Celiac Disease: Intestinal, Heart and Skin Interconnections

Aaron Lerner, Torsten Matthias

  Open Access OPEN ACCESS  Peer Reviewed PEER-REVIEWED

Celiac Disease: Intestinal, Heart and Skin Interconnections

Aaron Lerner1,, Torsten Matthias2

1Pediatric Gastroenterology and Nutrition Unit, Carmel Medical Center, B, Rappaport School of Medicine, Technion-Israel institute of Technology, Haifa, Israel

2Aesku.Kipp Institute, Wendelsheim, Germany

Abstract

The first description of celiac disease associated with dilated cardiomyopathy and pellagra in the same person, brings multiple interesting aspects to discuss. Celiac disease is prevalent in cardiac failure and vice versa, multiple cardiac manifestations exist in celiac disease. Pathophysiologically, autoimmune, nutritional, infectious and thrombophilic pathways can be involved. In some cases the cardiomyopathy respond to gluten free diet. Multiple cutaneous manifestations, including pellagra like rash, were described in CD. Autoimmune mechanisms and much more, (e.g. nutrient deficiencies) might aggravate the skin manifestation. The present editorial highlights the cardiac-cutaneous-intestinal cross talks in celiac disease in order to increase the awareness of the physician community to speed up celiac disease diagnosis in those extraintestinal manifestations.

Cite this article:

  • Lerner, Aaron, and Torsten Matthias. "Celiac Disease: Intestinal, Heart and Skin Interconnections." International Journal of Celiac Disease 3.1 (2015): 28-30.
  • Lerner, A. , & Matthias, T. (2015). Celiac Disease: Intestinal, Heart and Skin Interconnections. International Journal of Celiac Disease, 3(1), 28-30.
  • Lerner, Aaron, and Torsten Matthias. "Celiac Disease: Intestinal, Heart and Skin Interconnections." International Journal of Celiac Disease 3, no. 1 (2015): 28-30.

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1. Introduction

Celiac disease (CD) is an autoimmune inflammatory disorder of the small intestine, triggered by the ingestion of prolamins contained in wheat, barley, rye or oat in genetically susceptible individuals. It has been shown that the classic intestinal clinical picture of malnutrition, chronic diarrhea and nutritional deficiencies are disappearing and extraintestinal presentations are emerging. Skin, cardiological, endocrine, skeletal, hepatic, hematological, thrombophilic, gynecological, fertility, dental and behavioral abnormalities are often described [1, 2, 3, 4, 5].

All these extraintestinal presentations make the diagnosis of the disease more difficult and the reliance on the typical symptomatology more remote. These are some of the reasons why serological screening and diagnosis of CD have achieved prime importance and the high-risk CD populations were expanded to other conditions andto extraintestinal target organs symptomatologies [6, 7].

Cardiomyopathy represents a diverse and heterogeneous group of disorders affecting the myocardium and ultimately resulting in cardiac dysfunction. The prevalence of heart failure is high (5 million symptomatic patients in the United States) and increasing. Cardiomyopathy is the leading cause of hospitalization in patients older than 65 years of age, resulting in enormous healthcare expenditure and lost productivity. Dilated cardiomyopathy (DCM) is the most commonly seen type of cardiomyopathy. Ischemic cardiomyopathy accounts for about half of these patients, but in several large clinical trials the prevalence of potentially reversible non-ischemic cardiomyopathy is also significant, ranging from 20% to 50%. [8] Regarding the etiology, genetic causes, endocrine disorders, collagen vascular diseases, drugs, congenital metabolic abnormalities, muscular dystrophies, structural heart diseases, acute or chronic myocarditis and toxins can be presented.

Considered now as a vitamin deficiency state, pellagra has been linked to a chronic lack of niacin (vitamin B3 or nicotinic acid), an important constituent of coenzyme I and coenzyme II. Its clinical map is believed to include the classic 3 Ds: Dermatitis, Dementia and Diarrhea. The order of appearance and severity of these three sub-syndromes varies and some may not show at all.

In the present issue, Ben Ghorbel et al describe a young male presented with acute chest pains, myocardial infarction and dilated cardiomyopathy that 3 years later developed face and hands skin eruption, glossitis, photosensitivity and diarrhea. Based on positive CD associated serology and subtotal mucosal atrophy, the diagnosis of CD was established. Despite the fact that vitamin B3 and tryptophan were not measured, the clinical diagnosis of pellagra was done. It is the first description of CD, cardiomyopathy and pellagra in the same person, however, only associative linkscan be established, but not cause and effect relationships. Unfortunately, the patient was not diagnosed biochemically as pellagra and died before gluten free diet was initiated.

The present editorial will expand on the association between the above mention: celiac disease, cardiomyopathy and cutaneous eruptions, described by Ben Ghorbel et al. [9] and their pathophysiological interactions

2. Dilated Cardiomyopathy and CD

The association of the 2 conditions is well described [10, 11, 12]. The prevalence of CD in patients with sporadic or inherited DCM is substantially higher than in controls. Taking in account that 1% of the western population has CD, the percentage of DCM in the CD patients is around 5.0-6.75%.The largest Sweden patient register survey found that CD patients are at increased risk of idiopathic dilated cardiomyopathy with a hazard ratio of 1.73; 95% confidence interval, 1.00-3.00. [13] Regarding shared etiology between the two conditions, the autoimmune common trait, thatshares genes and the nutritional deficiencies are coming up. By having an autoimmune disease, CD patients are prone to develop additional autoimmune conditions during life, autoimmune myocarditis or cardiomyopathy, are some of them. [14] The recent expansion of the genome-wide association studies and exome sequencing technique sun revealed multiple shared mutations between the autoimmune diseases. It is possible that some of the 32 mutations identified in hereditary cardiomyopathies are shared with more than 40 non-HLA loci identified in CD. [15, 16] Being a malabsorptive state, multiple nutritional deficiencies can be expected in CD [17, 18]. Some of them like: hypocalcaemia, hypokalemia, carnitine, selenium, thiamine, zink, coenzyme Q10, taurine, vitamin E and C, riboflavin, pyridoxine and creatine were described in cardiomyopathy or associated with heart performance [19, 20, 21]. Unfortunately, those nutritional parameters weren’t checked in the case presented. It is conceivable that a person with “impaired general condition with moderate asthenia and weight loss” and chronic diarrhea with subtotal intestinal atrophy, will have multiple nutritional deficiencies, that might have affected his cardiac performance.

Several pathophysiological pathways can be suggested, relying heart pathology to CD: 1. Autoimmunogenesis shared between multiple autoimmune diseases [14], 2. Nutrient deficiencies, as mentioned above [22, 23, 24], 3. Autoantibodies against actin and myosin exist in CD and DCM and were postulated to participate in the damage to the target organs of both conditions [25, 26, 27]. In fact, impairment of protein trafficking by direct interaction of gliadin peptides with actin and actin-deficient cardiomyopathy coexisting with celiac disease, reinforce the interrelationship [28, 29]. 4. Hypercoagulability and thrombophilic autoantibodies like anticardiolipin and others are shared by both conditions [30, 31, 32, 33]. Can hypercoagulability be an additional factor aggravating intestinal and cardiac pathology? 5. Finally, Infections are considered as environmental etiologies for the two conditions. [34] Myocardial microabscesses detected by endomyocardial biopsy in a patient with dilated cardiomyopathy and celiac disease hint for the infectious avenue [35].

3. Pellagra and CD

The two diseases can be connected in two aspects. 58% of pellagra patients were shown to have malabsorption and many had intestinal pathology on biopsies [36, 37]. Alternatively, Pellagra was described in CD [38]. The skin manifestations in pellagra might have some additional etiologies, since multiple nutrient deficiencies are at the origin of the cutaneous manifestations in CD. The following nutritional deficiencies inducing skin rashes, were describe in CD: Zinc, Iron, Vitamin A, E, B12, niacin, folate, selenium and essential fatty acids [39, 40].

4. Does a Gluten Free Diet Ameliorate Cardiac and Skin Manifestations Associated with CD?

It goes without saying that the nutritional manifestations due to the malabsorptive state of CD improve on strict elimination of wheat, Barley, rye and oat. In severe deficiencies the deficient nutrient should be supplemented. A more challenging aspect is the reversibility of the cardiomyopathy on gluten avoidance. No large scaled studies exist in the literature on the subject, but there are some case presentations reporting complete or partial recovery or progression avoidance of the cardiomyopathy linked to CD [41, 42, 43, 44].

5. The Take Home Messages for the Clinicians

Speed up CD diagnosis in face of cardiomyopathy and look for associated autoimmune antibodies and nutritional deficiencies.

Speed up CD diagnosis in face of pellagra –like skin manifestations and look for additional CD nutritional deficiencies associated with cutaneous manifestations.

References

[1]  Lerner A. Factors affecting the clinical presentation and time diagnosis of celiac disease: The Jerusalem and the West Bank-Gaza experience. Isr J Med Sci. 1994; 11: 294-295.
In article      
 
[2]  Lerner A, Agmon-Levin N, Shapira Y, Gilburd B, Reuter S, Lavi I, Shoenfeld Y. The thrombophilic network of autoantibodies in celiac disease. BMC Med. 2013; 11: 89.
In article      CrossRefPubMed
 
[3]  Lerner A, Makhoul BF, Eliakim R. Neurological manifestations of celiac disease in children and adults. Europ Neurolog J. 2012; 4: 15-20.
In article      
 
[4]  Lerner A, Shapira Y, Agmon-Levin N, , Pacht A, Ben-Ami Shor D, López Hoyos M, Sanchez-CastanonM, Shoenfeld Y. The clinical significance of 25OH-vitamin D status in celiac disease. Crit Rev Allerg Immunol. 2012; 42: 322-330.
In article      CrossRefPubMed
 
[5]  Branski D, Ashkenazy A, Freier S, Lerner A, Dinari G et al.Extraintestinal manifestations and associated disorders of celiac disease. In: “Gluten-Sensitive Enteropathy”. Front Gastrointest Res.Eds. Branski D, Rozen P, Kagnoff MF. Karger , Basel. pp. 164-175. 1992.
In article      
 
[6]  Aggarwal S, Lebwohl B, Green PH. Screening for celiac disease in average-risk and high-risk populations. Therap Adv Gastroenterol. 2012; 5: 37-47.
In article      CrossRefPubMed
 
[7]  Lerner A. Serological Diagnosis of Celiac Disease –Moving Beyond the Tip of the Iceberg. International Journal of Celiac Disease 2014; 2(2): 64-66.
In article      
 
[8]  Nagarakanti R, Whellan D, Rubin S, Mather PJ. Reversible cardiomyopathies.Cardiol Rev. 2007 Jul-Aug; 15(4): 178-83.
In article      CrossRefPubMed
 
[9]  Ben Ghorbel I, Hajji R, Bel Feki N, Ben Salem T, Lamloum M, Habib Houman M. Two exceptional complications revealing celiac disease: ischemic cardiomyopathy and pellagra. International Journal of Celiac Disease 2015; 3(1): 31-32.
In article      
 
[10]  Curione M, Barbato M, De Biase L, Viola F, Lo Russo L, Cardi E. Prevalence of coeliac disease in idiopathic dilated cardiomyopathy. Lancet. 1999; 354: 222-3.
In article      CrossRef
 
[11]  De Bem RS, Da Ro Sa Utiyama SR, Nisihara RM, Fortunato JA, Tondo JA, Carmes ER, et al. Celiac disease prevalence in Brazilian dilated cardiomyopathy patients. Dig Dis Sci. 2006; 51: 1016-9.
In article      CrossRefPubMed
 
[12]  Not T, Faleschini E, Tommasini A, Repetto A, Pasotti M, Baldas V, Spano A, et al. Celiac disease in patients with sporadic and inherited cardiomyopathies and in their relatives. Eur Heart J. 2003; 24: 1455-61.
In article      CrossRef
 
[13]  Lerner A, Blank M, Shoenfeld Y. Celiac disease and autoimmunity. Isr J Med Sci 1996; 32: 33-36.
In article      PubMed
 
[14]  Frustaci A, Cuoco L, Chimenti C, Pieroni M, Fioravanti G, Gentiloni N, et al. Celiac disease associated with autoimmune myocarditis. Circulation. 2002; 105: 2611-8.
In article      CrossRefPubMed
 
[15]  Liu W, Liu W, Hu D, Zhu T, Ma Z, Yang J, Xie W, et al. Mutation spectrum in a large cohort of unrelated Chinese patients with hypertrophic cardiomyopathy.Am J Cardiol. 2013; 112: 585-9.
In article      CrossRefPubMed
 
[16]  Kumar V, Gutierrez-Achury J, Kanduri K, Almeida R, Hrdlickova B, Zhernakova DV et al Systematic annotation of celiac disease loci refines pathological pathways and suggests a genetic explanation for increased interferon-gamma levels.Hum Mol Genet. 2015; 24: 397-409.
In article      CrossRefPubMed
 
[17]  García-Manzanares A, Lucendo AJ. Nutritional and dietary aspects of celiac disease. Nutr Clin Pract. 2011; 26: 163-73.
In article      CrossRefPubMed
 
[18]  Wierdsma NJ, van Bokhorst-de van der Schueren MA, Berkenpas M, Mulder CJ, van Bodegraven AA. Vitamin and mineral deficiencies are highly prevalent in newly diagnosed celiac disease patients. Nutrients. 2013; 5: 3975-92.
In article      CrossRefPubMed
 
[19]  Marinescu V, McCullough PA. Nutritional and micronutrient determinants of idiopathic dilated cardiomyopathy: diagnostic and therapeutic implications. Expert Rev Cardiovasc Ther. 2011; 9: 1161-70.
In article      CrossRefPubMed
 
[20]  Allard ML, Jeejeebhoy KN, Sole MJ.The management of conditioned nutritional requirements in heart failure. Heart Fail Rev. 2006; 11: 75-82.
In article      CrossRefPubMed
 
[21]  Frustaci A, Sabbioni E, Fortaner S, Farina M, del Torchio R, Tafani M, et al. Selenium- and zinc-deficient cardiomyopathy in human intestinal malabsorption: preliminary results of selenium/zinc infusion. Eur J Heart Fail. 2012; 14: 202-10.
In article      CrossRefPubMed
 
[22]  Uslu N, Demir H, Karagöz T, Saltik-Temizel IN. Dilated cardiomyopathy in celiac disease: role of carnitine deficiency. Acta Gastroenterol Belg. 2010; 73: 530-1.
In article      PubMed
 
[23]  Lerner A, Gruener N, Iancu TC. Serum carnitine levels in coeliac disease. Gut 1993; 34: 933-935.
In article      CrossRefPubMed
 
[24]  Mavroudis K, Aloumanis K, Stamatis P, Antonakoudis G, Kifnidis K, Antonakoudis C.Irreversible end-stage heart failure in a young patient due to severe chronic hypocalcemia associated with primary hypoparathyroidism and celiac disease.Clin Cardiol. 2010; 33: E72-5.
In article      CrossRefPubMed
 
[25]  Konstadoulakis MM, Kroumbouzou H, Tsiamis E, Trikas A, Toutouzas P.Clinical significance of antibodies against tropomyosin, actin and myosin in patients with dilated cardiomyopathy.J Clin Lab Immunol. 1993; 40: 61-7.
In article      PubMed
 
[26]  Latif N, Smith J, Dunn MJ, Yacoub MH, Rose ML. Complement-mediated cytotoxic activity of anti-heart antibodies present in the sera of patients with dilated cardiomyopathy.Autoimmunity. 1994; 19: 99-104.
In article      CrossRefPubMed
 
[27]  Pedreira S, Sugai E, Moreno ML, Vázquez H, Niveloni S, Smecuol E, et al.Significance of smooth muscle/anti-actin autoantibodies in celiac disease. Acta Gastroenterol Latinoam. 2005; 35: 83-93.
In article      PubMed
 
[28]  Reinke Y, Behrendt M, Schmidt S, Zimmer KP, Naim HY. Impairment of protein trafficking by direct interaction of gliadin peptides with actin. Exp Cell Res. 2011; 317: 2124-35.
In article      CrossRefPubMed
 
[29]  Chuaqui B, Garrido J, Casanegra P. Actin-deficient cardiomyopathy coexisting with celiac disease: a chance association? Pathol Res Pract. 1986; 181: 604-14.
In article      CrossRef
 
[30]  Shamir R, Shoenfeld Y, Blank M, Eliakim R, Lahat N, Sobel E, Shinar E, Lerner A. The prevalence of coeliac disease antibodies in patients with the antiphospholipid syndrome. Lupus 2003; 12: 394-399.
In article      CrossRefPubMed
 
[31]  Lerner A, Agmon-Levin N, Shapira Y, Gilburd B, Reuter S, Lavi L, Shoenfeld Y. The thrombophylic network of autoantibodies in celiac disease. BMJ Medicine, 2013, 11; 89-95.
In article      CrossRefPubMed
 
[32]  Chen K, Williams S, Chan AK, Mondal TK. Thrombosis and embolism in pediatric cardiomyopathy. Blood Coagul Fibrinolysis. 2013; 24: 221-30.
In article      CrossRefPubMed
 
[33]  Makhdoom ZA, Randall NW.Dilated cardiomyopathy due to anticardiolipin syndrome in association with celiac sprue. J Clin Gastroenterol. 2000; 31: 91-2.
In article      CrossRef
 
[34]  Lerner A, Reif S. Celiac disease and infection. In: Infections and Autoimmunity. Eds: Shoenfeld Y and Rose N. 2nd Ed. Elsevier B.V. In press, 2015.
In article      
 
[35]  Mazurkiewicz L, Bilińska ZT, Witkowski A, Grzybowski J, Michalak E, Bieganowski A, et al. Myocardial microabscesses detected by endomyocardial biopsy in a patient with dilated cardiomyopathy and celiac disease: a case report. Kardiol Pol. 2006; 64: 733-6.
In article      PubMed
 
[36]  Halsted CH, Sheir S, Sourial N, Patwardhan VN. Small intestinal structure and absorption in Egypt. Influence of parasitism and pellagra. Am J Clin Nutr. 1969; 22: 744-54.
In article      PubMed
 
[37]  Mehta SK, Kaur S, Avasthi G, Wig NN, Chhuttani PN. Small intestinal deficit in pellagra.Am J Clin Nutr. 1972; 25: 545-9.
In article      PubMed
 
[38]  Schattner A.A 70-year-old man with isolated weight loss and a pellagra-like syndrome due to celiac disease. Yale J Biol Med. 1999; 72: 15-8.
In article      PubMed
 
[39]  Caproni M, Bonciolini V, D'Errico A, Antiga E, Fabbri P. Celiac disease and dermatologic manifestations: many skin clue to unfold gluten-sensitive enteropathy.Gastroenterol Res Pract. 2012; 2012: 952753.
In article      CrossRefPubMed
 
[40]  Haimi M, Lerner A. Nutritional Deficencies in the pediatric age group in a multicultural developed country- Israel. World Journal of Clinical Cases. 2014; 2: 120-125.
In article      CrossRefPubMed
 
[41]  Ouali S, Chabrak S, Larbi N, Kafsi N. Dilated cardiomyopathy and atrio-ventricular block in coeliac disease. Two case reports. Arch Mal Coeur Vaiss. 2006; 99: 1252-5.
In article      PubMed
 
[42]  Winter Del R JL, Gabrielli N L, Greig D, Inchauste G, Quezada F, Torres M J, et al.Dilated cardiomyopathy in celiac disease: report of one case. Rev Med Chil. 2009; 137: 1469-73.
In article      
 
[43]  Lodha A, Haran M, Hollander G, Frankel R, Shani J. Celiac disease associated with dilated cardiomyopathy. South Med J. 2009; 102: 1052-4.
In article      CrossRefPubMed
 
[44]  Milisavljević N, Cvetković M, Nikolić G, Filipović B, Milinić N. Dilated cardiomyopathy associated with celiac disease: case report and literature review. Srp Arh Celok Lek. 2012; 140: 641-3.
In article      CrossRefPubMed
 
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