Anania C, De Luca E, De Castro G, Chiesa C, Pacifico L. Liver involvement in pediatric celiac disease. World J Gastroenterol 2015; 21(19): 5813-5822 [PMID: 26019445 DOI: 10.3748/wjg.v21.i19.5813]
Corresponding Author of This Article
Lucia Pacifico, MD, Department of Pediatrics and Child Neuropsychiatry, Sapienza University of Rome, Rome, Viale Regina Elena, 324 00161 Rome, Italy. lucia.pacifico@uniroma1.it
Research Domain of This Article
Gastroenterology & Hepatology
Article-Type of This Article
Minireviews
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This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Caterina Anania, Ester De Luca, Giovanna De Castro, Lucia Pacifico, Department of Pediatrics and Child Neuropsychiatry, Sapienza University of Rome, Rome, Viale Regina Elena, 324 00161 Rome, Italy
Claudio Chiesa, Institute of Translational Pharmacology, National Research Council, Via Fosso del Cavaliere, 100 00133 Rome, Italy
ORCID number: $[AuthorORCIDs]
Author contributions: Anania C, Chiesa C and Pacifico L designed the study, analyzed the data and wrote the manuscript; De Castro G and De Luca E collected the data; all the authors participated in the critical review and in the final approval of the manuscript.
Conflict-of-interest: There are no potential conflicts of interest relevant to this article.
Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Correspondence to: Lucia Pacifico, MD, Department of Pediatrics and Child Neuropsychiatry, Sapienza University of Rome, Rome, Viale Regina Elena, 324 00161 Rome, Italy. lucia.pacifico@uniroma1.it
Telephone: +39-6-49979215 Fax: +39-6-49979216
Received: January 22, 2015 Peer-review started: January 24, 2015 First decision: February 10, 2015 Revised: February 27, 2015 Accepted: April 17, 2015 Article in press: April 17, 2015 Published online: May 21, 2015 Processing time: 118 Days and 0.3 Hours
Abstract
Celiac disease (CD) is an intestinal inflammatory disease that manifests in genetically susceptible individuals when exposed to dietary gluten. It is a common chronic disorder, with a prevalence of 1% in Europe and North America. Although the disease primarily affects the gut, the clinical spectrum of CD is remarkably varied, and the disease can affect many extraintestinal organs and systems, including the liver. The hepatic dysfunction presenting in CD ranges from asymptomatic liver enzyme elevations or nonspecific reactive hepatitis (cryptogenic liver disorders), to chronic liver disease. In this article, we review the clinical presentations and possible mechanisms of CD-related liver injury to identify strategies for the diagnosis and treatment of these disorders in childhood.
Core tip: Celiac disease (CD) is increasingly reported in children who are symptomless or present atypical symptoms and signs. Liver abnormalities are common extraintestinal manifestations in patients with CD and range from mild hepatic injury to severe liver disease. Awareness of this may help clinicians to improve strategies for the diagnosis and treatment of these disorders in childhood.
Citation: Anania C, De Luca E, De Castro G, Chiesa C, Pacifico L. Liver involvement in pediatric celiac disease. World J Gastroenterol 2015; 21(19): 5813-5822
Celiac disease (CD) is a chronic intestinal inflammatory disease that manifests in genetically susceptible individuals when exposed to dietary gluten[1]. The prevalence of CD is high in the European and North American population (1%), reaching 10% to 15% in patients who have first-degree relatives with this disease[1,2]. Genetic predisposition plays an important role in the development of CD. Ninety percent of affected individuals carry the HLA-DQ2 (e.g., DQA1*0501-DQB1*0201) haplotype, 5% the DQ8 haplotype (e.g., DQA1*0301-DQB1*0302), and the remaining 5% carry at least one of the two DQ2 alleles (frequently the DQB1*0201)[1,3]. Ingestion of gluten is necessary for the disease to develop[4]. Immunogenic peptides, created by deamidation of food-derived gliadin peptides by small intestinal tissue transglutaminase, are presented by antigen-presenting cells, mostly dendritic cells bearing HLA-DQ2 and DQ8 molecules, to proinflammatory CD4+ T cells, activating them[4]. Upon activation, the T cell produces a variety of cytokines like interferon-gamma as part of a Th1 response which results in clonal expansion of activated T cells, stimulation of cytotoxic T cells and B cell recruitment with subsequent production of anti-gliadin (AGA) and anti-transglutaminase antibodies (tTGA)[4]. Thus, intolerance to gluten is responsible for an immune-mediated damage of the intestinal mucosa, which resolves after a gluten-free diet (GFD)[4].
CD diagnosis still relies on serology and small intestinal biopsy. tTGA and anti-endomysial antibodies (EMA) of the immunoglobulin A (IgA) class have the highest diagnostic accuracy with a sensitivity of 98% and a specificity ranging from 90% to 99%. Deamidated gliadin peptide antibodies (DGP) of IgG class are a valuable diagnostic tool for identifying CD in patients with IgA deficiency and in children aged less than 2 years. Small bowel biopsy remains in adults the diagnostic gold standard, whereas in children and adolescents, as recently recommended, CD diagnosis can be accepted without the need for duodenal biopsy in symptomatic cases showing tTGA at high titer (> 10-times upper normal limit), backed up by EMA and HLA-DQ2 and/or positive DQ8[3].
Although CD primarily affects the gut, the clinical manifestations of the disease are remarkably wide, with many extraintestinal organs and systems, including the liver, affected[5,6]. Liver changes in patients with CD have been reported since 1977 by Hagander et al[7] who demonstrated that transaminases were often increased in untreated CD, normalizing upon a strict GFD. More recently, studies performed after CD was identified as an autoimmune disease, have underlined the strong relationship between CD and autoimmune liver disorders. In this article, we review the clinical presentations and possible mechanisms of CD-related liver injury in order to identify strategies for the diagnosis and treatment of these disorders in childhood.
CRYPTOGENIC LIVER DISORDER (CELIAC HEPATITIS)
An association between CD and cryptogenic liver damage was first reported in 1977 by Hagander et al[7] who found that 40% of adults with incipient CD had increased serum concentrations of transaminases, which returned to normal upon GFD in the majority of patients. One year later, Lindberg et al[8] reported elevation of serum aminotransferases in about one-third of pediatric patients with CD. Approximately one decade later, a mild to moderate hypertransaminasemia was observed in about 60% of symptomatic Italian children aged less than 2 years with newly diagnosed CD[9]. Prevalence studies have reported that transaminases are elevated in 39% to 47% of celiac adults[10-12] and in 26% to 57% of children at diagnosis of CD (Table 1)[9,13-15]. Frequently, elevation in transaminases is mild, and is not associated with hepatomegaly or splenomegaly. In those patients who had undergone liver biopsy[10,16-18], histological changes such as Kupffer cell hyperplasia, mononuclear cell infiltration, steatosis, and mild fibrosis have been reported. In most cases, transaminase values normalized upon a 1-year GFD.
Table 1 Studies reporting the prevalence of cryptogenic hypertransaminasemia in children and adolescents with celiac disease.
350 untreated children with suspected CD aged 1 to 16 yr
Serology and intestinal biopsy according to the ESPGHAN criteria
140 (40.0%) had elevated AST (≥ 38 U/L) and/or ALT (≥ 41 U/L); four with values > 5 times upper normal levels
Normalization of transaminases after 6 mo of GFD was achieved in 133 (97.8%) of 136 children with transaminase values < 5 times upper normal levels
The four children with transaminase values > 5 times upper normal levels as well as the 3 children with persistent elevated transaminases had further laboratory investigation and were found to be affected by autoimmune hepatitis
Conversely, CD is present in patients investigated because of chronic unexplained hypertransaminasemia. Volta et al[18] for the first time reported that adults with elevated concentrations of aminotransferases of unknown origin were affected by symptomless CD. Five of the 55 study patients with cryptogenic elevation of transaminases fulfilled the criteria for CD diagnosis. Other common causes of liver disease were excluded. Three of these patients showed histologically a picture of reactive hepatitis typical of CD patients with elevated transaminases. The importance of these findings has been confirmed by other investigators, who found a similar prevalence of CD in large patient populations with cryptogenic hypertransaminasemia[19].
Recently, Sainsbury et al[20] conducted a meta-analysis to estimate the prevalence of CD in adults with cryptogenic hypertransaminasemia, as well as the prevalence of hypertransaminasemia in those with incipient CD. The combined proportion with positive celiac serology and biopsy-proven CD in unexplained hypertransaminasemia were 6% (95%CI: 3%-10%) and 4% (1%-7%), respectively. However, there was significant heterogeneity between studies (P < 0.001). This is about four times the risk of CD, in the general population (about 1%)[20]. The combined proportion with abnormal serum aminotransferases in incipient CD was 27% (13%-44%). A 12-mo GFD normalized serum transaminase values in 63%-90% of patients. Discordant results were reported by Korpimäki et al[21] in a large population-based study including celiac patients with minor or atypical symptoms, and with or without GFD, as well as subjects without CD. The authors estimated that only 11% of the untreated celiac patients had elevated transaminase values. This prevalence was about the same as was found in treated CD cases and controls without CD. Variation in the CD clinical presentation and severity, as well as definition of the upper normal limits for serum transaminases may account for such discrepancies.
Also in children, hypertransaminasemia may represent the only manifestation of CD. In 1986 an 11-year-old girl with a chronic and unexplained elevated aminotransferases was reported. Liver histology evidenced slight inflammation of the portal tract[22]. CD was diagnosed on the basis of antireticulin antibodies and subsequently by intestinal biopsy. Seven years later six children with chronic hypertransaminasemia and histologic findings ranging from reactive hepatitis to moderately active chronic hepatitis, were reported[23]. They were asymptomatic and had jejunal histology consistent with CD diagnosis. In all subjects, transaminases normalized on a GFD. Resolution of hepatic histologic lesions occurred in two children, whereas aminotransferases increased in three children upon a gluten challenge[23]. Finally, in a prospective study involving 425 children and adolescents with isolated hypertransaminasemia, Iorio et al[24] found 166 patients with persistently (more than 6 mo) elevated transaminases of whom three (1.8%) were identified as having CD. Therefore, routine screening for CD is to be recommended in children with otherwise unexplained hypertransaminasemia.
AUTOIMMUNE LIVER DISORDERS ASSOCIATED WITH CELIAC DISEASE
Autoimmune liver disorders (AILD), including autoimmune hepatitis (AIH), primary sclerosing cholangitis (PSC), and primary biliary cirrhosis (PBC) have been shown to be associated with CD[25-28].
AIH is a progressive inflammatory liver disorder and is more common among females. It is associated serologically with high levels of aminotransferases and IgG, the presence of autoantibodies, and histologically with interface hepatitis in the absence of known etiology[29]. Hepatitis at the portal-parenchymal interface (“interface hepatitis”) is typical. The picture is characterized by a lymphoplasmacytic infiltrate crossing the limiting plate and invading the liver parenchyma. Other associated lesions are hepatocyte swelling and pycnotic necrosis. Fibrosis is found in all forms of the disease except the mildest ones[30]. Two types of AIH can be recognized: type 1 AIH is associated with antinuclear antibodies and/or smooth muscle antibodies and affects adult patients much more commonly, while type 2 AIH, characterized by antibodies to liver-kidney microsome type 1, is usually confined to childhood CD[18,31].
In the late 1970s, CD was occasionally reported in patients with AIH[18,32-34]. Then several studies established a relationship between CD and AIH of both types 1 and 2[26]. The first of these studies included the largest cohort of AIH patients (e.g., 181, of whom 157 with type 1 and 24 with type 2) who were screened for CD by serology[18]. Among these patients, eight [4.4% (3.8% with type 1 and 8.3% with type 2 AIH)] were found to have raised levels of EMA IgA. Of these 8 antibody-positive patients, five underwent jejunal biopsy which revealed a subtotal villous atrophy typical of CD. In a recent systematic review[26] performed in adults, the prevalence of CD in AIH ranged between 2% and 20% but was approximately 4% in most studies.
In children, at first the association between CD and AIH was only reported in isolated cases[35-37]. Subsequently pediatric surveys have reported a wide prevalence of CD in AIH ranging from 3.6% to 12% (Table 2)[38-43]. In an Italian retrospective (1990-2005) multicenter study, Caprai et al[39] found that among 140 children with AILD, 23 (16%) had CD [19 with AIH (12 with type 1; 4 with type 2; 3 seronegative), 2 with autoimmune cholangitis and 2 with overlap syndrome]. CD was diagnosed before liver disease in 18 of them, though raised aminotransferases were found in 16 at CD diagnosis. Conversely, five of the 23 patients had a diagnosis of AILD before the identification of CD. Nineteen patients had liver-related non-organ-specific autoantibodies. Hepatic biopsy showed inflammatory lesions with features of autoimmune damage and different degrees of fibrosis in all 19 subjects and cirrhosis in 4 of them. All patients on GFD achieved remission on immunosuppressive therapy, but 14 relapsed either because treatment ceased or because the GFD was not respected. Diamanti et al[40] retrospectively (1990-2006) evaluated the CD prevalence in 40 AIH children. There were five cases of CD in the 40 AIH patients (12.5%); all five CD patients had type 1 AIH. In four patients (80%), AIH preceded the diagnosis of CD. On GFD the level of transaminases mildly decreased, and never reached normal concentrations. Tosun et al[41] who retrospectively evaluated the presence of CD in 15 AIH patients, found a prevalence of 46% (95%CI: 21%-67%), being the highest ever reported in pediatric literature, although the sample size is small. In a prospective study involving 26 Egyptian patients (aged 3.5-21 years) with AIH, El-Shabrawi et al[42] reported an 11.5% prevalence of CD. Very recently, in a retrospective and prospective evaluation (1995-2000), Nastasio et al[43] reported that among 79 patients with AIH, CD was present in 15 (19%) of them (9 had type 1, 3 type 2, and 3 were seronegative). All these patients achieved sustained remission on a GFD when treated with immunosuppressive therapy.
Table 2 Studies reporting the prevalence of positive celiac serology or biopsy-proven celiac disease in children and adolescents with autoimmune liver diseases.
23 (16.4%) (19 with AIH; 2 with AIC; and 2 with overlap syndrome) had CD on the basis of serology (EMA IgA and/or tTGA IgA) Diagnosis of CD preceded the diagnosis of liver disease in 18 of the 23 patients
All patients achieved remission on GFD and immunosuppressive therapy, but 14 relapsed because of discontinuation of therapy or during spontaneous gluten challenge
15 (19.0%) had CD on the basis of serology and histological findings Diagnosis of CD preceded the diagnosis of liver disease in 8 of the 15 patients
All 15 patients on GFD achieved sustained remission when treated with immunosuppressive therapy
There are two studies providing prospective data on AIH in children with CD (Table 3)[15,44]. Di Biase et al[15] showed that isolated hypertransaminasemia was present in 40% of CD subjects on a gluten-containing diet, and that 2% had AIH, while there were no other AILD. Liver tests became normal after GFD only in CD patients with isolated hypertransaminasemia, but not in AIH cases who required GFD plus immunosuppressant therapy. Ventura et al[44] showed that AILD were more frequent in adolescents and young adults with CD than in the general population. In particular, out of 374 CD patients 10 (1.1%) had a diagnosis of AIH. They also reported that in patients with CD, AILD rates increased as age at diagnosis increased, suggesting a possible relationship with duration of exposure to gluten[44].
Table 3 Studies reporting the prevalence of autoimmune hepatitis in children and adolescents with celiac disease.
350 untreated children with suspected CD aged 1 to 16 yr
Serology and intestinal biopsy according to the ESPGHAN criteria
7 (2.0%) had AIH, of whom 5 type I AIH
During treatment with GFD, steroids and azathioprine for 5 yr, all AIH persistently normalized clinical and biochemical parameters. After withdrawal, 6 patients maintained a sustained remission (12-63 mo)
PSC is a cholestatic disorder characterized by inflammation and periductal fibrosis of the intrahepatic and/or extrahepatic bile ducts[45-47]. No characteristic autoantibody has been identified in PSC patients. The diagnosis depends on evidencing the characteristic biliary lesions in biopsy tissue or the intra and extrahepatic biliary tree abnormalities by cholangiography[47]. Many patients, especially children, have PSC-AIH overlap with features of both diseases, and this is termed autoimmune sclerosing cholangitis (ASC)[46,48]. ASC refers to cases with PSC who have positive autoantibodies and may have histological features overlapping with those seen in AIH[47]. In adults, PBC may also be found. This additional form of AILD is characterized by the presence of anti-mitochondrial antibodies. It progresses slowly and is more common in females. Histologically, PBC is characterized by portal inflammation and immune-mediated destruction of the intrahepatic bile ducts. Autoimmune cholangitis (AIC) is a cholestatic liver disorder with biochemical signs of cholestasis, histological features of inflammatory bile duct damage, and negativity for anti-mitochondrial antibodies. PSC, PBC, and AIC have been mainly described in adults with CD[21,49-53]. In children, the association between CD and PSC or AIH/ASC overlap syndrome or AIC has been only reported in two studies[39,54].
Nonalcoholic fatty liver disease (NAFLD) is a spectrum of liver conditions ranging from simple, uncomplicated steatosis, to nonalcoholic steatohepatitis (NASH), with inflammation and liver cell injury progressive to cryptogenic cirrhosis. NAFLD has become the most common cause of chronic liver disease in children and adolescents. Case reports and cross-sectional studies describe the association of various forms of fatty liver with CD[55-60]. Wigg et al[55] found that 3 of 22 adult patients with NASH had positive AGA IgA and IgG, and one of them had a histological diagnosis of CD. Grieco et al[56] reported histologically-diagnosed CD in 4 (13.3%) of 30 patients with laboratory diagnosis of NASH. After one year on GFD, the transaminase levels were normalized, and duodenal histology was improved. Nehra et al[57] investigating the relationship between NASH and CD, found that only one (2.1%) of the 47 study obese patients with NASH was positive for EMA IgA. In a study of 59 overweight patients undergoing liver biopsy for persistent hypertransaminasemia, NASH was detected in 38 (64%) whereas simple steatosis was found in 21 (36%)[58]. Six (10%) of the 59 patients showed positivity for tTGA and two (3.4%) of them also positivity for EMA IgA. Histology confirmed CD in the two patients positive for both markers. In both cases, liver enzymes went back to normal after a 6-mo GFD. In a study involving 121 patients with biopsy-proven NAFLD, Lo Iacono et al[59] reported that the prevalence of histologically-confirmed CD was 3.3%. In an Iranian population of 116 patients with NAFLD (as diagnosed on the basis of elevated transaminase levels, liver ultrasound and/or liver biopsy), Rahimi et al[60] found the prevalence of histologically-confirmed CD to be 2.2%. Interestingly, CD was more commonly diagnosed among NAFLD patients having body mass index (BMI) < 27 kg/m² compared to those with BMI > 27 kg/m² (5.83% vs 0%, P = 0.001). Very recently, in a nationwide study of more than 26000 children and adults with CD, Reilly et al[61] found an increased risk of NAFLD compared to the general population. Excess risks were highest in the first year after CD diagnosis, but persisted through 15 years beyond diagnosis with CD.
On the basis of the above findings, we conclude that there is an association between CD and fatty liver. However, since fatty liver is not an unusual finding in the general population of developed countries, the association of hepatic steatosis with CD may be a coincidental finding rather than a true association. To complicate matters further, fatty infiltration of the liver may be secondary to rapid weight loss or malabsorption, both etiologically linked to fatty liver. Future investigations should be undertaken to resolve this issue and should include pediatric populations for whom there are very few data at present.
SEVERE LIVER DAMAGE
Although rarely, severe liver disease has been described in adults with CD[62-64]. In a Finnish study, 4 patients with severe liver failure awaiting liver transplantation were discovered to have CD (one had congenital liver fibrosis; one, a massive hepatic steatosis; and two patients had progressive hepatitis with no apparent cause)[62]. Their liver disease improved after GFD. The Authors then screened 185 patients undergoing liver transplantation and found that 8 (4.3%) of them had CD, which is 4-10 times the population prevalence of CD in Finland. Most of these patients had AILD. Only 1 patient was on GFD. This suggests that in some cases of CD, GFD help to avoid end-stage liver disease. Subsequently, in a study from United States involving an ample cohort of individuals with end-stage AILD (n = 310) and non-AILD (n = 178) who underwent liver transplantation[64], the prevalence of tTGA and EMA was significantly greater in HLA-DQ2- or HLA-DQ8-positive patients with end-stage AILD compared with those with end-stage non-AILD (14.2% vs 5.4%, P = 0.0001 and 4.3% vs 0.78%, P = 0.01, respectively), while the co-occurrence of tTGA and EMA was increased five-fold in end-stage AILD (3% vs 0.6%). However, the study was retrospective, and apart from two patients, intestinal tissues were not available for re-review. Thus, a definite diagnosis of CD was not possible for most of the patients positive for CD-related autoantibodies. When serum samples were tested 6-12 or ≥ 24 mo post-transplantation, tTGA and EMA became normal in 94% and 100% of patients, respectively. This occurred without excluding gluten from the diet which implies no relationship between gluten and autoantibody kinetics. The suppression of tTGA and EMA after the transplant suggests that the lack of autoantibody positivity of post-transplant sera cannot exclude a diagnosis of CD, therefore supporting the pre-transplantation screening of patients with end-stage AILD[64].
In children, severe liver disease has been described in association with CD[65-68]. Demir et al[65] reported five celiac children with cryptogenic cirrhosis. In three patients with chronic diarrhea and hepatosplenomegaly, the diagnoses of CD and cirrhosis were concomitant, whereas in two patients, CD was diagnosed following that of cirrhosis. One to five years later, three patients on strict GDF had normal values of serum aminotransferases, and clinical improvement. The other two patients with poor dietary compliance had no improvement in liver function. Al-Hussaini et al[66] reported an 11-year-old girl with liver failure due to sclerosing cholangitis associated with CD. Treatment with ursodeoxycholic acid and GFD, and steroid tapered over three months, normalized the liver function tests. A few cases of CD with severe liver involvement requiring liver transplant have been also reported[67,68]. In a case-report, Pavone et al[67] described a 14-year-old girl with CD and mild gastrointestinal symptoms developing, after a long exposure to gluten, severe hepatic dysfunction requiring liver transplantation. Casswall et al[68] reported six 13- to 36-mo-old girls who within 1-24 mo of the diagnosis of CD developed severe liver damage. Four of these girls had acute liver failure and two needed a liver transplant.
PATHOGENESIS OF LIVER DYSFUNCTION IN CD
The pathogenesis of the hypertransaminasemia and liver damage in CD remains poorly understood. Probably they involve increased intestinal permeability and alterations in gut microbiota, chronic intestinal inflammation, and genetic predisposition (Figure 1).
Figure 1 Possible pathogenetic mechanisms between celiac disease and liver abnormalities.
Since the liver receives three quarters of its blood supply from the intestine, it is one of the organs most exposed to gut-derived toxic factors[69-72]. Cross-talk between the gut and the liver is an intriguing hypothesis that may explain the hepatobiliary changes associated with many intestinal inflammatory diseases including CD. The suggestion that increased intestinal permeability and altered gut microbiota may contribute to the development of several diseases was made since 1890 (Llewellyn Jones: “Theory of auto-intoxication from gut bacteria”)[72]. Gut epithelial cells are linked to one another with tight junctions (TJs), which play an essential role in maintaining the integrity of the intestinal barrier and in demarcating microbes in the gut from the host immune system. Zonulin, a human protein known to reversibly regulate intestinal permeability by modulating intercellular TJs[73], is augmented in autoimmune conditions associated with TJ dysfunction including CD[74].
Patients with CD and hypertransaminasemia have an important increase in intestinal permeability compared with those whose liver enzymes are normal[11]. The increased intestinal permeability may ease the entry of toxins, antigens, and inflammatory substances (cytokines and/or autoantibodies) to the portal circulation and these mediators may play a part in the pathogenesis of hepatic involvement in CD. Interestingly, increased intestinal permeability caused by disruption of intercellular TJs in the intestine as well as increased prevalence of small intestinal overgrowth has been reported in adult patients with NAFLD[75]. Moreover, it has been found that serum zonulin concentration is increased in children and adolescents with NAFLD and correlates with the severity of steatosis[76]. This may also explain hepatic fat deposition in CD. Autoantibodies directed against tTG are present in the liver and other extraintestinal tissues in CD. This raises the possibility of a pathogenic role for the humoral-mediated immune responses in liver injury observed in CD. It has also been suggested that an aberrant T lymphocyte homing to the liver may contribute to trigger immune hepatic damage. As matter of fact, an increased number of lymphocytes expressing molecules of intestinal origin have been discovered in hepatic sinusoidal endothelial cells in individuals with liver abnormalities[77]. Moreover, liver-primed T cells have been demonstrated to migrate into the intestine and into the gut-associated lymphoid tissue, suggesting an enterohepatic lymphocyte circulation[78]. The ability of T cells of homing both to the liver and the intestine may explain the link between CD and liver diseases.
Considerable progress has been made toward understanding the role of genetics in autoimmune liver damage. It is well known that CD and some autoimmune liver disorders share HLA class II molecules and haplotypes. The main genetic marker of CD is HLA-DQ2, which is present in about 95% of CD patients. HLA-DQ2 is in strong linkage disequilibrium with HLA-DR3, which is the major HLA risk factor for AIH[79].
CONCLUSION
CD is increasingly reported in children who are symptomless or present atypical symptoms and signs. Liver abnormalities are common extraintestinal manifestations in patients with CD and range from mild hepatic injury to severe liver disease. The so-called celiac hepatitis is a frequent, benign, clinically silent condition which resolves on a GFD. Autoimmune liver diseases are less common and are associated in the majority of cases with clinical signs and symptoms of chronic liver disease, which need specific immunosuppressive therapy, rather than just GFD. Although rarely, CD may be also associated with severe liver involvement requiring liver transplant. In light of this background early diagnosis and treatment of CD-associated chronic and severe liver diseases may play an important role in the prognosis of this clinical entities. To this end, screening for liver involvement in celiac children and for CD by means of tTGA and EMA in children with liver diseases should become routine practice.
Footnotes
P- Reviewer: Dore MP, Francavilla R, Quigley EMM, Ukleja A S- Editor: Ma YJ L- Editor: A E- Editor: Liu XM
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