidity)
Only placebo controlled studies on surrogate endpoints:cholesterol- endothelial function- carotis intima media thickness
( Razvi et al, J CEM, 2007)
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titel94 16-12-2007
The patient of the “vignette”
Surks et al., JAMA, 2004
Sufficient
Sufficient
Sufficient :Razvi et al, 2007
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Subclinical thyroid dysfunction and the heartDifficult exercise