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Published on: February 16, 2016
Thyroid function in heart failure and impact on mortality
Insights
Patients with heart failure (HF) and abnormal thyroid function face a significantly higher risk of death. This includes both hypothyroidism and hyperthyroidism, even after accounting for other risk factors.
Area of Science:
- Cardiology
- Endocrinology
- Clinical Research
Background:
- Thyroid hormone homeostasis is crucial for cardiovascular function.
- The independent prognostic impact of thyroid dysfunction in heart failure (HF) patients remains unclear.
Purpose of the Study:
- To determine if patients with systolic heart failure (HF) and abnormal thyroid function have an increased risk of mortality.
- To investigate the prognostic significance of thyroid abnormalities in HF.
Main Methods:
- Utilized data from the Sudden Cardiac Death in Heart Failure Trial (SCD-HeFT).
- Measured thyroid-stimulating hormone (TSH) at baseline and every 6 months in 2,225 HF patients over 5 years.
- Compared mortality rates between patients with normal and abnormal thyroid function.
Main Results:
- 13% of HF patients had abnormal TSH levels at baseline (12% hypothyroid, 1% hyperthyroid).
- Amiodarone treatment increased the risk of developing abnormal TSH levels.
- Both baseline and new-onset hypothyroidism and hyperthyroidism were associated with significantly higher mortality (HR 1.58 for hypo, HR 1.85 for hyper).
Conclusions:
- Abnormal thyroid function is a significant independent predictor of mortality in symptomatic HF patients with reduced ejection fraction.
- These findings highlight the importance of monitoring thyroid function in heart failure management.
Objectives:
The aim of this study was to investigate whether patients with systolic heart failure (HF) and abnormal thyroid function are at increased risk for death.
Background:
Thyroid hormone homeostasis is vital to the optimal functioning of the cardiovascular system, but an independent prognostic effect of thyroid abnormalities in patients with HF has not been established.
Methods:
In SCD-HeFT (Sudden Cardiac Death in Heart Failure Trial), which randomized patients with ischemic or nonischemic HF to placebo or amiodarone or implantable cardioverter-defibrillator therapy, thyroid-stimulating hormone (TSH) was measured at baseline and at 6-month intervals throughout the 5-year study.
Results:
Of 2,225 patients, the majority (87%) had normal TSH levels (0.3 to 5.0 μU/ml) at baseline, 12% had values suggestive of hypothyroidism, and 1% had values consistent with hyperthyroidism. Compared with euthyroid patients, those hypothyroid at baseline were older and included more women and Caucasians (all p values <0.05). Over the median follow-up period of 45.5 months, among patients euthyroid at baseline, 89 developed abnormally low TSH levels, and 341 developed abnormally high values. Patients randomized to amiodarone (median dose 300 mg) had an elevated risk for developing abnormal TSH levels compared with implantable cardioverter-defibrillator therapy or placebo (p < 0.0001). Patients with baseline or new-onset abnormal thyroid function had a higher mortality than those with normal thyroid function, even after controlling for other known mortality predictors (hazard ratio: 1.58; 95% confidence interval: 1.29 to 1.94; p < 0.0001 for hypothyroid; hazard ratio: 1.85; 95% confidence interval: 1.21 to 2.83; p = 0.0048 for hyperthyroid). Implantable cardioverter-defibrillator benefit did not vary with thyroid function.
Conclusions:
Abnormal thyroid function in patients with symptomatic HF and ejection fractions ≤35% is associated with significantly increased risk for death, even after controlling for known mortality predictors.
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