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. 2008 Sep 30;52(14):1152-9.
doi: 10.1016/j.jacc.2008.07.009.

Subclinical thyroid dysfunction, cardiac function, and the risk of heart failure. The Cardiovascular Health study

Affiliations

Subclinical thyroid dysfunction, cardiac function, and the risk of heart failure. The Cardiovascular Health study

Nicolas Rodondi et al. J Am Coll Cardiol. .

Abstract

Objectives: The goal of this study was to determine whether subclinical thyroid dysfunction was associated with incident heart failure (HF) and echocardiogram abnormalities.

Background: Subclinical hypothyroidism and hyperthyroidism have been associated with cardiac dysfunction. However, long-term data on the risk of HF are limited.

Methods: We studied 3,044 adults>or=65 years of age who initially were free of HF in the Cardiovascular Health Study. We compared adjudicated HF events over a mean 12-year follow-up and changes in cardiac function over the course of 5 years among euthyroid participants, those with subclinical hypothyroidism (subdivided by thyroid-stimulating hormone [TSH] levels: 4.5 to 9.9, >or=10.0 mU/l), and those with subclinical hyperthyroidism.

Results: Over the course of 12 years, 736 participants developed HF events. Participants with TSH>or=10.0 mU/l had a greater incidence of HF compared with euthyroid participants (41.7 vs. 22.9 per 1,000 person years, p=0.01; adjusted hazard ratio: 1.88; 95% confidence interval: 1.05 to 3.34). Baseline peak E velocity, which is an echocardiographic measurement of diastolic function associated with incident HF in the CHS cohort, was greater in those patients with TSH>or=10.0 mU/l compared with euthyroid participants (0.80 m/s vs. 0.72 m/s, p=0.002). Over the course of 5 years, left ventricular mass increased among those with TSH>or=10.0 mU/l, but other echocardiographic measurements were unchanged. Those patients with TSH 4.5 to 9.9 mU/l or with subclinical hyperthyroidism had no increase in risk of HF.

Conclusions: Compared with euthyroid older adults, those adults with TSH>or=10.0 mU/l have a moderately increased risk of HF and alterations in cardiac function but not older adults with TSH<10.0 mU/l. Clinical trials should assess whether the risk of HF might be ameliorated by thyroxine replacement in individuals with TSH>or=10.0 mU/l.

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Conflict of interest statement

Conflict of interest

No author has a financial interest in the subject matter or materials discussed in the manuscript.

Figures

Figure
Figure. Incident Heart Failure Events According to TSH Levels
Abbreviations: TSH: thyroid-stimulating hormone. Participants with TSH≥10.0–19.9 mU/L who were untreated by thyroxine replacement (participants censored at the time of first thyroxine use) had a greater incidence of HF events compared to euthyroid participants (41.7 vs. 22.9/1000 person-years, p=0.01), but rates were similar for those with subclinical hyperthyroidism or those with TSH between 4.5 and 9.9 mU/L.

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