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Thyroid Hormones-An Underestimated Player in Dilated Cardiomyopathy?
Karolina Zawadzka1, Radosław Dziedzic1, Andrzej Surdacki2
1Students' Scientific Group at the Second Department of Cardiology, Jagiellonian University Medical College, 2 Jakubowskiego Street, 30-688 Cracow, Poland.
Insights
Dilated cardiomyopathy patients often have low thyroid hormone (T3) levels, impacting prognosis. This review explores thyroid hormone status, myocardial gene expression, and potential T3 therapy for DCM treatment.
Area of Science:
- Cardiology
- Endocrinology
- Molecular Biology
Background:
- Dilated cardiomyopathy (DCM) is a primary heart muscle disease characterized by left ventricular dilation and impaired function.
- Altered thyroid status, particularly low free triiodothyronine (T3) and elevated thyroid-stimulating hormone, is common in DCM patients.
- Subtle thyroid dysfunction, especially low T3, correlates with poorer prognosis and increased mortality in DCM.
Purpose of the Study:
- To review current understanding of thyroid hormone (TH) status and its link to prognosis in DCM.
- To discuss the abnormal expression of genes involved in myocardial TH synthesis within DCM.
- To explore the potential therapeutic role of THs in managing DCM.
Main Methods:
- Literature review of studies on thyroid hormone status in DCM.
- Analysis of research on myocardial gene expression related to TH biosynthesis and metabolism.
- Synthesis of evidence regarding the efficacy of TH therapy in DCM.
Main Results:
- DCM patients frequently exhibit low T3 levels, associated with worse outcomes.
- Evidence suggests impaired local TH bioavailability in the myocardium of DCM patients.
- Genes for TH biosynthesis are expressed in the DCM myocardium, indicating local regulatory roles.
Conclusions:
- Thyroid hormone status is a critical prognostic factor in DCM.
- Local myocardial TH synthesis and metabolism are altered in DCM.
- Thyroid hormone therapy presents a potential future treatment strategy for DCM.
Abstract:
Dilated cardiomyopathy (DCM) is the most prevalent cardiomyopathy, typified by left ventricular dilation and systolic dysfunction. Many patients with DCM have altered thyroid status, especially lower levels of free triiodothyronine (T3) and elevated levels of thyroid-stimulating hormone. Moreover, growing evidence indicates that even subtle changes in thyroid status (especially low T3) are linked with a worse long-term prognosis and a higher risk of mortality. Notably, recent discoveries have shown that not only local myocardial thyroid hormones (THs) bioavailability could be diminished due to impaired expression of the activating deiodinase, but virtually all genes involved in TH biosynthesis are also expressed in the myocardium of DCM patients. Importantly, some studies have suggested beneficial effects of TH therapy in patients suffering from DCM. Our aim was to discuss new insights into the association between TH status and prognosis in DCM, abnormal expression of genes involved in the myocardial synthesis of TH in DCM, and the potential for TH use in the future treatment of DCM.
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