Heart Failure Clinical Trial
Official title:
Impact of Thyroid Hormone Replacement on Progression of Atherosclerosis : a Randomized Placebo-Controlled Trial in Older Adults With Subclinical Hypothyroidism.
Coronary heart disease (CHD) are the leading causes of mortality and morbidity, particularly with the current context of an aging population. Prospective cohort studies, as well as analyses of pooled individual participant data suggest up to a 60-90% increase in the risk of CHD or HF events among adults with severe SHypo. However, no large randomized controlled trials (RCT) have assessed the impact of thyroid replacement on cardiovascular (CV) imaging outcomes. The goals of this proposal are to address the impact of thyroid replacement on subclinical atherosclerosis. The investigators will conduct a RCT in 185 patients with subclinical hypothyroidism who will be randomly assigned to thyroxine or placebo with an average follow-up of 24 months from baseline. The main outcome will be CV imaging modalities measured by carotid ultrasound at the close-out visit. Assessment of the impact of thyroid replacement on subclinical atherosclerosis within a trial will aid decisions and evidence-based guidelines development to treat a potential modifiable risk factor, such as SHypo.
Background: Coronary heart disease (CHD) and heart failure (HF) are the leading causes of
mortality and morbidity, particularly with the current context of an aging population.
Subclinical hypothyroidism (SHypo), defined as elevated serum TSH levels with normal
thyroxine values, is common in older adults (5-10%). Prospective cohort studies, as well as
analyses of pooled individual participant data suggest up to a 60-90% increase in the risk
of CHD or HF events among adults with severe SHypo. However, no large randomized controlled
trials (RCT) have assessed the impact of thyroid replacement on cardiovascular (CV) imaging
outcomes (largest trial to date: 45 participants). Imaging endpoints are especially
well-suited for early trials with investigational therapies for HF treatment and prevention,
as well as validated and strong surrogate markers of clinical outcomes.
Specific Aims: The goals of this proposal are to address the impact of thyroid replacement
on subclinical atherosclerosis.
Methods: The investigators will conduct a RCT in 185 patients with subclinical
hypothyroidism who will be randomly assigned to thyroxine or placebo with an average
follow-up of 24 months from baseline (4 death and 17 withdrawal). The main outcome will be
CV imaging modalities measured by carotid ultrasound at the close-out visit. Ultrasound of
carotid intima media thickness (CIMT) will be used to assess subclinical atherosclerosis and
plaque burden. All images will be centralized at the core lab for a blinded and standardized
interpretation.
Expected value of the proposed project: Controversies persist regarding the indications for
screening and treatment of SHypo due to the lack of an appropriately powered RCT addressing
the impact of thyroid replacement on CV outcomes. Assessment of the impact of thyroid
replacement on subclinical atherosclerosis within a trial will aid decisions and
evidence-based guidelines development to treat a potential modifiable risk factor, such as
SHypo. The strengths of this study include the combination of: 1) High feasibility of the
project in collaboration with the largest RCT on SHypo making it possible to investigate the
mechanisms of associations with CV disease; 2) Innovative project with combined CV imaging
to assess subclinical atherosclerosis with thyroid replacement therapy vs. placebo; 3)
Excellent power given the large sample size and participants' older age. The sample size for
this proposal will be 5-fold higher than previous small trials of thyroid replacement on CV
outcomes and is comparable to statin trials showing a positive impact on CIMT. The
collaboration of CV imaging modalities expertise with the ongoing largest trial on SHypo, is
a unique opportunity to address the clinical and scientific issue of the impact of SHypo on
the CV system.
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