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Cardiology Research

Review

Volume 8, Number 2, April 2017, pages 31-35

Sub-Clinical Hypothyroidism and Its Association With Increased Cardiovascular Mortality: Call for Action

Thyroid hormones are responsible for regulating different functions regarding metabolism and performance in multiple organs. When the thyroid hormones axis is altered, it can lead to either hypo- or hyperthyroidism. Hypothyroidism is classified according to the clinical presentation as overt and subclinical. Subclinical hypothyroidism is defined as an increase in the levels of thyroid-stimulating hormone (TSH) with a normal level of T3 and T4 in the absence of symptoms. Overt hypothyroidism has been studied more than subclinical hypothyroidism and is well known to be associated with cardiovascular disease such as accelerated atherosclerosis and coronary artery disease. Both T3 and T4 seem to have beneficial effects in the cardiovascular system. T3 facilitates myocardial relaxation and decreases peripheral vascular resistance, whereas T4 replacement therapy has proven to be beneficial in improving hemodynamic effects in patients with subclinical hypothyroidism [1].

Currently, there exists a paucity of evidence on the beneficial effects of thyroxine hormone replacement on cardiovascular mortality outcomes in subclinical hypothyroidism. Also, the clinical relevance of measuring and treating supra-normal TSH levels in newly diagnosed heart failure patients with preserved ejection fraction requires further study. It has been proven beyond doubt that thyroid hormone metabolism can be altered in heart disease. Conversely, thyroid hormone dysfunction can result in altered ventricular contractility/relaxation dynamics and compromised cardiac function. This fact has important clinical implications in that thyroid dysfunction represents one of the few potentially reversible causes of heart failure [2].

T4 constitutes the major circulating fraction of thyroid hormone in the human body. T4 is transformed by iodothyronine deiodinase into T3, the biologically active form, responsible for thyroxine’s effects on target end organs. T3 affects the cardiac muscle through two different mechanisms, genomic and non-genomic. Genomic effects are achieved through upregulation in the expression of genes involved in the production of structural proteins including SERCA and cardiac myosin heavy chain [3]. Low thyroid hormone levels lead to decreased levels of SERCA2 activity, which controls the contraction and relaxation cycle through an ATPase with affinity for calcium, leading to myocardial stiffness and eventually left ventricular diastolic dysfunction [4]. T3 binds to the thyroid hormone receptors in the nucleus. These nuclear receptors bind themselves to thyroid hormone responsive elements located in the promoter regions of specific genes. In the heart, these types of receptors have been identified as TR alpha1, TR alpha2, TR beta1 and TR beta2 [5]. They have different functions and can act as positive or negative regulators. For instance, the TR alpha1 plays an important role in regulating some physiologic functions in the heart, while TR alpha2 has an antagonistic physiological role in exerting negative regulatory effects on TR alpha1 [6].

Thyroid hormones are involved in the regulation of hyperpolarization-activated cyclic nucleotide gated channels and proteins, and genes encoded in specialized pacemaker cells. Also, the angiotensin receptors in the smooth muscle cells of the vessels seem to be regulated by the T3 nuclear receptor [7]. Endothelial microprticles which have been linked to endothelial injury and dysfunction have also been found in patients with subclinical hypothyroidism and ischemic heart disease and congestive heart failure [2]. It has been observed that some of the involved genes encode for specific type of proteins that participate in the contraction process of the heart muscle such as alpha and beta (as mentioned above), the sodium calcium exchanger, phospholamban and the beta adrenergic receptor MHC. Once the expression of these genes is altered, there is a cascade of events where cardiac contractility, calcium cycling and diastolic relaxation can be affected with the subsequent development of heart failure [8].

Patients with low levels of thyroid hormones seem to fall into a cycle where the low levels of thyroid hormones lead to heart failure and at the same time heart failure can downregulate the signal of the thyroid hormones in the heart with a net effect of increasing overall mortality. If we combine this phenomenon with the effects on structures other than cardiac tissue, the overall mortality becomes significantly high [9]. One well known example to mention is the association between higher levels of cholesterol in patients with hypothyroidism either overt or subclinical and as we know hyperlipidemia is the main risk factor for coronary heart disease (CHD) that ultimately can lead to heart failure but more importantly some studies suggest that in more than 90% of patients with overt hypothyroidism and even patients with subclinical hypothyroidism, we can find derangements of the lipid profile including LDL and apolipoprotein A and treatment with thyroid hormones can lead to reversal of this derangements [10].

Another example to mention is the fact that some histological changes have been reported in some animal studies wherein animals have low levels of thyroid hormones; there is an accumulation of mucopolysaccharides in the heart which can lead to impairment of the myocardium similar to the one caused by other conditions that can lead to mucopolysaccharides accumulation in humans where most of them are genetic conditions and eventually lead to heart failure. Although strong evidence of this in humans lacks, there have been case reports reporting this association [11].

One last example of this ubiquitous interaction between hypothyroidism and heart failure is related to T3 levels which have shown a direct correlation with the degree of left ventricular dysfunction and levels of NT-pro beta natriuretic peptide, meaning the lower the T3 levels but more left ventricular dysfunction and the higher the biological marker. This correlation though did not exist with levels of T4 or TSH. At the clinical level there is correlation between low levels of T3 and idiopathic dilated cardiomyopathy [12].

This conclusion leads to an important question. If hypothyroidism is associated to increased mortality in heart failure, even subclinical hypothyroidism and some studies suggest that there is a benefit on replacing thyroid hormones, at what extent should we consider replacing them?

Regarding the question of whether subclinical hypothyroidism is associated to an increase or potentiation of risk factors for heart failure, we found in a study by Rodondi et al that the following risk factors have a statistically significant association with subclinical hypothyroidism: smoking, diabetes, presence of peripheral vascular disease and high cholesterol levels. In the same study, there was a direct association with congestive heart failure, although the levels of TSH were > 7 mIU/L to be statistically significant and also this was studied only in hospitalized patients [13].

Clinical signs and symptoms poorly predict thyroid status, especially in the elderly population, and the diagnosis of subclinical hypothyroidism is based purely on biochemical grounds of elevated TSH with normal free thyroxine. As the diagnosis rests on an elevated level of TSH, identifying the upper limit of reference range is critical in defining subclinical hypothyroidism. Observations from the composite of all age groups in the NHANES III study designated a TSH level of 4.5 mIU/L as upper range of normal [14]. Various studies have suggested an increase in the incidence of subclinical hypothyroidism with aging [14-16]. However, normal TSH distributions shift toward higher concentrations with age, a consequence leading to overestimation of this diagnosis in the elderly [17]. A longitudinal cohort study looking at elderly patients did not find an association between subclinical hypothyroidism and cardiovascular or all-cause mortality, raising concern for treating mildly supra-normal TSH levels based on currently recommended cut-off limits [18].

Patients with subclinical hypothyroidism represent a dimorphic population, either as pre-runners of overt hypothyroidism with risk factors of thyroid disease or with an indolent form of disease with preserved thyroid function reserve [19]. A prospective study observed that up to 55% of subclinical hypothyroid patients with TSH levels > 6 mIU/L eventually progressed to overt hypothyroidism over a 10-year follow-up period [20]. Clinical evidence of goiter and presence of anti-thyroid antibodies serve as predictive risk-stratifiers in determining progression towards overt hypothyroidism [20, 21].

The clinical importance of subclinical hypothyroidism in cardiovascular disease and mortality remains controversial, with most studies providing conflicting results. This may be explained by the selection of heterogenous patient populations, arbitrarily designated TSH reference limits in defining subclinical hypothyroidism, lack of stratification of study groups based on the degree of TSH elevation, varying study designs and paucity of randomized controlled trials directly addressing patient-outcome relationships.

Despite extensive research, there still exists clinical uncertainty on various aspects surrounding thyroid-related cardiovascular disease. The most recent ACC/AHA guidelines for the diagnosis and management of heart failure recommend measuring thyroid function in all patients with newly diagnosed heart failure, since it represents a potential reversible cause of cardiovascular disease. Nonetheless, no specific recommendations have been made with regard to the management of subclinical hypothyroidism in patients with heart failure [2].

Classification systems have been proposed grading subclinical hypothyroidism based on severity assessment into grade 1 (TSH levels < 10 mIU/L) and grade 2 (TSH > 10 mIU/L) [22]. The natural history may differ significantly between the two groups with grade 2 category patients having higher cardiovascular events and at higher rates of transition to overt hypothyroidism [23, 24]. A large prospective study involving elderly population (> 85 years) noted an association between grade 1 subclinical hyperthyroidism and decreased all-cause mortality [25]. This was later supported by a large retrospective cohort study which also noted lower mortality rates in grade 1 subclinical hypothyroidism patients, suggesting a protective benefit of mildly supra-normal TSH levels [26]. The same study observed an increase in myocardial infarction events in patients with grade 2 subclinical hypothyroidism. Similarly, an international prospective cohort study of 55,287 patients reported increased CHD events and CHD-related mortality in this subset of patients [20]. Individual participant data analysis did not identify statistically differing CHD outcomes across the age groups [20].

The higher cardiovascular mortality rates in group 2 subclinical hypothyroidism patients are related to known cardiovascular effects of thyroxine on heart function and metabolism. Cardiovascular alterations that occur in overt hypothyroidism have also been identified in subclinical hypothyroidism, effects varying only in the degree of derangement [27]. Of note, mouse model studies have demonstrated serum thyroxine levels not to reflect cardiac tissue T4 levels in mild hypothyroidism, with cardiac tissue hypothyroidism occurring in the presence of normal serum thyroxine levels [28]. Increased systemic vascular resistance, arterial stiffness, and altered endothelial function have been associated with subclinical thyroid dysfunction [27]. Enhanced cardiovascular risk can also be related to altered pro-atherogenic lipid profiles, an effect reversible with institution of levothyroxine replacement therapy [28]. The benefits of levothyroxine treatment on endothelial function and intima-media thickness have been well demonstrated in previous randomized trials [28, 29]. Whether these effects translate into improved patient-cardiovascular clinical outcomes awaits further study.

In the Health Aging and Body Composition population-based study, the authors investigated the levels of TSH effecting harmful cardiovascular effects by following patients prospectively over 4 years. The study concluded that patients with TSH levels more than 7 mIU/L and more than 10 mIU/L had a hazard ratio of 2.58 and 3.26, respectively for developing heart failure [30]. Another study conducted by Rodondi et al in over 55,000 individuals demonstrated a positive correlation between the degree of TSH elevations and cardiovascular event rates and mortality [23]. Collet et al collected data from 10 cohort studies which showed a hazard ratio for CHD-related mortality of 1.24 and 1.21 for CHD events [31]. Several studies suggest that the cutoff of TSH > 10 mIU/L may be used to define a patient with subclinical hypothyroidism with an increased risk for cardiovascular events. The Cardiovascular Health Study performed echocardiogram routinely for 6 years in a cohort of patients to determine patients at risk for developing heart failure. It was found that patients with a TSH > 10 mIU/L had higher risk of heart failure with low ejection fraction as compared to the population with normal thyroid function [7]. Collet et al also proved that the antibody status of an individual does not render higher risk for CHD since patients with clinical and subclinical hypothyroidism may or may not have positive antibodies [32].

The cardiac-ankle vascular index, an indicator of arteriosclerosis, has been studied in subclinical hypothyroidism and increased index values have been associated with elevated BNP levels, reflecting the effect of decreased tissue T3 in the alteration of the ventricular and arterial wall pressure dynamics [33]. While many studies identify the relation between heart disease and overt hypothyroidism, one study suggested that dilated cardiomyopathy is associated with subclinical hyperthyroidism [34].

It has also been noted that the levels of T3 correlate with the functional level (New York Heart Association (NYHA) class) and that lower hormone levels are associated with higher NYHA classification, making it a predictor of mortality in class III and IV of the NYHA [35]. In patients with heart failure with preserved ejection fraction, a study showed that up to 22% of these patients had altered thyroid function with low T3 levels [36]. However, available evidence, based on current literature, is still contradicting in certain groups of patients. In a study conducted on patients with heart failure and reduced ejection fraction, neither subclinical hyperthyroidism nor hypothyroidism was found to be significant prognostic factors [37].

The association between cardiovascular disease and subclinical hypothyroidism, though significant, is reversible with thyroxine hormone replacement, as reflected by improvement or reversal in some of the components such as diastolic dysfunction and carotid artery intima-media thickness (a marker of subclinical atherosclerosis) [38, 39]. In 2005, a consensus panel from three recognized organizations such as the American Association of Clinical Endocrinologist, the American Thyroid Association, and the Endocrine Society recommended against replacing thyroid hormones if TSH is < 10 mIU/L but that treatment was reasonable in patient with subclinical hypothyroidism if TSH was > 10 mIU/L [40]. Current clinical practice guidelines recommend treating subclinical hypothyroid patients with TSH levels with levels greater than 10 mIU/L [21, 41]. Thyroxine replacement for TSH levels less than 10 mIU/L should be patient-specific and tailored accordingly based on age characteristics and clinical symptoms consistent with hypothyroidism [39]. More studies need to be conducted in order to determine the appropriateness of thyroxine replacement by identifying select high risk subset of subclinical hypothyroid patients, including those likely to progress to overt hypothyroidism. Select patients with heart failure would benefit from thyroid hormone replacement if they are discovered to have subclinical hypothyroidism. This therapeutic benefit is more so in patients with heart failure with preserved ejection fraction, a relatively less well studied population.

To summarize, we may conclude that hypothyroidism and its subclinical counterpart have prognostic implications in patients with heart failure due to its association with increased cardiovascular mortality. Since there exists some evidence of a causal relationship, it may seem appropriate to perform a basic cardiac workup like an echocardiogram to assess for subclinical systolic and diastolic dysfunction as part of initial evaluation. Evidence of cardiac dysfunction may facilitate the determination of appropriateness of thyroxine replacement therapy in subclinical hypothyroidism.

Conflicts of Interest

We have no conflicts of interest to disclose.

Abbreviations

TSH: thyroid-stimulating hormone; T3: triiodothyronine; T4: tetraiodothyroxine; SERCA: sarco/endoplasmic reticulum Ca²⁺-ATPase; ATPase: adenosine 5'-triphosphatase; NYHA: New York Heart Association

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