Reversible dilated cardiomyopathy caused by hypothyroidism
© Khochtali et al; licensee BioMed Central Ltd. 2011
Received: 2 March 2011
Accepted: 21 June 2011
Published: 21 June 2011
The association between lack of thyroid hormones and cardiac dysfunction has been well described. We report two new cases of patients with dilated cardiomyopathy (DCM), revealing a periphery hypothyroidism and for whom cardiac function significantly improved after L thyroxin substitutive treatment. Our cases highlight the necessity to perform thyroid function testing to investigate the etiology of non ischemic DCM.
Dilated cardiomyopathy (DCM) is a heart muscle disorder defined by the presence of a dilated and poorly functioning left ventricle in the absence of abnormal loading conditions (hypertension, valve disease) or ischemic heart disease sufficient to cause global systolic impairment . In the majority of patients no identifiable cause is found hence the term "idiopathic" dilated cardiomyopathy (IDC). However, in a rare occasions DCM could be associated to variety of pathologies. A link between CMD and hypothyroidism was first reported in 1918 in four patients with heart failure refractory to digitalis and diuretics treated successfully with substitutive hormonal therapy . Since this first description few other cases have been published.
We report, two cases of hypothyroidism revealed by a DCM.
A 20 years old man, without any previous medical history, was admitted for chest pain and dyspnea. One year earlier, the patient developed an important muscle weakness and a weight gain. On examination the patient was obese, with a body mass index (BMI) at 35.4 kg/m2, his skin was pale, dry and infiltrated with edema. Blood pressure was at 120/80 mmHg, the pulse was at 50 b/mn and heart sounds were distant. Chest X ray showed moderate cardiomegaly with a cardiothoracic ratio of 0.59. Cardiac ultrasound revealed a DCM with a severe left ventricle dysfunction (ejection fraction at 20%) and a global hypokinesis. In addition, there was a moderate pericardial effusion.
Biological tests and cardiac ultrasound results before and after substitutive treatment for 2 patients
Before substitutive treatment
After substitutive treatment (12 weeks)
0,25 - 4 (mUI/l)
< 250 (UI/l)
< 5,5 (mmol/l)
A 34 years old man was hospitalized to investigate his DCM recently discovered. His medical history was marked by diabetes and heavy smoking. Four months ago, the patient reported weight gain, constipation and a nocturnal snoring developed. The physical exam revealed a patient with a BMI of 31.86 kg/m2, a blood pressure at 120/80 mmHg and a mild palpable goiter.
Thyroid hormones dosage revealed a peripheral hypothyroidism (TSH = 23.4 mUI/l and T4 = 10 ng/ml). Cardiac ultra sound showed a decrease of the left ventricle ejection fraction at 25% and a global hypokinesis. The patient was treated with thyroxin at a dose of 150 μg/day. After three months of follow up, TSH was at 4 mUI/l and echocardiography showed a substantial improvement of the left ventricule ejection fraction to 49% (table 1).
Thyroid hormones (TH) interact with the sympathovagal balance but act also on peripheral vascular resistances. The effect of TH on the cardiovascular system would be explained by the transcription's regulation of some genes implicated especially in the contractile system synthesis. More rapid non genomic effects of the TH on the ionic channels of cardiomyocyte's membrane were identified more recently 5. Hypothyroidism results in a bradycardia, a decrease of the myocardial contractility and an increase of the systemic peripheral vascular resistances. A pericardial effusion is the most frequent cardiac manifestation. Hypothyroidism is associated with an increased risk for atherosclerosis and ischemic heart disease and is now considered as proatherosclerosis factor[6, 7]. Many of the cardiac manifestations of thyroid dysfunction are associated with alterations in T3-mediated gene expression 8. In hypothyroidism, although cardiac output is reduced, heart failure is relatively rare because there is a lower oxygen demand in the periphery 9. In our two patients, family history was against inherited causes. There were no histories of drug abuse, nor alcohol or toxic substances addiction. Personal history and clinical exam ruled out nutritional deficiency, while negative HIV and HCV serologies eliminated potential viral causes. Our observation highlighted the importance of hormone dosage in first assessment of DCM even in the absence of major symptoms of TH, because clinical presentation is sometimes not obvious and the diagnosis can only be made by thyroid function testing. Fortunately, the diagnosis of hypothyroidism was clinically evident in our two patients and confirmed by hormone study. The second challenge is to know whether TH is an occasional association with DCM or a cause of it . The improvement of the cardiac function after hormonal treatment is an important argument in favor of the implication of hypothyroidism in the genesis of DCM in our patients.
DCM is usually idiopathic disease with progressive and an irreversible poor prognosis out come. In contrast, in some cases, DCM can be secondary to various causes such as hypothyroidism and hormonal treatment with L thyroxin can significantly improve myocardial function. Hence, thyroid function tests should be systematically performed in all patients with DCM in order to rule out a hypothyroidism.
Written informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
- Elliott P: Diagnosis and management of dilated cardiomyopathy. Heart 2000, 84:106–12.PubMedView ArticleGoogle Scholar
- Zondek H: Das myxodemherz. Munch Med Wochenschr 1918, 65:1180–83.Google Scholar
- Bezdah L, Slimène H, Kammoun M, Haddad A, Belhani A: Myocardiopathie dilatée d'origine myxoedémateuse. Ann Cardiol Angeiol 2004, 53:217–20.View ArticleGoogle Scholar
- Ladenson WP, Sherman SI, Kenneth L, Baughman T: Reversible alterations in myocardial gene expression in a young man with dilated cardiomyopathy and hypothyroidism. Proc Nat Acad Sci 1992, 89:5251–55.PubMedView ArticleGoogle Scholar
- Goichot B, Vinzio B: Troubles cardiovasculaires d'origine thyroïdienne. EMC (Elsevier Masson SAS), Endocrinologie-Nutrition, 10–003-B-10; 2007.Google Scholar
- Ichiki T: Thyroid hormone and atherosclerosis. Vascular Pharmacology 2010, 52:151–56.PubMedView ArticleGoogle Scholar
- François M, Delemer B: What's new in the couple thyroid and heart in 2008? Annales d'Endocrinologie 2008, S37-S43.Google Scholar
- Klein I, Danzi S: Thyroid Disease and the Heart. Circulation 2007, 116:1725–1735.PubMedView ArticleGoogle Scholar
- Stanescu C, Branidou K, Ranetti EA: Heart failure and dilated cardiomyopathy associated with severe longstanding untreated hypothyroidism. Rom J Intern Med 2007, 45:77–83.PubMedGoogle Scholar
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.