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Published on: April 30, 2020
Thyroid Dysfunction in Heart Failure and Cardiovascular Outcomes
Lakshmi Kannan1, Pamela A Shaw2, Michael P Morley3
1Division of Endocrinology, Diabetes, and Metabolism (L.K., A.R.C.) at the Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Insights
Thyroid dysfunction, specifically subclinical hypothyroidism and low T3 levels, is linked to worse outcomes in heart failure patients. Further research into thyroid hormone therapy for heart failure is warranted.
Area of Science:
- Cardiology
- Endocrinology
- Internal Medicine
Background:
- Thyroid dysfunction effects in heart failure patients are understudied.
- This study investigates thyroid dysfunction prevalence and cardiovascular outcomes in heart failure patients.
Purpose of the Study:
- To examine the association between thyroid dysfunction and heart failure severity.
- To determine the link between thyroid dysfunction and adverse cardiovascular events in heart failure patients.
Main Methods:
- A prospective cohort study of 1365 heart failure outpatients (Penn Heart Failure Study).
- Analysis of thyroid-stimulating hormone (TSH), free thyroxine (FT4), and total triiodothyronine (TT3) levels.
- Assessment of associations with New York Heart Association class, atrial fibrillation, and a composite endpoint (device placement, transplant, or death).
Main Results:
- More severe heart failure correlated with higher TSH, higher FT4, and lower TT3.
- Atrial fibrillation was associated with elevated FT4 levels.
- Subclinical hypothyroidism (TSH ≥7 mIU/L) and isolated low T3 were linked to increased risk of the composite endpoint.
Conclusions:
- Subclinical hypothyroidism (TSH ≥7 mIU/L) and isolated low T3 levels indicate a poor prognosis in heart failure patients.
- Clinical trials are recommended to evaluate the efficacy of T4 and T3 therapy in heart failure management.
Background:
The effects of thyroid dysfunction in patients with preexisting heart failure have not been adequately studied. We examined the prevalence of thyroid dysfunction and associations with cardiovascular outcomes in a large, prospective cohort of outpatients with preexisting heart failure.
Methods And Results:
We examined associations between thyroid dysfunction and New York Heart Association class, atrial fibrillation, and a composite end point of ventricular assist device placement, heart transplantation, or death in 1365 participants with heart failure enrolled in the Penn Heart Failure Study. Mean age was 57 years, 35% were women, and the majority had New York Heart Association class II (45%) or III (32%) symptoms. More severe heart failure was associated with higher thyroid-stimulating hormone (TSH), higher free thyroxine (FT4), and lower total triiodothyronine (TT3) concentrations ( P<0.001 all models). Atrial fibrillation was positively associated with higher levels of FT4 alone ( P≤0.01 all models). There were 462 composite end points over a median 4.2 years of follow-up. In adjusted models, compared with euthyroidism, subclinical hypothyroidism (TSH 4.51-19.99 mIU/L with normal FT4) was associated with an increased risk of the composite end point overall (hazard ratio, 1.82; 95% CI, 1.27-2.61; P=0.001) and in the subgroup with TSH ≥7.00 mIU/L (hazard ratio, 3.25; 95% CI, 1.96-5.39; P<0.001), but not in the subgroup with TSH 4.51-6.99 mIU/L (hazard ratio, 1.26; 95% CI, 0.78-2.06; P=0.34). Isolated low T3 was also associated with the composite end point (hazard ratio, 2.12; 95% CI, 1.65-2.72; P<0.001).
Conclusions:
In patients with preexisting heart failure, subclinical hypothyroidism with TSH ≥7 mIU/L and isolated low T3 levels are associated with poor prognosis. Clinical trials are needed to explore therapeutic effects of T4 and T3 administration in heart failure.
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