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3/2007
vol. 3
 
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Case report
A case of dilated cardiomyopathy associated with coeliac disease

Benedict M. Glover
,
Nuala J. Treanor
,
David J. McEneaney

Arch Med Sci 2007; 3, 3: 272-273
Online publish date: 2007/10/01
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Introduction

Coeliac disease is an autoimmune enteropathy caused by the ingestion of gluten by individuals with the DQ2/DQ8 haplotype [1]. Although there are several well known associations; dilated cardiomyopathy has been rarely reported. We report a case of a dilated cardiomyopathy in association with previously undiagnosed coeliac disease, in which the left ventricular function, dimensions and symptoms improved significantly with a gluten free diet.


Case report

A 36-year-old male attended hospital with a 6 month history of worsening dyspnoea (New York Heart Association (NYHA) Class IV). He had no significant past medical history, no gastrointestinal symptoms and no significant family history. He was a non-smoker, consumed minimal alcohol and was on no regular medication. There was no recent history of any viral illness. On examination he was tachypnoeic and hypoxic on room air. There was a pansystolic murmur audible throughout the praecordium and the jugular venous pressure was significantly elevated. Admission bloods revealed an iron deficiency anaemia and left bundle branch block was present on the electrocardiogram. A transthoracic echocardiogram revealed a dilated cardiomyopathy with an ejection fraction of 15% and a left ventricular end diastolic dimension of 64 mm.
The patient was initially treated with diuretics and subsequently commenced on an angiotensin converting enzyme and beta-adrenoceptor blockade. A coronary angiogram revealed normal coronary arteries.
The patient underwent further investigations for his anaemia. A coeliac screen revealed a positive IgA anti-endomysial antibody with elevated IgA anti-transglutaminse levels. A duodenal biopsy was performed which revealed atrophy of the villi and crypt hyperplasia was noted (Figure 1). Cardiac antibodies were negative and a micronutient screen was normal. The patient was subsequently commenced on a gluten free diet. At 12 month follow up the patient’s symptoms had improved (NYHA IV to NYHA II) and an echocardiogram showed a marked improvement in both the left ventricular ejection fraction (25%) as well as a significant reduction in left ventricular dimensions (left ventricular end diastolic diameter of 52 mm).


Discussion

The incidence of coeliac disease in patients with a dilated cardiomyopathy has been reported as 2.2% [2]. Like this case the majority of patients in previous reports had no prior history of gastrointestinal symptoms and the most commonly reported symptoms were dyspnoea related to the cardiomyopathy.
There have been several proposed mechanisms regarding the association between coeliac disease and dilated cardiomyopathy. A reduction in serum carnitine, a co-factor for the metabolism of fatty acids, has been reported in coeliac disease [3]. Low carnitine levels have also been reported in patients with idiopathic dilated cardiomyopathy compared with controls [4]. Carnitine levels return to normal after a gluten free diet.
There may also be an immune mediated reaction related to abnormalities of intestinal permeability resulting in an increased absorption of antigens or possibly infectious agents which may result in myocarditis through immune-mediated mechanisms which then develops into a cardiomyopathy [5]. In this case both cardiac antibodies and micronutrient screen were normal.
Although the number of cases described is small it appears that where a gluten free diet is strictly adhered to, there is a significant improvement in left ventricular ejection fraction and symptoms. Other important causes such as excess alcohol consumption [6] need to be excluded. This case demonstrates a dramatic improvement in left ventricular function with an improvement in symptoms. Although the medication (Angiotensin Converting Enzyme inhibitor and Beta adrenoceptor Blockage) may have also had an effect on these parameters it is still fundamental that this diagnosis be made and the association highlighted.



Conclusions

Although a dilated cardiomyopathy as a result of coeliac disease is rare it is an important finding as the patient’s left ventricular function, dimensions and symptoms may respond well to a gluten free diet resulting in an improved prognosis. The non-specific nature of this condition and often lack of symptoms would suggest that the association between these two conditions may be more common than previously reported. In patients with a dilated cardiomyopathy of uncertain cause and in particular in patients with anaemia screening for coeliac disease may be a useful investigation which could have significant implications on patient management.

References

1. Sollid LM, Thorsby E. HLA susceptibility genes in celiac disease: genetic mapping and role in pathogenesis. Gastroenterology 1993; 105: 910-22.
2. Prati D, Bardella MT, Peracchi M, Porretti L, Scalamogna M, Conte D. Antiendomysial antibodies in patients with end-satge heart failure. Am J Gastroenterology 2002;
97: 218-9.
3. Lerner A, Gruener N, Iancu TC. Serum carnitine concentrations in coeliac disease. Gut 1993; 34: 933-5.
4. Curione M, Danese C, Viola F, et al. Carnitine deficiency in patients with coeliac disease and idiopathic dilated cardiomyopathy. Nutr Metab Cardiovasc Dis 2005;
15: 279-83.
5. van Elburg RM, Uil JJ, Mulder CJ, Heymans HS. Intestinal permeability in patients with coeliac disease and relatives of patients with coeliac disease. Gut 1993; 34: 354-7.
6. Robert Irzmański, Ewa Serwa-Stępień, Marcin Barylski, et al. A 42-year-old patient with alcoholic cardiomyopathy. Arch Med Sci 2005; 1: 249-53.
Copyright: © 2007 Termedia & Banach. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
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