Key result
Subclinical hypothyroidism with TSH ≥ 10 linked to ~88% higher risk of incident HF.
Why the study?
Long-term data on the risk of heart failure associated with subclinical thyroid dysfunction, especially by TSH levels, were limited.
Does subclinical hypothyroidism with marked TSH elevation increase the risk of incident heart failure in older adults?
Cohort (n=3,044)
Yes
Does subclinical hypothyroidism with marked TSH elevation increase the risk of incident heart failure in older adults?
Hazard Ratio: 1.88 (95% CI 1.05–3.34)
Absolute Event Rate: 41.7% vs 22.9%
p-value: p=0.01
Markedly elevated TSH (≥10.0 mU/L) in subclinical hypothyroidism is associated with significantly increased long-term risk of heart failure, indicating it may be a clinically important threshold for thyroid replacement consideration.
Captured external expert commentary on this paper, strongest first. Original sources are linked where available.
“subclinical hypothyroid state results in a less efficient contraction of the heart”
TSH ≥10 mU/L subclinical hypothyroidism was associated with higher HF risk in older adults; extends prior observational data but leaves treatment benefit open.
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 3044 adults ≥65 years initially free of HF in the Cardiovascular Health Study (CHS). We compared adjudicated HF events over a mean 12-year follow-up and changes in cardiac function over 5 years among euthyroid participants, those with subclinical hypothyroidism (subdivided by TSH levels: 4.5–9.9, ≥10.0 mU/L), and those with subclinical hyperthyroidism. RESULTS Over 12 years, 736 participants developed HF events. Participants with TSH≥10.0 mU/L had a greater incidence of HF compared to euthyroid participants (41.7 vs. 22.9/1000 person years, p=0.01, adjusted hazard ratio=1.88, 95% confidence interval 1.05–3.34). Baseline peak E velocity, an echocardiographic measurement of diastolic function associated with incident HF in the CHS cohort, was higher in those with TSH≥10.0 compared to euthyroid participants (0.80 vs. 0.72 m/sec, p=0.002). Over 5 years, left ventricular mass increased among those with TSH≥10.0, but other echocardiographic measurements were unchanged. Those with TSH 4.5–9.9 or with subclinical hyperthyroidism had no increase in risk of HF. CONCLUSIONS Compared to euthyroid older adults, those with a TSH≥10.0 mU/L have a moderately elevated risk of HF and alterations in cardiac function, but not older adults with TSH<10. Clinical trials should assess whether the risk of HF might be ameliorated by thyroxine replacement in individuals with TSH≥10.0 mU/L.
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Rodondi et al. (2008) conducted a cohort in Subclinical thyroid dysfunction (n=3,044). Subclinical hypothyroidism with TSH ≥ 10.0 mU/L vs. Euthyroidism (normal TSH) was evaluated on Incident heart failure events (adjusted HR 1.88, 95% CI 1.05-3.34, p=0.01). Subclinical hypothyroidism with TSH ≥ 10.0 mU/L increased the risk of incident heart failure by 88% compared to euthyroidism (adjusted HR 1.88, 95% CI 1.05-3.34, p=0.01).
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