Low T3 syndrome predicts more adverse events in patients with hypertrophic cardiomyopathy
Chao-Jie He1, Chun-Yan Zhu2, Hong-Yan Fan1
1Department of Cardiology, The Affiliated Hospital of Jiaxing University, Jiaxing, Zhejiang, China.
Insights
Low thyroid hormone levels (low T3 syndrome) are common in hypertrophic cardiomyopathy (HCM) patients and predict a higher risk of sudden cardiac death and worsening heart failure.
Area of Science:
- Cardiology
- Endocrinology
- Genetics
Background:
- Hypertrophic cardiomyopathy (HCM) is a prevalent genetic heart disorder associated with sudden death and heart failure.
- Thyroid dysfunction increases cardiovascular risks, necessitating investigation into its role in HCM outcomes.
Purpose of the Study:
- To determine if thyroid hormones predict adverse events in patients with HCM.
- To investigate the association between low triiodothyronine (T3) syndrome and adverse cardiovascular events in HCM patients.
Main Methods:
- A cohort of 782 HCM patients with baseline thyroid hormone data was analyzed.
- Patients were classified into normal fT3 and low T3 syndrome groups (fT3 < 2.43 pmol/L, normal TSH).
- Kaplan-Meier and Cox regression analyses assessed sudden cardiac death (SCD) and worsening heart failure (WHF) events.
Main Results:
- Low T3 syndrome was associated with significantly higher cumulative incidence of SCD (log-rank p=.02) and WHF (log-rank p=.001) events.
- Multivariate Cox regression identified low T3 syndrome as a strong predictor of SCD (aHR: 1.53) and WHF (aHR: 3.87).
- The median follow-up was 52 months, with 75 SCD and 134 WHF events recorded.
Conclusions:
- Low T3 syndrome is prevalent in HCM patients and independently linked to increased risks of SCD and WHF.
- Routine assessment of serum free triiodothyronine (fT3) may aid in risk stratification for HCM patients.
Background:
Hypertrophic cardiomyopathy (HCM) is a common cardiac genetic disorder that clinically manifests with sudden death and progressive heart failure. Moreover, thyroid dysfunction is associated with increased cardiovascular morbidity and mortality risks. Therefore, this study aimed to clarify whether thyroid hormones could serve as an independent predictor of adverse events in patients with HCM.
Methods:
The cohort consisted of 782 patients with HCM who had thyroid hormones baseline data and were admitted to the Affiliated Hospital of Jiaxing University. Patients were divided into two groups according to serum levels of free triiodothyronine (fT3): the normal fT3 and low triiodothyronine (T3) syndrome groups. Low T3 syndrome was defined as fT3 < 2.43 pmol/L with a normal thyroid-stimulating hormone (TSH) level. Patients whose TSH levels were abnormally high or abnormally low were excluded from this study. The primary endpoint was the occurrence of sudden cardiac death (SCD) events, and the secondary endpoint was a composite of worsening heart failure (WHF) events, including heart failure death, cardiac decompensation, hospitalization for heart failure, and HCM-related stroke. The Kaplan-Meier and Cox regression were performed for the survival analysis.
Results:
After a median follow-up of 52 months, 75 SCD events and 134 WHF events were recorded. The Kaplan-Meier survival curves showed that the cumulative incidence of SCD events and WHF events were significantly higher in patients with low T3 syndrome (log-rank p = .02 and log-rank p = .001, respectively). Furthermore, multivariate Cox regression analysis demonstrated that low T3 syndrome is a strong predictor of SCD events and WHF events (adjusted hazard ratio [HR: 1.53, 95% confidence interval [CI]: 1.13-2.24, p < .01; HR: 3.87, 95% CI: 2.91-4.98, p < .001, respectively).
Conclusions:
Low T3 syndrome is highly prevalent among patients with HCM and was independently associated with an increased risk of SCD events and WHF events. The routine assessment of serum fT3 levels may provide risk stratification in this population.
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